(In)Distinctive Role of Long Non-Coding RNAs in Common and Rare Ovarian Cancers.

Cancers (Basel)

Laboratory for Hereditary Cancer, Division of Molecular Medicine, Ruđer Bošković Institute, HR-10000 Zagreb, Croatia.

Published: October 2021

AI Article Synopsis

  • Rare ovarian cancers (ROCs) have a low incidence rate, affecting fewer than 6 women per 100,000 annually, which can delay diagnosis and worsen prognosis.
  • The tumors are linked to changes in gene and protein expression that disrupt normal cellular processes, leading to dysregulation associated with cancer.
  • This review focuses on the role of long non-coding RNAs (lncRNAs) in ovarian cancer, particularly their mechanisms of action and influence on ROCs, highlighting the need for further research in this underexplored area.

Article Abstract

Rare ovarian cancers (ROCs) are OCs with an annual incidence of fewer than 6 cases per 100,000 women. They affect women of all ages, but due to their low incidence and the potential clinical inexperience in management, there can be a delay in diagnosis, leading to a poor prognosis. The underlying causes for these tumors are varied, but generally, the tumors arise due to alterations in gene/protein expression in cellular processes that regulate normal proliferation and its checkpoints. Dysregulation of the cellular processes that lead to cancer includes gene mutations, epimutations, non-coding RNA (ncRNA) regulation, posttranscriptional and posttranslational modifications. Long non-coding RNA (lncRNA) are defined as transcribed RNA molecules, more than 200 nucleotides in length which are not translated into proteins. They regulate gene expression through several mechanisms and therefore add another level of complexity to the regulatory mechanisms affecting tumor development. Since few studies have been performed on ROCs, in this review we summarize the mechanisms of action of lncRNA in OC, with an emphasis on ROCs.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8534192PMC
http://dx.doi.org/10.3390/cancers13205040DOI Listing

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