Genomic landscapes of ovarian clear cell carcinoma from latin countries reveal aberrations linked to survival and progression

Author:

Batista Mariana de Paiva,Roffé Martín,Romero Ignacio,López-Guerrero José Antonio,Illueca Carmen,Lopez Raquel,Balieiro Anastácio da Costa Alexandre André,De Brot Louise,Molina Juan Pablo,Barboza Laura,Peria Fernanda Maris,Chaud Fernando,Gouvêa Yamada Ana Silvia,Poveda Andres,Rego Eduardo Magalhães

Abstract

Abstract Background Ovarian clear cell carcinomas (OCCCs) are rare, aggressive and chemoresistant tumors. Geographical and ethnic differences in the incidence of OCCC have been reported with a higher incidence in Asiatic countries. There is a paucity of information regarding OCCC in Latin America (LA) and other countries. Methods Here, we characterized two cohorts of 33 patients with OCCC from LA (24 from Brazil and 9 from Costa Rica) and a cohort of 27 patients from Spain. Genomic analysis was performed for 26 OCCC using the OncoScan platform. Tumors were classified according to their genomic landscapes into subgroups. Clinical parameters were related to the frequency of genomic aberrations. Results The median overall survival (OS) was not significantly different between the cohorts. Genomic landscapes were characterized by different homologous recombination deficiency (HRD) levels. No difference in the distribution of genomic landscapes profiles was detected between patients from the different cohorts. OCCCs with MYC-amplified tumors harboring a concomitant loss of a region in chromosome 13q12-q13 that includes the BRCA2 gene had the longest OS. In contrast, patients carrying a high number (> 30) of total copy number (CN) aberrations with no concomitant alterations in MYC and BRCA2 genes presented the shortest OS. Furthermore, amplification of the ASH1L gene was also associated with a shorter OS. Initial-stage OCCCs with early progression were characterized by gains in the JNK1 and MKL1 genes. Conclusions Our results provide new data from understudied OCCC populations and reveal new potential markers for OCCCs.

Funder

Fundação de Amparo à Pesquisa do Estado de São Paulo

The Spanish Ovarian Cancer Research Group

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Genetics,Oncology

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