| Literature DB >> 9178817 |
N Yabunaka1, K Honke, A Ishii, Y Ogiso, N Kuzumaki, Y Agishi, A Makita.
Abstract
Glycolipid sulfotransferase activity in a human renal cell carcinoma cell line, SMKT-R3, is enhanced by epidermal growth factor (EGF); tyrosine kinase inhibitors suppress this enhancement. To investigate the involvement of Ras in the signal transduction pathway from the EGF receptor to the expression of glycolipid sulfotransferase, we introduced v-H-ras into SMKT-R3 cells. In a quiescent state, the percent GTP bound to Ras in v-H-ras-expressing cells increased about 2.5-fold compared with control cells, suggesting that v-Ras introduced into the renal cancer cells is in an active form without EGF stimulation. Glycolipid sulfotransferase activity in v-H-ras-expressing cells was higher than in control cells. The sulfotransferase activity was affected neither by EGF nor by genistein, a tyrosine kinase inhibitor, in v-H-ras-expressing cells, whereas it was enhanced by EGF and reduced by genistein in control cells. Our observations suggest that Ras mediates the regulation pathway of glycolipid sulfotransferase activity in SMKT-R3 cells.Entities:
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Year: 1997 PMID: 9178817 DOI: 10.1002/(sici)1097-0215(19970516)71:4<620::aid-ijc18>3.0.co;2-f
Source DB: PubMed Journal: Int J Cancer ISSN: 0020-7136 Impact factor: 7.396