Long non-coding RNA regulating androgen receptor signaling in breast and prostate cancer

dc.contributor.authorKumar, Shashank
dc.contributor.authorPrajapati, Kumari Sunita
dc.contributor.authorSingh, Atul Kumar
dc.contributor.authorKushwaha, Prem Prakash
dc.contributor.authorShuaib, Mohd
dc.contributor.authorGupta, Sanjay
dc.date.accessioned2024-01-16T14:23:06Z
dc.date.accessioned2024-08-13T10:34:57Z
dc.date.available2024-01-16T14:23:06Z
dc.date.available2024-08-13T10:34:57Z
dc.date.issued2021-02-07T00:00:00
dc.description.abstractThe human genome transcribe an array of RNAs that do not encode proteins and may act as mediators in the regulation of gene expression. Long non-coding RNAs (lncRNAs) are a group of non-coding RNAs consisting of more than 200 nucleotides of RNA transcripts that play important role in tumor development. Numerous lncRNAs have been characterized as functional transcripts associated with several biological processes and pathologic stages. Although the biological function and molecular mechanisms of lncRNAs remains to be explored, recent studies demonstrate aberrant expression of several lncRNAs linked with various human cancers. The present review summarizes the current knowledge of lncRNA expression patterns and mechanisms that contribute to carcinogenesis. In particular, we focus on lncRNAs regulating androgen receptor signaling pathways in prostate and breast cancer subtype having prognostic and therapeutic implications. � 2021 Elsevier B.V.en_US
dc.identifier.doi10.1016/j.canlet.2020.11.039
dc.identifier.issn3043835
dc.identifier.urihttps://doi.org/10.1016/j.canlet.2020.11.039
dc.identifier.urihttp://10.2.3.109/handle/32116/2840
dc.language.isoen_USen_US
dc.publisherElsevier Ireland Ltden_US
dc.subjectAndrogen receptoren_US
dc.subjectLong non-coding RNAsen_US
dc.subjectProstate canceren_US
dc.subjectSignaling pathwayen_US
dc.subjectTriple negative breast canceren_US
dc.titleLong non-coding RNA regulating androgen receptor signaling in breast and prostate canceren_US
dc.title.journalCancer Lettersen_US
dc.typeShort surveyen_US
dc.type.accesstypeOpen Accessen_US

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