Expression of Lgr5, a marker of intestinal stem cells, in colorectal cancer and its clinicopathological significance

被引:52
作者
He, Songbing [1 ,2 ,3 ]
Zhou, Hao [2 ]
Zhu, Xinguo [2 ]
Hu, Shuiqing [4 ]
Fei, Min [5 ]
Wan, Daiwei [6 ]
Gu, Wen [2 ]
Yang, Xiaodong [7 ]
Shi, Dongtao [8 ]
Zhou, Jian [2 ]
Zhou, Jin [2 ]
Zhu, Zheng [9 ]
Wang, Liang [2 ]
Li, Dechun [2 ]
Zhang, Yanyun [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Shanghai Inst Immunol, Shanghai 200025, Peoples R China
[2] Soochow Univ, Affiliated Hosp 1, Dept Gen Surg, Suzhou 215006, Peoples R China
[3] Washington Univ, Sch Med, St Louis, MO 63110 USA
[4] Shanghai Jiao Tong Univ, Sch Med, Peoples Hosp 9, Dept Clin Labs, Shanghai 200011, Peoples R China
[5] Soochow Univ, Affiliated Hosp 1, Jiangsu Inst Hematol, Suzhou 215006, Peoples R China
[6] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Gen Surg, Guangzhou 510000, Guangdong, Peoples R China
[7] Soochow Univ, Affiliated Hosp 2, Dept Gen Surg, Suzhou 215006, Peoples R China
[8] Soochow Univ, Affiliated Hosp 1, Dept Gastroenterol, Suzhou 215500, Peoples R China
[9] Jiangsu Shengze Hosp, Dept Gen Surg, Suzhou 215228, Peoples R China
基金
中国博士后科学基金;
关键词
Colorectal cancer; Lgr5; Cancer stem cells; beta-catenin; Prognosis; IN-VITRO; COLON; DIFFERENTIATION; ADENOCARCINOMA; PROLIFERATION; TUMORIGENESIS; SIGNATURE;
D O I
10.1016/j.biopha.2014.03.016
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Cancer stem cells (CSCs) have been the focus of intense investigations in cancer research although the cellular origin of CSCs has not been clearly determined. Lgr5 is a regulated target of Wnt/beta-catenin signaling, which was first identified as a marker of intestinal stem cells. However, the expression of Lgr5 in human colorectal cancer (CRC) and its clinical clinicopathological significance in CRC patients as well as its correlation with Wnt/beta-catenin pathway are not fully explored. Localization and expression of Lgr5 in CRC tissues was performed by immunohistochemical staining. The correlation between its expression levels and clinicopathological features as well as clinical outcomes of patients was analysed. The quantitative expression levels of Lgr5 in various CRC cell lines were determined using real-time RT-PCR. The relationship between Lgr5 expression and Wnt/beta-catenin pathway in CRC was also investigated. Obviously elevated expression of Lgr5 was observed in CRC tissues, compared to the paired nontumor tissues. mRNA expression levels of Lgr5 was positively correlated with the expression of beta-catenin in CRC tissues. The expression of Lgr5 was various in different CRC cell lines. Low and high expression levels of Lgr5 were significantly correlated with clinicopathological features such as TNM stage, lymph node metastasis and vascular invasion of CRC patients. More importantly, Lgr5 expression in CRC tissues was also associated with tumor angiogenesis as well as clinical outcomes. Taken together, these results suggest that elevated Lgr5 expression might contribute to the development and progression of CRC, and it could also be used a potential unfavorable prognostic biomarker for CRC. A better understanding of molecule mechanisms and the relevance of potential value for Lgr5 in the progression of CRC will help to identify a novel therapeutic strategy for CRC patients. (C) 2014 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:507 / 513
页数:7
相关论文
共 35 条
[1]  
Aoki Daisuke, 2005, Hum Cell, V18, P143
[2]   Identification of stem cells in small intestine and colon by marker gene Lgr5 [J].
Barker, Nick ;
van Es, Johan H. ;
Kuipers, Jeroen ;
Kujala, Pekka ;
van den Born, Maaike ;
Cozijnsen, Miranda ;
Haegebarth, Andrea ;
Korving, Jeroen ;
Begthel, Harry ;
Peters, Peter J. ;
Clevers, Hans .
NATURE, 2007, 449 (7165) :1003-U1
[3]   Crypt stem cells as the cells-of-origin of intestinal cancer [J].
Barker, Nick ;
Ridgway, Rachel A. ;
van Es, Johan H. ;
van de Wetering, Marc ;
Begthel, Harry ;
van den Born, Maaike ;
Danenberg, Esther ;
Clarke, Alan R. ;
Sansom, Owen J. ;
Clevers, Hans .
NATURE, 2009, 457 (7229) :608-U119
[4]   Lgr5, an intestinal stem cell marker, is abnormally expressed in Barrett's esophagus and esophageal adenocarcinoma [J].
Becker, L. ;
Huang, Q. ;
Mashimo, H. .
DISEASES OF THE ESOPHAGUS, 2010, 23 (02) :168-174
[5]  
Brenner H, 2013, LANCET, P61649
[6]   A microRNA miR-34a-Regulated Bimodal Switch Targets Notch in Colon Cancer Stem Cells [J].
Bu, Pengcheng ;
Chen, Kai-Yuan ;
Chen, Joyce Huan ;
Wang, Lihua ;
Walters, Jewell ;
Shin, Yong Jun ;
Goerger, Julian P. ;
Sun, Jian ;
Witherspoon, Mavee ;
Rakhilin, Nikolai ;
Li, Jiahe ;
Yang, Herman ;
Milsom, Jeff ;
Lee, Sang ;
Zipfel, Warren ;
Jin, Moonsoo M. ;
Guemues, Zeynep H. ;
Lipkin, Steven M. ;
Shen, Xiling .
CELL STEM CELL, 2013, 12 (05) :602-615
[7]   LGR5 Interacts and Cointernalizes with Wnt Receptors To Modulate Wnt/β-Catenin Signaling [J].
Carmon, Kendra S. ;
Lin, Qiushi ;
Gong, Xing ;
Thomas, Anthony ;
Liu, Qingyun .
MOLECULAR AND CELLULAR BIOLOGY, 2012, 32 (11) :2054-2064
[8]   TUMORIGENESIS Testing ground for cancer stem cells [J].
Delude, Cathryn .
NATURE, 2011, 480 (7377) :S43-S45
[9]   LGR5 deficiency deregulates Wnt signaling and leads to precocious Paneth cell differentiation in the fetal intestine [J].
Garcia, Marie Isabelle ;
Ghiani, Mariangela ;
Lefort, Anne ;
Libert, Frederick ;
Strollo, Sandra ;
Vassart, Gilbert .
DEVELOPMENTAL BIOLOGY, 2009, 331 (01) :58-67
[10]   Ambra1 Is an Essential Regulator of Autophagy and Apoptosis in SW620 Cells: Pro-Survival Role of Ambra1 [J].
Gu, Wen ;
Wan, Daiwei ;
Qian, Qinyi ;
Yi, Bin ;
He, Zhilong ;
Gu, Yilin ;
Wang, Liang ;
He, Songbing .
PLOS ONE, 2014, 9 (02)