TY - JOUR
T1 - Distinctive genomic features of human T-lymphotropic virus type 1-related adult T-cell leukemia-lymphoma in Western populations
AU - Myers, Caroline S.
AU - Williams, Eli
AU - Cornejo, Carlos Barrionuevo
AU - Pongas, Georgios
AU - Toomey, Ngoc L.
AU - Sanches, Jose A.
AU - Battistella, Maxime
AU - Mo, Samuel
AU - Pulitzer, Melissa
AU - Moskaluk, Cristopher A.
AU - Bhagat, Govind
AU - Ofori, Kenneth
AU - Davick, Jonathan J.
AU - Servitje, Octavio
AU - Miyashiro, Denis
AU - Climent, Fina
AU - Ringbloom, Kimberley
AU - Duenas, Daniela
AU - Law, Calvin
AU - Zambrano, Sandro Casavilca
AU - Malpica, Luis
AU - Beltran, Brady E.
AU - Castro, Denisse
AU - Barreto, Luciana
AU - Brites, Carlos
AU - Chapman, Jennifer R.
AU - Choi, Jaehyuk
AU - Gru, Alejandro A.
AU - Ramos, Juan C.
N1 - Publisher Copyright:
©2024 Ferrata Storti Foundation.
PY - 2024/12
Y1 - 2024/12
N2 - Adult T-cell leukemia-lymphoma (ATLL) is an aggressive malignancy driven by human T-cell leukemia virus type 1 (HTLV-1). Although patients from the Western hemisphere (Afro-Caribbean and South American) face worse prognoses, our understanding of ATLL molecular drivers derives mostly from Japanese studies. We performed multi-omic analyses to elucidate the genomic landscape of ATLL in Western cohorts. Recurrent deletions and/or damaging mutations involving FOXO3, ANKRD11, DGKZ, and PTPN6 implicate these genes as potential tumor suppressors. RNA-sequencing, published functional data and in vitro assays support the roles of ANKRD11 and FOXO3 as regulators of T-cell proliferation and apoptosis in ATLL, respectively. Survival data suggest that ANKRD11 mutation may confer a worse prognosis. Japanese and Western cohorts, in addition to acute and lymphomatous subtypes, demonstrated distinct molecular patterns. GATA3 deletion was associated with chronic cases with unfavorable outcomes. IRF4 and CARD11 mutations frequently emerged in relapses after interferon therapy. Our findings reveal novel putative ATLL driver genes and clinically relevant differences between Japanese and Western ATLL patients.
AB - Adult T-cell leukemia-lymphoma (ATLL) is an aggressive malignancy driven by human T-cell leukemia virus type 1 (HTLV-1). Although patients from the Western hemisphere (Afro-Caribbean and South American) face worse prognoses, our understanding of ATLL molecular drivers derives mostly from Japanese studies. We performed multi-omic analyses to elucidate the genomic landscape of ATLL in Western cohorts. Recurrent deletions and/or damaging mutations involving FOXO3, ANKRD11, DGKZ, and PTPN6 implicate these genes as potential tumor suppressors. RNA-sequencing, published functional data and in vitro assays support the roles of ANKRD11 and FOXO3 as regulators of T-cell proliferation and apoptosis in ATLL, respectively. Survival data suggest that ANKRD11 mutation may confer a worse prognosis. Japanese and Western cohorts, in addition to acute and lymphomatous subtypes, demonstrated distinct molecular patterns. GATA3 deletion was associated with chronic cases with unfavorable outcomes. IRF4 and CARD11 mutations frequently emerged in relapses after interferon therapy. Our findings reveal novel putative ATLL driver genes and clinically relevant differences between Japanese and Western ATLL patients.
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U2 - 10.3324/haematol.2024.285233
DO - 10.3324/haematol.2024.285233
M3 - Article
C2 - 39113648
AN - SCOPUS:85210958720
SN - 0390-6078
VL - 109
SP - 4021
EP - 4039
JO - Haematologica
JF - Haematologica
IS - 12
ER -