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The expression and clinical significance of β-catenin and colorectal cancer stem cells marker EpCAM^(high)/CD44^+ in colorectal cancer

β-catenin与大肠癌干细胞标记物EpCAM^(high)/CD44^+在大肠癌中的表达及临床意义(英文)
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摘要 Objective: The aim of the study was to explore the role of Wnt βcatenin signalling pathway in the maintenance, invasion and metastasis of colorectal cancer stem cells. Methods: Double immunohistochemical staining was used to detect the expression of EpCAMhigh/CD44~ which is regarded as the marker of colorectal cancer stem cells in 80 cases of colorectal cancer and their corresponding liver metastases. The SP method of immunohistochemistry was used to detect the expression of the key protein βcatenin in the Wnt pathway in these tissue. The expression and correlation of ^-catenin and EpCAMh^gh/ CD44+ in colorectal cancer were analyzed and their role on the biological behavior of colorectal cancer was explored. Results: The abnormal expression of βcatenin was significantly higher in colorectal cancer than in the paraneoplastic normal intes- tinal mucosa [55% (44/80) vs 10% (2/20), P 〈 0.05]. The positive expression of EpCAMhigh/CD44+ was significantly higher in colorectal cancer than in the paraneoplastic normal intestinal mucosa [66.25% (53/80) vs 0% (0/20), P 〈 0.05]. In the 80 cases of colorectal cancer, the abnormal expression of ^-catenin has no correlation with gender (P = 0.079), age (P = 0.416) and the magnitude (P = 0.816) of the tumor (P 〉 0.05), but it was significantly correlated with degree of differentiation (P = 0.001), depth of invasion (P = 0.001), clinical stage (P = 0.000) and metastasis (P = 0.000). In the colorectal cancer, the expression of EpCAMhi^h/CD44~ cells has no correlation with gender (P = 0.934) and the magnitude (P = 0.160) of the tumor (P 〉 0.05), but was significantly correlated with age (P = 0.021), degree of differentiation (P = 0.013), depth of invasion (P = 0.000), clinical stage (P = 0.000) and metastasis (P = 0.000). In the corresponding liver metastases, we could also detecte EpCAMhih/CD44+ cells. In cases with abnormal expression of βcatenin, the positive expression rate of EpCAMhigh/CD44+ was significantly higher than those with normal expression of β-catenin (84.1% vs 44.4%), and the difference was statistically significant (P 〈 0.05). Conclusion: The abnormal activation of Wnt β-catenin signalling pathway may prompt the abnormal proliferation of the colorectal cancer stem cells, which leads to the recurrence and metastasis of the cancer.
出处 《The Chinese-German Journal of Clinical Oncology》 CAS 2013年第12期581-585,共5页 中德临床肿瘤学杂志(英文版)
关键词 cancer stem cells double immunohistochemical staining βcatenin EpCAMhigh/CD44* 临床意义 大肠癌 干细胞 蛋白 标志物 免疫组织化学 免疫组化SP法 信号通路
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参考文献15

  • 1Shi H, Li S J, Zhang B, et al. Expression of MSP58 in human colorec- tal cancer and its correlation with prognosis. Med Oncol, 2012, 29: 3136-42.
  • 2Wu XZ. Origin of cancer stem cells: the role of self-renewal and dif- ferentiation. Ann Surg Oncol, 2008, 15: 407-414.
  • 3Li Z, Liu CP, He YL, et al. The expression and significance of multi- drug resistance genes in breast cancer stem cells. Chinese-German J Clin Oncol. 2008.7: 538-541.
  • 4Yang YM, Chang JW. Current status and issues in cancer stem cell study. Cancer Invest, 2008, 26: 741-755.
  • 5Kanwar SS, Yu Y, Nautiyal J, et al. The Wnt/β-catenin pathway regu- lates growth and maintenance of colono spheres. Mol Cancer, 2010, 9: 212.
  • 6Nodin B, Johannesson H, Wangefjord S, et al. Molecular correlates and prognostic significance of SATB1 expression in colorectal cancer. Diagn Pathol, 2012, 7: 115.
  • 7A1-Hajj M, Wicha M S, Benito-HernandezA, et al. Prospective identi- fication of tumorigenic breast cancer cells. Proc Natl Acad Sci U S A, 2003, 100: 3983-3988.
  • 8Khramtsov AI, Khramtsova GF, Tretiakova M, et al. Wnt/beta-catenin pathway activation is enriched in basal-like breast cancers and pre- dicts poor outcome. Am J Pathol, 2010, 176: 2911-2920.
  • 9Wang L, Cheng H, Liu Y, et al. Prognostic value of nuclear β-catenin overexpression at invasive front in colorectal cancer for synchronous liver metastasis. Ann Surg Oncol, 2011, 18: 1553-1559.
  • 10Dylla S J, Beviglia L, Park IK, et al. Colorectal cancer stem cells are enriched in xenogeneic tumors following chemotherapy. PLoS One, 2008, 3: e2428.

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