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Noncoding RNA (ncRNA) Profile Association with Patient Outcome in Epithelial Ovarian Cancer Cases.
Oliveira, Douglas V N P; Prahm, Kira P; Christensen, Ib J; Hansen, Anker; Høgdall, Claus K; Høgdall, Estrid V.
Afiliação
  • Oliveira DVNP; Department of Pathology, Herlev Hospital, University of Copenhagen, Herlev, Denmark.
  • Prahm KP; Department of Pathology, Herlev Hospital, University of Copenhagen, Herlev, Denmark.
  • Christensen IJ; Department of Pathology, Herlev Hospital, University of Copenhagen, Herlev, Denmark.
  • Hansen A; Oncology Venture, Hoersholm, Denmark.
  • Høgdall CK; Department of Gynecology, Juliane Marie Centre, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
  • Høgdall EV; Department of Pathology, Herlev Hospital, University of Copenhagen, Herlev, Denmark. estrid.hoegdall@regionh.dk.
Reprod Sci ; 28(3): 757-765, 2021 03.
Article em En | MEDLINE | ID: mdl-33125686
ABSTRACT
Ovarian cancer (OC) is the second most frequent type of gynecological cancers worldwide. In the past decades, the development of novel diagnostic and prognostic biomarkers available for OC has been limited, reflecting by the lack of specificity of such markers or very costly management. Microarray expression profiling has shown very effective results in exploring new molecular markers for patients with OC. Nonetheless, most screenings are focused on mutations or expression of molecules that are translated into proteins, corresponding to only 2% of the total human genome. In order to account for the vast majority of transcripts, in the present exploratory study, we assessed the expression levels of a comprehensive panel of noncoding RNA in different subtypes of OC. We further evaluated their association with patient overall survival (OS) and aggressive forms of the disease, such as tumor type, stage, and chemotherapy resistance. By microarray profiling in a total of 197 epithelial OC patients (162 serous carcinomas, 15 endometrioid carcinomas, 11 mucinous carcinomas, and 9 clear cell carcinomas), we found two candidates, SNORA68 and SNORD74, which associated with OS and poor clinicopathological features. The overexpression of those two targets combined was correlated with shorter OS and progression-free survival. That association was further observed to correlate with a more aggressive form of the disease. Overall, the results indicate that a panel comprised of SNORA68 and SNORD74 may be clinically relevant, where patients could be offered a more individualized, targeted follow-up, given its further validation on future prospective clinical studies.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Perfilação da Expressão Gênica / RNA não Traduzido / Transcriptoma / Carcinoma Epitelial do Ovário Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Perfilação da Expressão Gênica / RNA não Traduzido / Transcriptoma / Carcinoma Epitelial do Ovário Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article