APPLYCATION OF METHYLATED PCR TECHNIQUE TO DETECT METHYLATION OF RASSF1A DAPK GENE IN THE BLOOD SIMPLES OF NASOPHARYLGEAL CARCINOMA PATIENTS | Gấm | TNU Journal of Science and Technology

APPLYCATION OF METHYLATED PCR TECHNIQUE TO DETECT METHYLATION OF RASSF1A DAPK GENE IN THE BLOOD SIMPLES OF NASOPHARYLGEAL CARCINOMA PATIENTS

About this article

Published: 30/01/19

Authors

1. Nguyen Thi Hong Gam Email to author, University of Medicine and Pharmacy - TNU
2. Nguyen Thi Hai Yen, University of Medicine and Pharmacy - TNU
3. Nguyen Van Do, Hanoi Medical University
4. Nguyen Thanh Binh, Hanoi Medical University

Abstract


Methylation that reduces or does not express the cancer gene Rassf1A and DAPK has been shown in numerous studies on lung cancer. However, in Vietnam the research on methylation of tumor surpress gene have not much yet. Although 70% of human cancer is detected now, the last time and the extra time is very short. This relerve process to methylation of the genes of the genes of the genes in the blood of the package of the nasopharylgeal carcinoma. Cross-sectional descriptive study, non-probability sampling with 9 nasopharyngeal carcinoma and 9 normal patient. Meththylation Specipic PCR as methylation state is released tool: RASSF1A gene found for 100% (9/9) is methylated. The DAPK gene does not detect 100% methylation (9/9) in blood samples of patients with nasopharyngeal carcinoma. Both RASSF1A gene and DAPK gene are not found methyl in the normal blood pattern selected as an argument.

Keywords


MSP: Methylation-Specific Polymerase chain reaction; RASF1A: RAS association domain family member ; DAPK: Death-associated protein kinase

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