Evidence-Based Complementary and Alternative Medicine

Evidence-Based Complementary and Alternative Medicine / 2018 / Article

Research Article | Open Access

Volume 2018 |Article ID 1580427 | https://doi.org/10.1155/2018/1580427

Taiguo Liu, Lina Duo, Ping Duan, "Ginsenoside Rg3 Sensitizes Colorectal Cancer to Radiotherapy through Downregulation of Proliferative and Angiogenic Biomarkers", Evidence-Based Complementary and Alternative Medicine, vol. 2018, Article ID 1580427, 8 pages, 2018. https://doi.org/10.1155/2018/1580427

Ginsenoside Rg3 Sensitizes Colorectal Cancer to Radiotherapy through Downregulation of Proliferative and Angiogenic Biomarkers

Academic Editor: Jamal A. Mahajna
Received01 Sep 2017
Accepted27 Dec 2017
Published18 Mar 2018


Background. Radiation therapy is an important mode of colorectal cancer treatment. However, most people die of local recurrence after tumors become resistant to radiotherapy, and little progress has been made in treating radiotherapy-resistant colorectal cancer. Hence, novel agents that are nontoxic and can sensitize colorectal cancer to radiotherapy are urgently needed. Ginsenoside Rg3, a saponin extracted from ginseng, shows cytotoxicity against a variety of cancer cells through suppression of pathways linked to oncogenesis, including cell survival, proliferation, invasion, and angiogenesis. In this article, we investigated whether Rg3 can sensitize colorectal cancer to radiation in vivo. Methods and Materials. We established CT-26 xenografts in BALB/c mice and treated them with vehicle, Rg3, radiation, and combined Rg3 + radiation. Mouse quality of life, survival, tumor volumes, and inhibitive rates were estimated. NF-κB activation was ascertained using electrophoretic mobility shift assay and immunohistochemistry. We also tested for markers of proliferation, angiogenesis, and invasion using immunohistochemistry and Western blot analysis. Results. Rg3 significantly enhanced the efficacy of fractionated radiotherapy by improving the quality of life of mice. Moreover, tumors from mice xenografted with CT-26 cells and treated with combined Rg3 + radiotherapy showed significantly lower tumor volumes ( versus controls; versus radiation alone), NF-κB activation, and expression of NF-κB-regulated gene products (cyclin D1, survivin, cyclooxygenase-2 (COX-2), and vascular endothelial growth factor (VEGF)) compared with controls. The combination treatment was also effective in suppressing angiogenesis, as indicated by lower CD31+ microvessel density compared with controls (). Conclusion. Our results suggest that Rg3 enhances the antitumor effects of radiotherapy for colorectal cancer by suppressing NF-κB and NF-κB-regulated gene products, leading to inhibition of tumors and prolongation of the lifespan of CT-26 xenograft BALB/c mice.

1. Introduction

Colorectal cancer is the third most common type of cancer in western countries and is a significant cause of morbidity and mortality throughout the world [1]. Neoadjuvant chemoradiation therapy (CRT) is widely used to decrease local recurrence after surgical resection because colorectal cancer frequently presents at a locally advanced stage [2]. It can also improve disease-free and overall survival rates and increases the chances of anal sphincter preservation at the time of surgery [3, 4]. Unfortunately, more than one-third of patients do not respond or show only modest responses to CRT and optimal surgery treatment [5]. Furthermore, complete pathologic response to neoadjuvant CRT assessed at the time of surgical resection has become a surrogate marker for outcome. However, only about 10–20% of patients achieve a complete pathologic response to neoadjuvant CRT due to their resistance to radiation therapy [6, 7]. Developing a strategy to improve local control and pathologic response rates with novel radiosensitization may keep some patients from radical surgical resections.

It is not clear why the response to radiation is so limited. Recently, most reported studies have shown that the transcription factor NF-κB plays a critical role in the development of radiotherapy suppression on tumor [8]. NF-κB has been found to mediate tumor promotion, metastasis, angiogenesis, and treatment resistance in a wide range of tumors through the expression of genes involving in malignant transformation and tumor promotion [9, 10]. Previous study showed that NF-κB is constitutively active in colon cancer cells, but not in normal colorectal ductal epithelial cells [11]. Several studies have suggested that radiotherapy induces NF-κB activity upregulation [1214]. Therefore, agents that inhibit NF-κB activity could potentiate the radioresponse in colorectal cancer.

Panax ginseng has been frequently used to treat many disorders in traditional Chinese medicine for more than 2000 years. The principle biologically active ingredient of ginseng is ginsenoside, which has been found to have many biological activities, including anti-inflammatory and antineoplastic effects [15]. Ginsenoside Rg3 extracted from P. ginseng has been shown to inhibit a variety of tumors [1618].

It is not yet known whether Rg3 can sensitize colorectal tumors to radiotherapy. So, in this study, we measured the effect of Rg3 on the growth of colorectal cancer exposed to radiation, emphasizing combination therapy and inhibition of NF-κB as a molecular mechanism.

2. Methods and Materials

2.1. Materials

Ginsenoside Rg3 extracted from ginseng was supplied by the YaTai Pharmaceutical Company (China) with a purity of above 99.5%. Immunohistochemistry was performed by Liquid DAB+ substrate-chromogen system (Dako). Polyclonal antibodies against p65, cyclin D1, and survivin and monoclonal antibodies against VEGF, CD31, COX-2, and β-actin were purchased from Santa Cruz Biotechnology. Electrophoretic mobility shift assay (EMSA) kit was obtained from Promega. All other chemicals were purchased from the Beyotime Institute of Biotechnology (China), unless otherwise indicated.

2.2. Cell Culture

The CT-26 murine colon carcinoma cell line was supplied by the Cancer Research Institution at Sichuan University. The CT-26 cells were routinely cultured in RPMI1640 medium containing 10% fetal bovine serum (Gibco) with 100 U/mL penicillin and 100 μg/mL streptomycin and kept at 37°C in a humidified atmosphere of 5% CO2.

2.3. Animals and Experimental Protocol

Male BALB/c mice (aged 4 weeks) were used for experiments, which were obtained from the Experimental Animal Center of the West China School of Medicine, Sichuan University. The animals were housed (four mice per cage) under standard conditions (20–26 °C, 40–70% humidity, a 12-hour light/dark cycle) and were given food and water (ad libitum). None of the mice exhibited any lesions and all tested as pathogen-free. Cultured CT-26 colon cancer cells were washed with phosphate-buffered saline (PBS) and resuspended in a serum-free medium. The mouse was subcutaneously injected with the suspension (5 × 106 cells in 0.2 ml) under the armpits of the right anterior superior limbs. Seven days later, when the tumors were palpable, the mice were randomly divided into the following four groups (10 mice per group): (1) a control group receiving intragastric normal saline administration for 30 days, (2) a Rg3 group receiving intragastric administration of Rg3 (10 mg/kg) daily for 30 days, (3) a radiation group, which received radiotherapy delivered directly to the site of tumor twice weekly (2 Gy) for 2 weeks, and (4) a combination group (Rg3 + radiotherapy) treated with Rg3 (10 mg/kg) daily for 30 days and radiation delivered to the site of tumor twice weekly (2 Gy) for 2 weeks. For radiation treatment, mice were first anaesthetized with a volume of 70–100 μl mixture of ketamine (20 mg/ml) and xylazine (20 mg/ml) at a ratio of 6.7 : 1 and then placed onto a specially designed lead plate so as to radiate locally the tumors. The animals were euthanatized six weeks after tumor cell injection and tumor samples were immediately removed. All animal procedures were approved and performed in accordance with the guidelines of the Animal Care and Scientific Committee of Chengdu Integrated TCM & Western Medicine Hospital.

2.4. Electrophoretic Mobility Shift Assays (EMSA)

EMSA was performed to assess NF-κB activation. Briefly, cell nucleus extracted from tumor samples was incubated with 32P-labeled NF-κB consensus oligonucleotide for 20 min at room temperature. The resulting DNA-protein complex was separated from the free oligonucleotides on a nondenaturing 4% polyacrylamide gel and then visualized by the Imaging System.

2.5. Immunolocalization of NF-KB p65 in Tumor Samples

The nuclear localization and expression of p65 in cancer tissues and adjacent tissues were determined by immunohistochemical method. Briefly, colorectal tumor samples were fixed in 4% paraformaldehyde, embedded in paraffin, and sectioned. The biopsies were washed with PBS, blocked for 20 min in protein block solution, and incubated by the antibody to p65 (1 : 100). Biotinylated secondary antibodies were used and stained by Liquid DAB+. Finally, sections were counterstained with hematoxylin and microscopically analyzed with a FV1000 Laser Scanning Confocal Microscope (OLYMPUS).

2.6. Detection of Microvessel Density

Microvessel density (MVD) was assessed and determined by immunohistochemical examination using antibody to the endothelial marker CD31. Sections were fixed, embedded, and stained with rat anti-mouse CD31 monoclonal antibody (1 : 50). Areas of highest vessel density were then assessed under high magnification and capillaries and arterioles were counted. The average vessel count in three hot spots was blindly measured by three investigators and used as the MVD value. The consensus of microvessel counts was considered as the final score for analysis.

2.7. Western Blot Analysis

Colorectal tumor tissues (75–100 mg/mouse) from control and experimental mice were homogenized with 0.5 mL of ice-cold RIPA lysis buffer containing a proteinase inhibitor mixture (Roche) on ice for 30 min. The homogenate was rotated at 4°C for 20 min and centrifuged at 12,000/g at 4°C for 15 min and the supernatant was collected. Crude protein extracts (40 μg), the concentration of which were measured by BCA method, were denatured and fractionated by SDS-PAGE, electrotransferred onto nitrocellulose membranes (Millipore). The membranes were blotted in TBST (25 mM Tris, pH 7.4, 137 mM NaCl, 2.7 mM KCl, and 0.05% Tween 20) containing 5% nonfat milk or 5% BSA for 1 hour at room temperature and visualized using antibody against VEGF, COX-2, cyclin D1, survivin, and β-actin (1 : 1000, 1 : 500, 1 : 500, 1 : 500, and 1 : 2000, resp.) and detected by an enhanced chemiluminescence (ECL) detection system (Pierce). The density of the selected bands was quantified using ImageJ software.

2.8. Statistical Analysis

Data were analyzed using SPSS 19.0 software. Results were given as mean ± SEM, except for Figure 1 whose data are showed as mean only. was considered statistically significant. Two-way ANOVA followed by Bonferroni posttest was used to compare different groups. For all other statistical analyses a two-tailed unpaired -test was used.

3. Results

The goal of this study was, first, to determine whether Rg3 potentiates the antitumor effects of radiotherapy in vivo against colorectal cancer and, second, to delineate the mechanism by which Rg3 mediates its effects.

3.1. Rg3 Potentiates the Antitumor Effects of Radiation in Colorectal Cancers in Xenografted Mice

Based on tumor volume measurements on the seventh day after tumor cell implantation, we randomized animals into four groups and treated them as described in Animals and Experimental Protocol. The animals were sacrificed six weeks after tumor cell injection, five weeks from the date of treatment. Three mice from each of the groups were sacrificed on the 10th day and analyzed for NF-κB and other biomarkers. The lengths and widths of tumors were measured by caliper every five days to monitor tumor growth, and tumor volume (TV) was estimated using the formula: TV (mm3) = (width2  ×  length)/2. As shown in Figure 1, the tumor volume in the combined Rg3-radiation group was significantly lower than those of the other three groups by day 25 of treatment ( versus radiation; versus Rg3; versus control).

3.2. Rg3 Inhibits NF-κB Activation in Colorectal Cancers in Xenografted Mice

NF-κB contributes to the development and/or progression of malignancy by regulating the expression of genes involved in cell growth and proliferation, antiapoptosis, angiogenesis, and metastasis. Whether Rg3 can affect NF-κB p65 expression in vivo was first examined by immunohistochemical analysis. As shown in Figure 2, radiation activated NF-κB in tumor tissues; however NF-κB was inhibited by Rg3 alone or in combination with radiation. In addition, we also analyzed the effect of Rg3 and radiation on NF-κB activation in tumor tissues by EMSA, and the results showed that Rg3 downregulated NF-κB in tumor tissue (see Figure 3).

3.3. Rg3 Downregulates the NF-κB-Regulated Gene Products in Tumor Tissues

Because NF-κB regulates the expression of the antiapoptotic and proliferative proteins such as cyclin D1, COX-2, VEGF, and survivin, we tested whether Rg3 can modulate the expression of these gene products in tumor tissues in xenografts. As shown in Figure 4, Western blot revealed significant reductions in the expressions of these gene products in tumors of the Rg3-alone or radiation-combined treatment groups compared to controls.

3.4. Rg3 Potentiates the Effect of Radiation on a Biomarker of Angiogenesis

Antiangiogenesis can normalize the microvasculature of tumors, improve their lack of oxygen, and sensitize tumors to radiation. Our previous experiment showed that combining Rg3 with radiation can inhibit angiogenesis of lung cancer in mice [17]. We thus analyzed the effect of Rg3 on angiogenesis by examining the expression of CD31, which is a marker of microvessel density. The result showed that the combination of radiation and Rg3 treatments significantly suppressed the expression of CD31 in tumor tissues compared with radiation alone (see Figure 5).

3.5. Side Effects and Quality of Life of Mice

There were no significant abnormalities in psychosis, the status of activity, reaction to stimulation, loss of weight, appetite, or depilation of mice in the ginsenoside Rg3 group; however, this was not the case in the control, radiation, or combination groups. The quality of life of mice in the ginsenoside Rg3 group was the best, while the worst was found in the radiation group. The side effects were lower and quality of life better in the combination group compared with the gemcitabine group. The results showed that ginsenoside Rg3 might potently decrease the side effects of therapy and improve quality of life in tumor-bearing mice.

4. Discussion

Although radiotherapy has been frequently used to treat a variety of tumors, its success was limited by acquired resistance, which has posed a significant clinical challenge. Cellular resistance can be overcome by dose escalation, but it may result in severe cytotoxicity since radiotherapy has no choice except to damage normal tissue cells and tumor cells. Chemoradiation therapy can enhance the efficacy of radiotherapy, but it will increase toxicity, and some patients may even have to stop treatment [19]. Thus, researchers are increasingly taking an interest in exploring some nontoxic agents to increase efficacy for radiation-resistant cancer cells. The present study indicates that Rg3 sensitizes colorectal tumors to radiation therapy by inactivation of NF-κB in vivo. Moreover, Rg3 is a relatively safe medicine and can improve quality of life for mice with tumors.

NF-κB is found to be overexpressed in a variety of solid tumors implicating its aggressive characteristic, and some studies demonstrated that NF-κB increases apoptotic resistance and resistance to radiation treatment [20, 21]. NF-κB can be activated by radiation in both in vitro and in vivo models and then bind to specific DNA sequences in target genes to regulate the transcription of downstream genes, which involve in immunoregulation, growth regulation, inflammation, carcinogenesis, and cell survival [22]. Among these genes, some target genes containing NF-κB binding sites in their promotors, such as COX-2, cyclin D1, and survivin, have been shown to contribute radioresistance in various types of tumor cells [2325]. Therefore, the combination of radiation and an NF-κB inhibitor maybe a promising therapeutic strategy for tumor treatment. The majority of studies have demonstrated that inhibition of NF-κB activation increases radiation-induced apoptosis and enhances radiosensitivity in various tumor cells, including colorectal and cervical and melanoma [2628]. Recent reports have identified that a number of plants sensitize cancer cells to radiation. For example, curcumin has been found to modulate the radiation sensitivity of colorectal cancer cells through inhibiting constitutive and inducible NF-κB activity [29, 30].

Rg3 is an effective chemical trace component of ginseng with a C42H72O13 framework and 784 Da molecular weight, and it has pleiotropic capabilities, including antitumor effect. Previous studies have reported that Rg3 inhibits tumor cells to grow, invade, metastasize, and neovascularize. In another experiment, Kim et al. reported that Rg3 enhances the susceptibility of prostate and colon cancer cells to docetaxel via inhibition of NF-κB in vitro [18, 31]. Consistent with previous reports, our results confirmed that Rg3 enhances the antitumor effects of radiotherapy in CT-26 xenograft BALB/c mice by suppressing NF-κB activation and key downstream tumorigenic and angiogenic factors. In addition, we found that Rg3 suppresses angiogenesis, indicating its indirect (via angiogenic mechanisms) antitumor effect.

COX-2 has also been reported to mediate radiation resistance in various tumor cells, such as laryngeal tumors, oral squamous cell carcinomas, and glioblastoma multiforme cells [3234]. Cyclin D1 that controls the transition from G1 to S phase in the cell cycle is overexpressed in a wide variety of tumors and contributes chemoresistance and radioresistance [3537]. Survivin as a member of the family of apoptosis protein inhibitors is a key regulator of mitosis and programmed cell death [38]. Survivin overexpression has been found to be a predictive factor of response to chemotherapy and radiotherapy in patients with a wide variety of tumors [3941]. In our study, Western blot showed that Rg3 reduces the expression of NF-κB-regulated gene products (cyclin D1, survivin, and COX2) in cancer cells, indicating that Rg3 enhances radiosensitivity of colorectal cancer.

As the creation of new blood vessel supplies the metabolic needs of rapidly proliferating malignant cells, angiogenesis is a key step for tumor growth and metastasis. VEGF is one of the most critical proangiogenic growth factors and plays an important role in tumor angiogenesis. Decreased expression of VEGF may enhance tumor cells oxygenation through normalization of aberrant vessel. It has been reported that Rg3 blocks tumor growth by targeting VEGF [42]. We measured VEGF and MVD and observed that levels of these two markers were decreased by Rg3. The results suggest that Rg3 sensitizes colorectal cancer to radiotherapy, partly through the inhibition of angiogenesis.

Although Rg3 is considered a natural product, its safety and toxicity must be addressed. Consistent with previous reports, our results confirmed that ginsenoside Rg3 not only has no toxic side effects on the marrow, heart, lung, liver, kidney, and nervous system but can also enhances the living quality of mice with tumors.

In conclusion, our results show that Rg3 potentiates the antitumor effects of radiation by inhibiting NF-κB activation and its downstream targets. In addition, Rg3 involves suppression of proliferation and angiogenesis, suggesting that the underlying mechanisms seem to be multifaceted. Third, Rg3 provides a favorable safety profile and supports further research to explore it as a chemopreventive agent.

Conflicts of Interest

The authors declare that there are no conflicts of interest related to this paper.

Authors’ Contributions

Taiguo Liu and Lina Duo contributed equally to this work.


  1. J. Weitz, M. Koch, J. Debus, T. Höhler, P. R. Galle, and M. W. Büchler, “Colorectal cancer,” The Lancet, vol. 365, no. 9454, pp. 153–165, 2005. View at: Publisher Site | Google Scholar
  2. J.-F. Bosset, L. Collette, G. Calais et al., “Chemotherapy with preoperative radiotherapy in rectal cancer,” The New England Journal of Medicine, vol. 355, no. 11, pp. 1114–1123, 2006. View at: Publisher Site | Google Scholar
  3. C. Rödel, P. Martus, T. Papadoupolos et al., “Prognostic significance of tumor regression after preoperative chemoradiotherapy for rectal cancer,” Journal of Clinical Oncology, vol. 23, no. 34, pp. 8688–8696, 2005. View at: Publisher Site | Google Scholar
  4. N. A. Janjan, C. Crane, B. W. Feig et al., “Improved overall survival among responders to preoperative chemoradiation for locally advanced rectal cancer,” American Journal of Clinical Oncology, vol. 24, no. 2, pp. 107–112, 2001. View at: Publisher Site | Google Scholar
  5. G. C. Balch, A. De Meo, and J. G. Guillem, “Modern management of rectal cancer: A 2006 update,” World Journal of Gastroenterology, vol. 12, no. 20, pp. 3186–3195, 2006. View at: Publisher Site | Google Scholar
  6. S. Krishnan, N. A. Janjan, J. M. Skibber et al., “Phase II study of capecitabine (Xeloda®) and concomitant boost radiotherapy in patients with locally advanced rectal cancer,” International Journal of Radiation Oncology * Biology * Physics, vol. 66, no. 3, pp. 762–771, 2006. View at: Publisher Site | Google Scholar
  7. V. Velenik, J. Ocvirk, M. Music et al., “Neoadjuvant capecitabine, radiotherapy, and bevacizumab (CRAB) in locally advanced rectal cancer: results of an open-label phase II study,” Journal of Radiation Oncology, vol. 6, article 105, 2011. View at: Publisher Site | Google Scholar
  8. B. B. Aggarwal, “Nuclear factor-κB: the enemy within,” Cancer Cell, vol. 6, no. 3, pp. 203–208, 2004. View at: Publisher Site | Google Scholar
  9. M. Karin, “Nuclear factor-κB in cancer development and progression,” Nature, vol. 441, no. 7092, pp. 431–436, 2006. View at: Publisher Site | Google Scholar
  10. J.-I. Inoue, J. Gohda, T. Akiyama, and K. Semba, “NF-κB activation in development and progression of cancer,” Cancer Science, vol. 98, no. 3, pp. 268–274, 2007. View at: Publisher Site | Google Scholar
  11. L.-L. Yu, H.-G. Yu, J.-P. Yu, H.-S. Luo, X.-M. Xu, and J.-H. Li, “Nuclear factor-κB p65 (RelA) transcription factor is constitutively activated in human colorectal carcinoma tissue,” World Journal of Gastroenterology, vol. 10, no. 22, pp. 3255–3260, 2004. View at: Publisher Site | Google Scholar
  12. X. Chen, B. Shen, L. Xia et al., “Activation of nuclear factor kappaB in radioresistance of TP53-inactive human keratinocytes,” Cancer Res, vol. 62, pp. 1213–1221, 2002. View at: Google Scholar
  13. N. Cao, S. Li, Z. Wang et al., “NF-κB-mediated HER2 overexpression in radiation-adaptive resistance,” Journal of Radiation Research, vol. 171, no. 1, pp. 9–21, 2009. View at: Publisher Site | Google Scholar
  14. S. J. Veuger, J. E. Hunter, and B. W. Durkacz, “Ionizing radiation-induced NF-κB activation requires PARP-1 function to confer radioresistance,” Oncogene, vol. 28, no. 6, pp. 832–842, 2009. View at: Publisher Site | Google Scholar
  15. P. Y. K. Yue, N. K. Mak, Y. K. Cheng et al., “Pharmacogenomics and the Yin/Yang actions of ginseng: anti-tumor, angiomodulating and steroid-like activities of ginsenosides,” Chinese Medicine, vol. 2, article 6, 2007. View at: Publisher Site | Google Scholar
  16. B.-C. He, J.-L. Gao, X. Luo et al., “Ginsenoside Rg3 inhibits colorectal tumor growth through the down-regulation of Wnt/β-catenin signaling,” International Journal of Oncology, vol. 38, no. 2, pp. 437–445, 2011. View at: Publisher Site | Google Scholar
  17. T.-G. Liu, Y. Huang, D.-D. Cui et al., “Inhibitory effect of ginsenoside Rg3 combined with gemcitabine on angiogenesis and growth of lung cancer in mice,” BMC Cancer, vol. 9, article 250, 2009. View at: Publisher Site | Google Scholar
  18. S. M. Kim, S. Y. Lee, J. S. Cho et al., “Combination of ginsenoside Rg3 with docetaxel enhances the susceptibility of prostate cancer cells via inhibition of NF-B,” European Journal of Pharmacology, vol. 631, no. 1–3, pp. 1–9, 2010. View at: Publisher Site | Google Scholar
  19. J. M. Kirwan, P. Symonds, J. A. Green, J. Tierney, M. Collingwood, and C. J. Williams, “A systematic review of acute and late toxicity of concomitant chemoradiation for cervical cancer,” Radiotherapy & Oncology, vol. 68, no. 3, pp. 217–226, 2003. View at: Publisher Site | Google Scholar
  20. K. M. Ahmed, S. Dong, M. Fan, and J. J. Li, “Nuclear factor-κB p65 inhibits mitogen-activated protein kinase signaling pathway in radioresistant breast cancer cells,” Molecular Cancer Research, vol. 4, no. 12, pp. 945–955, 2006. View at: Publisher Site | Google Scholar
  21. K. N. Rithidech, M. Tungjai, E. Arbab, and S. R. Simon, “Activation of NF-κB in bone marrow cells of BALB/cJ mice following exposure in vivo to low doses of 137Cs γ-rays,” Radiation and Environmental Biophysics, vol. 44, no. 2, pp. 139–143, 2005. View at: Publisher Site | Google Scholar
  22. F. Li and G. Sethi, “Targeting transcription factor NF-κB to overcome chemoresistance and radioresistance in cancer therapy,” Biochimica et Biophysica Acta (BBA) - Reviews on Cancer, vol. 1805, no. 2, pp. 167–180, 2010. View at: Publisher Site | Google Scholar
  23. K. Yamamoto, T. Arakawa, N. Ueda, and S. Yamamoto, “Transcriptional roles of nuclear factor κB and nuclear factor-interleukin-6 in the tumor necrosis factor α-dependent induction of cyclooxygenase-2 in MC3T3-E1 cells,” The Journal of Biological Chemistry, vol. 270, no. 52, pp. 31315–31320, 1995. View at: Publisher Site | Google Scholar
  24. D. C. Guttridge, C. Albanese, J. Y. Reuther, R. G. Pestell, and A. S. Baldwin Jr., “NF-κB controls cell growth and differentiation through transcriptional regulation of cyclin D1,” Molecular and Cellular Biology, vol. 19, no. 8, pp. 5785–5799, 1999. View at: Publisher Site | Google Scholar
  25. L. Zhu, S. Fukuda, G. Cordis, D. K. Das, and N. Maulik, “Anti-apoptotic protein survivin plays a significant role in tubular morphogenesis of human coronary arteriolar endothelial cells by hypoxic preconditioning,” FEBS Letters, vol. 508, no. 3, pp. 369–374, 2001. View at: Publisher Site | Google Scholar
  26. S. M. Russo, J. E. Tepper, A. S. Baldwin et al., “Enhancement of radiosensitivity by proteasome inhibition: implications for a role of NF-κB,” International Journal of Radiation Oncology * Biology * Physics, vol. 50, pp. 183–193, 2001. View at: Google Scholar
  27. C. M. Bradbury, S. Markovina, S. J. Wei et al., “Indomethacin-induced radiosensitization and inhibition of ionizing radiation-induced NF-kappaB activation in HeLa cells occur via a mechanism involving p38 MAP kinase,” Cancer Res, vol. 61, pp. 7689–7696, 2001. View at: Google Scholar
  28. A. Munshi, J. F. Kurland, T. Nishikawa et al., “Inhibition of constitutively activated nuclear factor-kappaB radiosensitizes human melanoma cells,” Mol Cancer Ther, vol. 3, pp. 985–992, 2004. View at: Google Scholar
  29. A. B. Kunnumakkara, P. Diagaradjane, S. Guha et al., “Curcumin sensitizes human colorectal cancer xenografts in nude mice to γ-radiation by targeting nuclear factor-κB-regulated gene products,” Clinical Cancer Research, vol. 14, no. 7, pp. 2128–2136, 2008. View at: Publisher Site | Google Scholar
  30. S. K. Sandur, A. Deorukhkar, M. K. Pandey et al., “Curcumin modulates the radiosensitivity of colorectal cancer cells by suppressing constitutive and inducible NF-κB activity,” International Journal of Radiation Oncology * Biology * Physics, vol. 75, no. 2, pp. 534–542, 2009. View at: Publisher Site | Google Scholar
  31. S. M. Kim, S. Y. Lee, D. Y. Yuk et al., “Inhibition of NF-κB by ginsenoside Rg3 enhances the susceptibility of colon cancer cells to docetaxel,” Archives of Pharmacal Research, vol. 32, no. 5, pp. 755–765, 2009. View at: Publisher Site | Google Scholar
  32. W.-C. Chen, W. H. McBride, S.-M. Chen et al., “Prediction of poor survival by cyclooxygenase-2 in patients with T4 nasopharyngeal cancer treated by radiation therapy: Clinical and in vitro studies,” Head & Neck, vol. 27, no. 6, pp. 503–512, 2005. View at: Publisher Site | Google Scholar
  33. N. Terakado, S. Shintani, J. Yano et al., “Overexpression of cyclooxygenase-2 is associated with radioresistance in oral squamous cell carcinoma,” Oral Oncology, vol. 40, no. 4, pp. 383–389, 2004. View at: Publisher Site | Google Scholar
  34. A. Karim, K. McCarthy, A. Jawahar, D. Smith, B. Willis, and A. Nanda, “Differential cyclooxygenase-2 enzyme expression in radiosensitive versus radioresistant glioblastoma multiforme cell lines,” Anticancer Reseach, vol. 25, no. 1 B, pp. 675–679, 2005. View at: Google Scholar
  35. K. M. Ahmed, M. Fan, D. Nantajit, N. Cao, and J. J. Li, “Cyclin D1 in low-dose radiation-induced adaptive resistance,” Oncogene, vol. 27, no. 53, pp. 6738–6748, 2008. View at: Publisher Site | Google Scholar
  36. H. Biliran Jr., Y. Wang, S. Banerjee et al., “Overexpression of cyclin D1 promotes tumor cell growth and confers resistance to cisplatin-mediated apoptosis in an elastase-myc transgene-expressing pancreatic tumor cell line,” Clinical Cancer Research, vol. 11, no. 16, pp. 6075–6086, 2005. View at: Publisher Site | Google Scholar
  37. K. I. M. Jong Kyong and J. Alan Diehl, “Nuclear cyclin D1: An oncogenic driver in human cancer,” Journal of Cellular Physiology, vol. 220, no. 2, pp. 292–296, 2009. View at: Publisher Site | Google Scholar
  38. A. C. Mita, M. M. Mita, S. T. Nawrocki, and F. J. Giles, “Survivin: key regulator of mitosis and apoptosis and novel target for cancer therapeutics,” Clinical Cancer Research, vol. 14, no. 16, pp. 5000–5005, 2008. View at: Publisher Site | Google Scholar
  39. K. Asanuma, R. Moriai, T. Yajima et al., “Survivin as a radioresistance factor in pancreatic cancer,” Japanese Journal of Cancer Research, vol. 91, no. 11, pp. 1204–1209, 2000. View at: Publisher Site | Google Scholar
  40. F. Rödel, J. Hoffmann, L. Distel et al., “Survivin as a radioresistance factor, and prognostic and therapeutic target for radiotherapy in rectal cancer,” Cancer Research, vol. 65, no. 11, pp. 4881–4887, 2005. View at: Publisher Site | Google Scholar
  41. C. Cao, Y. Mu, D. E. Hallahan, and B. Lu, “XIAP and survivin as therapeutic target's for radiation sensitization in preclinical models of lung cancer,” Oncogene, vol. 23, no. 42, pp. 7047–7052, 2004. View at: Publisher Site | Google Scholar
  42. Q. Zhang, X. Kang, B. Yang, J. Wang, and F. Yang, “Antiangiogenic effect of capecitabine combined with ginsenoside Rg3 on breast cancer in mice,” Cancer Biotherapy and Radiopharmaceuticals, vol. 23, no. 5, pp. 647–653, 2008. View at: Publisher Site | Google Scholar

Copyright © 2018 Taiguo Liu 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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