Telomeres are involved in processes like cellular growth, chromosomal stability, and proper segregation to daughter cells. Telomere length measured in leukocytes (LTL) has been investigated in different cancer types, including multiple myeloma (MM). However, LTL measurement is prone to heterogeneity due to sample handling and study design (retrospective vs. prospective). LTL is genetically determined; genome-wide association studies identified 11 SNPs that, combined in a score, can be used as a genetic instrument to measure LTL and evaluate its association with MM risk. This approach has been already successfully attempted in various cancer types but never in MM. We tested the “teloscore” in 2407 MM patients and 1741 controls from the International Multiple Myeloma rESEarch (IMMeNSE) consortium. We observed an increased risk for longer genetically determined telomere length (gdTL) (OR = 1.69; 95% CI 1.36–2.11; P = 2.97 × 10−6 for highest vs. lowest quintile of the score). Furthermore, in a subset of 1376 MM patients we tested the relationship between the teloscore and MM patients survival, observing a better prognosis for longer gdTL compared with shorter gdTL (HR = 0.93; 95% CI 0.86–0.99; P = 0.049). In conclusion, we report convincing evidence that longer gdTL is a risk marker for MM risk, and that it is potentially involved in increasing MM survival.

Genetically determined telomere length and multiple myeloma risk and outcome

Giaccherini M.
Primo
;
Buda G.;Gemignani F.;Campa D.
Ultimo
2021-01-01

Abstract

Telomeres are involved in processes like cellular growth, chromosomal stability, and proper segregation to daughter cells. Telomere length measured in leukocytes (LTL) has been investigated in different cancer types, including multiple myeloma (MM). However, LTL measurement is prone to heterogeneity due to sample handling and study design (retrospective vs. prospective). LTL is genetically determined; genome-wide association studies identified 11 SNPs that, combined in a score, can be used as a genetic instrument to measure LTL and evaluate its association with MM risk. This approach has been already successfully attempted in various cancer types but never in MM. We tested the “teloscore” in 2407 MM patients and 1741 controls from the International Multiple Myeloma rESEarch (IMMeNSE) consortium. We observed an increased risk for longer genetically determined telomere length (gdTL) (OR = 1.69; 95% CI 1.36–2.11; P = 2.97 × 10−6 for highest vs. lowest quintile of the score). Furthermore, in a subset of 1376 MM patients we tested the relationship between the teloscore and MM patients survival, observing a better prognosis for longer gdTL compared with shorter gdTL (HR = 0.93; 95% CI 0.86–0.99; P = 0.049). In conclusion, we report convincing evidence that longer gdTL is a risk marker for MM risk, and that it is potentially involved in increasing MM survival.
2021
Giaccherini, M.; Macauda, A.; Orciuolo, E.; Rymko, M.; Gruenpeter, K.; Dumontet, C.; Razny, M.; Moreno, V.; Buda, G.; Beider, K.; Varkonyi, J.; Avet-Loiseau, H.; Martinez-Lopez, J.; Marques, H.; Watek, M.; Sarasquete, M. E.; Andersen, V.; Karlin, L.; Suska, A.; Kruszewski, M.; Abildgaard, N.; Dudzinski, M.; Butrym, A.; Nagler, A.; Vangsted, A. J.; Kadar, K.; Waldemar, T.; Jamroziak, K.; Jacobsen, S. E. H.; Ebbesen, L. H.; Taszner, M.; Mazur, G.; Lesueur, F.; Pelosini, M.; Garcia-Sanz, R.; Jurczyszyn, A.; Demangel, D.; Reis, R. M.; Iskierka-Jazdzewska, E.; Markiewicz, M.; Gemignani, F.; Subocz, E.; Zawirska, D.; Druzd-Sitek, A.; Stepien, A.; Alonso, M. H.; Sainz, J.; Canzian, F.; Campa, D.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/1105316
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