a 2023

Molecular response of chronic lymphocytic leukemia cells to targeted therapy.

HLAVÁČ, Kryštof, Laura ONDRIŠOVÁ, Václav ŠEDA, Petra PAVELKOVÁ, Eva HOFERKOVÁ et. al.

Basic information

Original name

Molecular response of chronic lymphocytic leukemia cells to targeted therapy.

Authors

HLAVÁČ, Kryštof, Laura ONDRIŠOVÁ, Václav ŠEDA, Petra PAVELKOVÁ, Eva HOFERKOVÁ, Daniel FILIP and Marek MRÁZ

Edition

XXII. Interdisciplinary Meeting of Young Life Scientists, Milovy, 2023

Other information

Language

English

Type of outcome

Konferenční abstrakta

Country of publisher

Czech Republic

Confidentiality degree

is not subject to a state or trade secret

References:

Organization

Středoevropský technologický institut – Repository – Repository

Keywords in English

Chronic lymphocytic leukemia; BTK inhibitor; ibrutinib; PI3K inhibitor; idelalisib;

Links

LM2018132, research and development project. LX22NPO5102, research and development project. MUNI/A/1224/2022, interní kód Repo. MUNI/C/0086/2022, interní kód Repo.
Changed: 26/3/2024 03:18, RNDr. Daniel Jakubík

Abstract

V originále

amp;Run assay, an alternative to ChIPseq, in the MEC1 cell line, to characterize genes directly regulated by this transcription factor. Apart from the regulation of the BCR signaling pathway, we noticed its potential in response to other drugs such as the BH3 mimetic (BCL2 inhibitor) venetoclax that has been recently approved for CLL therapy. Altogether, we thoroughly describe particular changes in CLL transcriptome, that provide increase in survival of leukemic cells during the BCR inhibitors therapy in both primary CLL cells and cell lines. Based on these results, we further suggest a rational combinatorial treatment of ibrutinib/idelalisib with an inhibitor targeting the transcription factor as a potential therapeutic strategy to eliminate mechanism of adaptation to BCR inhibitors.