Literature DB >> 24222114

MCP-1 promotes invasion and adhesion of human ovarian cancer cells.

Shigenori Furukawa1, Shu Soeda, Yuichiro Kiko, Osamu Suzuki, Yuko Hashimoto, Takafumi Watanabe, Hiroshi Nishiyama, Kazuhiro Tasaki, Hiroshi Hojo, Masafumi Abe, Keiya Fujimori.   

Abstract

BACKGROUND: Monocyte chemoattractant protein-1 (MCP-1) can accelerate tumor progression by attracting tumor-associated macrophages. We studied the effects of MCP-1 on SKOV-3 cells in order to investigate MCP-1 biological activity ovarian cancer.
MATERIALS AND METHODS: A SKOV-3 cell invasion assay (Transwell assay) and cell adhesion assay (96-well assay) were performed. Immunohistochemical staining for C-C motif chemokine receptor-2 (CCR2), a receptor for MCP-1, was also performed on cultured SKOV-3 cells.
RESULTS: Migration and adhesion of MCP-1-treated SKOV-3 cells were significantly increased compared to untreated cells (p<0.01). A CCR2 antagonist attenuated the invasion and adhesion of MCP-1-treated cells. CCR2 was expressed in the cytoplasm of SKOV-3 cells.
CONCLUSION: MCP-1 promoted invasion and adhesion of ovarian cancer cells, and a CCR2 antagonist attenuated the effects of MCP-1 in vitro. These data suggest that MCP-1 is a potential therapeutic target for ovarian cancer therapy.

Entities:  

Keywords:  C-C motif chemokine receptor-2 (CCR2) antagonist; Ovarian cancer; SKOV-3 cell line; monocyte chemoattractant protein-1 (MCP-1); tumor-associated macrophages (TAMs)

Mesh:

Substances:

Year:  2013        PMID: 24222114

Source DB:  PubMed          Journal:  Anticancer Res        ISSN: 0250-7005            Impact factor:   2.480


  33 in total

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