Mitogenic Signaling Mediated by Oxidants in Ras-Transformed Fibroblasts

Abstract

NIH 3T3 fibroblasts stably transformed with a constitutively active isoform of p21 Ras , H-Ras V12 (v-H-Ras or EJ-Ras), produced large amounts of the reactive oxygen species superoxide (·O 2 − ). ·O 2 − production was suppressed by the expression of dominant negative isoforms of Ras or Rac1, as well as by treatment with a farnesyltransferase inhibitor or with diphenylene iodonium, a flavoprotein inhibitor. The mitogenic activity of cells expressing H-Ras V12 was inhibited by treatment with the chemical antioxidant N -acetyl-L-cysteine. Mitogen-activated protein kinase (MAPK) activity was decreased and c-Jun N-terminal kinase (JNK) was not activated in H-Ras V12 -transformed cells. Thus, H-Ras V12 -induced transformation can lead to the production of ·O 2 − through one or more pathways involving a flavoprotein and Rac1. The implication of a reactive oxygen species, probably ·O 2 − , as a mediator of Ras-induced cell cycle progression independent of MAPK and JNK suggests a possible mechanism for the effects of antioxidants against Ras-induced cellular transformation.

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Affiliated Institutions

• University of Michigan US
• National Heart Lung and Blood Institute US
• Johns Hopkins Medicine US
• Johns Hopkins University US
• University of North Carolina at Chapel Hill US
• Ann Arbor VA Medical Center US
• National Institutes of Health US

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