期刊
JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY
卷 20, 期 7, 页码 1163-1173出版社
SPRINGER
DOI: 10.1007/s00775-015-1297-8
关键词
Anticancer drug; Heavy metal; Biomedicine; Molecular dynamics
资金
- Callerio Foundation Onlus
- University of Padua (Italy)
The ruthenium-based drug NAMI-A, characterised by its selectivity against solid tumour metastases, promotes TGF-beta 1-dependent fibrosis and the reduction of the release of MMPs in the primary tumour. The aim of the study was to examine the interaction of NAMI-A with TGF-beta 1 in the process of metastasis formation. NAMI-A (1) affects the secretion of TGF-beta 1 in metastatic MDA-MB-231 cells rather than in non-tumorigenic HBL-100 cells, (2) prevails over TGF-beta 1 with regard to the invasive capacity of the treated cells, and (3) contrasts integrin-dependent migration stimulated by TGF-beta 1. It, thus, appears that the effects of NAMI-A on cell invasion and migration are best summarised as an interference with TGF-beta 1 and a reduction of its activity in these events. At a molecular level, the similar activity of NAMI-A and TGF-beta 1 on RhoA GTPase supports its interaction with cell surface integrins while TGF-beta 1 can activate it by interaction with its TGF beta R receptor. The inhibition of TGF-beta 1-induced migration of MDA-MB-231 cells by NAMI-A cannot simply be attributed to a modulation of the Smad2 and p38MAPK pathways. In conclusion, the effects of NAMI-A on the biological role of TGF-beta 1 in cancer metastasis are insufficient to attribute the responsibility for the anti-metastatic activity of the ruthenium-based drug to this target alone.
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