Nicholas Dyson Explained

Nicholas Dyson
Workplaces:Massachusetts General Hospital Cancer Center
Academic Advisors:Ed Harlow
Doctoral Students:Simon Boulton
Adam Brook
Known For:E2F and pRB

Nicholas Dyson is Professor of Medicine at Harvard Medical School, the James and Shirley Curvey MGH Research Scholar and Scientific Director of the Massachusetts General Hospital Cancer Center.[1]

Research

The Dyson Lab studies the retinoblastoma protein.

Working as a post-doctoral fellow in the laboratory of Dr. Ed Harlow, Dyson demonstrated that the retinoblastoma protein can form complexes in vitro with the E7 oncoprotein of Human papilloma virus type-16.[2] This result implicated pRB binding to E7 as a step in human papilloma virus-associated carcinogenesis.

More recently, Dyson's group has shown that the transcription factor E2F1 is a potent and specific inhibitor of beta-catenin/T-cell factor (TCF)-dependent transcription, and that this function contributes to E2F1-induced apoptosis.[3]

As of 2015, Professor Dyson has 140 publications in leading peer-reviewed journals.

Notes and References

  1. Web site: Dyson Lab - Massachusetts General Hospital, Boston, MA. www.massgeneral.org. Massachusetts General Hospital.
  2. Dyson. N. Howley. PM. Munger. K. Harlow. E. The human papilloma virus-16 E7 oncoprotein is able to bind to the retinoblastoma gene product.. Science. 1989. 243. 4893. 934–7. 2537532. 10.1126/science.2537532. 1989Sci...243..934D.
  3. Morris. E. Ji. J. Yang. F. Di Stefano. L. Herr. A. Moon. N. Kwon. E. Haigis. K. Naar. A. Dyson. N. E2F1 represses beta-catenin transcription and is antagonized by both pRB and CDK8.. Nature. 2008. 455. 7212. 552–6. 18794899. 10.1038/nature07310. 3148807. 2008Natur.455..552M.