Defective expression of transforming growth factor beta receptor type II is associated with CpG methylated promoter

Hong-Tao Zhang1, Xiao-Feng Chen, Ming-Hua Wang

  • 1Laboratory of Population and Quantitative Genetics, Institute of Genetics, The State Key Laboratory of Genetic Engineering, Morgan-Tan International Center for Life Sciences, Fudan University, Shanghai, People's Republic of China.

Abstract

Insights

Transforming growth factor beta receptor type II (TGF beta RII) is a tumor suppressor in non-small cell lung cancer (NSCLC). Aberrant promoter methylation frequently causes its down-regulation, contributing to NSCLC progression.

Area of Science:

  • Oncology
  • Molecular Biology
  • Cancer Genetics

Background:

  • Transforming growth factor beta receptor type II (TGF beta RII) acts as a tumor suppressor gene, inhibiting epithelial cell growth.
  • Reduced TGF beta RII expression is observed in various cancers, including non-small cell lung cancer (NSCLC).

Purpose of the Study:

  • To investigate the role and molecular mechanisms of TGF beta RII in NSCLC carcinogenesis.
  • To explore the significance of TGF beta RII gene alterations in the development of NSCLC.

Main Methods:

  • Analysis of 43 NSCLC tumor and paracarcinoma tissue pairs.
  • Screening for TGF beta RII gene variants using PCR-denaturing gradient gel electrophoresis.
  • Assessing TGF beta RII expression via immunohistochemistry, promoter methylation by methylation-specific PCR, and mRNA levels by RT-PCR.

Main Results:

  • No DNA variants were detected in the TGF beta RII coding sequence.
  • Reduced or lost TGF beta RII expression was found in 44% of NSCLC tumors.
  • Frequent promoter methylation of TGF beta RII was observed in tumor tissues, correlating significantly with reduced expression (P < 10(-4)).

Conclusions:

  • TGF beta RII functions as a crucial tumor suppressor in NSCLC.
  • Defective TGF beta RII expression, particularly due to aberrant 5' CpG promoter methylation, is a key mechanism in NSCLC progression.
  • Methylation-driven down-regulation of TGF beta RII contributes significantly to the transcriptional alterations in NSCLC.

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