Mesenchymal Stromal Cells Promote Tumor Growth through the Enhancement of Neovascularization

被引:189
|
作者
Suzuki, Kazuhiro [1 ,2 ]
Sun, Ruowen [1 ,3 ]
Origuchi, Makoto [4 ]
Kanehira, Masahiko [4 ]
Takahata, Takenori [1 ]
Itoh, Jugoh [1 ]
Umezawa, Akihiro [5 ]
Kijima, Hiroshi [6 ]
Fukuda, Shinsaku [2 ]
Saijo, Yasuo [1 ]
机构
[1] Hirosaki Univ, Grad Sch Med, Dept Med Oncol, Hirosaki, Aomori 0368562, Japan
[2] Hirosaki Univ, Grad Sch Med, Dept Gastroenterol & Hematol, Hirosaki, Aomori 0368562, Japan
[3] China Med Univ, Shengjing Hosp, Dept Rheumatol & Immunol, Shenyang, Peoples R China
[4] Tohoku Univ, Grad Sch Med, Dept Mol Med, Sendai, Miyagi 980, Japan
[5] Natl Inst Child Hlth & Dev, Dept Reprod Biol, Tokyo, Japan
[6] Hirosaki Univ, Grad Sch Med, Dept Pathol & Biosci, Hirosaki, Aomori 0368562, Japan
关键词
BREAST-CANCER METASTASIS; STEM-CELLS; BONE-MARROW; PROGRESSION; EXPRESSION; FIBROBLASTS; CARCINOMA; DIFFERENTIATION; LINE; MYOFIBROBLASTS;
D O I
10.2119/molmed.2010.00157
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
Mesenchymal stromal cells (MSCs), also called mesenchymal stem cells, migrate and function as stromal cells in tumor tissues. The effects of MSCs on tumor growth are controversial. In this study, we showed that MSCs increase proliferation of tumor cells in vitro and promote tumor growth in vivo. We also further analyzed the mechanisms that underlie these effects. For use in in vitro and in vivo experiments, we established a bone marrow-derived mesenchymal stromal cell line from cells isolated in C57BL/6 mice. Effects of murine MSCs on tumor cell proliferation in vitro were analyzed in a coculture model with B16-LacZ cells. Both coculture with MSCs and treatment with MSC-conditioned media led to enhanced growth of B16-LacZ cells, although the magnitude of growth stimulation in cocultured cells was greater than that of cells treated with conditioned media. Co-injection of B16-LacZ cells and MSCs into syngeneic mice led to increased tumor size compared with injection of B16-LacZ cells alone. Identical experiments using Lewis lung carcinoma (LLC) cells instead of B16-LacZ cells yielded similar results. Consistent with a role for neovascularization in MSC-mediated tumor growth, tumor vessel area was greater in tumors resulting from co-injection of B16-LacZ cells or LLCs with MSCs than in tumors induced by injection of cancer cells alone, Co-injected MSCs directly supported the tumor vasculature by localizing close to vascular walls and by expressing an endothelial marker. Furthermore, secretion of leukemia inhibitory factor, macrophage colony-stimulating factor, macrophage inflammatory protein-2 and vascular endothelial growth factor was increased in cocultures of MSCs and B16-LacZ cells compared with B16-LacZ cells alone. Together, these results indicate that MSCs promote tumor growth both in vitro and in vivo and suggest that tumor promotion in vivo may be attributable in part to enhanced angiogenesis. (C) 2011 The Feinstein Institute for Medical Research, www.feinsteininstitute.org
引用
收藏
页码:579 / 587
页数:9
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