Epigenetic Alteration and its Association With Downregulated FOXP3 Gene in Indian Breast Cancer Patients

gene, known to be a potential tumor suppressor, has been identified to interact with HER2 in mammary cancer. Moreover, the high expression of serves as a good predictor of the survival of patients in breast cancer, prostate cancer, and gastric cancer. The expression and epigenetic alterations were e...

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Veröffentlicht in:Frontiers in genetics 2021-11, Vol.12, p.781400-781400
Hauptverfasser: Sadaf, Akhter, Naseem, Alharbi, Raed A, Sindi, Abdulmajeed A A, Najm, Mohammad Zeeshan, Alhumaydhi, Fahad A, Khan, Mohammad Aasif, Deo, S V S, Husain, Syed Akhtar
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Sprache:eng
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Zusammenfassung:gene, known to be a potential tumor suppressor, has been identified to interact with HER2 in mammary cancer. Moreover, the high expression of serves as a good predictor of the survival of patients in breast cancer, prostate cancer, and gastric cancer. The expression and epigenetic alterations were evaluated in female breast cancer patients. Expression studies at the mRNA level and protein level were conducted in 140 breast cancer cases by real-time PCR and immunohistochemistry, respectively. Epigenetic studies were also conducted by analyzing the methylation status at the promoter region of the gene using MS-PCR. mRNA expression and protein expression were downregulated in breast cancer patients. The absence of protein expression is significantly associated with promoter methylation, where 70 methylated cases exhibited protein loss (70/95, 73.6%). Statistically, we also found a significant correlation between protein expression and TNM stage, promoter methylation, and histological grade. The methylated cases that did not express protein were also significantly associated with positive lymph node metastasis and HER-2 status. The expression profile of may serve as a prognostic factor. In short, may stand in the most crucial list of biomarkers for breast cancer, bringing compelling results in terms of treatment and management of the disease.
ISSN:1664-8021
1664-8021
DOI:10.3389/fgene.2021.781400