Formation of Solid Tumors by a Single Multinucleated Cancer Cell

被引:111
作者
Zhang Weihua [1 ]
Lin, Qingtang [2 ]
Ramoth, Asa J. [1 ]
Fan, Dominic [2 ]
Fidler, Isaiah J. [2 ]
机构
[1] Univ Houston, Coll Nat Sci & Math, Dept Biol & Biochem, Ctr Nucl Receptors & Cell Signaling, Houston, TX 77204 USA
[2] Univ Texas MD Anderson Canc Ctr, Canc Metastasis Res Ctr, Dept Canc Biol, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
multinucleated cells; senescent-like cancer cells; cancer-initiating cells; GIANT-CELL; STEM-CELL; IN-VIVO; CARCINOMA; ADENOCARCINOMA; IDENTIFICATION; SPECIMENS; STRAINS; VARIANT; FUSION;
D O I
10.1002/cncr.26021
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Large multinucleated cells (MNCs) commonly exist in tumorigenic cancer cell lines that are used widely in research. However, the contributions of MNCs to tumorigenesis are unknown. METHODS: In this study, MNCs were characterized in the murine fibrosarcoma cell line UV-2237 in vitro and in vivo at the single-cell level. RESULTS: The authors observed that MNCs originated from a rare subpopulation of mononuclear cells and were positive for a senescent marker, b-galactosidase. In addition, MNCs were responsible for the majority of clonogenic activity when cultured in hard agar; they were more resistant to chemotherapeutic agents than mononuclear cells; they could undergo asymmetric division (producing mononuclear cells) and self-renewal in vitro and in vivo; and, most important; a single MNC produced orthotopic, subcutaneous tumors (composed mainly of mononuclear cells) that gave rise to spontaneous lung metastases in nude mice. CONCLUSIONS: The current results indicated that the growth of MNCs may be arrested under stress and that MNCs are highly resistant to chemotherapy and can generate clonal, orthotopic, metastatic tumors. Cancer 2011;117:4092-9. (C) 2011 American Cancer Society.
引用
收藏
页码:4092 / 4099
页数:8
相关论文
共 31 条
[11]   PULMONARY BLASTOMA - AN ULTRASTRUCTURAL AND HISTOCHEMICAL-STUDY [J].
JACKSON, MD ;
ALBRECHT, R ;
ROGGLI, VL ;
SHELBURNE, JD .
ULTRASTRUCTURAL PATHOLOGY, 1984, 7 (04) :259-268
[12]   ENDOMETRIAL ADENOCARCINOMA WITH A COMPONENT OF GIANT-CELL CARCINOMA [J].
JONES, MA ;
YOUNG, RH ;
SCULLY, RE .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL PATHOLOGY, 1991, 10 (03) :260-270
[13]   Multinucleated epithelial giant cells in colorectal polyps - A potential mimic of viropathic and/or dysplastic changes [J].
Kambham, N ;
Troxell, M ;
Longacre, TA .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2005, 29 (07) :912-919
[14]  
KAWANO H, 1995, CLIN NEUROPATHOL, V14, P118
[15]  
KRIPKE ML, 1977, CANCER RES, V37, P1395
[16]   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
[17]   CORRELATION OF GROWTH CAPACITY OF HUMAN-TUMOR CELLS IN HARD AGAROSE WITH THEIR INVIVO PROLIFERATIVE CAPACITY AT SPECIFIC METASTATIC SITES [J].
LI, LM ;
PRICE, JE ;
FAN, D ;
ZHANG, RD ;
BUCANA, CD ;
FIDLER, IJ .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1989, 81 (18) :1406-1412
[18]   Isolation and identification of mesenchymal stem cells from human lipoma tissue [J].
Lin, Tsai-Ming ;
Chang, Hsueh-Wei ;
Wang, Kai-Hung ;
Kao, An-Pei ;
Chang, Chia-Cheng ;
Wen, Cheng-Hao ;
Lai, Chung-Sheng ;
Lin, Sin-Daw .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2007, 361 (04) :883-889
[19]  
Moore JG, 1998, DIAGN CYTOPATHOL, V19, P44, DOI 10.1002/(SICI)1097-0339(199807)19:1<44::AID-DC9>3.0.CO
[20]  
2-O