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Recent advances in studies of 15-PGDH as a key enzyme for the degradation of prostaglandins
•15-PGDH degrades PGs to attenuate PG-mediated signaling and activity.•15-PGDH suppresses tumor progression and development through its targeting of PGs.•15-PGDG is a marker and potential therapeutic target for aging-associated diseases. 15-hydroxyprostaglandin dehydrogenase (15-PGDH; encoded by HPG...
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Published in: | International immunopharmacology 2021-12, Vol.101 (Pt B), p.108176-108176, Article 108176 |
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description | •15-PGDH degrades PGs to attenuate PG-mediated signaling and activity.•15-PGDH suppresses tumor progression and development through its targeting of PGs.•15-PGDG is a marker and potential therapeutic target for aging-associated diseases.
15-hydroxyprostaglandin dehydrogenase (15-PGDH; encoded by HPGD) is ubiquitously expressed in mammalian tissues and catalyzes the degradation of prostaglandins (PGs; mainly PGE2, PGD2, and PGF2α) in a process mediated by solute carrier organic anion transport protein family member 2A1 (SLCO2A1; also known as PGT, OATP2A1, PHOAR2, or SLC21A2). As a key enzyme, 15-PGDH catalyzes the rapid oxidation of 15-hydroxy-PGs into 15-keto-PGs with lower biological activity. Increasing evidence suggests that 15-PGDH plays a key role in many physiological and pathological processes in mammals and is considered a potential pharmacological target for preventing organ damage, promoting bone marrow graft recovery, and enhancing tissue regeneration. Additionally, results of whole-exome analyses suggest that recessive inheritance of an HPGD mutation is associated with idiopathic hypertrophic osteoarthropathy. Interestingly, as a tumor suppressor, 15-PGDH inhibits proliferation and induces the differentiation of cancer cells (including those associated with colorectal, lung, and breast cancers). Furthermore, a recent study identified 15-PGDH as a marker of aging tissue and a potential novel therapeutic target for resisting the complex pathology of aging-associated diseases. Here, we review and summarise recent information on the molecular functions of 15-PGDH and discuss its pathophysiological implications. |
doi_str_mv | 10.1016/j.intimp.2021.108176 |
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15-hydroxyprostaglandin dehydrogenase (15-PGDH; encoded by HPGD) is ubiquitously expressed in mammalian tissues and catalyzes the degradation of prostaglandins (PGs; mainly PGE2, PGD2, and PGF2α) in a process mediated by solute carrier organic anion transport protein family member 2A1 (SLCO2A1; also known as PGT, OATP2A1, PHOAR2, or SLC21A2). As a key enzyme, 15-PGDH catalyzes the rapid oxidation of 15-hydroxy-PGs into 15-keto-PGs with lower biological activity. Increasing evidence suggests that 15-PGDH plays a key role in many physiological and pathological processes in mammals and is considered a potential pharmacological target for preventing organ damage, promoting bone marrow graft recovery, and enhancing tissue regeneration. Additionally, results of whole-exome analyses suggest that recessive inheritance of an HPGD mutation is associated with idiopathic hypertrophic osteoarthropathy. Interestingly, as a tumor suppressor, 15-PGDH inhibits proliferation and induces the differentiation of cancer cells (including those associated with colorectal, lung, and breast cancers). Furthermore, a recent study identified 15-PGDH as a marker of aging tissue and a potential novel therapeutic target for resisting the complex pathology of aging-associated diseases. Here, we review and summarise recent information on the molecular functions of 15-PGDH and discuss its pathophysiological implications.</description><identifier>ISSN: 1567-5769</identifier><identifier>EISSN: 1878-1705</identifier><identifier>DOI: 10.1016/j.intimp.2021.108176</identifier><identifier>PMID: 34655851</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>15-Hydroxyprostaglandin dehydrogenase (NAD+) ; 15-PGDH ; Aging ; Biological activity ; Biomedical materials ; Bone marrow ; Breast cancer ; Cancer ; Cell differentiation ; Cell proliferation ; Damage prevention ; Degradation ; Degrades ; Enzymes ; Heredity ; Mammals ; Mutation ; Organic anion transporting polypeptide ; Osteoarthropathy ; Oxidation ; Pathology ; Physiology ; Prostaglandin ; Prostaglandin E2 ; Prostaglandins ; Protein transport ; Regeneration ; Therapeutic targets ; Tissue engineering ; Tissues ; Tumor suppressor genes ; Tumors</subject><ispartof>International immunopharmacology, 2021-12, Vol.101 (Pt B), p.108176-108176, Article 108176</ispartof><rights>2021</rights><rights>Copyright © 2021. Published by Elsevier B.V.</rights><rights>Copyright Elsevier BV Dec 2021</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-a06b75b0a515a8f609d75cd5d2a6f17b7068dfe312d0d7b51bd3ce9a89da3eaf3</citedby><cites>FETCH-LOGICAL-c390t-a06b75b0a515a8f609d75cd5d2a6f17b7068dfe312d0d7b51bd3ce9a89da3eaf3</cites><orcidid>0000-0002-8104-7753</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34655851$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sun, Chen-Chen</creatorcontrib><creatorcontrib>Zhou, Zuo-qiong</creatorcontrib><creatorcontrib>Yang, Dong</creatorcontrib><creatorcontrib>Chen, Zhang-lin</creatorcontrib><creatorcontrib>Zhou, Yun-yi</creatorcontrib><creatorcontrib>Wen, Wei</creatorcontrib><creatorcontrib>Feng, Chen</creatorcontrib><creatorcontrib>Zheng, Lan</creatorcontrib><creatorcontrib>Peng, Xi-Yang</creatorcontrib><creatorcontrib>Tang, Chang-Fa</creatorcontrib><title>Recent advances in studies of 15-PGDH as a key enzyme for the degradation of prostaglandins</title><title>International immunopharmacology</title><addtitle>Int Immunopharmacol</addtitle><description>•15-PGDH degrades PGs to attenuate PG-mediated signaling and activity.•15-PGDH suppresses tumor progression and development through its targeting of PGs.•15-PGDG is a marker and potential therapeutic target for aging-associated diseases.
15-hydroxyprostaglandin dehydrogenase (15-PGDH; encoded by HPGD) is ubiquitously expressed in mammalian tissues and catalyzes the degradation of prostaglandins (PGs; mainly PGE2, PGD2, and PGF2α) in a process mediated by solute carrier organic anion transport protein family member 2A1 (SLCO2A1; also known as PGT, OATP2A1, PHOAR2, or SLC21A2). As a key enzyme, 15-PGDH catalyzes the rapid oxidation of 15-hydroxy-PGs into 15-keto-PGs with lower biological activity. Increasing evidence suggests that 15-PGDH plays a key role in many physiological and pathological processes in mammals and is considered a potential pharmacological target for preventing organ damage, promoting bone marrow graft recovery, and enhancing tissue regeneration. Additionally, results of whole-exome analyses suggest that recessive inheritance of an HPGD mutation is associated with idiopathic hypertrophic osteoarthropathy. Interestingly, as a tumor suppressor, 15-PGDH inhibits proliferation and induces the differentiation of cancer cells (including those associated with colorectal, lung, and breast cancers). Furthermore, a recent study identified 15-PGDH as a marker of aging tissue and a potential novel therapeutic target for resisting the complex pathology of aging-associated diseases. Here, we review and summarise recent information on the molecular functions of 15-PGDH and discuss its pathophysiological implications.</description><subject>15-Hydroxyprostaglandin dehydrogenase (NAD+)</subject><subject>15-PGDH</subject><subject>Aging</subject><subject>Biological activity</subject><subject>Biomedical materials</subject><subject>Bone marrow</subject><subject>Breast cancer</subject><subject>Cancer</subject><subject>Cell differentiation</subject><subject>Cell proliferation</subject><subject>Damage prevention</subject><subject>Degradation</subject><subject>Degrades</subject><subject>Enzymes</subject><subject>Heredity</subject><subject>Mammals</subject><subject>Mutation</subject><subject>Organic anion transporting polypeptide</subject><subject>Osteoarthropathy</subject><subject>Oxidation</subject><subject>Pathology</subject><subject>Physiology</subject><subject>Prostaglandin</subject><subject>Prostaglandin E2</subject><subject>Prostaglandins</subject><subject>Protein transport</subject><subject>Regeneration</subject><subject>Therapeutic targets</subject><subject>Tissue engineering</subject><subject>Tissues</subject><subject>Tumor suppressor genes</subject><subject>Tumors</subject><issn>1567-5769</issn><issn>1878-1705</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kEtr3DAQgEVoaB7tPwhF0Esv3kj26uFLoCRtEgi0hOaUgxhL41SbtbyV5MDm11eLkxx66GmG4ZvXR8gJZwvOuDxdLXzIftgsalbzUtJcyT1yyLXSFVdMvCu5kKoSSrYH5CilFWOlvuTvyUGzlEJowQ_J_S1aDJmCe4JgMVEfaMqT8yUde8pF9fPy4opCokAfcUsxPG8HpP0Yaf6N1OFDBAfZj2GHb-KYMjysITgf0gey38M64ceXeEzuvn_7dX5V3fy4vD7_elPZpmW5AiY7JToGggvQvWStU8I64WqQPVedYlK7HhteO-ZUJ3jnGost6NZBg9A3x-TLPLes_zNhymbwyeK6nIHjlEwtdK2ZEkIW9PM_6GqcYijXmVrWy1bLRqlCLWfKln9SxN5soh8gbg1nZiffrMws3-zkm1l-afv0MnzqBnRvTa-2C3A2A1hsPHmMJlmPRbvzEW02bvT_3_AXff6Wmw</recordid><startdate>202112</startdate><enddate>202112</enddate><creator>Sun, Chen-Chen</creator><creator>Zhou, Zuo-qiong</creator><creator>Yang, Dong</creator><creator>Chen, Zhang-lin</creator><creator>Zhou, Yun-yi</creator><creator>Wen, Wei</creator><creator>Feng, Chen</creator><creator>Zheng, Lan</creator><creator>Peng, Xi-Yang</creator><creator>Tang, Chang-Fa</creator><general>Elsevier B.V</general><general>Elsevier BV</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7T5</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-8104-7753</orcidid></search><sort><creationdate>202112</creationdate><title>Recent advances in studies of 15-PGDH as a key enzyme for the degradation of prostaglandins</title><author>Sun, Chen-Chen ; Zhou, Zuo-qiong ; Yang, Dong ; Chen, Zhang-lin ; Zhou, Yun-yi ; Wen, Wei ; Feng, Chen ; Zheng, Lan ; Peng, Xi-Yang ; Tang, Chang-Fa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-a06b75b0a515a8f609d75cd5d2a6f17b7068dfe312d0d7b51bd3ce9a89da3eaf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>15-Hydroxyprostaglandin dehydrogenase (NAD+)</topic><topic>15-PGDH</topic><topic>Aging</topic><topic>Biological activity</topic><topic>Biomedical materials</topic><topic>Bone marrow</topic><topic>Breast cancer</topic><topic>Cancer</topic><topic>Cell differentiation</topic><topic>Cell proliferation</topic><topic>Damage prevention</topic><topic>Degradation</topic><topic>Degrades</topic><topic>Enzymes</topic><topic>Heredity</topic><topic>Mammals</topic><topic>Mutation</topic><topic>Organic anion transporting polypeptide</topic><topic>Osteoarthropathy</topic><topic>Oxidation</topic><topic>Pathology</topic><topic>Physiology</topic><topic>Prostaglandin</topic><topic>Prostaglandin E2</topic><topic>Prostaglandins</topic><topic>Protein transport</topic><topic>Regeneration</topic><topic>Therapeutic targets</topic><topic>Tissue engineering</topic><topic>Tissues</topic><topic>Tumor suppressor genes</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sun, Chen-Chen</creatorcontrib><creatorcontrib>Zhou, Zuo-qiong</creatorcontrib><creatorcontrib>Yang, Dong</creatorcontrib><creatorcontrib>Chen, Zhang-lin</creatorcontrib><creatorcontrib>Zhou, Yun-yi</creatorcontrib><creatorcontrib>Wen, Wei</creatorcontrib><creatorcontrib>Feng, Chen</creatorcontrib><creatorcontrib>Zheng, Lan</creatorcontrib><creatorcontrib>Peng, Xi-Yang</creatorcontrib><creatorcontrib>Tang, Chang-Fa</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Immunology Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>International immunopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sun, Chen-Chen</au><au>Zhou, Zuo-qiong</au><au>Yang, Dong</au><au>Chen, Zhang-lin</au><au>Zhou, Yun-yi</au><au>Wen, Wei</au><au>Feng, Chen</au><au>Zheng, Lan</au><au>Peng, Xi-Yang</au><au>Tang, Chang-Fa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Recent advances in studies of 15-PGDH as a key enzyme for the degradation of prostaglandins</atitle><jtitle>International immunopharmacology</jtitle><addtitle>Int Immunopharmacol</addtitle><date>2021-12</date><risdate>2021</risdate><volume>101</volume><issue>Pt B</issue><spage>108176</spage><epage>108176</epage><pages>108176-108176</pages><artnum>108176</artnum><issn>1567-5769</issn><eissn>1878-1705</eissn><abstract>•15-PGDH degrades PGs to attenuate PG-mediated signaling and activity.•15-PGDH suppresses tumor progression and development through its targeting of PGs.•15-PGDG is a marker and potential therapeutic target for aging-associated diseases.
15-hydroxyprostaglandin dehydrogenase (15-PGDH; encoded by HPGD) is ubiquitously expressed in mammalian tissues and catalyzes the degradation of prostaglandins (PGs; mainly PGE2, PGD2, and PGF2α) in a process mediated by solute carrier organic anion transport protein family member 2A1 (SLCO2A1; also known as PGT, OATP2A1, PHOAR2, or SLC21A2). As a key enzyme, 15-PGDH catalyzes the rapid oxidation of 15-hydroxy-PGs into 15-keto-PGs with lower biological activity. Increasing evidence suggests that 15-PGDH plays a key role in many physiological and pathological processes in mammals and is considered a potential pharmacological target for preventing organ damage, promoting bone marrow graft recovery, and enhancing tissue regeneration. Additionally, results of whole-exome analyses suggest that recessive inheritance of an HPGD mutation is associated with idiopathic hypertrophic osteoarthropathy. Interestingly, as a tumor suppressor, 15-PGDH inhibits proliferation and induces the differentiation of cancer cells (including those associated with colorectal, lung, and breast cancers). Furthermore, a recent study identified 15-PGDH as a marker of aging tissue and a potential novel therapeutic target for resisting the complex pathology of aging-associated diseases. Here, we review and summarise recent information on the molecular functions of 15-PGDH and discuss its pathophysiological implications.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>34655851</pmid><doi>10.1016/j.intimp.2021.108176</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-8104-7753</orcidid></addata></record> |
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subjects | 15-Hydroxyprostaglandin dehydrogenase (NAD+) 15-PGDH Aging Biological activity Biomedical materials Bone marrow Breast cancer Cancer Cell differentiation Cell proliferation Damage prevention Degradation Degrades Enzymes Heredity Mammals Mutation Organic anion transporting polypeptide Osteoarthropathy Oxidation Pathology Physiology Prostaglandin Prostaglandin E2 Prostaglandins Protein transport Regeneration Therapeutic targets Tissue engineering Tissues Tumor suppressor genes Tumors |
title | Recent advances in studies of 15-PGDH as a key enzyme for the degradation of prostaglandins |
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