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
[1]   Anaplastic variant of spermatocytic seminoma [J].
AlboresSaavedra, J ;
Huffman, H ;
AlvaradoCabrero, I ;
Avala, AG .
HUMAN PATHOLOGY, 1996, 27 (07) :650-655
[2]   Multinucleation followed by an acytokinetic cell division in myxofibrosarcoma with giant cell proliferation [J].
Ariizumi, Takashi ;
Ogose, Akira ;
Kawashima, Hiroyuki ;
Hotta, Tetsuo ;
Umezu, Hajime ;
Endo, Naoto .
JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH, 2009, 28
[3]   Cancer stem cell and cancer stemloids [J].
Blagosklonny, Mikhail V. .
CANCER BIOLOGY & THERAPY, 2007, 6 (11) :1684-1690
[4]   Therapeutic Implications of the Cancer Stem Cell Hypothesis [J].
Diehn, Maximilian ;
Cho, Robert W. ;
Clarke, Michael F. .
SEMINARS IN RADIATION ONCOLOGY, 2009, 19 (02) :78-86
[5]   A BIOMARKER THAT IDENTIFIES SENESCENT HUMAN-CELLS IN CULTURE AND IN AGING SKIN IN-VIVO [J].
DIMRI, GP ;
LEE, XH ;
BASILE, G ;
ACOSTA, M ;
SCOTT, C ;
ROSKELLEY, C ;
MEDRANO, EE ;
LINSKENS, M ;
RUBELJ, I ;
PEREIRASMITH, O ;
PEACOCKE, M ;
CAMPISI, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (20) :9363-9367
[6]  
DOUGLASJONES AG, 1989, ACTA CYTOL, V33, P109
[7]   METASTASIS RESULTS FROM PREEXISTING VARIANT CELLS WITHIN A MALIGNANT-TUMOR [J].
FIDLER, IJ ;
KRIPKE, ML .
SCIENCE, 1977, 197 (4306) :893-895
[8]   SERIAL CULTIVATION OF HUMAN DIPLOID CELL STRAINS [J].
HAYFLICK, L ;
MOORHEAD, PS .
EXPERIMENTAL CELL RESEARCH, 1961, 25 (03) :585-+
[9]   Giant cell formation through fusion of cells derived from a human giant cell tumor of tendon sheath [J].
Hosaka, M ;
Hatori, M ;
Smith, R ;
Kokubun, S .
JOURNAL OF ORTHOPAEDIC SCIENCE, 2004, 9 (06) :581-584
[10]   Replicative senescence and senescence-like state induced in cancer-derived cells [J].
Hwang, ES .
MECHANISMS OF AGEING AND DEVELOPMENT, 2002, 123 (12) :1681-1694