2'-Hydroxyflavanone: A promising molecule for kidney cancer prevention

Biochem Pharmacol. 2015 Aug 1;96(3):151-8. doi: 10.1016/j.bcp.2015.04.022. Epub 2015 May 6.

Abstract

Kidney cancer, also known as renal cell carcinoma (RCC), is one of the top 10 diagnosed cancers in the USA, and the incidence is rising. Despite major improvements in drug therapy strategies, RCC remains a deadly malignancy if not found and removed in its early stages. RCC is so highly drug-resistant that no effective life-prolonging regimen of cytotoxic chemotherapy has been demonstrated for RCC, despite several decades of effort. It is also highly radiation-resistant, thus circumventing therapies to prevent local recurrence or to control metastatic disease. In the last few years, extensive research has been conducted to elucidate the functional significance of the plant-derived compounds, and their derivatives, as anticancer agents. This review is focussed on a chemo-dietary prevention strategy against RCC using a citrus-derived compound called 2'-hydroxyflavanone. RCC is frequently caused by VHL gene mutations, which contribute to 75% of all RCCs. These mutations are positively linked to cigarette smoking, and exposure to the tobacco carcinogen, N-nitrosodimethylamine and benzopyrene, can disrupt VHL. According to in vitro and preclinical mouse studies, 2'-hydroxyflavanone can both protect the VHL locus and prevent the progression of VHL-mutant cancer. Human clinical trials examining the effect of supplementation of 2'-hydroxyflavanone, either alone or in combination with chemotherapeutic drugs, on RCC prevention have not been conducted, although there is considerable potential for 2'-hydroxyflavanone and its derivatives to be developed as RCC chemoprevention agents. Therefore, the discovery of plant-derived cancer therapies, such as 2'-hydroxyflavanone, offers a new strategy for combating this highly resistant cancer.

Keywords: 2-Hydroxyflavanone; Aldo-keto reductase; Chemoprevention; Glutathione-S-transferase; Renal cell carcinoma; von Hippel–Lindau.

Publication types

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

MeSH terms

  • Animals
  • Antineoplastic Agents, Phytogenic / pharmacology*
  • Benzopyrenes / toxicity
  • Carcinogens / toxicity
  • Carcinoma, Renal Cell / chemically induced
  • Carcinoma, Renal Cell / genetics
  • Carcinoma, Renal Cell / pathology
  • Carcinoma, Renal Cell / prevention & control*
  • Dimethylnitrosamine / toxicity
  • Drug Resistance, Neoplasm / genetics
  • Flavanones / pharmacology*
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Kidney Neoplasms / chemically induced
  • Kidney Neoplasms / genetics
  • Kidney Neoplasms / pathology
  • Kidney Neoplasms / prevention & control*
  • Mice
  • Mutation
  • Signal Transduction
  • Von Hippel-Lindau Tumor Suppressor Protein / genetics*
  • Von Hippel-Lindau Tumor Suppressor Protein / metabolism

Substances

  • 2'-hydroxyflavanone
  • Antineoplastic Agents, Phytogenic
  • Benzopyrenes
  • Carcinogens
  • Flavanones
  • Von Hippel-Lindau Tumor Suppressor Protein
  • VHL protein, human
  • Dimethylnitrosamine