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Investigation of Decitabine Effects on HDAC3 and HDAC7 mRNA Expression in NALM-6 and HL-60 Cancer Cell Lines
Decitabine is a potent anticancer hypomethylating agent and changes the gene expression through the gene's promoter demethylation and also independently from DNA demethylation. So, the present study was designed to distinguish whether Decitabine, in addition to inhibitory effects on DNA methylt...
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Published in: | Reports of biochemistry and molecular biology 2021-10, Vol.10 (3), p.420-428 |
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creator | Dalvand, Sina Namdari, Amin Sepahvand, Farzad Meshkibaf, Mohammad Hassan Ahmadpour, GholamReza |
description | Decitabine is a potent anticancer hypomethylating agent and changes the gene expression through the gene's promoter demethylation and also independently from DNA demethylation. So, the present study was designed to distinguish whether Decitabine, in addition to inhibitory effects on DNA methyltransferase, can change HDAC3 and HDAC7 mRNA expression in NALM-6 and HL-60 cancer cell lines.
HL-60, NALM-6, and normal cells were cultured, and the Decitabine treatment dose was obtained (1 µM) through the MTT assay. Finally, HDAC3 and HDAC7 mRNA expression were measured by Real-Time PCR in HL-60 and NALM-6 cancerous cells before and after treatment. Furthermore, HDAC3 and HDAC7 mRNA expression in untreated HL-60 and NALM-6 cancerous cells were compared to normal cells.
Our results revealed that the expression of HDAC3 and HDAC7 in HL-60 and NALM-6 cells increases as compared to normal cells. After treatment of HL-60 and NALM-6 cells with Decitabine, HDAC3, and HDAC7 mRNA expression were decreased significantly.
Our data confirmed that the effects of Decitabine are not limited to direct hypomethylation of DNMTs, but it can indirectly affect other epigenetic factors, such as HDACs activity, through converging pathways. |
doi_str_mv | 10.52547/rbmb.10.3.420 |
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HL-60, NALM-6, and normal cells were cultured, and the Decitabine treatment dose was obtained (1 µM) through the MTT assay. Finally, HDAC3 and HDAC7 mRNA expression were measured by Real-Time PCR in HL-60 and NALM-6 cancerous cells before and after treatment. Furthermore, HDAC3 and HDAC7 mRNA expression in untreated HL-60 and NALM-6 cancerous cells were compared to normal cells.
Our results revealed that the expression of HDAC3 and HDAC7 in HL-60 and NALM-6 cells increases as compared to normal cells. After treatment of HL-60 and NALM-6 cells with Decitabine, HDAC3, and HDAC7 mRNA expression were decreased significantly.
Our data confirmed that the effects of Decitabine are not limited to direct hypomethylation of DNMTs, but it can indirectly affect other epigenetic factors, such as HDACs activity, through converging pathways.</description><identifier>ISSN: 2322-3480</identifier><identifier>EISSN: 2322-3480</identifier><identifier>DOI: 10.52547/rbmb.10.3.420</identifier><identifier>PMID: 34981019</identifier><language>eng</language><publisher>Iran: Varastegan Institute for Medical Sciences</publisher><subject>Original</subject><ispartof>Reports of biochemistry and molecular biology, 2021-10, Vol.10 (3), p.420-428</ispartof><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-1114bdf2fac8141f970f32c4b9ad37340c46f8663cc79e70783387b04e9247ef3</citedby><cites>FETCH-LOGICAL-c390t-1114bdf2fac8141f970f32c4b9ad37340c46f8663cc79e70783387b04e9247ef3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8718785/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8718785/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27922,27923,53789,53791</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34981019$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dalvand, Sina</creatorcontrib><creatorcontrib>Namdari, Amin</creatorcontrib><creatorcontrib>Sepahvand, Farzad</creatorcontrib><creatorcontrib>Meshkibaf, Mohammad Hassan</creatorcontrib><creatorcontrib>Ahmadpour, GholamReza</creatorcontrib><creatorcontrib>Department of Clinical Biochemistry, Fasa University of Medical Sciences, Fasa, Fars, Iran</creatorcontrib><creatorcontrib>Department of Medical Parasitology and Mycology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran</creatorcontrib><creatorcontrib>International Campus, Department of Biochemistry and Molecular Biology, Shahid Sadoughi University of Medical Sciences, Yazd, Iran</creatorcontrib><title>Investigation of Decitabine Effects on HDAC3 and HDAC7 mRNA Expression in NALM-6 and HL-60 Cancer Cell Lines</title><title>Reports of biochemistry and molecular biology</title><addtitle>Rep Biochem Mol Biol</addtitle><description>Decitabine is a potent anticancer hypomethylating agent and changes the gene expression through the gene's promoter demethylation and also independently from DNA demethylation. So, the present study was designed to distinguish whether Decitabine, in addition to inhibitory effects on DNA methyltransferase, can change HDAC3 and HDAC7 mRNA expression in NALM-6 and HL-60 cancer cell lines.
HL-60, NALM-6, and normal cells were cultured, and the Decitabine treatment dose was obtained (1 µM) through the MTT assay. Finally, HDAC3 and HDAC7 mRNA expression were measured by Real-Time PCR in HL-60 and NALM-6 cancerous cells before and after treatment. Furthermore, HDAC3 and HDAC7 mRNA expression in untreated HL-60 and NALM-6 cancerous cells were compared to normal cells.
Our results revealed that the expression of HDAC3 and HDAC7 in HL-60 and NALM-6 cells increases as compared to normal cells. After treatment of HL-60 and NALM-6 cells with Decitabine, HDAC3, and HDAC7 mRNA expression were decreased significantly.
Our data confirmed that the effects of Decitabine are not limited to direct hypomethylation of DNMTs, but it can indirectly affect other epigenetic factors, such as HDACs activity, through converging pathways.</description><subject>Original</subject><issn>2322-3480</issn><issn>2322-3480</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNpVUU1LAzEQDaKoqFePkqOXrflqkr0IZa1aWBVEzyGbJhrZzdZkW_Tfm1otepoZ3ps3Hw-AU4xGYzJm4iI2XTPKFR0xgnbAIaGEFJRJtPsnPwAnKb0hhDAZc17yfXBAWSkxwuUhaGdhZdPgX_Tg-wB7B6-s8YNufLBw6pw1Q4IZuL2aVBTqMP_OBOwe7ydw-rGINqV1ow_wflLfFXzDqQuOYKWDsRFWtm1hnfXSMdhzuk325Ccegefr6VN1W9QPN7NqUheGlmgoMMasmTvitJGYYVcK5CgxrCn1nArKkGHcSc6pMaK0AglJqRQNYrYkTFhHj8DlRnexbDo7NzYMUbdqEX2n46fqtVf_keBf1Uu_UlJgKeQ4C5z_CMT-fZn_ozqfTL5DB9svkyIcc54fSEimjjZUE_uUonXbMRipb5fU2qV1RVV2KTec_V1uS__1hH4BQtCLKA</recordid><startdate>20211001</startdate><enddate>20211001</enddate><creator>Dalvand, Sina</creator><creator>Namdari, Amin</creator><creator>Sepahvand, Farzad</creator><creator>Meshkibaf, Mohammad Hassan</creator><creator>Ahmadpour, GholamReza</creator><general>Varastegan Institute for Medical Sciences</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20211001</creationdate><title>Investigation of Decitabine Effects on HDAC3 and HDAC7 mRNA Expression in NALM-6 and HL-60 Cancer Cell Lines</title><author>Dalvand, Sina ; Namdari, Amin ; Sepahvand, Farzad ; Meshkibaf, Mohammad Hassan ; Ahmadpour, GholamReza</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-1114bdf2fac8141f970f32c4b9ad37340c46f8663cc79e70783387b04e9247ef3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Original</topic><toplevel>online_resources</toplevel><creatorcontrib>Dalvand, Sina</creatorcontrib><creatorcontrib>Namdari, Amin</creatorcontrib><creatorcontrib>Sepahvand, Farzad</creatorcontrib><creatorcontrib>Meshkibaf, Mohammad Hassan</creatorcontrib><creatorcontrib>Ahmadpour, GholamReza</creatorcontrib><creatorcontrib>Department of Clinical Biochemistry, Fasa University of Medical Sciences, Fasa, Fars, Iran</creatorcontrib><creatorcontrib>Department of Medical Parasitology and Mycology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran</creatorcontrib><creatorcontrib>International Campus, Department of Biochemistry and Molecular Biology, Shahid Sadoughi University of Medical Sciences, Yazd, Iran</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Reports of biochemistry and molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dalvand, Sina</au><au>Namdari, Amin</au><au>Sepahvand, Farzad</au><au>Meshkibaf, Mohammad Hassan</au><au>Ahmadpour, GholamReza</au><aucorp>Department of Clinical Biochemistry, Fasa University of Medical Sciences, Fasa, Fars, Iran</aucorp><aucorp>Department of Medical Parasitology and Mycology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran</aucorp><aucorp>International Campus, Department of Biochemistry and Molecular Biology, Shahid Sadoughi University of Medical Sciences, Yazd, Iran</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Investigation of Decitabine Effects on HDAC3 and HDAC7 mRNA Expression in NALM-6 and HL-60 Cancer Cell Lines</atitle><jtitle>Reports of biochemistry and molecular biology</jtitle><addtitle>Rep Biochem Mol Biol</addtitle><date>2021-10-01</date><risdate>2021</risdate><volume>10</volume><issue>3</issue><spage>420</spage><epage>428</epage><pages>420-428</pages><issn>2322-3480</issn><eissn>2322-3480</eissn><abstract>Decitabine is a potent anticancer hypomethylating agent and changes the gene expression through the gene's promoter demethylation and also independently from DNA demethylation. So, the present study was designed to distinguish whether Decitabine, in addition to inhibitory effects on DNA methyltransferase, can change HDAC3 and HDAC7 mRNA expression in NALM-6 and HL-60 cancer cell lines.
HL-60, NALM-6, and normal cells were cultured, and the Decitabine treatment dose was obtained (1 µM) through the MTT assay. Finally, HDAC3 and HDAC7 mRNA expression were measured by Real-Time PCR in HL-60 and NALM-6 cancerous cells before and after treatment. Furthermore, HDAC3 and HDAC7 mRNA expression in untreated HL-60 and NALM-6 cancerous cells were compared to normal cells.
Our results revealed that the expression of HDAC3 and HDAC7 in HL-60 and NALM-6 cells increases as compared to normal cells. After treatment of HL-60 and NALM-6 cells with Decitabine, HDAC3, and HDAC7 mRNA expression were decreased significantly.
Our data confirmed that the effects of Decitabine are not limited to direct hypomethylation of DNMTs, but it can indirectly affect other epigenetic factors, such as HDACs activity, through converging pathways.</abstract><cop>Iran</cop><pub>Varastegan Institute for Medical Sciences</pub><pmid>34981019</pmid><doi>10.52547/rbmb.10.3.420</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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title | Investigation of Decitabine Effects on HDAC3 and HDAC7 mRNA Expression in NALM-6 and HL-60 Cancer Cell Lines |
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