Detailed Information on Publication Record
2023
CRISPR/Cas9 technology as a useful tool in the study of chronic lymphocytic leukemia.
PESCHELOVÁ, Helena, Veronika KOZLOVÁ, Veronika MANČÍKOVÁ, Lenka DOSTÁLOVÁ, Adriana LADUNGOVÁ et. al.Basic information
Original name
CRISPR/Cas9 technology as a useful tool in the study of chronic lymphocytic leukemia.
Authors
PESCHELOVÁ, Helena (203 Czech Republic, belonging to the institution), Veronika KOZLOVÁ (203 Czech Republic, belonging to the institution), Veronika MANČÍKOVÁ (703 Slovakia, belonging to the institution), Lenka DOSTÁLOVÁ (203 Czech Republic, belonging to the institution), Adriana LADUNGOVÁ (703 Slovakia, belonging to the institution), Dominika ŠKRNOVÁ (203 Czech Republic, belonging to the institution), Václav HEJRET (203 Czech Republic, belonging to the institution) and Michal ŠMÍDA (203 Czech Republic, guarantor, belonging to the institution)
Edition
PhD and PostDoc RETREAT, Sněžné, Milovy, 2023
Other information
Language
English
Type of outcome
Konferenční abstrakt
Field of Study
30204 Oncology
Country of publisher
Czech Republic
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
RIV identification code
RIV/00216224:14740/23:00132849
Organization unit
Central European Institute of Technology
Keywords in English
Chronic lymphocytic leukemia; somatic mutations; CRISPR/Cas9 screening
Tags
Tags
Reviewed
Změněno: 30/3/2024 14:06, Mgr. Eva Dubská
Abstract
V originále
Chronic lymphocytic leukemia (CLL) is characterized by genetic heterogeneity and a variety of somatic mutations, the most frequent of which targeting ATM, TP53, NOTCH1, MYD88 and SF3B1 genes. A thorough exploration of these mutations could shed light on the disease etiology, or even lead to the discovery of potential novel drug targets. However, CLL cells extracted from patients do not proliferate ex vivo and thus preclude lengthy experiments, such as CRISPR/Cas9 screening. 76 The aim of this study was to generate stable knockout (ATM, TP53) and knock-in (NOTCH1, SF3B1 and MYD88) CLL cell lines and subsequently use them to investigate unique vulnerabilities specific to these mutations
Links
LX22NPO5102, research and development project |
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MUNI/A/1224/2022, interní kód MU |
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