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Published on: October 27, 2020
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.
Purpose:
Reduced expression of the transforming growth factor beta receptor type II (TGF beta RII), a key inhibitor of epithelial cell growth and tumor suppressor gene, was reported frequently in many types of tumors including non-small cell lung cancer (NSCLC). This study explored the significance of the TGF beta RII gene in NSCLC carcinogenesis.
Experimental Design:
With 43 independent pairs of tumor and paracarcinoma tissue samples from patients with primary NSCLC, we carried out PCR-denaturing gradient gel electrophoresis screening for DNA variants over the coding sequence of the TGF beta RII gene, immunohistochemical assay of TGF beta RII expression, methylation-specific PCR analysis, and semiquantitative reverse transcription-PCR.
Results:
The PCR-denaturing gradient gel electrophoresis did not detect variation in the whole coding sequence of the TGF beta RII gene, but the immunohistochemistry experiment revealed reduced or lost expression of the gene in 44% (19 of 43) of the tumor samples. The methylation analysis on the 19 pairs detected the frequent occurrence of methylated TGF beta RII promoter in tumor tissues, whereas most of the paracarcinoma tissues were free of methylation. The reduced TGF beta RII expression was highly significantly associated with the methylation event (P < 10(-4)). The reverse transcription-PCR analysis demonstrated a clear agreement between reduced TGF beta RII expression and decreased mRNA level of the gene in the tumor tissue samples.
Conclusions:
TGF beta RII plays an important role as a tumor suppressor in NSCLC carcinogenesis. The defective expression may serve as one of most important molecular mechanisms in explaining progression of the disease. In particular, aberrant 5' CpG methylation of the gene has explained the down-regulation of the gene at a transcriptional level.
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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