NAVRKALOVÁ, Veronika, Terézia KURUCOVÁ, Kamila RÉBLOVÁ, Michaela BOHÚNOVÁ, Karla PLEVOVÁ, Michael DOUBEK, Jitka MALČÍKOVÁ, Šárka PAVLOVÁ, Jana KOTAŠKOVÁ and Šárka POSPÍŠILOVÁ. Tracking CLL cells with aberrations in the TP53 gene using scRNA-seq in relapsed/refractory patients. In XX. International Workshop on CLL (iwCLL 2023), Boston, USA. 2023.
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Basic information
Original name Tracking CLL cells with aberrations in the TP53 gene using scRNA-seq in relapsed/refractory patients.
Authors NAVRKALOVÁ, Veronika, Terézia KURUCOVÁ, Kamila RÉBLOVÁ, Michaela BOHÚNOVÁ, Karla PLEVOVÁ, Michael DOUBEK, Jitka MALČÍKOVÁ, Šárka PAVLOVÁ, Jana KOTAŠKOVÁ and Šárka POSPÍŠILOVÁ.
Edition XX. International Workshop on CLL (iwCLL 2023), Boston, USA, 2023.
Other information
Original language English
Type of outcome Konferenční abstrakta
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
WWW URL
Organization Středoevropský technologický institut – Repository – Repository
Keywords in English TP53 gene aberrations; CCL; resistance
Links LX22NPO5102, research and development project. MUNI/A/1224/2022, interní kód Repo. NU20-08-00314, research and development project.
Changed by Changed by: RNDr. Daniel Jakubík, učo 139797. Changed: 27/3/2024 04:12.
Abstract
TP53 gene aberrations (mutation and/or deletion 17p) are the most important adverse prognostic and predictive markers in CLL • Low-burden TP53 mutations are often detectable in CLL cells prior to the therapy and expand upon the selective pressure of chemoimmunotherapy • Other genomic alterations accompany aberrations in the TP53 gene • Bulk analysis (such as whole genome/exome sequencing or genomic array) cannot precisely determine the co-occurrence of abnormalities in individual cells • Expression profiles of cells bearing TP53 mutation are altered and may be distinguished from expression profiles of unaffected cells using single-cell RNA sequencing (scRNA-seq). We aimed to explore the possibility to identify and characterize populations of CLL cells resistant to treatment and causing refractoriness in samples from patients with disease relapse. We tried to trace back the refractory cells in samples prior to the therapy using scRNA-seq in patients with TP53 mutations
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