Whole-exome and whole-genome sequencing in chronic lymphocytic leukemia: new biomarkers to target.

Abstract:

:Many biomarkers indicate prognosis in chronic lymphocytic leukemia; such as fluorescence in situ hybridization testing: 17p or 11q deletions have a worse prognosis than trisomy 12, 13q deletion or normal result, or the mutational status of the immunoglobulin heavy chain (IGHV): unmutated IGHV have a worse prognosis than mutated IGHV. Recently, many gene mutations (TP53, NOTCH1 etc.,) have been linked to a worse prognosis. With the new era of high-throughput sequencing, it has become easier to study gene mutations and their implication in predicting prognosis. In this review, we aim to review all the studies that performed whole-exome sequencing or whole-genome sequencing on chronic lymphocytic leukemia cells and explore the implication of various genes in disease prognosis.

journal_name

Pharmacogenomics

journal_title

Pharmacogenomics

authors

Hobeika C,Rached G,Chebly A,Chouery E,Kourie HR

doi

10.2217/pgs-2020-0022

subject

Has Abstract

pub_date

2020-08-01 00:00:00

pages

957-962

issue

13

eissn

1462-2416

issn

1744-8042

journal_volume

21

pub_type

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