CD133 Expression and the Prognosis of Colorectal Cancer: A Systematic Review and Meta-Analysis

被引:98
作者
Chen, Shicai [1 ]
Song, Xinming [2 ]
Chen, Zhihui [2 ]
Li, Xinxin [2 ]
Li, Mingzhe [2 ]
Liu, Haiying [1 ]
Li, Jianchang [1 ]
机构
[1] Guangzhou Med Univ, Affiliated Tumor Hosp, Dept Gastrointestinal Tumor Surg, Guangzhou, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Gastrointestinal & Pancreat Surg, Guangzhou 510275, Guangdong, Peoples R China
关键词
CELL MARKERS CD133; STEM-LIKE CELLS; DUKES STAGE B; RECTAL-CANCER; COLON-CANCER; PREOPERATIVE CHEMORADIOTHERAPY; CLINICAL-SIGNIFICANCE; HEMATOPOIETIC STEM; PANCREATIC-CANCER; TUMOR-REGRESSION;
D O I
10.1371/journal.pone.0056380
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Objective: CD133 has recently been reported as a marker of cancer stem-like cells in colorectal cancer (CRC). However, its predictive value in CRC still remains controversial. In this study, we aimed to evaluate the association between the expression of CD133 and clinicopathological features and the outcome of CRC patients by performing a meta-analysis. Methods: A comprehensive literature search for relevant studies published up to December 2012 was performed using PubMed, MEDLINE and ISI Web of Science. Only articles in which CD133 antigen was detected in situ localisation by immunohistochemical staining were included. This meta-analysis was done using RevMan 4.2 software. Results: We found that a total of 15 studies involving 810 CD133-high and 1487 CD133-low patients met the inclusion criteria for the analysis of 5-year overall survival (OS) rate. In a random-effects model, the results showed that CD133-high expression in colorectal cancer was an independent prognostic marker correlating with both OS rate (RR = 0.67, 95% CI 0.54-0.82, P<0.01) and disease free survival (DFS) rate (RR = 0.71, 95% CI 0.52-0.96, P = 0.03). CD133-high expression was also associated with more T3,4 tumor invasion, N positive and vascular invasion cases, corresponding to a risk difference of 1.12 (95% CI 1.01-1.23, P = 0.03), 1.31 (95% CI 1.06-1.63, P = 0.01) and 1.24 (95% CI 1.08-1.41, P<0.01), respectively. However, when types of histology, lymphatic invasion and distant metastasis were considered, CD133 overexpression was not significantly related with these clinicopathological parameters. Conclusion: Our meta-analysis results suggest that CD133 is an efficient prognostic factor in CRC. Higher CD133 expression is significantly associated with poorer clinical outcome and some clinicopathological factors such as T category, N category and vascular invasion in CRC patients.
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页数:9
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