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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 |
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container_title | Prostate cancer and prostatic diseases |
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creator | Mouraviev, V Lee, B Patel, V Albala, D Johansen, T E B Partin, A Ross, A Perera, R J |
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 |
format | article |
fullrecord | <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_1773829286</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A443654121</galeid><sourcerecordid>A443654121</sourcerecordid><originalsourceid>FETCH-LOGICAL-c586t-9f8bae93600695fe083dfd037be562a592db30349d35f25470608ce377b69d183</originalsourceid><addsrcrecordid>eNqNkk2LFDEQhhtR3HX15lkaBPFgj_nu5DgMuyosCqLnkE5Xz2TtScakW_DfW-2suiuLSA4JlafequKtqnpKyYoSrl8fvIsrRqhcCX2vOqWiVY1URN_HN1eyabVkJ9WjUq4IIYYa8rA6YUoSTik5rXabMcTg3VgfcioH8FOp01CPKW7rmKJPfcDXx_frUruCkW8w1l1Ie5e_QMZY7OtpB9kdYJ6CryeXt4ASIf7Um9wENfbnIT-uHgxuLPDk-j6rPl-cf9q8bS4_vHm3WV82Xmo1NWbQnQPDFSHKyAGI5v3QE952IBVz0rC-44QL03M5MClagqN64G3bKdNTzc-ql0ddrP91hjLZfSgextFFSHOxtG25ZoZp9R-oElxQLRiiz_9Cr9KcIw5imRKSU6PQjH9QqMWVbluj_1BbN4INcUhTdn4pbddCoGWCMorU6g4KTw_74FOEIWD8VsKLGwk7cOO0K2lEW1Ist8FXR9CjQyXDYA85oKHfLSV2WSm7rJRdVsqKpd1n10PN3R763_CvHUKgOQIFv-IW8o2p7xL8AUDz0dY</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1763687798</pqid></control><display><type>article</type><title>Clinical prospects of long noncoding RNAs as novel biomarkers and therapeutic targets in prostate cancer</title><source>Springer Link</source><creator>Mouraviev, V ; Lee, B ; Patel, V ; Albala, D ; Johansen, T E B ; Partin, A ; Ross, A ; Perera, R J</creator><creatorcontrib>Mouraviev, V ; Lee, B ; Patel, V ; Albala, D ; Johansen, T E B ; Partin, A ; Ross, A ; Perera, R J</creatorcontrib><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.</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.
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><subject>13/105</subject><subject>13/51</subject><subject>13/89</subject><subject>38/43</subject><subject>38/89</subject><subject>38/90</subject><subject>45/43</subject><subject>45/90</subject><subject>45/91</subject><subject>692/308</subject><subject>692/53</subject><subject>Antisense oligonucleotides</subject><subject>Antisense RNA</subject><subject>Biological markers</subject><subject>Biomarkers</subject><subject>Biomarkers, Tumor - genetics</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer Research</subject><subject>Cell proliferation</subject><subject>Deoxyribozymes</subject><subject>Development and progression</subject><subject>Diagnosis</subject><subject>Epithelial cells</subject><subject>Epithelium</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Genetic aspects</subject><subject>Health aspects</subject><subject>Health services</subject><subject>Humans</subject><subject>Male</subject><subject>Metastases</subject><subject>Molecular Targeted Therapy - methods</subject><subject>Non-coding RNA</subject><subject>Oligonucleotides</subject><subject>Prognosis</subject><subject>Prostate cancer</subject><subject>Prostatic Neoplasms - genetics</subject><subject>Prostatic Neoplasms - pathology</subject><subject>Prostatic Neoplasms - therapy</subject><subject>review</subject><subject>Ribozymes</subject><subject>RNA, Long Noncoding - genetics</subject><subject>Therapeutic applications</subject><subject>Therapeutic targets</subject><subject>Transient receptor potential proteins</subject><subject>Tumor markers</subject><subject>Tumors</subject><issn>1365-7852</issn><issn>1476-5608</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqNkk2LFDEQhhtR3HX15lkaBPFgj_nu5DgMuyosCqLnkE5Xz2TtScakW_DfW-2suiuLSA4JlafequKtqnpKyYoSrl8fvIsrRqhcCX2vOqWiVY1URN_HN1eyabVkJ9WjUq4IIYYa8rA6YUoSTik5rXabMcTg3VgfcioH8FOp01CPKW7rmKJPfcDXx_frUruCkW8w1l1Ie5e_QMZY7OtpB9kdYJ6CryeXt4ASIf7Um9wENfbnIT-uHgxuLPDk-j6rPl-cf9q8bS4_vHm3WV82Xmo1NWbQnQPDFSHKyAGI5v3QE952IBVz0rC-44QL03M5MClagqN64G3bKdNTzc-ql0ddrP91hjLZfSgextFFSHOxtG25ZoZp9R-oElxQLRiiz_9Cr9KcIw5imRKSU6PQjH9QqMWVbluj_1BbN4INcUhTdn4pbddCoGWCMorU6g4KTw_74FOEIWD8VsKLGwk7cOO0K2lEW1Ist8FXR9CjQyXDYA85oKHfLSV2WSm7rJRdVsqKpd1n10PN3R763_CvHUKgOQIFv-IW8o2p7xL8AUDz0dY</recordid><startdate>20160301</startdate><enddate>20160301</enddate><creator>Mouraviev, V</creator><creator>Lee, B</creator><creator>Patel, V</creator><creator>Albala, D</creator><creator>Johansen, T E B</creator><creator>Partin, A</creator><creator>Ross, A</creator><creator>Perera, R J</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>M7Z</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>7TM</scope></search><sort><creationdate>20160301</creationdate><title>Clinical prospects of long noncoding RNAs as novel biomarkers and therapeutic targets in prostate cancer</title><author>Mouraviev, V ; Lee, B ; Patel, V ; Albala, D ; Johansen, T E B ; Partin, A ; Ross, A ; Perera, R J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c586t-9f8bae93600695fe083dfd037be562a592db30349d35f25470608ce377b69d183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>13/105</topic><topic>13/51</topic><topic>13/89</topic><topic>38/43</topic><topic>38/89</topic><topic>38/90</topic><topic>45/43</topic><topic>45/90</topic><topic>45/91</topic><topic>692/308</topic><topic>692/53</topic><topic>Antisense oligonucleotides</topic><topic>Antisense RNA</topic><topic>Biological markers</topic><topic>Biomarkers</topic><topic>Biomarkers, Tumor - genetics</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cancer Research</topic><topic>Cell proliferation</topic><topic>Deoxyribozymes</topic><topic>Development and progression</topic><topic>Diagnosis</topic><topic>Epithelial cells</topic><topic>Epithelium</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Genetic aspects</topic><topic>Health aspects</topic><topic>Health services</topic><topic>Humans</topic><topic>Male</topic><topic>Metastases</topic><topic>Molecular Targeted Therapy - methods</topic><topic>Non-coding RNA</topic><topic>Oligonucleotides</topic><topic>Prognosis</topic><topic>Prostate cancer</topic><topic>Prostatic Neoplasms - genetics</topic><topic>Prostatic Neoplasms - pathology</topic><topic>Prostatic Neoplasms - therapy</topic><topic>review</topic><topic>Ribozymes</topic><topic>RNA, Long Noncoding - genetics</topic><topic>Therapeutic applications</topic><topic>Therapeutic targets</topic><topic>Transient receptor potential proteins</topic><topic>Tumor markers</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>Nucleic Acids Abstracts</collection><jtitle>Prostate cancer and prostatic diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mouraviev, V</au><au>Lee, B</au><au>Patel, V</au><au>Albala, D</au><au>Johansen, T E B</au><au>Partin, A</au><au>Ross, A</au><au>Perera, R J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical prospects of long noncoding RNAs as novel biomarkers and therapeutic targets in prostate cancer</atitle><jtitle>Prostate cancer and prostatic diseases</jtitle><stitle>Prostate Cancer Prostatic Dis</stitle><addtitle>Prostate Cancer Prostatic Dis</addtitle><date>2016-03-01</date><risdate>2016</risdate><volume>19</volume><issue>1</issue><spage>14</spage><epage>20</epage><pages>14-20</pages><issn>1365-7852</issn><eissn>1476-5608</eissn><abstract>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.</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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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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