Site-selective 8-chloroadenosine 3',5'-cyclic monophosphate inhibits transformation and transforming growth factor alpha production in Ki-ras-transformed rat fibroblasts.

Abstract:

:A site-selective cAMP analog, 8-chloroadenosine 3',5'-cyclic monophosphate (8-Cl-cAMP), was demonstrated to be a potent inhibitor of both the monolayer and soft agar growth of normal rat kidney (NRK) fibroblasts that had been transformed with the v-Ki-ras oncogene or treated with transforming growth factor alpha (TGF alpha). The growth inhibition was dose dependent and reversible and was accompanied by reversion of the transformed phenotype, suppression of TGF alpha production, and a decrease in p21 ras protein levels. These effects of 8-Cl-cAMP were linked to the cAMP analog's selective modulation of the type I and type II cAMP-dependent protein kinase regulatory subunits, RI and RII, present in Ki-ras-transformed and TGF alpha-treated NRK cells.

journal_name

FEBS Lett

journal_title

FEBS letters

authors

Tortora G,Ciardiello F,Ally S,Clair T,Salomon DS,Cho-Chung YS

doi

10.1016/0014-5793(89)80502-2

subject

Has Abstract

pub_date

1989-01-02 00:00:00

pages

363-7

issue

2

eissn

0014-5793

issn

1873-3468

pii

0014-5793(89)80502-2

journal_volume

242

pub_type

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