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RNA-based ovarian cancer research from 'a gene to systems biomedicine' perspective

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dc.contributor.author Gov, Esra
dc.contributor.author Kori, Medi
dc.contributor.author Arga, Kazim Yalcin
dc.date.accessioned 2019-11-14T05:22:17Z
dc.date.available 2019-11-14T05:22:17Z
dc.date.issued 2017
dc.identifier.citation Gov, E., Kori, M., & Arga, K. Y. (2017). RNA-based ovarian cancer research from “a gene to systems biomedicine” perspective. Systems Biology in Reproductive Medicine, 63(4), 219-238. https://doi.org/10.1080/19396368.2017.1330368 tr_TR
dc.identifier.issn 1939-6368
dc.identifier.issn 1939-6376
dc.identifier.uri http://openaccess.adanabtu.edu.tr:8080/xmlui/handle/123456789/559
dc.identifier.uri https://doi.org/10.1080/19396368.2017.1330368
dc.description DT: Review tr_TR
dc.description WOS indeksli yayınlar koleksiyonu. / WOS indexed publications collection.
dc.description.abstract Ovarian cancer remains the leading cause of death from a gynecologic malignancy, and treatment of this disease is harder than any other type of female reproductive cancer. Improvements in the diagnosis and development of novel and effective treatment strategies for complex pathophysiologies, such as ovarian cancer, require a better understanding of disease emergence and mechanisms of progression through systems medicine approaches. RNA-level analyses generate new information that can help in understanding the mechanisms behind disease pathogenesis, to identify new biomarkers and therapeutic targets and in new drug discovery. Whole RNA sequencing and coding and non-coding RNA expression array datasets have shed light on the mechanisms underlying disease progression and have identified mRNAs, miRNAs, and lncRNAs involved in ovarian cancer progression. In addition, the results from these analyses indicate that various signalling pathways and biological processes are associated with ovarian cancer. Here, we present a comprehensive literature review on RNA-based ovarian cancer research and highlight the benefits of integrative approaches within the systems biomedicine concept for future ovarian cancer research. We invite the ovarian cancer and systems biomedicine research fields to join forces to achieve the interdisciplinary caliber and rigor required to find real-life solutions to common, devastating, and complex diseases such as ovarian cancer.Abbreviations: CAF: cancer-associated fibroblasts; COG: Cluster of Orthologous Groups; DEA: disease enrichment analysis; EOC: epithelial ovarian carcinoma; ESCC: oesophageal squamous cell carcinoma; GSI: gamma secretase inhibitor; GO: Gene Ontology; GSEA: gene set enrichment analyzes; HAS: Hungarian Academy of Sciences; lncRNAs: long non-coding RNAs; MAPK/ERK: mitogen-activated protein kinase/extracellular signal-regulated kinases; NGS: next-generation sequencing; ncRNAs: non-coding RNAs; OvC: ovarian cancer; PI3K/Akt/mTOR: phosphatidylinositol-3-kinase/protein kinase B/mammalian target of rapamycin; RT-PCR: real-time polymerase chain reaction; SNP: single nucleotide polymorphism; TF: transcription factor; TGF-: transforming growth factor- tr_TR
dc.language.iso en tr_TR
dc.publisher SYSTEMS BIOLOGY IN REPRODUCTIVE MEDICINE / TAYLOR & FRANCIS INC tr_TR
dc.relation.ispartofseries 2017;Volume: 63 Issue: 4
dc.subject Non-coding RNAs tr_TR
dc.subject ovarian cancer
dc.subject systems biomedicine
dc.subject transcriptome
dc.subject LONG NONCODING RNA
dc.subject DIFFERENTIALLY EXPRESSED GENES
dc.subject PROTEIN-INTERACTION NETWORKS
dc.subject WNT/BETA-CATENIN PATHWAY
dc.subject PREDICTS POOR-PROGNOSIS
dc.subject TRANSCRIPTIONAL REGULATION
dc.subject CISPLATIN RESISTANCE
dc.subject MICRORNA REGULATION
dc.subject THERAPEUTIC TARGET
dc.subject METABOLIC NETWORK
dc.subject Andrology
dc.subject Reproductive Biology
dc.title RNA-based ovarian cancer research from 'a gene to systems biomedicine' perspective tr_TR
dc.type Article tr_TR


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