Identification of cancer stem cell markers in human malignant mesothelioma cells

被引:65
作者
Ghani, Farhana Ishrat [1 ]
Yamazaki, Hiroto [1 ]
Iwata, Satoshi [1 ]
Okamoto, Toshihiro [1 ]
Aoe, Keisuke [2 ]
Okabe, Kazunori [2 ]
Mimura, Yusuke [2 ]
Fujimoto, Nobukazu [3 ]
Kishimoto, Takumi [3 ]
Yamada, Taketo [4 ]
Xu, C. Wilson [5 ]
Morimoto, Chikao [1 ,5 ]
机构
[1] Univ Tokyo, Inst Med Sci, Div Clin Immunol, Tokyo, Japan
[2] Yamaguchi Ube Med Ctr, Dept Med Oncol, Yamaguchi, Japan
[3] Okayama Rosai Hosp, Dept Resp Med, Okayama, Japan
[4] Keio Univ, Sch Med, Dept Pathol, Tokyo 160, Japan
[5] Nevada Canc Inst, Drug Dev Program, Las Vegas, NV USA
关键词
Side population; CD9; CD24; CD26; Cancer stem cells; Malignant mesothelioma; ANTI-CD26; MONOCLONAL-ANTIBODY; SIDE-POPULATION; DOWN-REGULATION; IN-VITRO; CD9; EXPRESSION; LEUKEMIA; TUMORS; SUBPOPULATION; ARREST;
D O I
10.1016/j.bbrc.2010.12.054
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Malignant mesothelioma (MM) is an aggressive and therapy-resistant neoplasm arising from the pleural mesothelial cells and usually associated with long-term asbestos exposure. Recent studies suggest that tumors contain cancer stem cells (CSCs) and their stem cell characteristics are thought to confer therapy-resistance. However, whether MM cell has any stem cell characteristics is not known. To understand the molecular basis of MM, we first performed serial transplantation of surgical samples into NOD/SCID mice and established new cell lines. Next, we performed marker analysis of the MM cell lines and found that many of them contain SP cells and expressed several putative CSC markers such as CD9, CD24, and CD26. Interestingly, expression of CD26 closely correlated with that of CD24 in some cases. Sorting and culture assay revealed that SP and CD24(+) cells proliferated by asymmetric cell division-like manner. In addition, CD9(+) and CD24(+) cells have higher potential to generate spheroid colony than negative cells in the stem cell medium. Moreover, these marker-positive cells have clear tendency to generate larger tumors in mouse transplantation assay. Taken together, our data suggest that SP, CD9, CD24, and CD26 are CSC markers of MM and could be used as novel therapeutic targets. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:735 / 742
页数:8
相关论文
共 31 条
[1]   Infrequent existence of simian virus 40 large T antigen DNA in malignant mesothelioma in Japan [J].
Aoe, K ;
Hiraki, A ;
Murakami, T ;
Toyooka, S ;
Shivapurkar, N ;
Gazdar, AF ;
Sueoka, N ;
Taguchi, K ;
Kamei, T ;
Takeyama, H ;
Sugi, K ;
Kishimoto, T .
CANCER SCIENCE, 2006, 97 (04) :292-295
[2]   THE EXPRESSION OF CD26 AND CD40 LIGAND IS MUTUALLY EXCLUSIVE IN HUMAN T-CELL NON-HODGKINS-LYMPHOMAS LEUKEMIAS [J].
CARBONE, A ;
GLOGHINI, A ;
ZAGONEL, V ;
ALDINUCCI, D ;
GATTEI, V ;
DEGAN, M ;
IMPROTA, S ;
SORIO, R ;
MONFARDINI, S ;
PINTO, A .
BLOOD, 1995, 86 (12) :4617-4626
[3]  
Corson Joseph M, 2004, Thorac Surg Clin, V14, P447
[4]   The therapeutic promise of the cancer stem cell concept [J].
Frank, Natasha Y. ;
Schatton, Tobias ;
Frank, Markus H. .
JOURNAL OF CLINICAL INVESTIGATION, 2010, 120 (01) :41-50
[5]   Down-regulation of CD9 in human ovarian carcinoma cell might contribute to peritoneal dissemination:: Morphologic alteration and reduced expression of β1 integrin subsets [J].
Furuya, M ;
Kato, F ;
Nishimura, N ;
Ishiwata, I ;
Ikeda, H ;
Ito, R ;
Yoshiki, T ;
Ishikura, H .
CANCER RESEARCH, 2005, 65 (07) :2617-2625
[6]   CD24+ cells from hierarchically organized ovarian cancer are enriched in cancer stem cells [J].
Gao, M-Q ;
Choi, Y-P ;
Kang, S. ;
Youn, J. H. ;
Cho, N-H .
ONCOGENE, 2010, 29 (18) :2672-2680
[7]  
Ho L, 2001, CLIN CANCER RES, V7, P2031
[8]   Side population in human lung cancer cell lines and tumors is enriched with stem-like cancer cells [J].
Ho, Maria M. ;
Ng, Alvin V. ;
Lam, Stephen ;
Hung, Jaclyn Y. .
CANCER RESEARCH, 2007, 67 (10) :4827-4833
[9]   Humanized anti-CD26 monoclonal antibody as a treatment for malignant mesothelioma tumors [J].
Inamoto, Teruo ;
Yamada, Taketo ;
Ohnuma, Kei ;
Kina, Shinichiro ;
Takahashi, Nozomu ;
Yamochi, Tadanori ;
Inamoto, Sakiko ;
Katsuoka, Yoji ;
Hosono, Osamu ;
Tanaka, Hirotoshi ;
Dang, Nam H. ;
Morimoto, Chikao .
CLINICAL CANCER RESEARCH, 2007, 13 (14) :4191-4200
[10]   Anti-CD26 monoclonal antibody-mediated G1-S arrest of human renal clear cell carcinoma Caki-2 is associated with retinoblastoma substrate dephosphorylation, cyclin-dependent kinase 2 reduction, p27kip1 enhancement, and disruption of binding to the extracellular matrix [J].
Inamoto, Teruo ;
Yamochi, Tadanori ;
Ohnuma, Kei ;
Iwata, Satoshi ;
Kina, Shinichiro ;
Inamoto, Sakiko ;
Tachibana, Masaaki ;
Katsuoka, Yoji ;
Dang, Nam H. ;
Morimoto, Chikao .
CLINICAL CANCER RESEARCH, 2006, 12 (11) :3470-3477