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Differentially regulated gene expression in quiescence versus senescence and identification of ARID5A as a quiescence associated marker
In multicellular organisms majority of the cells remain in a non‐dividing states of either quiescence (reversible) or senescence (irreversible). In the present study, gene expression signatures unique to quiescence and senescence were identified using microarray in osteosarcoma cell line, U2OS. It w...
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Published in: | Journal of cellular physiology 2018-05, Vol.233 (5), p.3695-3712 |
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container_title | Journal of cellular physiology |
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creator | Anwar, Tarique Sen, Bijoya Aggarwal, Savera Nath, Rhisita Pathak, Niteen Katoch, Ajay Aiyaz, Mohamed Trehanpati, Nirupma Khosla, Sanjeev Ramakrishna, Gayatri |
description | In multicellular organisms majority of the cells remain in a non‐dividing states of either quiescence (reversible) or senescence (irreversible). In the present study, gene expression signatures unique to quiescence and senescence were identified using microarray in osteosarcoma cell line, U2OS. It was noted that certain genes and pathways like NOD pathway was shared by both the growth arrest conditions. A major highlight of the present study was increased expression of number of chemokines and cytokines in both quiescence and senescence. While senescence‐associated secretory phenotype (SASP) is well known, the quiescence‐associated secretory phenotype (QASP) is relatively unknown and appeared novel in this study. ARID5A, a subunit of SWI/SNF complex was identified as a quiescence associated gene. The endogenous expression of ARID5A increased during serum starved condition of quiescence. Overexpression of ARID5A resulted in more number of cells in G0/G1 phase of cell cycle. Further ARID5A overexpressing cells when subjected to serum starvation showed a pronounced secretory phenotype. Overall, the present work has identified gene expression signatures which can distinguish quiescence from senescence.
The present work has identified gene expression signatures which can distinguish quiescence from senescence. Additionally the work has identified ARID5A as a quiescence associated gene. |
doi_str_mv | 10.1002/jcp.26227 |
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The present work has identified gene expression signatures which can distinguish quiescence from senescence. Additionally the work has identified ARID5A as a quiescence associated gene.</description><identifier>ISSN: 0021-9541</identifier><identifier>EISSN: 1097-4652</identifier><identifier>DOI: 10.1002/jcp.26227</identifier><identifier>PMID: 29044508</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>ARID5A ; Biocompatibility ; Biomarkers - metabolism ; Biomedical materials ; Bone cancer ; Cell cycle ; Cell Cycle - genetics ; Cell Cycle Checkpoints - genetics ; Cell Division - genetics ; Cell Line, Tumor ; Cellular Senescence - genetics ; Chemokines ; Cytokines ; Cytokines - metabolism ; DNA microarrays ; G1 phase ; Gene expression ; Humans ; inflammasome ; Nuclear Proteins - genetics ; Osteosarcoma ; Phenotype ; Phenotypes ; quiescence ; Sarcoma ; secretory phenotype ; Senescence ; Signal Transduction ; Signatures ; SWI/SNF complex</subject><ispartof>Journal of cellular physiology, 2018-05, Vol.233 (5), p.3695-3712</ispartof><rights>2017 Wiley Periodicals, Inc.</rights><rights>2018 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3537-d638220395173f4a224eef957c569ee67b41df666359d32d58aa3573794d48bc3</citedby><cites>FETCH-LOGICAL-c3537-d638220395173f4a224eef957c569ee67b41df666359d32d58aa3573794d48bc3</cites><orcidid>0000-0003-4345-294X</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/29044508$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Anwar, Tarique</creatorcontrib><creatorcontrib>Sen, Bijoya</creatorcontrib><creatorcontrib>Aggarwal, Savera</creatorcontrib><creatorcontrib>Nath, Rhisita</creatorcontrib><creatorcontrib>Pathak, Niteen</creatorcontrib><creatorcontrib>Katoch, Ajay</creatorcontrib><creatorcontrib>Aiyaz, Mohamed</creatorcontrib><creatorcontrib>Trehanpati, Nirupma</creatorcontrib><creatorcontrib>Khosla, Sanjeev</creatorcontrib><creatorcontrib>Ramakrishna, Gayatri</creatorcontrib><title>Differentially regulated gene expression in quiescence versus senescence and identification of ARID5A as a quiescence associated marker</title><title>Journal of cellular physiology</title><addtitle>J Cell Physiol</addtitle><description>In multicellular organisms majority of the cells remain in a non‐dividing states of either quiescence (reversible) or senescence (irreversible). In the present study, gene expression signatures unique to quiescence and senescence were identified using microarray in osteosarcoma cell line, U2OS. It was noted that certain genes and pathways like NOD pathway was shared by both the growth arrest conditions. A major highlight of the present study was increased expression of number of chemokines and cytokines in both quiescence and senescence. While senescence‐associated secretory phenotype (SASP) is well known, the quiescence‐associated secretory phenotype (QASP) is relatively unknown and appeared novel in this study. ARID5A, a subunit of SWI/SNF complex was identified as a quiescence associated gene. The endogenous expression of ARID5A increased during serum starved condition of quiescence. Overexpression of ARID5A resulted in more number of cells in G0/G1 phase of cell cycle. Further ARID5A overexpressing cells when subjected to serum starvation showed a pronounced secretory phenotype. Overall, the present work has identified gene expression signatures which can distinguish quiescence from senescence.
The present work has identified gene expression signatures which can distinguish quiescence from senescence. Additionally the work has identified ARID5A as a quiescence associated gene.</description><subject>ARID5A</subject><subject>Biocompatibility</subject><subject>Biomarkers - metabolism</subject><subject>Biomedical materials</subject><subject>Bone cancer</subject><subject>Cell cycle</subject><subject>Cell Cycle - genetics</subject><subject>Cell Cycle Checkpoints - genetics</subject><subject>Cell Division - genetics</subject><subject>Cell Line, Tumor</subject><subject>Cellular Senescence - genetics</subject><subject>Chemokines</subject><subject>Cytokines</subject><subject>Cytokines - metabolism</subject><subject>DNA microarrays</subject><subject>G1 phase</subject><subject>Gene expression</subject><subject>Humans</subject><subject>inflammasome</subject><subject>Nuclear Proteins - genetics</subject><subject>Osteosarcoma</subject><subject>Phenotype</subject><subject>Phenotypes</subject><subject>quiescence</subject><subject>Sarcoma</subject><subject>secretory phenotype</subject><subject>Senescence</subject><subject>Signal Transduction</subject><subject>Signatures</subject><subject>SWI/SNF complex</subject><issn>0021-9541</issn><issn>1097-4652</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kctqGzEUhkVpqF2ni75AEHTTLibRdTRaGru5EUgp6XqQpSMjZzzjSJ60foK8duRLQglkJZC-8-mc8yP0lZJTSgg7W9jVKSsZUx_QkBKtClFK9hEN8xsttBR0gD6ntCCEaM35JzRgmgghSTVET9PgPURo18E0zQZHmPeNWYPDc2gBw79VhJRC1-LQ4oc-QLLQWsCPEFOfcMrQ4ca0Dge3FflgzXpb0nk8_n01lWNsEjb_l5uUOht2_yxNvId4jI68aRJ8OZwj9Of8593ksri5vbiajG8KyyVXhSt5xRjhWlLFvTCMCQCvpbKy1AClmgnqfFmWXGrHmZOVMVwqrrRwoppZPkLf995V7B56SOt6GXJPTWNa6PpUUy2Z5KTKixqhb2_QRdfHNneXKa1ppciO-rGnbOxSiuDrVQx5pk1NSb1Np87p1Lt0MntyMPazJbhX8iWODJztgb-hgc37pvp68muvfAarnpmN</recordid><startdate>201805</startdate><enddate>201805</enddate><creator>Anwar, Tarique</creator><creator>Sen, Bijoya</creator><creator>Aggarwal, Savera</creator><creator>Nath, Rhisita</creator><creator>Pathak, Niteen</creator><creator>Katoch, Ajay</creator><creator>Aiyaz, Mohamed</creator><creator>Trehanpati, Nirupma</creator><creator>Khosla, Sanjeev</creator><creator>Ramakrishna, Gayatri</creator><general>Wiley Subscription Services, Inc</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>7TK</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-4345-294X</orcidid></search><sort><creationdate>201805</creationdate><title>Differentially regulated gene expression in quiescence versus senescence and identification of ARID5A as a quiescence associated marker</title><author>Anwar, Tarique ; Sen, Bijoya ; Aggarwal, Savera ; Nath, Rhisita ; Pathak, Niteen ; Katoch, Ajay ; Aiyaz, Mohamed ; Trehanpati, Nirupma ; Khosla, Sanjeev ; Ramakrishna, Gayatri</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3537-d638220395173f4a224eef957c569ee67b41df666359d32d58aa3573794d48bc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>ARID5A</topic><topic>Biocompatibility</topic><topic>Biomarkers - metabolism</topic><topic>Biomedical materials</topic><topic>Bone cancer</topic><topic>Cell cycle</topic><topic>Cell Cycle - genetics</topic><topic>Cell Cycle Checkpoints - genetics</topic><topic>Cell Division - genetics</topic><topic>Cell Line, Tumor</topic><topic>Cellular Senescence - genetics</topic><topic>Chemokines</topic><topic>Cytokines</topic><topic>Cytokines - metabolism</topic><topic>DNA microarrays</topic><topic>G1 phase</topic><topic>Gene expression</topic><topic>Humans</topic><topic>inflammasome</topic><topic>Nuclear Proteins - genetics</topic><topic>Osteosarcoma</topic><topic>Phenotype</topic><topic>Phenotypes</topic><topic>quiescence</topic><topic>Sarcoma</topic><topic>secretory phenotype</topic><topic>Senescence</topic><topic>Signal Transduction</topic><topic>Signatures</topic><topic>SWI/SNF complex</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Anwar, Tarique</creatorcontrib><creatorcontrib>Sen, Bijoya</creatorcontrib><creatorcontrib>Aggarwal, Savera</creatorcontrib><creatorcontrib>Nath, Rhisita</creatorcontrib><creatorcontrib>Pathak, Niteen</creatorcontrib><creatorcontrib>Katoch, Ajay</creatorcontrib><creatorcontrib>Aiyaz, Mohamed</creatorcontrib><creatorcontrib>Trehanpati, Nirupma</creatorcontrib><creatorcontrib>Khosla, Sanjeev</creatorcontrib><creatorcontrib>Ramakrishna, Gayatri</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of cellular physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Anwar, Tarique</au><au>Sen, Bijoya</au><au>Aggarwal, Savera</au><au>Nath, Rhisita</au><au>Pathak, Niteen</au><au>Katoch, Ajay</au><au>Aiyaz, Mohamed</au><au>Trehanpati, Nirupma</au><au>Khosla, Sanjeev</au><au>Ramakrishna, Gayatri</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differentially regulated gene expression in quiescence versus senescence and identification of ARID5A as a quiescence associated marker</atitle><jtitle>Journal of cellular physiology</jtitle><addtitle>J Cell Physiol</addtitle><date>2018-05</date><risdate>2018</risdate><volume>233</volume><issue>5</issue><spage>3695</spage><epage>3712</epage><pages>3695-3712</pages><issn>0021-9541</issn><eissn>1097-4652</eissn><abstract>In multicellular organisms majority of the cells remain in a non‐dividing states of either quiescence (reversible) or senescence (irreversible). In the present study, gene expression signatures unique to quiescence and senescence were identified using microarray in osteosarcoma cell line, U2OS. It was noted that certain genes and pathways like NOD pathway was shared by both the growth arrest conditions. A major highlight of the present study was increased expression of number of chemokines and cytokines in both quiescence and senescence. While senescence‐associated secretory phenotype (SASP) is well known, the quiescence‐associated secretory phenotype (QASP) is relatively unknown and appeared novel in this study. ARID5A, a subunit of SWI/SNF complex was identified as a quiescence associated gene. The endogenous expression of ARID5A increased during serum starved condition of quiescence. Overexpression of ARID5A resulted in more number of cells in G0/G1 phase of cell cycle. Further ARID5A overexpressing cells when subjected to serum starvation showed a pronounced secretory phenotype. Overall, the present work has identified gene expression signatures which can distinguish quiescence from senescence.
The present work has identified gene expression signatures which can distinguish quiescence from senescence. Additionally the work has identified ARID5A as a quiescence associated gene.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>29044508</pmid><doi>10.1002/jcp.26227</doi><tpages>18</tpages><orcidid>https://orcid.org/0000-0003-4345-294X</orcidid></addata></record> |
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subjects | ARID5A Biocompatibility Biomarkers - metabolism Biomedical materials Bone cancer Cell cycle Cell Cycle - genetics Cell Cycle Checkpoints - genetics Cell Division - genetics Cell Line, Tumor Cellular Senescence - genetics Chemokines Cytokines Cytokines - metabolism DNA microarrays G1 phase Gene expression Humans inflammasome Nuclear Proteins - genetics Osteosarcoma Phenotype Phenotypes quiescence Sarcoma secretory phenotype Senescence Signal Transduction Signatures SWI/SNF complex |
title | Differentially regulated gene expression in quiescence versus senescence and identification of ARID5A as a quiescence associated marker |
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