期刊
CANCER LETTERS
卷 313, 期 1, 页码 108-121出版社
ELSEVIER IRELAND LTD
DOI: 10.1016/j.canlet.2011.08.033
关键词
Ovarian cancer; Transforming growth factor beta; Activin; Bone morphogenetic protein; Epithelial-to-mesenchymal transition; Motility
类别
资金
- Canadian Cancer Society (National Cancer Institute of Canada) [15303]
- Marsha Rivkin Center for Ovarian Cancer Research [037732]
- Nova Scotia Health Research Foundation
- Canadian Cancer Society through National Cancer Institute of Canada
TGF beta superfamily signalling participates in normal and pathophysiologic cellular processes. Despite several reports demonstrating active TGF beta superfamily signalling pathways in OvCa cell lines and primary cultures, few studies examine their functional outcome. Herein we show that primary human ovarian cancer cells possess intact autocrine BMP, TGF beta and activin signalling. Blocking autocrine signalling resulted in differential cellular responses affecting cellular morphology, motility and proliferation. Additionally, BMP4-induced alterations in morphology and motility are dependent on Smad signalling. These results suggest that a balance between BMP and TGF beta/activin signalling may be altered to favour BMP signalling during ovarian cancer metastatic progression. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
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