Please use this identifier to cite or link to this item: https://doi.org/10.1158/0008-5472.CAN-13-2309
Title: CD44v8-10 Is a Cancer-Specific Marker for Gastric Cancer Stem Cells
Authors: Lau, Wen Min 
Teng, Eileen 
Chong, Hui Shan
Lopez, Kirsten Anne Pagaduan 
Tay, Amy Yuh Ling 
Salto-Tellez, Manuel 
Shabbir, Asim 
So, Jimmy Bok Yan 
Chan, Shing Leng 
Keywords: Science & Technology
Life Sciences & Biomedicine
Oncology
CD44 VARIANT PROTEINS
DE-NOVO EXPRESSION
ADHESION MOLECULE
SIDE POPULATION
TUMOR-GROWTH
ADENOCARCINOMA
CARCINOMA
IDENTIFICATION
TUMORIGENESIS
GLYCOPROTEIN
Issue Date: 1-May-2014
Publisher: AMER ASSOC CANCER RESEARCH
Citation: Lau, Wen Min, Teng, Eileen, Chong, Hui Shan, Lopez, Kirsten Anne Pagaduan, Tay, Amy Yuh Ling, Salto-Tellez, Manuel, Shabbir, Asim, So, Jimmy Bok Yan, Chan, Shing Leng (2014-05-01). CD44v8-10 Is a Cancer-Specific Marker for Gastric Cancer Stem Cells. CANCER RESEARCH 74 (9) : 2630-2641. ScholarBank@NUS Repository. https://doi.org/10.1158/0008-5472.CAN-13-2309
Abstract: 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. © 2014 AACR.
Source Title: CANCER RESEARCH
URI: https://scholarbank.nus.edu.sg/handle/10635/155006
ISSN: 0008-5472
1538-7445
DOI: 10.1158/0008-5472.CAN-13-2309
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