| Literature DB >> 12212807 |
Elena Blishchenko1, Olga Sazonova, Andrei Surovoy, Sergei Khaidukov, Yury Sheikine, Dmitry Sokolov, Irina Freidlin, Marina Philippova, Arpad Vass, Andrei Karelin, Vadim Ivanov.
Abstract
The antiproliferative effects of the haemoglobin beta-chain fragment (33-39) (valorphin or VV-haemorphin-5) were studied in a panel of tumour cell lines and normal cells of different origin, using various methods of activity determination (trypan blue inclusion test, sulphorhodamine B staining, MTT staining, flow cytometry and clonogenic test). Valorphin suppressed the proliferation of tumour cells by 25%-95%, depending on the cell line. The maximal valorphin activity was detected in transformed cells of fibroblastic (L929) and epithelial (MCF-7) origin, transformed haematopoietic cells (K562, HL-60) being less sensitive. In normal cells, valorphin activity was several fold lower (10%-15%). A study of the dynamics of cell proliferation in L929 cells using a visual cell count and flow cytometry showed that valorphin induced reversible and relatively short (24 h) S-phase arrest of cell proliferation, accompanied by a reversible increase of cell size. The proliferation delay was followed by a comparatively long period of reversible resistance of the cells to the peptide (96 h) when the cells are dividing at normal rate. The same dynamics were demonstrated for A549, MCF-7 and primary murine breast carcinoma cells. On the basis of the data obtained, a pattern of regulation of cell growth by valorphin is suggested.Entities:
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Year: 2002 PMID: 12212807 DOI: 10.1002/psc.402
Source DB: PubMed Journal: J Pept Sci ISSN: 1075-2617 Impact factor: 1.905