Formation of Polyploid Giant Cancer Cells Involves in the Prognostic Value of Neoadjuvant Chemoradiation in Locally Advanced Rectal Cancer

Fei, Fei; Zhang, Mingqing; Li, Bo; Zhao, Lizhong; Wang, Hui; Liu, Lina; Li, Yuwei; Ding, Po; Gu, Yanjun; Zhang, Xipeng; Jiang, Tao; Zhu, Siwei; Zhang, Shiwu

doi:https://doi.org/10.1155/2019/2316436

Journal of Oncology

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Abstract Introduction Materials and Methods Results Discussion Conclusions Abbreviations Data Availability Ethical Approval Consent Conflicts of Interest Authors’ Contributions Acknowledgments Supplementary Materials References Copyright Related Articles

Research Article | Open Access

Volume 2019 | Article ID 2316436 | https://doi.org/10.1155/2019/2316436

Formation of Polyploid Giant Cancer Cells Involves in the Prognostic Value of Neoadjuvant Chemoradiation in Locally Advanced Rectal Cancer

Fei Fei,^1,2Mingqing Zhang,³Bo Li,⁴Lizhong Zhao,^1,5Hui Wang,⁴Lina Liu,^1,5Yuwei Li,³Po Ding,⁶Yanjun Gu,⁷Xipeng Zhang,³Tao Jiang,⁸and Siwei Zhu⁹ et al.

Academic Editor: Maria S. Tretiakova

Received26 Apr 2019

Revised09 Jul 2019

Accepted30 Jul 2019

Published29 Aug 2019

Abstract

We previously reported that polyploid giant cancer cells (PGCCs) exhibit cancer stem cell properties and can generate daughter cells with the epithelial-mesenchymal transition phenotype. This study investigated the role of PGCC formation in the prognostic value of neoadjuvant chemoradiation therapy (nCRT) in locally advanced rectal cancer (LARC). The morphological characteristics were observed in patients with LARC after nCRT. Colorectal cancer cell lines were treated with irradiation or chemotherapeutic drugs, and the metastasis-related proteins were detected. 304 nCRT cases and 301 paired non-nCRT cases were collected for analysis. More PGCCs and morphologic characteristics related to invasion and metastasis appeared in tumor tissue after nCRT. Irradiation or chemicals could induce the formation of PGCCs with daughter cells exhibiting strong migratory, invasive, and proliferation abilities. In patients after nCRT, pathologic complete remission, partial remission, stable disease, and progressive disease were observed in 29 (9.54%), 125 (41.12%), 138 (45.39%), and 12 (3.95%) patients, respectively. Mucinous adenocarcinomas (MCs) occurred more frequently in nCRT than in non-nCRT patients (χ² = 29.352, ), and the prognosis in MC patients was worse than that in non-MC patients (χ² = 24.617, ). The difference in survival time had statistical significance for 60 days (χ² = 5.357, ) and 70 days (χ² = 18.830, ) rest interval time. On multivariable analysis, 60 days rest interval, Duke’s stage, and recurrence and/or distant metastasis remained significant predictors of survival. In conclusion, irradiation or chemicals induce the formation of PGCCs and PGCCs produce daughter cells with strong migration and invasion abilities after a long incubation period. Appropriate rest interval (incubation period) is very important for patients with LARC who will receive nCRT.

1. Introduction

In China, of those cancers that affect both men and women, colorectal cancer (CRC) is the second most common (12.2%) and rectal cancer ranks the seventh most common cause of cancer death [1]. Rectal cancer differs substantially from colon cancer, particularly in terms of clinical management [2]. Population-based cancer statistics provide an indicator of the overall effectiveness of the healthcare system in the context of effectiveness of screening, early diagnosis, and treatment services for patients with rectal cancer.

Polyploid giant cancer cells (PGCCs) are a special subpopulation of cancer cells that contribute to solid tumor heterogeneity. PGCCs differ from diploid cancer cells in size, tumorigenic ability, radioresistance, and chemoresistance. PGCCs possess functions of cancer stem cells and promote tumor maintenance and recurrence [3]. Our previous study showed that PGCC formation can be induced by CoCl₂, paclitaxel, and other drugs. The polyploid nature of PGCCs was confirmed by fluorescence in situ hybridization and flow cytometry. Based on the long-term experimental data and observation, we defined the PGCC as a cancer cell that was at least three times larger in size than that of regular cancer cells [4–8]. PGCCs can generate daughter cells via asymmetric division, and these daughter cells show stronger migratory and invasive capacities than diploid cells, express less epithelial markers, and acquire mesenchymal phenotype [5, 7]. During the process of cancer development and progression, cancer cells gradually lose epithelial characteristics and acquire mesenchymal phenotype, called epithelial-mesenchymal transition, which is vital to cancer invasion and metastasis [9]. The number of PGCCs positively correlates with the malignant degree of cancer. In cancer, antimitotic chemotherapy drugs, radiotherapy, and hypoxia can increase the number of PGCCs. The formation of PGCCs can be involved in reactivation of embryonic developmental stages escaped from initial courses of treatment [10, 11]. Also, some other researchers have observed the rapid emergence of numerous PGCCs in a high-drug environment attributed to diploid epithelial cells converting to PGCCs, which suggests that PGCCs may be mediators of resistance in response to chemotherapeutic stress [12]. The number of PGCCs correlates with the recurrence, lymph node metastasis, chemoresistance, and poor prognosis of CRCs and is a good indicator to predict the metastasis and aggressiveness in CRCs [8].

Annually, more than 2000 radical CRC surgeries are performed at our hospital, of which 80% are performed for rectal cancer. For locally advanced rectal cancer (LARC), treatment includes neoadjuvant chemoradiation therapy (nCRT) followed by total mesorectal excision (TME) which comprises resection of the rectal tumor together with the fatty tissue surrounding the rectum [13], and this treatment methodology has been recommended for inclusion in clinical practice guidelines [14]. As of Aug 31, 2018, more than 300 LARC patients have received nCRT at our hospital. nCRT is currently the standard-of-care in stage II-III rectal cancer, resulting in tumor downstaging for patients with treatment-responsive disease. However, the prognosis of the downstaged patients treated with nCRT remains controversial. Furthermore, the optimal timing of surgery after nCRT (rest interval time) is unclear [13, 15, 16]. Rombouts et al. report that rest intervals of 9–12 weeks between surgery and CRT may improve the chances of pathologic complete response (pCR) in LARC patients, without an effect on overall survival (OS) [13]. Sun et al. reported that a rest interval of eight weeks after completion of nCRT appears to be the critical threshold for optimal tumor response [15]. Furthermore, prognoses in patients treated with nCRT and non-nCRT regimens have not been compared with a follow-up time of more than five years. The results of our study showed that differences in survival rates between patients treated with and without nCRT (nCRT and non-nCRT patients) increased gradually with time, when compared at three, five, six, seven, and eight years. A pathologic diagnosis of MC was more incident in nCRT cases, which may be related to the poor prognosis associated with nCRT.

In this study, we confirmed that irradiation and chemicals could induce the formation of PGCCs, and these PGCCs can generate daughter cells with strong migratory and invasive capacities. Furthermore, this paper also provides a comprehensive overview of nCRT in LARC, including the rest interval time, treatment response, and overall survival beyond five years, and discusses possible molecular mechanisms. A rest interval of less than 50 days may improve survival since nCRT may induce the formation of PGCCs and daughter cells with a strong migration and invasion capability; this may be related to the poor prognosis observed in patients treated with nCRT.

2. Materials and Methods

2.1. Culture of Cancer Cell Lines and Treatment

The human colorectal cancer cell lines LoVo and HCT116 were purchased from American Type Culture Collection (USA) and cultured in the RPMI-1640 medium supplemented with 10% fetal bovine serum, 100 U/mL penicillin, and 100 g/mL streptomycin. When the confluence of LoVo and HCT116 cells reached 90%, they were treated with radiation, capecitabine, oxaliplatin, and irinotecan. For irradiation, 9 Gy at a dose of 1.0 Gy/min with a ¹³⁷Cs source was used. Detailed information about the chemotherapeutic drugs used is listed in Supplementary Table S1.

2.2. Hematoxylin-Eosin Staining and Immunocytochemical (ICC) Staining

The detailed information is provided in the supplementary Materials and Methods. In order to quantify protein expression of ICC, the sum of the staining intensity and the percentage of positive cell scores was performed to indicate the protein expression indexes for each section. The staining intensity was scored as follows: 0, no staining; 1, faint yellow staining; 2, moderate positive staining; and 3, strong positive staining. The percentage of positive cells was scored as follows: 0, <5% positive cells; 1, 6%–50% positive cells; 2, 51%–100% positive cells.

2.3. Plate Colony Formation Assay

The detailed information is provided in the supplementary Materials and Methods.

2.4. Wound-Scratch Assay, Cell Migration, and Invasion Assay

The detailed information is provided in the supplementary Materials and Methods.

2.5. Western Blotting

Western blot analyses were performed as described previously [5, 7]. Simply, total protein was extracted from the LoVo and HCT116 cells before and after treatment. The total protein was then separated on sodium dodecyl sulfate polyacrylamide gels and transferred to polyvinylidene fluoride membranes (Amersham Hybond-P PVDF Membrane; GE Healthcare). Information about the primary antibodies used is listed in Supplementary Table S2.

2.6. PGCC Definition and Counting

PGCCs are defined as a subpopulation of cancer cells with a nucleus that is at least three times larger than that of a regular diploid cancer cell, which was first described by Zhang et al. [7]. We counted the number of PGCCs per 100 tumor cells in five hot spots of each tumor sample. The size of each PGCC nucleus was measured using a micrometer. The average PGCCs number per 100 tumor cells was calculated for statistical analyses.

2.7. Patient Population

LARC patients (n = 605) (T3/4 and/or N1 disease confirmed by magnetic resonance imaging, MRI), including patients treated with neoadjuvant chemoradiation (nCRT) (n = 304) and those not treated with nCRT (non-nCRT patients) (n = 301), followed by surgery (radical or palliative operation) and postoperative chemotherapy at the Tianjin Union Medical Center between 2009 and 2018, were enrolled. The paired 301 non-nCRT patients who did not receive nCRT, mainly due to the poor compliance, such as financial burden, traffic inconvenience for outside patients, and nCRT-refusal patients. All patients had complete pathologic or survival data. The follow-ups of all these patients were completed in August 2018. Data of patients with surgery completed prior to August 30, 2015, were used for survival analysis. Furthermore, paraffin-embedded tissue samples with locally advanced rectal cancer after nCRT were obtained from the Tumor Tissue Bank of Tianjin Union Medical Center. Morphologic characteristics were observed in the liver metastases, and recurrence was seen in some patients. Furthermore, the 301 non-nCRT patients were used as paired controls and were matched based on the MRI stage, tumor differentiation, sex, operation time, surgical procedures, and age (the difference in age of one-by-one matched patient between the nCRT and non-nCRT was less than 5 years), to minimize potential for bias. Three patients in the nCRT group were not paired because of lack of patients who met the inclusion criteria. There was no history of inflammatory bowel disease and familial colorectal cancer in these patients. Patients with perioperative mortalities were also excluded. The clinicopathologic data for each patient, including age, sex, MRI stage, start and end time of nCRT, tumor characteristics, surgery details, administration of postoperative chemotherapy, date of the last follow-up, date of recurrence, and date of death, were collected. This study was approved by the Hospital Review Board, and the confidentiality of patient information was maintained.

2.8. Treatment Characteristics

All patients in the nCRT and non-nCRT groups received surgery and/or nCRT at our hospital. At our hospital, nCRT is offered to most patients with MRI stage II (T3-4, node-negative disease with tumor penetration through the muscle wall) or MRI stage III (node positive disease without distant metastasis) disease according to the National Comprehensive Cancer Network (NCCN) Clinical Practice Guidelines in Oncology [14, 17]. All the 605 patients were offered adjuvant chemotherapy after surgery.

2.9. Neoadjuvant Chemoradiation

The nCRT regimen for rectal cancer consists of chemotherapy combined with medium-dose radiotherapy before surgery. Radiotherapy for rectal cancer was performed with three-dimensional conformal radiotherapy (3DCRT) or intensity-modulated radiotherapy (IMRT). After affixing a body mask, computed tomography (CT) scans were performed on patients in a prone or supine position. The CT images were then transmitted to the radiotherapy planning system for three-dimensional reconstruction and target mapping. Gross tumor volume (GTV) included primary tumors and metastatic lymph nodes. Clinical target volumes (CTV) included the perimesenteric lymphatic drainage area, obturator lymphatic drainage area, and the iliac lymphatic drainage area. The presacral lymphatic drainage area, if necessary, included the external iliac lymph drainage area. Radiation doses were as follows: planning target volume (PTV), 45 Gy in 25 fractions to the pelvis, and gross tumor volume (GTV), 48 Gy in 25 fractions to the tumor. Patients were irradiated for five weeks, five times a week, on weekdays. Chemotherapy was administered for five weeks and synchronized with radiotherapy. The patients were treated with capecitabine monotherapy or with two cycles of the CAPOX regimen (capecitabine (trade name Xeloda) combined with oxaliplatin). All patients who received adjuvant chemotherapy were examined by a medical oncologist. The final decision and choice of regimen was made on an individualized basis.

2.10. Scoring Pathologic Response

Pathologic responses to nCRT were scored using the American Joint Committee on Cancer (AJCC) and the College of American Pathologists (CAP) guidelines [18], defined as follows: complete response (CR), no viable cancer cells; partial response (PR), single or small groups of cancer cells; minimal response (stable disease, SD), residual cancer outgrown by fibrosis; poor response (progressive disease, PD), minimal or no tumor kill, and extensive residual cancer [19, 20]. Scoring was performed by two pathologists at our hospital who were blinded to the clinical treatments.

2.11. Statistical Analyses

Statistical software SPSS 17.0 (IBM Corporation, USA) was used to evaluate the data, and a 2-tailed value of less than 0.05 was defined as statistically significant. Pearson’s chi-square (χ²) test was used to analyze the differences in clinicopathologic characteristics between patients in the nCRT and non-nCRT groups. Survival time was analyzed using the Kaplan–Meier method, and differences were assessed using the log-rank test.

3. Results

3.1. Morphologic Observation in CRCs after nCRT

Many PGCCs appeared in tumor tissue after nCRT (Figure 1(a)), and different morphologic characteristics related with tumor invasion and metastasis in cancer cells appeared in tumor tissue after nCRT. The average number of PGCCs per 100 tumor cells for all tumor tissues in nCRT (exclusion of pathologic CR patients in nCRT) was significantly more than that in non-CRT patients (F = 35.38, ; Table 1). Tumor emboli in blood or lymphatic vessels (Figure 1(b)) and perineural invasion of cancer cells (Figure 1(c)) could also be observed in tumor tissue after nCRT. The incidence of tumor emboli was higher in nCRT patients than in non-nCRT patients (χ² = 5.117, ; Table 2). Furthermore, as described above, MC occurred more frequently in nCRT than in non-nCRT patients (χ² = 29.352, ; Table 2). Mucus often appeared in the cytoplasm of cancer cells after nCRT (Figure 1(d)). There were more PGCCs appearing in the liver metastatic rectal cancer than the primary tumor (Figure 1(e)). More PGCCs were observed in anastomotic recurrent rectal cancer after nCRT than before nCRT (Figure 1(f)). In the tumor tissues, PGCCs were usually located in the necrosis margin and infiltrating front, resulting from the environment of PGCCs formation.

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Figure 1

The number of PGCCs increased in colorectal cancers (CRCs) after neoadjuvant chemoradiation therapy (nCRT). (a) Many PGCCs appeared in the tumor after nCRT (black arrow heads, H&E, 100x). (b) Tumor emboli (black arrow heads, H&E, 100x). (c) Perineural invasion of cancer cells (black arrow heads, H&E, 100x). (d) Mucinous adenocarcinomas (black arrow heads) and PGCCs (red arrow heads) occurred after nCRT (H&E, 100x). (e) Many PGCCs (black arrow heads) appeared in the liver (red arrow heads represent the liver tissue) metastatic rectal cancer in patients after nCRT (H&E, 100x). (f) Many PGCCs appeared in the anastomotic recurrence in patients with locally advanced rectal cancer after nCRT (black arrow heads, H&E, 100x).

3.2. Formation of PGCCs in Response to Radiation and Chemotherapeutics Treatment In Vitro

Colon cancer cell lines LoVo and HCT116 were cultured in medium and treated with radiation and chemotherapeutics (capecitabine, oxaliplatin, and irinotecan) when the confluency reached 90%. Two days after treatment with radiation (Figure 2(a)-A and F) and chemotherapeutics (Figures 2(b)-A, E, and I and 2(c)-A, E, and I), most diploid LoVo and HCT116 cells died, whereas scattered PGCCs could be clearly visualized after removing floating dead cells. A PGCC was defined as a tumor cell with a nucleus at least 3 times larger than that of a diploid tumor cell, and such cells exhibited properties of cancer stem cells [7]. As described in our previously published papers [5, 7, 8], LoVo and HCT116 PGCCs treated with radiation and chemotherapeutic agents can generate small daughter cells through asymmetric cell division. The cellular dynamics of the radiation-treated LoVo and HCT116 were recorded with a microscope over the course of 18 days in a fixed field (Figures 2(a)–2(c)). Eighteen days (incubation period) after radiation, single PGCCs generated hundreds of daughter cells (Figures 2(a)-E and J; 2(b)-C, G, and K; 2(c)-C, G, and K). These cells recovered from the treatment with radiation and chemotherapeutics once and were then treated for the second time. Two days after the second treatment, only a few cells died, while most cells survived the treatment (Figures 2(b)-D, H, and I and 2(c)-D, H, and L); this meant that cells which recovered from the first treatment were resistant to the second treatment.

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Figure 2

(a) Time-lapse observation of cultured LoVo and HCT116 cells after irradiation (40x): (A and F) morphologic characteristics of LoVo and HCT116 before irradiation (B and G), 7 days after irradiation (C and H), 11 days after irradiation (D and I), 14 days after irradiation (E and J), and 18 days after irradiation. (b) Time-lapse observation of LoVo after chemotherapeutic treatment (40x): (A) 2 days after capecitabine treatment, (B) 11 days after capecitabine treatment, (C) 18 days after capecitabine treatment, (D) 2 days after a second capecitabine treatment, (E) 2 days after oxaliplatin treatment, (F) 11 days after oxaliplatin treatment, (G) 18 days after oxaliplatin treatment, (H) 2 days after a second oxaliplatin treatment, (I) 2 days after irinotecan treatment, (J) 11 days after irinotecan treatment, (K) 18 days after irinotecan treatment, and (L) 2 days after a second irinotecan treatment. (c) Time-lapse observation of HCT116 after chemotherapeutic treatment (40x): (A) 2 days after capecitabine treatment, (B) 11 days after capecitabine treatment, (C) 18 days after capecitabine treatment, (D) 2 days after a second capecitabine treatment, (E) 2 days after oxaliplatin treatment, (F) 11 days after oxaliplatin treatment, (G) 18 days after oxaliplatin treatment, (H) 2 days after a second oxaliplatin treatment, (I) 2 days after irinotecan treatment. (J) 11 days after irinotecan treatment, (K) 18 days after irinotecan treatment, and (L) 2 days after a second irinotecan treatment.

3.3. PGCCs and Their Daughter Cells Exhibit Strong Migration, Invasion, and Proliferation Capabilities

To determine whether PGCCs and their daughter cells had stronger migration, invasion, and proliferation capabilities than did the control cells, wound healing, cell migration, and invasion assays using matrigel-coated transwell inserts and plate colony formation assays were performed. Figures 3(a) and 3(b) depict the results of the wound-scratch assay at various incubation periods. The spaces covering the scratched surface in the panels were observed to gradually become narrower at 26 h incubation periods. The cell migration and invasion capabilities of PGCCs and their daughter cells were found to increase. Moreover, results of the transwell migration and invasion assays showed that compared to control cells, a higher number of treated PGCCs and their daughter cells showed migration and invasion capabilities (Figures 3(c) and 3(d)). Furthermore, we examined the proliferation abilities of cells before and after treatment. Results of the plate colony formation assay showed that cells subjected to treatment exhibited more clone formation compared to control cells (Figures 3(e) and 3(f)). Figures 3(g) and 3(h) show that the number of clones increased with increasing incubation time.

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Figure 3

(a) Wound-scratch assay of LoVo cells at 0 hours and 26 hours after irradiation (40x). (b) Wound-scratch assay of HCT116 cells at 0 hours and 26 hours after irradiation (40x). (c) Migration and invasion assay of LoVo cells before and after irradiation (40x). (d) Migration and invasion assay of HCT116 cells before and after irradiation (40x). (e) Plate colony formation assay of 50, 100, and 200 LoVo cells/well before and after irradiation (40x). (f) Plate colony formation assay of 50, 100, and 200 HCT116 cells/well before and after irradiation (40x). (g) Bar graph depicting the number of clones in wells containing 50, 100, and 200 LoVo cells/well, before and after irradiation. (h) Bar graph depicting the number of clones in wells containing 50, 100, and 200 LoVo cells/well, before and after irradiation.

3.4. PGCCs and Their Daughter Cells Exhibit a Mesenchymal Phenotype

PGCCs with budding daughter cells and the control cells were cultured on coverslips for ICC staining. Results of E-cadherin, N-cadherin, vimentin, fibronectin, Snail and Slug, Twist-1, and CK7 staining showed that the control LoVo cells were negative for N-cadherin and vimentin. A few PGCCs and their daughter cells were positive for N-cadherin (Figures 4(a)-A and 4(b)-A) and vimentin (Figures 4(a)-B, 4(b)-B). E-cadherin expression in the control cells was higher than that in treated cells (Figures 4(a)-C and 4(b)-C). The expression levels of fibronectin, Snail and Slug, Twist-1, and CK7 in the LoVo and HCT116 PGCCs and their daughter cells were higher than those in the control cells (Figures 4(a) and 4(b)). The quantitative results of N-cadherin, Vimentin, E-cadherin, Fibronectin, Snail + Slug, Twist-1, and CK7 of ICC staining in PGCCs with budding daughter cells and the control cells of LoVo and HCT116 are showed in Supplementary Figures S1 and S2. Furthermore, the subcellular location of Slug and Snail and Twist after treatment was different from that in the control cells. The nuclei of PGCCs were positive for Slug and Snail and Twist with ICC staining. Western blot analysis confirmed greater levels of Slug and Snail, Twist, and CK7 expression in PGCCs and in their budding daughter cells than those in control cells. The expression level of E-cadherin in control cells was higher than that in the PGCCs and their budding daughter cells (Figures 4(c) and 4(d)).

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Figure 4

(a) Immunocytochemical (ICC) staining of N-cadherin, vimentin, E-cadherin, Fibronectin, Snail and Slug, Twist-1, and CK7 in LoVo cells before and after irradiation (100x). (b) ICC staining of N-cadherin, vimentin, E-cadherin, fibronectin, Snail and Slug, Twist-1, and CK7 in HCT116 cells before and after irradiation (100x). (c) Western blot assay of E-cadherin, Twist-1, Snail and Slug, fibronectin, and CK7 expression in LoVo cells before and after irradiation (-C, -cytoplasm; -N, -nuclear; 100x). (d) Western blot assay of E-cadherin, Twist-1, Snail and Slug, fibronectin, and CK7 expression in HCT116 cells before and after irradiation (-C, -cytoplasm; -N, -nuclear; 100x).

3.5. Comparison of Long-Term Follow-Up Prognosis in Patients with Locally Advanced Rectal Cancer with and without nCRT

Six hundred and five LARC cases (T3/4 and/or N1) including 304 patients treated with nCRT and 301 patients treated without nCRT followed by surgery were analyzed. The mean patient age at the time of surgery was 60.21 years (range 29–84 years), and 32.23% were women. For patients treated with nCRT, the mean patient age at surgery was 60.02 years (range 32–84 years) and 32.24% (98/304) were women. Radical surgery was performed in 292 patients, and palliative operation was performed in 12 patients. For the paired group (non-nCRT group), the mean age at surgery was 60.40 years (range 29–83 years), and 32.22% (97/304) were women. After nCRT, of 304 patients, 29 patients (9.54%) achieved pathologic CR, and 125 (41.12%), 138 (45.39%), and 12 (3.95%) patients achieved PR, SD, and PD, respectively. R0 resection was not performed in 12 patients (3.95%). Clinicopathologic characteristics of patients treated with nCRT are summarized in Table 3. After surgery (radical and palliative surgeries), all 605 patients received adjuvant chemotherapy. In the nCRT group, therapeutic response did not differ significantly based on age, sex, and histological differentiation. The differences in therapeutic response showed statistically significant differences as per T stage (χ² = 440.12, ) and N stage (χ² = 18.007, ). After nCRT, the prognosis of MC cases was worse than that of non-MC cases (χ² = 24.617, ).

There was no significant difference in the survival rate between the nCRT and non-nCRT groups. However, differences in survival rates increased gradually over time between the nCRT and non-nCRT groups (survival rates: three year (χ² = 0.075, ), five year (χ² = 0.094, ), six year (χ² = 0.722, ), seven year (χ² = 1.376, ), and eight year (χ² = 2.995, ) (Table 4) (Figure 5(a)). Furthermore, survival time in the nCRT group was associated with the rest interval. With a rest interval time of less than 50 days, the difference in survival time was not statistically significant (χ² = 2.634, ) (Figure 5(b)). The difference in survival time was statistically significant for a rest interval time of 60 days (χ² = 5.357, , Figure 5(c)) and 70 days (χ² = 10.830, , Figure 5(d)) (Table 5). MC after surgery was more frequent in the nCRT group than it was in the non-nCRT group, and the difference was statistically significant (χ² = 29.352, ) (Table 2) (Figure 6(a)). There were no differences in lymph node metastasis rates between the nCRT and non-nCRT groups (Table 2).

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Figure 5

(a) Comparison of overall survival in patients treated with neoadjuvant chemoradiation therapy (nCRT) and those not treated with nCRT (non-nCRT). (b) Comparison of overall survival in nCRT patients with less than 50 days rest interval and no less than 50 days rest interval. (c) Comparison of overall survival in nCRT patients with less than 60 days rest interval and no less than 60 days rest interval. (d) Comparison of overall survival in nCRT patients with less than 70 days rest interval and no less than 70 days rest interval.

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Figure 6

(a) Overall survival of patients with mucinous adenocarcinoma and nonmucinous adenocarcinoma after neoadjuvant chemoradiation therapy (nCRT). (b) Overall survival of in patients at different T stages (T1 + T2 vs. T3 + T4) after nCRT. (c) Overall survival of patients with and without lymph node metastasis after nCRT. (d) Overall survival of patients with N0, N1, and N2 disease after nCRT. (e) Overall survival of nCRT patients with positive recurrence and/or distant metastasis and nonpositive recurrence and/or distant metastasis. (f) Overall survival of nCRT patients at different Duke’s stages.

The association of clinicopathologic and treatment characteristics with overall survival (OS) is detailed in Table 6. Response to nCRT in the nCRT group was associated with OS on univariable analysis (log rank). pCR, pPR, and pSD were significantly different between the study groups, and hence, these parameters were grouped together and compared against pPD during analysis (χ² = 7.773, ). More than 60 days rest interval (χ² = 5.357, ), higher T stage (Tis + T1 + T2 vs. T3: χ² = 7.553, , T3 vs. T4: χ² = 30.120, , Tis + T1 + T2 vs. T4: χ² = 39.765, ) (Figure 6(b)), positive lymph node metastasis (χ² = 13.722, ) (Figures 6(c) and 6(d)), positive recurrence and/or distant metastasis (χ² = 66.532, ) (Figure 6(e)), and higher Duke’s stage (A + B vs. C: χ² = 13.527, , C vs. D: χ² = 7.415, , A + B vs. D: χ² = 38.719, ) (Figure 6(f)) were associated with poor survival. On multivariable (Cox proportional hazards) analysis, rest interval (60 days), Duke’s stage, and recurrence and/or distant metastasis remained significant predictors of survival (Table 6).

4. Discussion

Tumor invasion and metastasis are the main causes of tumor recurrence and patient mortality [21]. Treatments used for CRC include surgery, chemotherapy, radiation, and targeted therapy. For patients with LARC, nCRT has become the standard treatment strategy over the past decade [22] and has been recommended by major guidelines [14]. Our previous studies have confirmed that chemotherapeutic drugs could induce the formation of PGCCs, and PGCCs can produce daughter cells with strong abilities of tumor infiltration and metastasis in vitro [4, 5, 7, 23, 24]. Morphologic observation of human locally advanced rectal cancer after nCRT showed that there were many PGCCs in tumor tissue after nCRT and different morphologic characteristics related with tumor invasion and metastasis appeared in tumor tissue. In this study, we showed that irradiation and chemicals could induce the formation of PGCCs in vitro and PGCCs with their generated daughter cells exhibited strong migratory, invasive, and proliferation abilities, associating with the therapeutic effect of nCRT for LARC patients.

Most clinical studies have shown that the main benefits of nCRT lie in improving staging and cancer resectability though long-term OS and progression-free survival are not affected significantly [25]. At present, the most commonly used nCRT is radiotherapy and synchronized adjuvant chemotherapy for five weeks followed by surgery 6–8 weeks after radiotherapy [26]. However, different rest interval time between radiotherapy and surgery may affect the survival of patients with nCRT [3]. Several clinical studies have suggested that prolonging the time interval may help to increase the rate of pathologic CR and reduce the clinical stage. Retrospective studies have reported that a 9–12-week rest interval time after nCRT can improve the rate of pCR in LARC patients though there is no effect on OS. Compared with <8 weeks rest interval time, >8 weeks rest interval time after CRT can reduce tumor staging and increase pCR rate [27]. In 2016, the European Society for Medical Oncology (ESMO) reported a randomized controlled study of more than 200 patients. Compared with those who had a 6-week rest interval time, the pCR rate in patients with a 12-week rest interval time was significantly higher and the mrT staging was significantly lower [28]. However, these studies have focused on pathological remission or a decline in tumor staging, even though pCR or magnetic resonance tumor regression grade (mrTRG) is only a predictor of long-term prognosis. Differences in OS and disease-free survival have nevertheless been observed among patients after nCRT [29, 30]. Patients with a long rest interval time after nCRT therapy may have a higher rate of pCR, but the survival benefits need to be studied with a long-term follow-up. Another randomized controlled study comparing 11 weeks and 7 weeks of rest interval time showed that there was no statistically significant difference in pCR rates. In contrast, patients with 11 weeks of rest interval time had a higher incidence of complications and incomplete mesorectal excisions, which may be related to difficulties during surgery after a long rest interval time [31]. Another retrospective study of more than 10,000 nCRT-treated cases showed that 8 weeks of rest interval time may be optimum and the risk of positive margins increased when the rest interval time was more than 8 weeks [15]. Kwak et al. studied 1785 cases of LARC and found that the rate of tumor downstaging peaked at 6-7 weeks of rest interval after nCRT and decreased thereafter [32]. Here, by analyzing the clinicopathologic characteristics of 304 patients treated with nCRT and those of paired 301 patients not treated with nCRT, we concluded that the survival time of LARC patients treated with nCRT was related to the rest interval. For a rest interval time of more than 50 days, the difference in survival time was not statistically significant. When the rest interval time was more than 60 days, the difference in survival time was statistically significant. Results of multivariable analysis showed that 60 days rest interval, Duke’s stage, and recurrence and/or distant metastasis remained significant predictors of survival. Furthermore, in patients after nCRT, MC (a highly metastatic malignant tumor) occurred more frequently in nCRT after surgery than in non-nCRT patients. MC has been reported to be associated with a higher risk of death when located in the rectum [33]. The differences in survival rates between the nCRT and non-nCRT groups increased gradually with time, though the differences in three-year, five-year, six-year, seven-year, and eight-year survival rates were not significant.

To further study the possible mechanisms by which nCRT affects the survival of patients with LARC, chemotherapeutic drugs and irradiation were used to treat colon cancer cell lines LoVo and HCT116. Results showed that chemotherapeutic drugs and irradiation can induce the formation of PGCCs. We have previously demonstrated that PGCCs induced with CoCl₂ and paclitaxel exhibit cancer stem cell properties and asymmetrically generate daughter cells via budding [5–7]. The number of PGCCs correlates positively with the degree of malignancy. Presence of PGCC-enriched tumor tissue correlates with a high recurrence rate, lymph node metastasis, chemoresistance, and poor prognosis. Furthermore, daughter cells produced by PGCCs via asymmetric cell division have strong migration and invasion capabilities [5–7, 34]. In contrast to control cells, daughter cells generated by PGCCs after irradiation and chemicals acquired a mesenchymal phenotype and expressed epithelial-mesenchymal transition-related proteins including N-cadherin, vimentin, Twist, Slug, Snail, and CK7.

PGCCs have been reported in different types of cancer cell lines including those of ovarian cancer [7], colon cancer [35], and breast cancer [36]. After chemotherapeutic drug and radiation treatment, a long incubation period is required before daughter cells are generated and the length of this period depends on the chemotherapy dose and intensity of radiotherapy. We previously treated SKOv3 cells with1 μM paclitaxel for 48 hours and observed that SKOv3 PGCCs generated daughter cells four months later. The long incubation period may be related to the increasing differences in survival rates of the nCRT and non-nCRT groups observed in this study at three-year, five-year, six-year, seven-year, and eight-year time periods. Furthermore, when cells were treated with chemotherapeutic drugs and radiation for the first time, the surviving PGCCs recovered and generated daughter cells, which were resistant to a second treatment with the same dose of chemotherapeutic drugs and intensity of irradiation. Compared with first time treatment, more PGCCs survived and the recovery time was also shortened after the second treatment.

5. Conclusions

Taken together, compared to patients not treated with nCRT, those treated with nCRT did not show improved long-term survival rates in LARC. The detailed molecular mechanisms by which chemotherapeutic drugs and irradiation induce the formation of PGCCs with daughter cells resistant to treatment need to be studied further.

Abbreviations

LARC:	Locally advanced rectal cancer
CRT:	Neoadjuvant chemoradiation therapy
MC:	Mucinous adenocarcinomas
PGCCs:	Polyploid giant cancer cells
CoCl₂:	Cobalt chloride
CRC:	Colorectal cancer
TME:	Total mesorectal excision
pCR:	Pathologic complete response
OS:	Overall survival
PR:	Partial response
SD:	Stable disease
PD:	Progressive disease
ICC:	Immunocytochemical
WB:	Western blot
GTV:	Gross tumor volume
CTV:	Clinical target volumes
PTV:	Planning target volume
mrTRG:	Magnetic resonance tumor regression grade.

Data Availability

All data supporting the findings of this study are available within the article and its supplementary files and are available from the corresponding author upon reasonable request.

Ethical Approval

The research has been carried out in accordance with the World Medical Association Declaration of Helsinki, and all subjects provided written informed consent. The use of human tissue samples was approved by the Hospital Review Board, and the confidentiality of patient information was maintained.

All authors have read and agreed to publish this manuscript.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Authors’ Contributions

FF and MZ equally contributed to the paper. SZ designed the study; collected, analyzed, and interpreted data; contributed to manuscript writing; and approved the manuscript before submission. FF, MZ, and BL collected and analyzed data and approved the manuscript before submission. LZ, HW, and LL collected, analyzed, and interpreted data; contributed to manuscript writing; and approved the manuscript before submission. YL, PD, and YG managed the study, collected data, gave constructive comments on the manuscript, and approved the manuscript before submission. XZ, TJ, and SZ collected data, gave constructive comments on the manuscript, and approved the manuscript before submission.

Acknowledgments

We acknowledge Editage service for language editing. This work was supported in part by grants from the National Natural Science Foundation of China (81672426) and the Foundation of Committee on Science and Technology of Tianjin (17ZXMFSY00120 and 17YFZCSY00700).

Supplementary Materials

Supplementary Figure S1: quantitative results of the expression differences of N-cadherin, vimentin, E-cadherin, fibronectin, Snail + Slug, Twist-1, and CK7 in LoVo control cells and treatment cells are shown as histograms. Each bar represents the mean ± SD of three independent experiments (). Supplementary Figure S2: quantitative results of the expression differences of N-cadherin, vimentin, E-cadherin, fibronectin, Snail + Slug, Twist-1, and CK7 in HCT116 control cells and treatment cells are shown as histograms. Each bar represents the mean ± SD of three independent experiments (). Supplementary Table S1: different concentrations and durations of chemotherapeutic treatment in different cell lines. Supplementary Table S2: detailed information of antibodies used in this study. (Supplementary Materials)

References

F. Bray, J. Ferlay, I. Soerjomataram, R. L. Siegel, L. A. Torre, and A. Jemal, “Global cancer statistics 2018: globocan estimates of incidence and mortality worldwide for 36 cancers in 185 countries,” CA: A Cancer Journal for Clinicians, vol. 68, no. 6, pp. 394–424, 2018.
View at: Publisher Site | Google Scholar
D. A. Joseph, C. J. Johnson, A. White, M. Wu, and M. P. Coleman, “Rectal cancer survival in the United States by race and stage, 2001 to 2009: findings from the CONCORD-2 study,” Cancer, vol. 123, no. 24, pp. 5037–5058, 2017.
View at: Publisher Site | Google Scholar
J. Liu, “The dualistic origin of human tumors,” Seminars in Cancer Biology, vol. 53, pp. 1–16, 2018.
View at: Publisher Site | Google Scholar
L. Zhang, P. Ding, H. Lv et al., “Number of polyploid giant cancer cells and expression of EZH2 are associated with VM formation and tumor grade in human ovarian tumor,” BioMed Research International, vol. 2014, Article ID 903542, 9 pages, 2014.
View at: Publisher Site | Google Scholar
S. Zhang, I. Mercado-Uribe, and J. Liu, “Tumor stroma and differentiated cancer cells can be originated directly from polyploid giant cancer cells induced by paclitaxel,” International Journal of Cancer, vol. 134, no. 3, pp. 508–518, 2014.
View at: Publisher Site | Google Scholar
S. Zhang, I. Mercado-Uribe, A. Sood, R. C. Bast, and J. Liu, “Coevolution of neoplastic epithelial cells and multilineage stroma via polyploid giant cells during immortalization and transformation of mullerian epithelial cells,” Genes & Cancer, vol. 7, no. 3-4, pp. 60–72, 2016.
View at: Publisher Site | Google Scholar
S. Zhang, I. Mercado-Uribe, Z. Xing, B. Sun, J. Kuang, and J. Liu, “Generation of cancer stem-like cells through the formation of polyploid giant cancer cells,” Oncogene, vol. 33, no. 1, pp. 116–128, 2014.
View at: Publisher Site | Google Scholar
S. Zhang, D. Zhang, Z. Yang, and X. Zhang, “Tumor budding, micropapillary pattern, and polyploidy giant cancer cells in colorectal cancer: current status and future prospects,” Stem Cells International, vol. 2016, Article ID 4810734, 8 pages, 2016.
View at: Publisher Site | Google Scholar
D. D. Tran, C. A. S. Corsa, H. Biswas, R. L. Aft, and G. D. Longmore, “Temporal and spatial cooperation of Snail1 and Twist1 during epithelial-mesenchymal transition predicts for human breast cancer recurrence,” Molecular Cancer Research, vol. 9, no. 12, pp. 1644–1657, 2011.
View at: Publisher Site | Google Scholar
S. White-Gilbertson, P. Lu, J. S. Norris, and C. Voelkel-Johnson, “Genetic and pharmacological inhibition of acid ceramidase prevents asymmetric cell division by neosis,” Journal of Lipid Research, vol. 60, no. 7, pp. 1225–1235, 2019.
View at: Publisher Site | Google Scholar
N. Niu, J. Zhang, N. Zhang et al., “Linking genomic reorganization to tumor initiation via the giant cell cycle,” Oncogenesis, vol. 5, no. 12, p. e281, 2016.
View at: Publisher Site | Google Scholar
K.-C. Lin, G. Torga, Y. Sun et al., “The role of heterogeneous environment and docetaxel gradient in the emergence of polyploid, mesenchymal and resistant prostate cancer cells,” Clinical & Experimental Metastasis, vol. 36, no. 2, pp. 97–108, 2019.
View at: Publisher Site | Google Scholar
A. J. M. Rombouts, N. Hugen, M. A. G. Elferink, I. D. Nagtegaal, and J. H. W. de Wilt, “Treatment interval between neoadjuvant chemoradiotherapy and surgery in rectal cancer patients: a population-based study,” Annals of Surgical Oncology, vol. 23, no. 11, pp. 3593–3601, 2016.
View at: Publisher Site | Google Scholar
R. W. Burt, J. S. Barthel, K. B. Dunn et al., “Colorectal cancer screening,” Journal of the National Comprehensive Cancer Network, vol. 8, no. 1, pp. 8–61, 2010.
View at: Publisher Site | Google Scholar
Z. Sun, M. A. Adam, J. Kim, M. Shenoi, J. Migaly, and C. R. Mantyh, “Optimal timing to surgery after neoadjuvant chemoradiotherapy for locally advanced rectal cancer,” Journal of the American College of Surgeons, vol. 222, no. 4, pp. 367–374, 2016.
View at: Publisher Site | Google Scholar
F. A. Calvo, V. Morillo, M. Santos et al., “Interval between neoadjuvant treatment and definitive surgery in locally advanced rectal cancer: impact on response and oncologic outcomes,” Journal of Cancer Research and Clinical Oncology, vol. 140, no. 10, pp. 1651–1660, 2014.
View at: Publisher Site | Google Scholar
G. L. Jackson, L. L. Zullig, S. Y. Zafar et al., “Using NCCN clinical practice guidelines in oncology to measure the quality of colorectal cancer care in the veterans health administration,” Journal of the National Comprehensive Cancer Network, vol. 11, no. 4, pp. 431–441, 2013.
View at: Publisher Site | Google Scholar
S. B. Edge and C. C. Compton, “The American Joint Committee on Cancer: the 7th edition of the AJCC cancer staging manual and the future of TNM,” Annals of Surgical Oncology, vol. 17, no. 6, pp. 1471–1474, 2010.
View at: Publisher Site | Google Scholar
G. Karagkounis, L. Thai, A. G Mace et al., “Prognostic implications of pathological response to neoadjuvant chemoradiation in pathologic stage III rectal cancer,” Annals of Surgery, vol. 269, no. 6, pp. 1117–1123, 2019.
View at: Publisher Site | Google Scholar
M. K. Washington, J. Berlin, P. Branton et al., “Protocol for the examination of specimens from patients with primary carcinoma of the colon and rectum,” Archives of Pathology & Laboratory Medicine, vol. 133, no. 10, pp. 1539–1551, 2009.
View at: Google Scholar
N. Khan and H. Mukhtar, “Cancer and metastasis: prevention and treatment by green tea,” Cancer and Metastasis Reviews, vol. 29, no. 3, pp. 435–445, 2010.
View at: Publisher Site | Google Scholar
R. Sauer, H. Becker, W. Hohenberger et al., “Preoperative versus postoperative chemoradiotherapy for rectal cancer,” New England Journal of Medicine, vol. 351, no. 17, pp. 1731–1740, 2004.
View at: Publisher Site | Google Scholar
D. Zhang, Y. Wang, and S. Zhang, “Asymmetric cell division in polyploid giant cancer cells and low eukaryotic cells,” BioMed Research International, vol. 2014, Article ID 432652, 8 pages, 2014.
View at: Publisher Site | Google Scholar
S. Zhang, I. Mercado-Uribe, S. Hanash, and J. Liu, “iTRAQ-based proteomic analysis of polyploid giant cancer cells and budding progeny cells reveals several distinct pathways for ovarian cancer development,” PLoS One, vol. 8, no. 11, Article ID e80120, 2013.
View at: Publisher Site | Google Scholar
R. Sauer, T. Liersch, S. Merkel et al., “Preoperative versus postoperative chemoradiotherapy for locally advanced rectal cancer: results of the German CAO/ARO/AIO-94 randomized phase III trial after a median follow-up of 11 years,” Journal of Clinical Oncology, vol. 30, no. 16, pp. 1926–1933, 2012.
View at: Publisher Site | Google Scholar
J. D. Foster, E. L. Jones, S. Falk, E. J. Cooper, and N. K. Francis, “Timing of surgery after long-course neoadjuvant chemoradiotherapy for rectal cancer,” Diseases of the Colon & Rectum, vol. 56, no. 7, pp. 921–930, 2013.
View at: Publisher Site | Google Scholar
M. Mihmanli, E. Kabul Gurbulak, I. E Akgun et al., “Delaying surgery after neoadjuvant chemoradiotherapy improves prognosis of rectal cancer,” World Journal of Gastrointestinal Oncology, vol. 8, no. 9, pp. 695–706, 2016.
View at: Publisher Site | Google Scholar
J. Evans, J. Bhoday, B Sizer et al., “Results of a prospective randomised control 6 vs 12 trial: is greater tumour downstaging observed on post treatment MRI if surgery is delayed to 12-weeks versus 6-weeks after completion of neoadjuvant chemoradiotherapy?” Annals of Oncology, vol. 27, no. 6, p. 452O, 2016.
View at: Publisher Site | Google Scholar
F. Dossa, S. A. Acuna, A. S. Rickles et al., “Association between adjuvant chemotherapy and overall survival in patients with rectal cancer and pathological complete response after neoadjuvant chemotherapy and resection,” JAMA Oncology, vol. 4, no. 7, pp. 930–937, 2018.
View at: Publisher Site | Google Scholar
P. M. Polanco, A. A. Mokdad, H. Zhu, M. A. Choti, and S. Huerta, “Association of adjuvant chemotherapy with overall survival in patients with rectal cancer and pathologic complete response following neoadjuvant chemotherapy and resection,” JAMA Oncology, vol. 4, no. 7, pp. 938–943, 2018.
View at: Publisher Site | Google Scholar
J. H. Lefevre, L. Mineur, S. Kotti et al., “Effect of interval (7 or 11 weeks) between neoadjuvant radiochemotherapy and surgery on complete pathologic response in rectal cancer: a multicenter, randomized, controlled trial (GRECCAR-6),” Journal of Clinical Oncology, vol. 34, no. 31, pp. 3773–3780, 2016.
View at: Publisher Site | Google Scholar
Y.-K. Kwak, K. Kim, J. H. Lee et al., “Timely tumor response analysis after preoperative chemoradiotherapy and curative surgery in locally advanced rectal cancer: a multi-institutional study for optimal surgical timing in rectal cancer,” Radiotherapy and Oncology, vol. 119, no. 3, pp. 512–518, 2016.
View at: Publisher Site | Google Scholar
N. Hugen, R. H. A. Verhoeven, S. A. Radema et al., “Prognosis and value of adjuvant chemotherapy in stage III mucinous colorectal carcinoma,” Annals of Oncology, vol. 24, no. 11, pp. 2819–2824, 2013.
View at: Publisher Site | Google Scholar
H. Lv, Y. Shi, L. Zhang et al., “Polyploid giant cancer cells with budding and the expression of cyclin E, S-phase kinase-associated protein 2, stathmin associated with the grading and metastasis in serous ovarian tumor,” BMC Cancer, vol. 14, no. 1, p. 576, 2014.
View at: Publisher Site | Google Scholar
L. M. Lopez-Sanchez, C. Jimenez, A. Valverde et al., “CoCl₂, a mimic of hypoxia, induces formation of polyploid giant cells with stem characteristics in colon cancer,” PLoS One, vol. 9, no. 6, Article ID e99143, 2014.
View at: Publisher Site | Google Scholar
F. Fei, D. Zhang, Z. Yang et al., “The number of polyploid giant cancer cells and epithelial-mesenchymal transition-related proteins are associated with invasion and metastasis in human breast cancer,” Journal of Experimental & Clinical Cancer Research, vol. 34, no. 1, p. 158, 2015.
View at: Publisher Site | Google Scholar

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Copyright © 2019 Fei Fei et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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