The von Hippel-Lindau Tumor Suppressor Gene: Implications and Therapeutic Opportunities

Cancer J. 2020 Sep/Oct;26(5):390-398. doi: 10.1097/PPO.0000000000000480.

Abstract

The discovery of the von Hippel-Lindau (VHL) gene marked a milestone in our understanding of clear cell renal cell carcinoma (ccRCC) pathogenesis. VHL inactivation is not only a defining feature of ccRCC, but also the initiating event. Herein, we discuss canonical and noncanonical pVHL functions, as well as breakthroughs shaping our understanding of ccRCC evolution and evolutionary subtypes. We conclude by presenting evolving strategies to therapeutically exploit effector mechanisms downstream of pVHL.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • Carcinoma, Renal Cell* / genetics
  • Carcinoma, Renal Cell* / therapy
  • Genes, Tumor Suppressor
  • Humans
  • Kidney Neoplasms* / genetics
  • Kidney Neoplasms* / therapy
  • Von Hippel-Lindau Tumor Suppressor Protein / genetics*

Substances

  • Von Hippel-Lindau Tumor Suppressor Protein
  • VHL protein, human