M
Michael B. Sporn
Researcher at Dartmouth College
Publications - 561
Citations - 96644
Michael B. Sporn is an academic researcher from Dartmouth College. The author has contributed to research in topics: Transforming growth factor & Transforming growth factor beta. The author has an hindex of 157, co-authored 559 publications receiving 94605 citations. Previous affiliations of Michael B. Sporn include Cornell University & Reata Pharmaceuticals.
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Isolation and identification of 4-hydroxy- and 4-oxoretinoic acid. In vitro metabolites of all-trans-retinoic acid in hamster trachea and liver.
Charles A. Frolik,Anita B. Roberts,Thomas E. Tavela,Peter P. Roller,Dianne L. Newton,Michael B. Sporn +5 more
TL;DR: Two metabolites produced in a cell-free liver incubation reaction also migrate on a high-pressure liquid chromatography column together with metabolites isolated from a tracheal organ culture system both in ultraviolet absorption and mass spectral characteristics and in migration rates on two different reverse-phase high- pressure liquid chromatographic systems.
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Structural and functional characterization of the transforming growth factor beta 3 promoter. A cAMP-responsive element regulates basal and induced transcription.
Robert Lafyatis,Robert J. Lechleider,Seong-Jin Kim,Sonia B. Jakowlew,Anita B. Roberts,Michael B. Sporn +5 more
TL;DR: Since the TGF-beta s have activity in promoting or inhibiting proliferation and differentiation of multiple cell types, it seems likely that the differential and tissue-specific transcriptional regulation of these genes is of fundamental importance in the induction and maintenance of differentiated cell types in various tissues.
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Transcriptional regulation of the AP-1 and Nrf2 target gene sulfiredoxin
Francesc X. Soriano,Paul Baxter,Lyndsay M. Murray,Michael B. Sporn,Thomas H. Gillingwater,Giles E. Hardingham +5 more
TL;DR: It is illustrated here that sulfiredoxin can be rapidly induced in vivo by administration of CDDO-TFEA, a synthetic triterpenoid inducer of endogenous Nrf2, which may offer a way of reversing peroxiredoxin hyperoxidation in vivo following chronic or acute oxidative stress.
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Complex regulation of TGF beta expression by retinoic acid in the vitamin A-deficient rat.
Adam B. Glick,Bryan K. McCune,N. Abdulkarem,Kathleen C. Flanders,Jeanne A. Lumadue,J.M. Smith,Michael B. Sporn +6 more
TL;DR: The results show for the first time the widespread regulation of TGF beta expression by retinoic acid in vivo, and suggest a possible mechanism by which retinoics regulate the functions of both normal and pre-neoplastic epithelia.
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Role of Retinoids in Differentiation and Carcinogenesis
TL;DR: It has been shown that retinoids can exert effects on certain fully transformed, invasive, neoplastic cells, leading in certain instances to a suppression of proliferation and in other instances to terminal differentiation of these cells, resulting in a more benign, nonneoplastic pheno type.