Ovarian cancer stem-like side-population cells are tumourigenic and chemoresistant

被引:243
作者
Hu, L. [1 ]
McArthur, C. [2 ]
Jaffe, R. B. [1 ]
机构
[1] Univ Calif San Francisco, Dept Obstet Gynecol & Reprod Sci, Ctr Reprod Sci, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Med, Sandler Sorting Facil, San Francisco, CA 94143 USA
关键词
side population; ovarian cancer stem-like cells; tumourigenesis; drug resistance; ABCG2; MULTIDRUG-RESISTANCE TRANSPORTER; GENE-EXPRESSION; HOECHST-33342; IDENTIFICATION; SUBPOPULATION; PLURIPOTENCY; MITOXANTRONE; MAINTENANCE; CLONING; TUMORS;
D O I
10.1038/sj.bjc.6605626
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Ovarian cancer is the most lethal gynaecological malignancy. Although ovarian cancer patients often respond initially to chemotherapy, they usually develop chemoresistance. We hypothesised that a small portion of ovarian cancer cells have stem-like cell properties that contribute to tumourigenesis and drug resistance. METHODS: Flow cytometry and Hoechst 33342 efflux isolated side-population (SP) cells from ascites derived from ovarian cancer patients and from mice inoculated with human ovarian cancer cell lines. The SP cells were examined for stem cell markers OCT4, NANOG, STELLAR, and ABCG2/BCRP1 by immunocytochemistry and RT-PCR. The SP cells and non-SP cells were studied for tumourigenesis and chemoresistance in vitro and in vivo. RESULTS: The SP cells expressed ABCG2/BCRP1, OCT4, STELLAR, and NANOG, detected by immunocytochemistry and RT-PCR. ABCG2/BCRP1 expression was higher in SP than in non-SP cells. Xenogeneic mice inoculated with SP cells yielded more tumours than did mice inoculated with non-SP cells. In parallel, SP cell culture resulted in extensive cell proliferation, which was markedly more than in non-SP cells. SP cells resisted chemotherapy compared with non-SP cells, both in vivo and in vitro. CONCLUSION: Ovarian cancer SP cells are tumourigenic and chemoresistant. ABCG2/BCRP1 has an important role in chemoresistance, which has implications for new therapeutic approaches. British Journal of Cancer (2010) 102, 1276-1283. doi: 10.1038/sj.bjc.6605626 www.bjcancer.com Published online 30 March 2010 (C) 2010 Cancer Research UK
引用
收藏
页码:1276 / 1283
页数:8
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