Silencing mutated β-catenin inhibits cell proliferation and stimulates apoptosis in the adrenocortical cancer cell line H295R

PLoS One. 2013;8(2):e55743. doi: 10.1371/journal.pone.0055743. Epub 2013 Feb 7.

Abstract

Context: Adrenocortical carcinoma (ACC) is a rare and highly aggressive endocrine neoplasm, with limited therapeutic options. Activating β-catenin somatic mutations are found in ACC and have been associated with a poor clinical outcome. In fact, activation of the Wnt/β-catenin signaling pathway seems to play a major role in ACC aggressiveness, and might, thus, represent a promising therapeutic target.

Objective: Similar to patient tumor specimen the H295 cell line derived from an ACC harbors a natural activating β-catenin mutation. We herein assess the in vitro and in vivo effect of β-catenin inactivation using a doxycyclin (dox) inducible shRNA plasmid in H295R adrenocortical cancer cells line (clone named shβ).

Results: Following dox treatment a profound reduction in β-catenin expression was detectable in shβ clones in comparison to control clones (Ctr). Accordingly, we observed a decrease in Wnt/βcatenin-dependent luciferase reporter activity as well as a decreased expression of AXIN2 representing an endogenous β-catenin target gene. Concomitantly, β-catenin silencing resulted in a decreased cell proliferation, cell cycle alterations with cell accumulation in the G1 phase and increased apoptosis in vitro. In vivo, on established tumor xenografts in athymic nude mice, 9 days of β-catenin silencing resulted in a significant reduction of CTNNB1 and AXIN2 expression. Moreover, continous β-catenin silencing, starting 3 days after tumor cell inoculation, was associated with a complete absence of tumor growth in the shβ group while tumors were present in all animals of the control group.

Conclusion: In summary, these experiments provide evidences that Wnt/β-catenin pathway inhibition in ACC is a promising therapeutic target.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenal Cortex Neoplasms / genetics*
  • Adrenal Cortex Neoplasms / metabolism
  • Adrenocortical Carcinoma / genetics*
  • Adrenocortical Carcinoma / metabolism
  • Animals
  • Apoptosis / genetics*
  • Cell Cycle / genetics
  • Cell Line, Tumor
  • Cell Proliferation
  • Disease Models, Animal
  • Female
  • Gene Silencing*
  • Humans
  • Mice
  • Mutation*
  • RNA Interference
  • Signal Transduction
  • TCF Transcription Factors / metabolism
  • Transcription, Genetic
  • Transplantation, Heterologous
  • Wnt Proteins / metabolism
  • beta Catenin / genetics*

Substances

  • TCF Transcription Factors
  • Wnt Proteins
  • beta Catenin

Grants and funding

This work was supported in part by the Contrat d'Initiation à la Recherche Clinique (grant CIRC 05045 – AP-HP), the Plan Hospitalier de Recherche Clinique (AOM06179) to the COMETE Network, the Recherche Translationnelle DHOS/INCA 2009 (RTD09024), ESF (07-RNP-067), Association pour la Recherche sur le Cancer (SFI20111203542), the Weigand Trust Germany, the Sander Stiftung (2011.003.1) and the Ligue contre le cancer (RS12/75–105). Furthermore, research leading to these results has received funding from the Seventh Framework Programme (FP7/2007–2013) under grant agreement number 259735 (ENS@T-CANCER). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.