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Clinical prospects of long noncoding RNAs as novel biomarkers and therapeutic targets in prostate cancer

Background: The lack of sensitive and specific biomarkers for prostate cancer (PCa) has led to over-diagnosis and overtreatment with uncertain benefit. Therefore, biomarkers for early diagnosis that can distinguish aggressive from indolent tumors and that can detect metastatic or recurrent disease a...

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Published in:Prostate cancer and prostatic diseases 2016-03, Vol.19 (1), p.14-20
Main Authors: Mouraviev, V, Lee, B, Patel, V, Albala, D, Johansen, T E B, Partin, A, Ross, A, Perera, R J
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container_title Prostate cancer and prostatic diseases
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description Background: The lack of sensitive and specific biomarkers for prostate cancer (PCa) has led to over-diagnosis and overtreatment with uncertain benefit. Therefore, biomarkers for early diagnosis that can distinguish aggressive from indolent tumors and that can detect metastatic or recurrent disease are needed. Long noncoding RNAs (lncRNAs) are non-protein-coding RNA species. lncRNAs are dysregulated in many diseases including PCa and are emerging as major players in cancer development. lncRNAs have several features that make then suitable as both biomarkers and therapeutics, and lncRNAs regulate critical cancer hallmarks in prostate epithelial cells including proliferation and survival. Methods: The PubMed database was searched using the terms 'long noncoding RNA', 'biomarker' and 'prostate cancer'. Known lncRNAs implicated as biomarkers and potential therapeutic targets in PCa are reviewed. Results: We comprehensively review several lncRNAs with potential as biomarkers for PCa. lncRNAs including PCA3 , PCAT s, SChLAP1 , SPRY4-IT1 and TRPM2-AS are upregulated in PCa and are cancer specific; they are, therefore, attractive lead candidate biomarkers for clinical application. Several lncRNA therapeutics are currently being investigated by several companies for the treatment of various cancers including PCa. Small interfering RNAs, antisense oligonucleotides, ribozymes, deoxyribozymes and aptemers are few promising technologies for future lncRNA bases therapeutics. Conclusion: lncRNA expression is altered in cancer. Aberrant regulation promotes tumor formation, progression and metastasis. lncRNAs can use as tumor markers for PCa and may be attractive novel therapeutic targets for the diagnosis and treatment of PCa.
doi_str_mv 10.1038/pcan.2015.48
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Therefore, biomarkers for early diagnosis that can distinguish aggressive from indolent tumors and that can detect metastatic or recurrent disease are needed. Long noncoding RNAs (lncRNAs) are non-protein-coding RNA species. lncRNAs are dysregulated in many diseases including PCa and are emerging as major players in cancer development. lncRNAs have several features that make then suitable as both biomarkers and therapeutics, and lncRNAs regulate critical cancer hallmarks in prostate epithelial cells including proliferation and survival. Methods: The PubMed database was searched using the terms 'long noncoding RNA', 'biomarker' and 'prostate cancer'. Known lncRNAs implicated as biomarkers and potential therapeutic targets in PCa are reviewed. Results: We comprehensively review several lncRNAs with potential as biomarkers for PCa. lncRNAs including PCA3 , PCAT s, SChLAP1 , SPRY4-IT1 and TRPM2-AS are upregulated in PCa and are cancer specific; they are, therefore, attractive lead candidate biomarkers for clinical application. Several lncRNA therapeutics are currently being investigated by several companies for the treatment of various cancers including PCa. Small interfering RNAs, antisense oligonucleotides, ribozymes, deoxyribozymes and aptemers are few promising technologies for future lncRNA bases therapeutics. Conclusion: lncRNA expression is altered in cancer. Aberrant regulation promotes tumor formation, progression and metastasis. lncRNAs can use as tumor markers for PCa and may be attractive novel therapeutic targets for the diagnosis and treatment of PCa.</description><identifier>ISSN: 1365-7852</identifier><identifier>EISSN: 1476-5608</identifier><identifier>DOI: 10.1038/pcan.2015.48</identifier><identifier>PMID: 26503110</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13/105 ; 13/51 ; 13/89 ; 38/43 ; 38/89 ; 38/90 ; 45/43 ; 45/90 ; 45/91 ; 692/308 ; 692/53 ; Antisense oligonucleotides ; Antisense RNA ; Biological markers ; Biomarkers ; Biomarkers, Tumor - genetics ; Biomedical and Life Sciences ; Biomedicine ; Cancer Research ; Cell proliferation ; Deoxyribozymes ; Development and progression ; Diagnosis ; Epithelial cells ; Epithelium ; Gene Expression Regulation, Neoplastic ; Genetic aspects ; Health aspects ; Health services ; Humans ; Male ; Metastases ; Molecular Targeted Therapy - methods ; Non-coding RNA ; Oligonucleotides ; Prognosis ; Prostate cancer ; Prostatic Neoplasms - genetics ; Prostatic Neoplasms - pathology ; Prostatic Neoplasms - therapy ; review ; Ribozymes ; RNA, Long Noncoding - genetics ; Therapeutic applications ; Therapeutic targets ; Transient receptor potential proteins ; Tumor markers ; Tumors</subject><ispartof>Prostate cancer and prostatic diseases, 2016-03, Vol.19 (1), p.14-20</ispartof><rights>Macmillan Publishers Limited 2016</rights><rights>COPYRIGHT 2016 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Mar 2016</rights><rights>Macmillan Publishers Limited 2016.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c586t-9f8bae93600695fe083dfd037be562a592db30349d35f25470608ce377b69d183</citedby><cites>FETCH-LOGICAL-c586t-9f8bae93600695fe083dfd037be562a592db30349d35f25470608ce377b69d183</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26503110$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mouraviev, V</creatorcontrib><creatorcontrib>Lee, B</creatorcontrib><creatorcontrib>Patel, V</creatorcontrib><creatorcontrib>Albala, D</creatorcontrib><creatorcontrib>Johansen, T E B</creatorcontrib><creatorcontrib>Partin, A</creatorcontrib><creatorcontrib>Ross, A</creatorcontrib><creatorcontrib>Perera, R J</creatorcontrib><title>Clinical prospects of long noncoding RNAs as novel biomarkers and therapeutic targets in prostate cancer</title><title>Prostate cancer and prostatic diseases</title><addtitle>Prostate Cancer Prostatic Dis</addtitle><addtitle>Prostate Cancer Prostatic Dis</addtitle><description>Background: The lack of sensitive and specific biomarkers for prostate cancer (PCa) has led to over-diagnosis and overtreatment with uncertain benefit. Therefore, biomarkers for early diagnosis that can distinguish aggressive from indolent tumors and that can detect metastatic or recurrent disease are needed. Long noncoding RNAs (lncRNAs) are non-protein-coding RNA species. lncRNAs are dysregulated in many diseases including PCa and are emerging as major players in cancer development. lncRNAs have several features that make then suitable as both biomarkers and therapeutics, and lncRNAs regulate critical cancer hallmarks in prostate epithelial cells including proliferation and survival. Methods: The PubMed database was searched using the terms 'long noncoding RNA', 'biomarker' and 'prostate cancer'. Known lncRNAs implicated as biomarkers and potential therapeutic targets in PCa are reviewed. 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Results: We comprehensively review several lncRNAs with potential as biomarkers for PCa. lncRNAs including PCA3 , PCAT s, SChLAP1 , SPRY4-IT1 and TRPM2-AS are upregulated in PCa and are cancer specific; they are, therefore, attractive lead candidate biomarkers for clinical application. Several lncRNA therapeutics are currently being investigated by several companies for the treatment of various cancers including PCa. Small interfering RNAs, antisense oligonucleotides, ribozymes, deoxyribozymes and aptemers are few promising technologies for future lncRNA bases therapeutics. Conclusion: lncRNA expression is altered in cancer. Aberrant regulation promotes tumor formation, progression and metastasis. lncRNAs can use as tumor markers for PCa and may be attractive novel therapeutic targets for the diagnosis and treatment of PCa.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>26503110</pmid><doi>10.1038/pcan.2015.48</doi><tpages>7</tpages></addata></record>
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identifier ISSN: 1365-7852
ispartof Prostate cancer and prostatic diseases, 2016-03, Vol.19 (1), p.14-20
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subjects 13/105
13/51
13/89
38/43
38/89
38/90
45/43
45/90
45/91
692/308
692/53
Antisense oligonucleotides
Antisense RNA
Biological markers
Biomarkers
Biomarkers, Tumor - genetics
Biomedical and Life Sciences
Biomedicine
Cancer Research
Cell proliferation
Deoxyribozymes
Development and progression
Diagnosis
Epithelial cells
Epithelium
Gene Expression Regulation, Neoplastic
Genetic aspects
Health aspects
Health services
Humans
Male
Metastases
Molecular Targeted Therapy - methods
Non-coding RNA
Oligonucleotides
Prognosis
Prostate cancer
Prostatic Neoplasms - genetics
Prostatic Neoplasms - pathology
Prostatic Neoplasms - therapy
review
Ribozymes
RNA, Long Noncoding - genetics
Therapeutic applications
Therapeutic targets
Transient receptor potential proteins
Tumor markers
Tumors
title Clinical prospects of long noncoding RNAs as novel biomarkers and therapeutic targets in prostate cancer
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