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Cited by 188

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Growth inhibition by transforming growth factor beta (TGF-beta) type I is restored in TGF-beta-resistant hepatoma cells after expression of TGF-beta receptor type II cDNA.

Open access
Inagaki, M, Moustakas, A, Lin, H Y, Lodish, H F, Carr, B I·1993·Proceedings of the National Academy of Sciences

Abstract

The growth of human hepatoma Hep 3B cells is potently inhibited by TGF-beta 1 (ID50 = 0.2 ng/ml, 8 pM). A mutant cell line was derived that was not inhibited in growth by TGF-beta 1 at 5 ng/ml (200 pM) and that lacked TGF-beta receptor type II (TGF-beta RII) gene. Transfection of the cloned cDNA for human TGF-beta RII to this mutant cell line restored receptor expression as well as the inhibition in growth by TGF-beta 1. In both wild-type and mutant cells stably transfected with TGF-beta RII cDNA, TGF-beta RII coimmunoprecipitated with TGF-beta receptor type I in the presence of ligand. These experiments provide direct evidence for the role of TGF-beta RII in the inhibitory effect of TGF-beta on growth and suggest that TGF-beta RII acts by means of a heteromeric surface complex with TGF-beta receptor type I.

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Metadata

Authors
Inagaki, M., Moustakas, A., Lin, H. Y., Lodish, H. F., & Carr, B. I.
Venue
Proceedings of the National Academy of Sciences
Published
1993-06
Volume
90
Issue
11
Pages
5359-5363
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2036143395
Cited by
188
References
0
FWCI
9.37
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Growth inhibition by transforming growth factor beta (TGF-beta) type I is restored in TGF-beta-resistant hepatoma cells after expression of TGF-beta receptor type II cDNA. https://app.cochat.ai/papers/10.1073/pnas.90.11.5359
The paper
Inagaki, M., Moustakas, A., Lin, H. Y., Lodish, H. F., & Carr, B. I. (1993). Growth inhibition by transforming growth factor beta (TGF-beta) type I is restored in TGF-beta-resistant hepatoma cells after expression of TGF-beta receptor type II cDNA. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.90.11.5359

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