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Updated: Apr 3, 2026

Methyl-binding DNA capture Sequencing for Patient Tissues
Published on: October 31, 2016
Integrin α9 gene promoter is hypermethylated and downregulated in nasopharyngeal carcinoma
Imran Nawaz1,2, Li-Fu Hu1, Zi-Ming Du1,3
1Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden.
Abstract:
Epigenetic silencing of tumor suppressor genes (TSGs) by promoter methylation can be an early event in the multi-step process of carcinogenesis. Human chromosome 3 contains clusters of TSGs involved in many cancer types including nasopharyngeal carcinoma (NPC), the most common cancer in Southern China. Among ten candidate TSGs identified in chromosome 3 using NotI microarray, ITGA9 and WNT7A could be validated. 5'-aza-2' deoxycytidine treatment restored the expression of ITGA9 and WNT7A in two NPC cell lines. Immunostaining showed strong expression of these genes in the membrane and cytoplasm of adjacent control nasopharyngeal epithelium cells, while they were weakly expressed in NPC tumor cells. The ITGA9 promoter showed marked differentially methylation between tumor and control tissue, whereas no differentially methylation could be detected for the WNT7A promoter. The expression level of ITGA9 in NPC tumors was downregulated 4.9-fold, compared to the expression in control. ITGA9 methylation was detected by methylation specific PCR (MSP) in 56% of EBV positive NPC-cases with 100% specificity. Taken together, this suggests that ITGA9 might be a TSG in NPC that is involved in tumor cell biology. The possibility of using ITGA9 methylation as a marker for early detection of NPC should further be explored.
Insights
Integrin alpha 9 (ITGA9) is a tumor suppressor gene silenced by promoter methylation in nasopharyngeal carcinoma (NPC). ITGA9 methylation may serve as a potential biomarker for early NPC detection.
Area of Science:
- Oncology
- Molecular Biology
- Epigenetics
Background:
- Epigenetic silencing of tumor suppressor genes (TSGs) via promoter methylation is an early event in carcinogenesis.
- Human chromosome 3 harbors TSGs implicated in various cancers, including nasopharyngeal carcinoma (NPC).
Purpose of the Study:
- To identify and validate candidate TSGs on chromosome 3 in NPC.
- To investigate the role of ITGA9 and WNT7A in NPC development and their potential as diagnostic markers.
Main Methods:
- NotI microarray analysis to identify candidate TSGs.
- 5'-aza-2' deoxycytidine treatment to assess gene expression restoration.
- Immunostaining for protein expression analysis.
- Methylation-specific PCR (MSP) to detect promoter methylation.
Main Results:
- ITGA9 and WNT7A were validated as candidate TSGs; their expression was restored by demethylation treatment.
- ITGA9 showed significant promoter hypermethylation and a 4.9-fold downregulation in NPC tumors compared to adjacent normal tissue.
- ITGA9 methylation was detected in 56% of EBV-positive NPC cases with 100% specificity.
Conclusions:
- ITGA9 functions as a tumor suppressor gene in NPC, with its silencing mediated by promoter methylation.
- ITGA9 methylation represents a promising biomarker for the early detection of nasopharyngeal carcinoma.
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