A methylation-specific dot blot assay for improving specificity and sensitivity of methylation-specific PCR on DNA methylation analysis

Verfasser / Beitragende:
[Vo Lan, Nguyen Trang, Doan Van, Ta Thuan, Ta Van To, Vuong Linh, Nguyen Uyen]
Ort, Verlag, Jahr:
2015
Enthalten in:
International Journal of Clinical Oncology, 20/4(2015-08-01), 839-845
Format:
Artikel (online)
ID: 605491291
LEADER caa a22 4500
001 605491291
003 CHVBK
005 20210128100509.0
007 cr unu---uuuuu
008 210128e20150801xx s 000 0 eng
024 7 0 |a 10.1007/s10147-014-0780-5  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1007/s10147-014-0780-5 
245 0 2 |a A methylation-specific dot blot assay for improving specificity and sensitivity of methylation-specific PCR on DNA methylation analysis  |h [Elektronische Daten]  |c [Vo Lan, Nguyen Trang, Doan Van, Ta Thuan, Ta Van To, Vuong Linh, Nguyen Uyen] 
520 3 |a Background and objectives: Developing a methylation-specific dot blot assay (MSP-DB) to increase the sensitivity and specificity of simultaneous methylation analysis of multiple genes is the goal of the present study to evaluate the methylation status of GSTP1 and RASSF1A from prostate cancer in Vietnamese males. Methods: The methylation of GSTP1 and RASSF1A was investigated by using the MSP in 50 prostate cancer and 17 benign prostate hyperplasia specimens. The MSP-DB assay that uses a single or multiple probes specifically detected the methylation status of a particular gene or of the two genes GSTP1 and RASSF1A at the same time in a series of samples. The sensitivity and specificity of the MSP-DB were compared to those of the MSP. Results: The probes specifically hybridized with the methylated targets only in the MSP-DB, which allowed detecting GSTP1 and RASSF1A methylation in 23 of 50 and 14 of 50 patients with prostate cancer and in 2 of 17 and 4 of 17 patients with benign prostate hyperplasia. MSP-DB following the MSP assay improved the sensitivity of detection to more than 0.01% methylated status of a given high CpG-rich region. One methylated MSP product corresponding to the GSTP1, lack of methylated cytosine, was clearly detected on gel electrophoresis but barely visible on MSP-DB. Thus, the MSP-DB is suitable to eliminate the risk of false-positive results. Conclusion: The MSP-DB dispels the weakness of MSP and increases the sensitivity to simultaneous methylation analysis of multiple genes. The MSP-DB is advantageous for the promotion of DNA methylation markers in progressing quickly toward clinical application. 
540 |a Japan Society of Clinical Oncology, 2015 
690 7 |a DNA methylation  |2 nationallicence 
690 7 |a Glutathione S-transferase P1 (GSTP1)  |2 nationallicence 
690 7 |a RAS - association domain family member 1 (RASSF1A)  |2 nationallicence 
690 7 |a Methylation-specific polymerase chain reaction (MSP)  |2 nationallicence 
690 7 |a Methylation-specific dot blot assay (MSP-DB)  |2 nationallicence 
700 1 |a Lan  |D Vo  |u Faculty of Biology, VNU University of Science, 334, Nguyen Trai, Thanh Xuan, Hanoi, Vietnam  |4 aut 
700 1 |a Trang  |D Nguyen  |u Faculty of Biology, VNU University of Science, 334, Nguyen Trai, Thanh Xuan, Hanoi, Vietnam  |4 aut 
700 1 |a Van  |D Doan  |u Faculty of Biology, VNU University of Science, 334, Nguyen Trai, Thanh Xuan, Hanoi, Vietnam  |4 aut 
700 1 |a Thuan  |D Ta  |u Faculty of Biology, VNU University of Science, 334, Nguyen Trai, Thanh Xuan, Hanoi, Vietnam  |4 aut 
700 1 |a Van To  |D Ta  |u Department of Cytology and Pathology, National Cancer Hospital K, 43 Quan Su, Hoan Kiem, Hanoi, Vietnam  |4 aut 
700 1 |a Linh  |D Vuong  |u Department of Cytology and Pathology, National Cancer Hospital K, 43 Quan Su, Hoan Kiem, Hanoi, Vietnam  |4 aut 
700 1 |a Uyen  |D Nguyen  |u Institute of Microbiology and Biotechnology, Vietnam National University Hanoi, 144, Xuan Thuy, Cau Giay, Hanoi, Vietnam  |4 aut 
773 0 |t International Journal of Clinical Oncology  |d Springer Japan  |g 20/4(2015-08-01), 839-845  |x 1341-9625  |q 20:4<839  |1 2015  |2 20  |o 10147 
856 4 0 |u https://doi.org/10.1007/s10147-014-0780-5  |q text/html  |z Onlinezugriff via DOI 
898 |a BK010053  |b XK010053  |c XK010000 
900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a research-article  |2 jats 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-springer 
950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1007/s10147-014-0780-5  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Lan  |D Vo  |u Faculty of Biology, VNU University of Science, 334, Nguyen Trai, Thanh Xuan, Hanoi, Vietnam  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Trang  |D Nguyen  |u Faculty of Biology, VNU University of Science, 334, Nguyen Trai, Thanh Xuan, Hanoi, Vietnam  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Van  |D Doan  |u Faculty of Biology, VNU University of Science, 334, Nguyen Trai, Thanh Xuan, Hanoi, Vietnam  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Thuan  |D Ta  |u Faculty of Biology, VNU University of Science, 334, Nguyen Trai, Thanh Xuan, Hanoi, Vietnam  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Van To  |D Ta  |u Department of Cytology and Pathology, National Cancer Hospital K, 43 Quan Su, Hoan Kiem, Hanoi, Vietnam  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Linh  |D Vuong  |u Department of Cytology and Pathology, National Cancer Hospital K, 43 Quan Su, Hoan Kiem, Hanoi, Vietnam  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Uyen  |D Nguyen  |u Institute of Microbiology and Biotechnology, Vietnam National University Hanoi, 144, Xuan Thuy, Cau Giay, Hanoi, Vietnam  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t International Journal of Clinical Oncology  |d Springer Japan  |g 20/4(2015-08-01), 839-845  |x 1341-9625  |q 20:4<839  |1 2015  |2 20  |o 10147