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Published on: June 18, 2015
CMTM8 is Frequently Downregulated in Multiple Solid Tumors
Wenjuan Zhang1, Hui Qi, Xiaoning Mo
1*Department of Immunology, School of Basic Medical Sciences, Key Laboratory of Immunology, Ministry of Health, Peking University Health Science Center †National Institutes for Food and Drug Control ‡Peking University People's Hospital, Beijing, P.R. China.
Abstract:
Previous studies have demonstrated that overexpression of CMTM8 inhibits cell growth and induces apoptosis in multiple types of cancer cells, whereas the downregulation of CMTM8 induces the epithelial-to-mesenchymal (EMT)-like phenotype in hepatocyte carcinoma cells, implying its important roles in tumorigenesis and tumor metastasis. No extensive studies on the expression of CMTM8 in either normal or tumorous human tissues have been reported to date. Here, using real-time quantitative polymerase chain reaction, we analyzed CMTM8 expression in multiple normal human tissue samples. Moreover, by applying high-throughput immunohistochemical staining of tissue microarrays with homemade anti-CMTM8 antibodies, we studied CMTM8 expression in carcinoma samples and adjacent normal samples of 6 types of human tissues. CMTM8 is widely expressed in many normal human tissues and is frequently downregulated or absent in multiple solid tumors (liver, lung, colon, rectum, esophagus, stomach). χ tests revealed a significant negative correlation between CMTM8 expression and tumorigenesis: liver, lung (squamous carcinoma), colon, rectum, P<0.0001; esophagus, P<0.001; stomach, P<0.01. Real-time quantitative polymerase chain reaction analysis of samples from esophageal carcinomas and the adjacent normal tissues revealed that CMTM8 mRNA levels are reduced in carcinomas compared with normal tissues, indicating that CMTM8 is potentially downregulated at the mRNA level (P<0.01). This is the first extensive study of CMTM8 expression in both normal and tumorous human tissues. Our findings strongly supported the potential role of CMTM8 as a novel tumor suppressor and may shape further functional studies on this gene.
Insights
CMTM8 is widely expressed in normal human tissues but often lost in solid tumors like liver and lung cancer. This study reveals CMTM8
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Previous studies suggest CMTM8 influences cell growth, apoptosis, and epithelial-to-mesenchymal transition (EMT).
- The expression pattern of CMTM8 in normal versus tumorous human tissues remains largely uncharacterized.
- Understanding CMTM8 expression is crucial for its potential role in tumorigenesis and metastasis.
Purpose of the Study:
- To extensively analyze the expression of CMTM8 in various normal human tissues.
- To investigate the expression levels of CMTM8 in multiple types of human solid tumors compared to adjacent normal tissues.
- To determine the correlation between CMTM8 expression and tumorigenesis.
Main Methods:
- Real-time quantitative polymerase chain reaction (RT-qPCR) for mRNA expression analysis in normal tissues.
- High-throughput immunohistochemical (IHC) staining of tissue microarrays (TMAs) to assess protein expression in tumor and normal samples.
- Statistical analysis (Chi-squared tests) to evaluate the association between CMTM8 expression and tumorigenesis.
Main Results:
- CMTM8 is broadly expressed across many normal human tissues.
- CMTM8 expression is frequently downregulated or absent in solid tumors, including liver, lung, colon, rectum, esophagus, and stomach.
- A significant negative correlation was observed between CMTM8 expression and the presence of tumors in multiple cancer types (P<0.0001 to P<0.01).
- RT-qPCR confirmed reduced CMTM8 mRNA levels in esophageal carcinomas compared to adjacent normal tissues (P<0.01).
Conclusions:
- This is the first comprehensive study detailing CMTM8 expression in both normal and cancerous human tissues.
- The findings strongly support a potential role for CMTM8 as a novel tumor suppressor gene.
- Downregulation of CMTM8 may be a significant event in the development of various solid tumors.
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