Inhibition of coding region determinant binding protein sensitizes melanoma cells to chemotherapeutic agents

Pigment Cell Melanoma Res. 2012 Jan;25(1):83-7. doi: 10.1111/j.1755-148X.2011.00921.x. Epub 2011 Oct 28.

Abstract

We previously reported that malignant melanomas express high levels of the mRNA binding protein coding region determinant binding protein (CRD-BP). This molecule is important for the activation of anti-apoptotic pathways, a mechanism often linked to insensitivity to therapeutics. However, it is not known whether CRD-BP plays a role in the resistance of melanomas to anti-cancer treatment. Here we demonstrate that knockdown of CRD-BP with a specific sh-RNA enhances the effect of dacarbazine, temozolomide, vinblastine, and etoposide on both primary and metastatic melanoma cell lines. CRD-BP down-regulation contributes to cell sensitization by increasing apoptosis and diminishing melanoma cell growth in response to chemotherapeutic agents. Furthermore, inhibition of CRD-BP decreases microphthalmia-associated transcription factor (MITF) expression and reintroduction of MITF partially compensates for the absence of CRD-BP. These findings suggest that high expression of CRD-BP in melanoma cells confers resistance to chemotherapy and that these CRD-BP responses are mediated, at least in part, by MITF.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Antineoplastic Agents / pharmacology*
  • Apoptosis / drug effects
  • Cell Line, Tumor / drug effects
  • Dacarbazine / analogs & derivatives
  • Dacarbazine / pharmacology
  • Down-Regulation
  • Drug Resistance, Neoplasm / genetics*
  • Etoposide / pharmacology
  • Gene Knockdown Techniques
  • Humans
  • Melanoma / pathology*
  • Microphthalmia-Associated Transcription Factor / physiology
  • Neoplasm Proteins / antagonists & inhibitors
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / physiology*
  • RNA, Small Interfering / pharmacology
  • RNA-Binding Proteins / antagonists & inhibitors
  • RNA-Binding Proteins / genetics
  • RNA-Binding Proteins / physiology*
  • Temozolomide
  • Vinblastine / pharmacology

Substances

  • Antineoplastic Agents
  • IGF2BP1 protein, human
  • MITF protein, human
  • Microphthalmia-Associated Transcription Factor
  • Neoplasm Proteins
  • RNA, Small Interfering
  • RNA-Binding Proteins
  • Vinblastine
  • Etoposide
  • Dacarbazine
  • Temozolomide