Sphere-forming stem-like cell populations with drug resistance in human sarcoma cell lines

被引:178
作者
Fujii, Hiromasa [1 ]
Honoki, Kanya [1 ]
Tsujiuchi, Toshifumi [2 ]
Kido, Akira [1 ]
Yoshitani, Kazuhiro [1 ]
Takakura, Yoshinori [1 ]
机构
[1] Nara Med Univ, Dept Orthoped Surg, Nara 6348521, Japan
[2] Kinki Univ, Fac Sci & Technol, Dept Life Sci, Osaka 5778502, Japan
关键词
cancer stem cell; osteosarcoma; Ewing's sarcoma; fibrosarcoma; drug resistance; DNA repair; ACUTE MYELOID-LEUKEMIA; IN-VIVO; BRAIN-TUMORS; CANCER CELLS; EXPRESSION; IDENTIFICATION; NANOG; CARCINOGENESIS; PLURIPOTENCY; MARKERS;
D O I
10.3892/ijo_00000265
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The presence of cancer stem cells in both solid and hematopoietic malignancies, has been recently linked to their pathogenesis. Sarcomas are rare, and diversely characterized by degrees of mesenchymal differentiation. The aim of the current study was to demonstrate whether the human sarcoma cell lines, osteosarcoma MG63, Ewing's sarcoma HTB166, fibrosarcoma HT1080, possess the stem-like properties which may contribute to the drug-resistance. All cell lines possessed an ability to form spherical, clonal expanding colonies (sarcospheres) in anchorage-independent, serum-starved conditions. Sarcospheres showed the stem-like properties with the ability of self-renewal, and increased expression of the stem cell-related genes such as Nanog, OCT3/4 SOX2 and DNA repair enzyme genes, MLH1 and MSH2. Sarcospheres showed strong resistance to doxorubicin and cisplatin, and caffeine, a DNA repair inhibitor, enhanced the efficacy of those drugs, suggesting that the drug resistance in sarcosphere cells was partly related to the efficient DNA repair ability. These results indicate that human sarcoma cell lines contain stem-like cell populations with strong drug resistance, and DNA repair inhibitor could enhance the efficacy of chemo-drugs against sarcomas.
引用
收藏
页码:1381 / 1386
页数:6
相关论文
共 40 条
[11]   Prostate cancer cells with stem cell characteristics reconstitute the original human tumor in vivo [J].
Gu, Guangyu ;
Yuan, Jialing ;
Wils, Marcia ;
Kasper, Susan .
CANCER RESEARCH, 2007, 67 (10) :4807-4815
[12]   Cancerous stem cells can arise from pediatric brain tumors [J].
Hemmati, HD ;
Nakano, I ;
Lazareff, JA ;
Masterman-Smith, M ;
Geschwind, DH ;
Bronner-Fraser, M ;
Kornblum, HI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (25) :15178-15183
[13]  
HONOKI K, 2007, CANC STEM CELL CLUST, P9
[14]   Sox10 is required for the early development of the prospective neural crest in Xenopus embryos [J].
Honoré, SM ;
Aybar, MJ ;
Mayor, R .
DEVELOPMENTAL BIOLOGY, 2003, 260 (01) :79-96
[15]   DNA mismatch repair: Molecular mechanism, cancer, and ageing [J].
Hsieh, Peggy ;
Yamane, Kazuhiko .
MECHANISMS OF AGEING AND DEVELOPMENT, 2008, 129 (7-8) :391-407
[16]   Selective targeting of cancer stem cells - A new concept in cancer therapeutics [J].
Korkaya, Hasan ;
Wicha, Max S. .
BIODRUGS, 2007, 21 (05) :299-310
[17]   A CELL INITIATING HUMAN ACUTE MYELOID-LEUKEMIA AFTER TRANSPLANTATION INTO SCID MICE [J].
LAPIDOT, T ;
SIRARD, C ;
VORMOOR, J ;
MURDOCH, B ;
HOANG, T ;
CACERESCORTES, J ;
MINDEN, M ;
PATERSON, B ;
CALIGIURI, MA ;
DICK, JE .
NATURE, 1994, 367 (6464) :645-648
[18]   Identification of pancreatic cancer stem cells [J].
Li, Chenwei ;
Heidt, David G. ;
Dalerba, Piero ;
Burant, Charles F. ;
Zhang, Lanjing ;
Adsay, Volkan ;
Wicha, Max ;
Clarke, Michael F. ;
Simeone, Diane M. .
CANCER RESEARCH, 2007, 67 (03) :1030-1037
[19]   Mammary stem cells, self-renewal pathways, and carcinogenesis [J].
Liu, SL ;
Dontu, G ;
Wicha, MS .
BREAST CANCER RESEARCH, 2005, 7 (03) :86-95
[20]   CD133+ HCC cancer stem cells confer chemoresistance by preferential expression of the Akt/PKB survival pathway [J].
Ma, S. ;
Lee, T. K. ;
Zheng, B-J ;
Chan, K. W. ;
Guan, X-Y .
ONCOGENE, 2008, 27 (12) :1749-1758