期刊
BRITISH JOURNAL OF CANCER
卷 90, 期 2, 页码 463-470出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/sj.bjc.6601533
关键词
TIMP-1; metalloproteinases; proliferation; ERK; p38 kinase
类别
TIMP-1, an similar to30 kDa glycosylated protein found predominantly in extracellular compartments, is involved in the regulation of a variety of developmental, remodelling, and pathological processes. One function of TIMP-I is to inhibit certain members of a group of extracellular and cell surface enzymes known collectively as metalloproteinases (MP). These include the matrix metalloproteinases and the adamalysin-like disintegrin and metalloproteinases (ADAMs). Additional activities of TIMP-I include potentiating the activity of erythroid precursors and stimulating proliferation of certain cancer cell lines. Published evidence suggests that the apparent proliferative action of TIMP-I is independent of its MP-inhibitory activity; however, reports of a cell surface receptor for TIMP-I have not been confirmed. We have utilised a baculovirus-based system to produce TIMP-1. Data presented here show that TIMP-I and synthetic hydroxamate (GM6001) IMP inhibitors stimulate proliferation and metabolic activity of MDA-MB-435 cancer cells with similar kinetics. An inactive hydroxamate derivative was ineffective. The TIMP-I-induced increase in proliferation and metabolic activity was not the consequence of the inhibition of apoptosis by TIMP-I in the serum-free medium. These data taken together imply that the mechanism by which TIMP-I enhances cell growth depends on its ability to inhibit a metalloproteinase, rather than to stimulate a cell surface receptor by a process independent of its MP-inhibitory activity. Inhibitor's of extracellular regulated kinase (UO 126) and p38 (SB203580), and to a lesser extent the phosphatidylinositol-3-kinase inhibitor LY294002, suppressed the action of TIMP-1. Assays for ERK1/2 and p38 showed that both were activated by TIMP-I and GM6001. Mechanisms by which TIMP-I might act to stimulate cell proliferation are described.
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