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ARMS-PCR combined with capillary electrophoresis can be a sensitive and quantitative method for detection of MYD88-L265P mutation in lymphoma / 中国实验血液学杂志
Journal of Experimental Hematology ; (6): 1663-1667, 2018.
Article Dans Chinois | WPRIM | ID: wpr-773039
ABSTRACT
OBJECTIVE@#To investigate the feasibility of sensitive and quantitative detection of MYD88 gene L265P mutation in lymphoma patients by using ARMS-PCR combined with capillary electrophoresis.@*METHODS@#ARMS-PCR amplified MYD88 gene was analyzed by capillary electrophoresis in ABI 3730 sequencer; Exon 5 of the same gene was sequenced bi-directionally as reported.@*RESULTS@#The sensitivity of detection L265P mutations by the ARMS-PCR combined with capillary electrophoresis and direct sequencing was 0.2% and 5%, respectively, according to the detection of the gradient-diluted plasmid standards. The detection rate of 184 patients was 13.59% and 8.28%, respectively (p<0.001). Moreover, the former method can successfully detect the mutation ratio(R=0.979), and the repeatabilities (CV=2.86%, 1.94%, 5.49%) are acceptable.@*CONCLUSION@#ARMS-PCR combined with capillary electrophoresis can quantitatively detect the MYD88 gene L265P mutation, and the detection sensitivity is significantly higher than sanger sequencing. As a supplement to the latter, it can effectively lead to the earlier diagnose and monitoring of minimal residual disease.
Sujets)
Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Analyse de mutations d&apos;ADN / Réaction de polymérisation en chaîne / Électrophorèse capillaire / Facteur de différenciation myéloïde-88 / Génétique / Lymphomes / Mutation Type d'étude: Etude diagnostique / Guide de pratique Limites du sujet: Humains langue: Chinois Texte intégral: Journal of Experimental Hematology Année: 2018 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Analyse de mutations d&apos;ADN / Réaction de polymérisation en chaîne / Électrophorèse capillaire / Facteur de différenciation myéloïde-88 / Génétique / Lymphomes / Mutation Type d'étude: Etude diagnostique / Guide de pratique Limites du sujet: Humains langue: Chinois Texte intégral: Journal of Experimental Hematology Année: 2018 Type: Article