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BioMed Research International
Volume 2013 (2013), Article ID 648420, 9 pages
PSCA and Oct-4 Expression in the Benign and Malignant Lesions of Gallbladder: Implication for Carcinogenesis, Progression, and Prognosis of Gallbladder Adenocarcinoma
1Department of Pathology, Third Xiangya Hospital, Central South University, Changsha, Hunan 410013, China
2Research Laboratory of Hepatobiliary Diseases, Second Xiangya Hospital, Central South University, Changsha, Hunan 410011, China
Received 13 September 2012; Accepted 9 June 2013
Academic Editor: Sachidanand Pandey
Copyright © 2013 Qiong Zou 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.
- A. T. Collins, P. A. Berry, C. Hyde, M. J. Stower, and N. J. Maitland, “Prospective identification of tumorigenic prostate cancer stem cells,” Cancer Research, vol. 65, no. 23, pp. 10946–10951, 2005.
- C.-C. Chang, “Recent translational research: stem cells as the roots of breast cancer,” Breast Cancer Research, vol. 8, no. 1, article 103, 2006.
- L. Ricci-Vitiani, D. G. Lombardi, E. Pilozzi et al., “Identification and expansion of human colon-cancer-initiating cells,” Nature, vol. 445, no. 7123, pp. 111–115, 2007.
- C. Li, D. G. Heidt, P. Dalerba et al., “Identification of pancreatic cancer stem cells,” Cancer Research, vol. 67, no. 3, pp. 1030–1037, 2007.
- M. E. Prince, R. Sivanandan, A. Kaczorowski et al., “Identification of a subpopulation of cells with cancer stem cell properties in head and neck squamous cell carcinoma,” Proceedings of the National Academy of Sciences of the United States of America, vol. 104, no. 3, pp. 973–978, 2007.
- R. E. Reiter, Z. Gu, T. Watabe et al., “Prostate stem cell antigen: a cell surface marker overexpressed in prostate cancer,” Proceedings of the National Academy of Sciences of the United States of America, vol. 95, no. 4, pp. 1735–1740, 1998.
- S. Ross, S. D. Spencer, I. Holcomb et al., “Prostate stem cell antigen as therapy target: tissue expression and in vivo efficacy of an immunoconjugate,” Cancer Research, vol. 62, no. 9, pp. 2546–2553, 2002.
- Z. Gu, G. Thomas, J. Yamashiro et al., “Prostate stem cell antigen (PSCA) expression increases with high gleason score, advanced stage and bone metastasis in prostate cancer,” Oncogene, vol. 19, no. 10, pp. 1288–1296, 2000.
- K.-R. Han, D. B. Seligson, X. Liu et al., “Prostate stem cell antigen expression is associated with gleason score, seminal vesicle invasion and capsular invasion in prostate cancer,” Journal of Urology, vol. 171, no. 3, pp. 1117–1121, 2004.
- N. Amara, G. S. Palapattu, M. Schrage et al., “Prostate stem cell antigen is overexpressed in human transitional cell carcinoma,” Cancer Research, vol. 61, no. 12, pp. 4660–4665, 2001.
- P. Argani, C. Rosty, R. E. Reiter et al., “Discovery of new markers of cancer through serial analysis of gene expression: prostate stem cell antigen is overexpressed in pancreatic adenocarcinoma,” Cancer Research, vol. 61, no. 11, pp. 4320–4324, 2001.
- M. N. Wente, A. Jain, E. Kono et al., “Prostate stem cell antigen is a putative target for immunotherapy in pancreatic cancer,” Pancreas, vol. 31, no. 2, pp. 119–125, 2005.
- E. Elsamman, T. Fukumori, T. Kasai et al., “Prostate stem cell antigen predicts tumour recurrence in superficial transitional cell carcinoma of the urinary bladder,” BJU International, vol. 97, no. 6, pp. 1202–1207, 2006.
- C. A. Iacobuzio-Donahue, A. Maitra, G. L. Shen-Ong et al., “Discovery of novel tumor markers of pancreatic cancer using global gene expression technology,” American Journal of Pathology, vol. 160, no. 4, pp. 1239–1249, 2002.
- E. M. Elsamman, T. Fukumori, S. Tanimoto et al., “The expression of prostate stem cell antigen in human clear cell renal cell carcinoma: a quantitative reverse transcriptase-polymerase chain reaction analysis,” BJU International, vol. 98, no. 3, pp. 668–673, 2006.
- H. Sakamoto, K. Yoshimura, N. Saeki et al., “Genetic variation in PSCA is associated with susceptibility to diffuse-type gastric cancer,” Nature Genetics, vol. 40, no. 6, pp. 730–740, 2008.
- D. F. Stroncek, L. Caruccio, and M. Bettinotti, “CD177: a member of the Ly-6 gene superfamily involved with neutrophil proliferation and polycythemia vera,” Journal of Translational Medicine, vol. 2, article 8, 2004.
- A. Hänninen, I. Jaakkola, M. Salmi, O. Simell, and S. Jalkanen, “Ly-6C regulates endothelial adhesion and homing of CD8+ T cells by activating integrin-dependent adhesion pathways,” Proceedings of the National Academy of Sciences of the United States of America, vol. 94, no. 13, pp. 6898–6903, 1997.
- S.-K. Lee, B. Su, S. E. Maher, and A. L. M. Bothwell, “Ly-6A is required for T cell receptor expression and protein tyrosine kinase fyn activity,” The EMBO Journal, vol. 13, no. 9, pp. 2167–2176, 1994.
- W. L. Stanford, S. Haque, R. Alexander et al., “Altered proliferative response by T lymphocytes of Ly-6A (Sca-1) null mice,” Journal of Experimental Medicine, vol. 186, no. 5, pp. 705–717, 1997.
- H. R. Schöler, S. Ruppert, N. Suzuki, K. Chowdhury, and P. Gruss, “New type of POU domain in germ line-specific protein Oct-4,” Nature, vol. 344, no. 6265, pp. 435–439, 1990.
- M. H. Rosner, M. A. Vigano, K. Ozato et al., “A POU-domain transcription factor in early stem cells and germ cells of the mammalian embryo,” Nature, vol. 345, no. 6277, pp. 686–692, 1990.
- J. Nichols, B. Zevnik, K. Anastassiadis et al., “Formation of pluripotent stem cells in the mammalian embryo depends on the POU transcription factor Oct4,” Cell, vol. 95, no. 3, pp. 379–391, 1998.
- H. Niwa, J.-I. Miyazaki, and A. G. Smith, “Quantitative expression of Oct-3/4 defines differentiation, dedifferentiation or self-renewal of ES cells,” Nature Genetics, vol. 24, no. 4, pp. 372–376, 2000.
- M. Monk and C. Holding, “Human embryonic genes re-expressed in cancer cells,” Oncogene, vol. 20, no. 56, pp. 8085–8091, 2001.
- T. Jin, D. R. Branch, X. Zhang, S. Qi, B. Youngson, and P. E. Goss, “Examination of POU homeobox gene expression in human breast cancer cells,” International Journal of Cancer, vol. 81, no. 1, pp. 104–112, 1999.
- Y.-C. Chen, H.-S. Hsu, Y.-W. Chen et al., “Oct-4 expression maintained cancer stem-like properties in lung cancer-derived CD133-positive cells,” PLoS ONE, vol. 3, no. 7, Article ID e2637, 2008.
- C.-C. Chang, G.-S. Shieh, P. Wu, C.-C. Lin, A.-L. Shiau, and C.-L. Wu, “Oct-3/4 expression reflects tumor progression and regulates motility of bladder cancer cells,” Cancer Research, vol. 68, no. 15, pp. 6281–6291, 2008.
- N. Monsef, M. Soller, M. Isaksson, P. A. Abrahamsson, and I. Panagopoulos, “The expression of pluripotency marker oct 3/4 in prostate cancer and benign prostate hyperplasia,” Prostate, vol. 69, no. 9, pp. 909–916, 2009.
- S.-H. Chiou, C.-C. Yu, C.-Y. Huang et al., “Positive correlations of Oct-4 and Nanog in oral cancer stem-like cells and high-grade oral squamous cell carcinoma,” Clinical Cancer Research, vol. 14, no. 13, pp. 4085–4095, 2008.
- U. I. Ezeh, P. J. Turek, R. A. Reijo Pera, and A. T. Clark, “Human embryonic stem cell genes OCT4, NANOG, STELLAR, and GDF3 are expressed in both seminoma and breast carcinoma,” Cancer, vol. 104, no. 10, pp. 2255–2265, 2005.
- Z. Du, R. Qin, C. Wei et al., “Pancreatic cancer cells resistant to chemoradiotherapy rich in “stem-cell-like” tumor cells,” Digestive Diseases and Sciences, vol. 56, no. 3, pp. 741–750, 2011.
- M.-H. Tai, C.-C. Chang, L. K. Olson, and J. E. Trosko, “Oct4 expression in adult human stem cells: evidence in support of the stem cell theory of carcinogenesis,” Carcinogenesis, vol. 26, no. 2, pp. 495–502, 2005.
- M. Al-Hajj and M. F. Clarke, “Self-renewal and solid tumor stem cells,” Oncogene, vol. 23, no. 43, pp. 7274–7282, 2004.
- A. Jemal, R. Siegel, E. Ward et al., “Cancer statistics, 2006,” Ca-A Cancer Journal for Clinicians, vol. 56, no. 2, pp. 106–130, 2006.
- C.-P. Chan, H.-C. Chang, Y.-L. Chen et al., “A 10-year experience of unsuspected gallbladder cancer after laparoscopic cholecystectomy,” International Surgery, vol. 88, no. 3, pp. 175–179, 2003.
- D. L. Bartlett, Y. Fong, J. G. Fortner, M. F. Brennan, and L. H. Blumgart, “Long-term results after resection for gallbladder cancer: implications for staging and management,” Annals of Surgery, vol. 224, no. 5, pp. 639–646, 1996.
- C. Wullstein, G. Woeste, S. Barkhausen, E. Gross, and U. T. Hopt, “Do complications related to laparoscopic cholecystectomy influence the prognosis of gallbladder cancer?” Surgical Endoscopy and Other Interventional Techniques, vol. 16, no. 5, pp. 828–832, 2002.
- S. Jayaraman and W. R. Jarnagin, “Management of gallbladder cancer,” Gastroenterology Clinics of North America, vol. 39, no. 2, pp. 331–342, 2010.
- H. Yamagiwa, H. Tomiyama, and H. Yoshimura, “Histogenesis of carcinoma of gallbladder. Histological study of serial sections of 1000 cases of resected gallbladder,” Rinsho Byori, vol. 34, no. 4, pp. 475–480, 1986.
- G. P. Dowling and J. K. Kelly, “The histogenesis of adenocarcinoma of the gallbladder,” Cancer, vol. 58, no. 8, pp. 1702–1708, 1986.
- E. Leonardo, G. Valente, S. Cappia et al., “Immunohistochemical evaluation of P-glycoprotein in human malignancies by monoclonal antibody MC57,” International Journal of Cancer, vol. 57, no. 6, pp. 841–846, 1994.
- H. Khalid, A. Yasunaga, M. Kishikawa, and S. Shibata, “Immunohistochemical expression of the estrogen receptor-r elated antigen (ER-D5) in human intracranial tumors,” Cancer, vol. 75, pp. 2571–2578, 1995.
- E. Sasatomi, O. Tokunaga, and K. Miyazaki, “Precancerous conditions of gallbladder carcinoma: overview of histopathologic characteristics and molecular genetic findings,” Journal of Hepato-Biliary-Pancreatic Surgery, vol. 7, no. 6, pp. 556–567, 2000.
- I. Roa, J. C. Araya, M. Villaseca et al., “Preneoplastic lesions and gallbladder cancer: an estimate of the period required for progression,” Gastroenterology, vol. 111, no. 1, pp. 232–236, 1996.
- D. L. Bartlett, “Gallbladder cancer,” Seminars in Surgical Oncology, vol. 19, pp. 145–155, 2000.
- X. Q. Wang, W. M. Ongkeko, L. Chen et al., “Octamer 4 (Oct4) mediates chemotherapeutic drug resistance in liver cancer cells through a potential Oct4-AKT-ATP-binding cassette G2 pathway,” Hepatology, vol. 52, no. 2, pp. 528–539, 2010.
- T. Hu, S. Liu, D. R. Breiter, F. Wang, Y. Tang, and S. Sun, “Octamer 4 small interfering RNA results in cancer stem cell-like cell apoptosis,” Cancer Research, vol. 68, no. 16, pp. 6533–6540, 2008.
- T. Kawaguchi, M. Sho, T. Tojo et al., “Clinical significance of prostate stem cell antigen expression in non-small cell lung cancer,” Japanese Journal of Clinical Oncology, vol. 40, no. 4, pp. 319–326, 2010.
- D. C. Saffran, A. B. Raitano, R. S. Hubert, O. N. Witte, R. E. Reiter, and A. Jakobovits, “Anti-PSCA mAbs inhibit tumor growth and metastasis formation and prolong the survival of mice bearing human prostate cancer xenografts,” Proceedings of the National Academy of Sciences of the United States of America, vol. 98, no. 5, pp. 2658–2663, 2001.
- Z. Gu, J. Yamashiro, E. Kono, and R. E. Reiter, “Anti-prostate stem cell antigen monoclonal antibody 1G8 induces cell death in vitro and inhibits tumor growth in vivo via a Fc-independent mechanism,” Cancer Research, vol. 65, no. 20, pp. 9495–9500, 2005.
- S. Matsueda, K. Kobayashi, Y. Nonaka, M. Noguchi, K. Itoh, and M. Harada, “Identification of new prostate stem cell antigen-derived peptides immunogenic in HLA-A2+ patients with hormone-refractory prostate cancer,” Cancer Immunology, Immunotherapy, vol. 53, no. 6, pp. 479–489, 2004.
- M. D. L. L. Garcia-Hernandez, A. Gray, B. Hubby, O. J. Klinger, and W. M. Kast, “Prostate stem cell antigen vaccination induces a long-term protective immune response against prostate cancer in the absence of autoimmunity,” Cancer Research, vol. 68, no. 3, pp. 861–869, 2008.