Prognostic impact of CD44-positive cancer stem-like cells at the invasive front of gastric cancer

被引:59
作者
Kodama, Hirokazu [1 ]
Murata, Satoshi [1 ]
Ishida, Mitsuaki [2 ,3 ]
Yamamoto, Hiroshi [1 ]
Yamaguchi, Tsuyoshi [1 ]
Kaida, Sachiko [1 ]
Miyake, Tohru [1 ]
Takebayashi, Katsushi [1 ]
Kushima, Ryoji [2 ]
Tani, Masaji [1 ]
机构
[1] Shiga Univ Med Sci, Dept Surg, Otsu, Shiga, Japan
[2] Shiga Univ Med Sci, Div Diagnost Pathol, Dept Clin Lab Med, Otsu, Shiga, Japan
[3] Kansai Med Univ, Div Diagnost Pathol, Osaka, Japan
关键词
CD44; cancer stem cells; prognosis; gastrectomy; recurrence; survival; EPITHELIAL-MESENCHYMAL TRANSITION; LYMPH-NODE METASTASIS; PROSPECTIVE IDENTIFICATION; CD44; EXPRESSION; TUMOR; MARKERS; GASTRECTOMY; MMP-7; CD133;
D O I
10.1038/bjc.2016.401
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The invasive tumour front may provide prognostic information. We examined the relationship between the presence of cancer stem cells (CSCs) at the invasive tumour front and prognosis in gastric cancer (GC). Methods: CD44 is a CSC marker; accordingly, CD44 standard (CD44s), CD44 variant-6 (CD44v6), and CD44 variant-9 (CD44v9) expression were examined in 123 resected primary GCs and the clinical significance of CSCs at the invasive tumour front was analysed. Results: Thirteen (10.6%), 79 (64.2%), and 47 (38.2%) GCs were CD44s-, CD44v6-, and CD44v9-positive, respectively. Patients with CD44-positive expression at the invasive tumour front had significantly poorer disease-specific survival than those with negative expression (CD44s: P < 0.00001, CD44v6: P = 0.013, CD44v9: P = 0.0002). CD44s expression at the invasive tumour front was an independent prognostic factor in resectable GC patients (hazard ratio = 3.13; 95% confidence interval, 1.09-9.01; P = 0.035) and was significantly associated with peritoneal (P < 0.001), lymphatic (P < 0.001), and haematogenous recurrences (P < 0.008). In addition, the number of CD44 isoforms expressed in cancer cells at the invasive tumour front was associated with patient prognosis. No conventional clinicopathological factors were independently associated with CD44 expression at the invasive tumour front. Conclusions: CD44-positive cancer stem-like cells at the invasive tumour front indicate poor survival and can be a unique biological prognostic factor for GC.
引用
收藏
页码:186 / 194
页数:9
相关论文
共 35 条
[1]   Prospective identification of tumorigenic breast cancer cells [J].
Al-Hajj, M ;
Wicha, MS ;
Benito-Hernandez, A ;
Morrison, SJ ;
Clarke, MF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (07) :3983-3988
[2]   Prognostic and predictive factors in oral cancer:: the role of the invasive tumour front [J].
Bànkfalvi, A ;
Piffkò, J .
JOURNAL OF ORAL PATHOLOGY & MEDICINE, 2000, 29 (07) :291-298
[3]   CD44 splice isoform switching in human and mouse epithelium is essential for epithelial-mesenchymal transition and breast cancer progression [J].
Brown, Rhonda L. ;
Reinke, Lauren M. ;
Damerow, Mann S. ;
Perez, Denise ;
Chodosh, Lewis A. ;
Yang, Jing ;
Cheng, Chonghui .
JOURNAL OF CLINICAL INVESTIGATION, 2011, 121 (03) :1064-1074
[4]   CD44 but not CD24 expression is related to poor prognosis in non-cardia adenocarcinoma of the stomach [J].
Cao, Xueyuan ;
Cao, Donghui ;
Jin, MeiShan ;
Jia, Zhifang ;
Kong, Fei ;
Ma, Hongxi ;
Wang, Yinping ;
Jiang, Jing .
BMC GASTROENTEROLOGY, 2014, 14
[5]   Prospective identification of tumorigenic prostate cancer stem cells [J].
Collins, AT ;
Berry, PA ;
Hyde, C ;
Stower, MJ ;
Maitland, NJ .
CANCER RESEARCH, 2005, 65 (23) :10946-10951
[6]   Phenotypic characterization of human colorectal cancer stem cells [J].
Dalerba, Piero ;
Dylla, Scott J. ;
Park, In-Kyung ;
Liu, Rui ;
Wang, Xinhao ;
Cho, Robert W. ;
Hoey, Timothy ;
Gurney, Austin ;
Huang, Emina H. ;
Simeone, Diane M. ;
Shelton, Andrew A. ;
Parmiani, Giorgio ;
Castelli, Chiara ;
Clarke, Michael F. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (24) :10158-10163
[7]   Prognostic role of CD10+ myeloid cells in association with tumor budding at the invasion front of colorectal cancer [J].
Do Trong Khanh ;
Mekata, Eiji ;
Mukaisho, Ken-ichi ;
Sugihara, Hiroyuki ;
Shimizu, Tomoharu ;
Shiomi, Hisanori ;
Murata, Satoshi ;
Naka, Shigeyuki ;
Yamamoto, Hiroshi ;
Endo, Yoshihiro ;
Tani, Tohru .
CANCER SCIENCE, 2011, 102 (09) :1724-1733
[8]  
Ishigami S, 2010, ANTICANCER RES, V30, P2453
[9]   CD44 Variant Regulates Redox Status in Cancer Cells by Stabilizing the xCT Subunit of System xc- and Thereby Promotes Tumor Growth [J].
Ishimoto, Takatsugu ;
Nagano, Osamu ;
Yae, Toshifumi ;
Tamada, Mayumi ;
Motohara, Takeshi ;
Oshima, Hiroko ;
Oshima, Masanobu ;
Ikeda, Tatsuya ;
Asaba, Rika ;
Yagi, Hideki ;
Masuko, Takashi ;
Shimizu, Takatsune ;
Ishikawa, Tomoki ;
Kai, Kazuharu ;
Takahashi, Eri ;
Imamura, Yu ;
Baba, Yoshifumi ;
Ohmura, Mitsuyo ;
Suematsu, Makoto ;
Baba, Hideo ;
Saya, Hideyuki .
CANCER CELL, 2011, 19 (03) :387-400
[10]   CD44+ slow-cycling tumor cell expansion is triggered by cooperative actions of Wnt and prostaglandin E2 in gastric tumorigenesis [J].
Ishimoto, Takatsugu ;
Oshima, Hiroko ;
Oshima, Masanobu ;
Kai, Kazuharu ;
Torii, Ryota ;
Masuko, Takashi ;
Baba, Hideo ;
Saya, Hideyuki ;
Nagano, Osamu .
CANCER SCIENCE, 2010, 101 (03) :673-678