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.
Papers
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Journal Article
Antagonistic Actions of Retinoic Acid and Dexamethasone on Anchorage-independent Growth and Epidermal Growth Factor Binding of Normal Rat Kidney Cells
TL;DR: The abilities of retinoic acid and dexamethasone to alter expression of the transformed phenotype induced by treatment of normal rat kidney cells with TGF-beta and EGF are mediated at least in part through their effects on the EGF receptor.
Journal ArticleDOI
Antibodies to transforming growth factor-β2 peptides: Specific detection of TGF-β2 in immunoassays
Kathleen C. Flanders,David S. Cissel,Larry T. Mullen,David Danielpour,Michael B. Sporn,Anita B. Roberts +5 more
TL;DR: None of the TGF-β2 peptide antibodies was able to block receptor binding of either TGF -β1 or 2, and both anti-P 50–75(2) andAnti-P 79–108 (2) specifically immunoprecipitated TGF,β2 under reducing conditions only.
Patent
Therapeutic compounds and methods of use
TL;DR: In this article, the authors present a list of compounds and methods useful for chemopreventive treatment of diseases such as cancer, Alzheimer's disease, Parkinson disease, inflammatory bowel diseases and multiple sclerosis.
Journal ArticleDOI
Aberrant TGF-β Production and Regulation in Metastatic Malignancy
Lois C. Schwarz,Jim A. Wright,Marie-Claude Gingras,Paturu Kondaiah,David Danielpour,Mark Pimentel,Michael B. Sporn,Arnold H. Greenberg +7 more
TL;DR: Despite the greatly enhanced rate of secretion of activated T GF-β, metastatic cells exhibited markedly altered responses of TGF-β1, and TGF -β2., being unable to either increase collagen sec...
Journal ArticleDOI
Triterpenoids CDDO-Methyl Ester or CDDO-Ethyl Amide and Rexinoids LG100268 or NRX194204 for Prevention and Treatment of Lung Cancer in Mice
Karen T. Liby,Renee Risingsong,Darlene B. Royce,Charlotte R. Williams,Tian Ma,Mark M. Yore,Michael B. Sporn +6 more
TL;DR: It is shown for the first time that these drugs also were highly effective for treatment of experimental lung cancer, and all triterpenoid and rexinoid combinations reduced ATB 85% to 87% compared with the control group.