Dysregulated Expression of Long Intergenic Non-coding RNAs (LincRNAs) in Urothelial Bladder Carcinoma

Long intergenic non-coding RNA (lincRNA) has been introduced as key regulators of diverse biological processes, including transcription, chromatin organization, cell growth and tumorigenesis. With regard to the potential role of lincRNAs in cancer development, one may postulate that differential exp...

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Bibliographic Details
Published in:International journal of molecular and cellular medicine Vol. 6; no. 4; pp. 212 - 221
Main Authors: Ousati Ashtiani, Zahra, Pourmand, Gholamreza, Salami, Seyed Alireza, Ayati, Mohsen, Tavakkoly-Bazzaz, Javad
Format: Journal Article
Language:English
Published: Iran Babol University of Medical Sciences 2017
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ISSN:2251-9637, 2251-9645
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Summary:Long intergenic non-coding RNA (lincRNA) has been introduced as key regulators of diverse biological processes, including transcription, chromatin organization, cell growth and tumorigenesis. With regard to the potential role of lincRNAs in cancer development, one may postulate that differential expression of lincRNAs could be employed as a tool in cancer diagnosis, prognosis, and targeted therapy. In this study, we aimed to explore the putative correlation between the expression levels of two lincRNAs: and in the bladder cancer (BC), in comparison with its adjacent non-cancerous tissue. Fifty Iranian subjects diagnosed with BC, representing in different stages and grades participated in this study The mRNA expression levels of the abovementioned lincRNAs were comparatively analyzed in cancerous and their adjacent non-cancerous counterpart tissues, of each subject by Real-Time PCR. The expression levels of , and were significantly lower in tumor tissues in comparison with their adjacent normal tissues (P<0.001). More notably, in the case of the reduced expression was differentiated by the muscle invasiveness pattern of the tumor (P= 0.05). Our study presents a new finding about the tumor suppressor potentiality of these lincRNAs in BC development that in turn may suggest them as candidate biomarkers. Replicating this study in higher number of BC subjects, coupled with functional analysis, is necessary to investigate interconnections between these RNAs and cancer development, leading to better understanding of cancer biology.
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ISSN:2251-9637
2251-9645
DOI:10.22088/BUMS.6.4.212