CD44v8-10 Is a Cancer-Specific Marker for Gastric Cancer Stem Cells

被引:175
作者
Lau, Wen Min [1 ]
Teng, Eileen [1 ]
Chong, Hui Shan [1 ]
Lopez, Kirsten Anne Pagaduan [1 ]
Tay, Amy Yuh Ling [2 ]
Salto-Tellez, Manuel [1 ,3 ]
Shabbir, Asim [2 ]
So, Jimmy Bok Yan [2 ]
Chan, Shing Leng [1 ]
机构
[1] Natl Univ Singapore, Canc Sci Inst Singapore, Singapore 117548, Singapore
[2] Natl Univ Singapore, Dept Surg, Singapore 117548, Singapore
[3] Queens Univ Belfast, Ctr Canc Res & Cell Biol, Belfast, Antrim, North Ireland
基金
新加坡国家研究基金会;
关键词
CD44 VARIANT PROTEINS; DE-NOVO EXPRESSION; ADHESION MOLECULE; SIDE POPULATION; TUMOR-GROWTH; ADENOCARCINOMA; CARCINOMA; IDENTIFICATION; TUMORIGENESIS; GLYCOPROTEIN;
D O I
10.1158/0008-5472.CAN-13-2309
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The surface marker CD44 has been identified as one of several markers associated with cancer stem cells (CSC) in solid tumors, but its ubiquitous expression in many cell types, including hematopoietic cells, has hindered its use in targeting CSCs. In this study, 28 paired primary tumor and adjacent nontumor gastric tissue samples were analyzed for cell surface protein expression. Cells that expressed pan-CD44 were found to occur at significantly higher frequency in gastric tumor tissues. We identified CD44v8-10 as the predominant CD44 variant expressed in gastric cancer cells and verified its role as a gastric CSC marker by limiting dilution and serial transplantation assays. Parallel experiments using CD133 failed to enrich for gastric CSCs. Analyses of another 26 primary samples showed significant CD44v8-10 upregulation in gastric tumor sites. Exogenous expression of CD44v8-10 but not CD44 standard (CD44s) increased the frequency of tumor initiation in immunocompromised mice. Reciprocal silencing of total CD44 resulted in reduced tumor-initiating potential of gastric cancer cells that could be rescued by CD44v8-10 but not CD44s expression. Our findings provide important functional evidence that CD44v8-10 marks human gastric CSCs and contributes to tumor initiation, possibly through enhancing oxidative stress defense. In addition, we showed that CD44v8-10 expression is low in normal tissues. Because CD44 also marks CSCs of numerous human cancers, many of which may also overexpress CD44v8-10, CD44v8-10 may provide an avenue to target CSCs in other human cancers. (C) 2014 AACR.
引用
收藏
页码:2630 / 2641
页数:12
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