Evidence for aldosterone-dependent growth of renal cell carcinoma

Int J Exp Pathol. 2014 Aug;95(4):244-50. doi: 10.1111/iep.12074. Epub 2014 May 7.

Abstract

The aim if this study was to investigate the hypothesis that K-RAS 4A is upregulated in a mineralocorticoid-dependent manner in renal cell carcinoma and that this supports the proliferation and survival of some renal cancers. Expression of the K-RAS in renal tumour tissues and cell lines was examined by real-time PCR and Western blot and mineralocorticoid receptor, and its gatekeeper enzyme 11β-hydroxysteroid dehydrogenase-2 was examined by immunocytochemistry on a tissue microarray of 27 cases of renal cell carcinoma. Renal cancer cells lines 04A018 (RCC4 plus VHL) and 04A019 (RCC4 plus vector alone) were examined for the expression of K-RAS4A and for the effect on K-RAS expression of spironolactone blockade of the mineralocorticoid receptor. K-RAS4A was suppressed by siRNA, and the effect on cell survival, proliferation and activation of the Akt and Raf signalling pathways was investigated in vitro. K-RAS4A was expressed in RCC tissue and in the renal cancer cell lines but K-RAS was downregulated by spironolactone and upregulated by aldosterone. Spironolactone treatment and K-RAS suppression both led to a reduction in cell number in vitro. Both Akt and Raf pathways showed activation which was dependent on K-RAS expression. K-RAS expression in renal cell carcinoma is at least partially induced by aldosterone. Aldosterone supports the survival and proliferation of RCC cells by upregulation of K-RAS acting through the Akt and Raf pathways.

Keywords: K-RAS; aldosterone; mineralocorticoid receptor; renal cell carcinoma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 11-beta-Hydroxysteroid Dehydrogenases / metabolism
  • Aldosterone / metabolism*
  • Biomarkers, Tumor / metabolism
  • Carcinoma, Renal Cell / metabolism*
  • Carcinoma, Renal Cell / pathology*
  • Cell Line, Tumor
  • Cell Proliferation*
  • Cell Survival / physiology
  • Humans
  • In Vitro Techniques
  • Kidney Neoplasms / metabolism*
  • Kidney Neoplasms / pathology*
  • Proto-Oncogene Proteins / metabolism*
  • Proto-Oncogene Proteins c-akt / metabolism
  • Proto-Oncogene Proteins p21(ras)
  • Receptors, Mineralocorticoid / drug effects
  • Signal Transduction / drug effects
  • Spironolactone / pharmacology
  • Tissue Array Analysis
  • raf Kinases / metabolism
  • ras Proteins / metabolism*

Substances

  • Biomarkers, Tumor
  • KRAS protein, human
  • Proto-Oncogene Proteins
  • Receptors, Mineralocorticoid
  • Spironolactone
  • Aldosterone
  • 11-beta-Hydroxysteroid Dehydrogenases
  • Proto-Oncogene Proteins c-akt
  • raf Kinases
  • Proto-Oncogene Proteins p21(ras)
  • ras Proteins