Evolution of TP53 abnormalities during CLL disease course is associated with telomere length changes

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Publikace nespadá pod Ekonomicko-správní fakultu, ale pod Lékařskou fakultu. Oficiální stránka publikace je na webu muni.cz.
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OLBERTOVÁ Helena PLEVOVÁ Karla PAVLOVÁ Šárka MALCIKOVA Jitka KOTAŠKOVÁ Jana STRÁNSKÁ Kamila ŠPUNAROVÁ Michaela TRBUŠEK Martin NAVRKALOVÁ Veronika DVOŘÁČKOVÁ Barbara TOM Nikola PÁL Karol JAROŠOVÁ Marie BRYCHTOVÁ Yvona PANOVSKÁ Anna DOUBEK Michael POSPÍŠILOVÁ Šárka

Rok publikování 2022
Druh Článek v odborném periodiku
Časopis / Zdroj BMC Cancer
Fakulta / Pracoviště MU

Lékařská fakulta

Citace
www https://bmccancer.biomedcentral.com/articles/10.1186/s12885-022-09221-z
Doi http://dx.doi.org/10.1186/s12885-022-09221-z
Klíčová slova Chronic Lymphocytic Leukemia; Telomere; TP53; Clonal evolution; BCR signaling
Popis Background Telomeres are protective structures at chromosome ends which shorten gradually with increasing age. In chronic lymphocytic leukemia (CLL), short telomeres have been associated with unfavorable disease outcome, but the link between clonal evolution and telomere shortening remains unresolved. Methods We investigated relative telomere length (RTL) in a well-characterized cohort of 198 CLL patients by qPCR and focused in detail on a subgroup 26 patients who underwent clonal evolution of TP53 mutations (evolTP53). In the evolTP53 subgroup we explored factors influencing clonal evolution and corresponding changes in telomere length through measurements of telomerase expression, lymphocyte doubling time, and BCR signaling activity. Results At baseline, RTL of the evolTP53 patients was scattered across the entire RTL spectrum observed in our CLL cohort. RTL changed in the follow-up samples of 16/26 (62%) evolTP53 cases, inclining to reach intermediate RTL values, i.e., longer telomeres shortened compared to baseline while shorter ones prolonged. For the first time we show that TP53 clonal shifts are linked to RTL change, including unexpected RTL prolongation. We further investigated parameters associated with RTL changes. Unstable telomeres were significantly more frequent among younger patients (P = 0.032). Shorter telomeres were associated with decreased activity of the B-cell receptor signaling components p-ERK1/2, p-ZAP-70/SYK, and p-NF kappa B (P = 0.04, P = 0.01, and P = 0.02, respectively). Conclusions Our study revealed that changes of telomere length reflect evolution in leukemic subclone proportion, and are associated with specific clinico-biological features of the explored cohort.
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