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8-Hydroxyquinoline a natural chelating agent from Streptomyces spp. inhibits A549 lung cancer cell lines via BCL2/STAT3 regulating pathways
Biomolecules from Streptomyces spp. are emerging sources of natural drugs and have been focused on over the decade. The discovery of bioactive chemotherapeutic molecules from soil Streptomyces spp. has opened the medium for the search for natural drugs. In the current study, 8-HOQ was extracted and...
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Published in: | World journal of microbiology & biotechnology 2022-10, Vol.38 (10), p.182-182, Article 182 |
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container_title | World journal of microbiology & biotechnology |
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creator | Balthazar, Joseph Devadass Soosaimanickam, Maria Packiam Emmanuel, C. Krishnaraj, Thirugnansambantham Sheikh, Abdullah Alghafis, Saleh Fahad Ibrahim, Hairul-Islam Mohamed |
description | Biomolecules from
Streptomyces
spp. are emerging sources of natural drugs and have been focused on over the decade. The discovery of bioactive chemotherapeutic molecules from soil
Streptomyces
spp. has opened the medium for the search for natural drugs. In the current study, 8-HOQ was extracted and purified from soil
Streptomyces
spp. and was evaluated on A549 and BEAS cell lines. The apoptotic and caspase mediated pathways were evaluated using cell proliferation, dual fluorescent staining, migration, invasion and mRNA as well as protein quantification of apoptotic markers. In vitro cytotoxicity test revealed that 8-HOQ possesses potent cytotoxicity activities with IC
50
values of 26 µM, 5 µM, 7.2 µM at 24 h, 48 h, and 72 h respectively against A549 lung cancer cell lines. The result also demonstrated that 8-HOQ from
Streptomyces
spp significantly inhibited the A549 lung cancer cell lines and activated the intrinsic pathways of apoptosis. The caspase-3 and caspase-8 activities were potentially elevated in 8-HOQ treated A549 cell lines and confirmed that 8-HOQ mediated A549 cancer cell death through the intrinsic pathway. The results explored caspase-mediated apoptosis as a mechanism underlying the inhibition of cancer cell viability in a dose-dependent manner. The expression of P53, BCL2 and STAT3 were inhibited in A549 cell lines and confirmed the metastasis inhibitory potential of 8-HOQ by blocking migration and invasion in A549 cell lines. These results indicated that 8-HOQ from
Streptomyces
spp. potentially inhibited growth and migration of A549 lung cancer cell lines. |
doi_str_mv | 10.1007/s11274-022-03368-4 |
format | article |
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Streptomyces
spp. are emerging sources of natural drugs and have been focused on over the decade. The discovery of bioactive chemotherapeutic molecules from soil
Streptomyces
spp. has opened the medium for the search for natural drugs. In the current study, 8-HOQ was extracted and purified from soil
Streptomyces
spp. and was evaluated on A549 and BEAS cell lines. The apoptotic and caspase mediated pathways were evaluated using cell proliferation, dual fluorescent staining, migration, invasion and mRNA as well as protein quantification of apoptotic markers. In vitro cytotoxicity test revealed that 8-HOQ possesses potent cytotoxicity activities with IC
50
values of 26 µM, 5 µM, 7.2 µM at 24 h, 48 h, and 72 h respectively against A549 lung cancer cell lines. The result also demonstrated that 8-HOQ from
Streptomyces
spp significantly inhibited the A549 lung cancer cell lines and activated the intrinsic pathways of apoptosis. The caspase-3 and caspase-8 activities were potentially elevated in 8-HOQ treated A549 cell lines and confirmed that 8-HOQ mediated A549 cancer cell death through the intrinsic pathway. The results explored caspase-mediated apoptosis as a mechanism underlying the inhibition of cancer cell viability in a dose-dependent manner. The expression of P53, BCL2 and STAT3 were inhibited in A549 cell lines and confirmed the metastasis inhibitory potential of 8-HOQ by blocking migration and invasion in A549 cell lines. These results indicated that 8-HOQ from
Streptomyces
spp. potentially inhibited growth and migration of A549 lung cancer cell lines.</description><identifier>ISSN: 0959-3993</identifier><identifier>EISSN: 1573-0972</identifier><identifier>DOI: 10.1007/s11274-022-03368-4</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>8-Hydroxyquinoline ; Apoptosis ; Applied Microbiology ; Biochemistry ; Biocompatibility ; Biomedical and Life Sciences ; Biomolecules ; Biotechnology ; Caspase-3 ; Caspase-8 ; Cell death ; Cell proliferation ; Cell viability ; Chelating agents ; Chelation ; Cytotoxicity ; Drug development ; Drugs ; Environmental Engineering/Biotechnology ; Fluorescence ; Hydroxyquinoline ; In vitro methods and tests ; Life Sciences ; Lung cancer ; Metastases ; Microbiology ; mRNA ; p53 Protein ; Soils ; Stat3 protein ; Streptomyces ; Toxicity testing ; Tumor cell lines</subject><ispartof>World journal of microbiology & biotechnology, 2022-10, Vol.38 (10), p.182-182, Article 182</ispartof><rights>The Author(s), under exclusive licence to Springer Nature B.V. 2022. Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c352t-8e3fc42ecdf40cef863d47a3d2669d5c9f9b909115a43290888c8dd7c7050c833</citedby><cites>FETCH-LOGICAL-c352t-8e3fc42ecdf40cef863d47a3d2669d5c9f9b909115a43290888c8dd7c7050c833</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2700906679/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$H</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2700906679?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,780,784,11688,27924,27925,36060,36061,44363,74895</link.rule.ids></links><search><creatorcontrib>Balthazar, Joseph Devadass</creatorcontrib><creatorcontrib>Soosaimanickam, Maria Packiam</creatorcontrib><creatorcontrib>Emmanuel, C.</creatorcontrib><creatorcontrib>Krishnaraj, Thirugnansambantham</creatorcontrib><creatorcontrib>Sheikh, Abdullah</creatorcontrib><creatorcontrib>Alghafis, Saleh Fahad</creatorcontrib><creatorcontrib>Ibrahim, Hairul-Islam Mohamed</creatorcontrib><title>8-Hydroxyquinoline a natural chelating agent from Streptomyces spp. inhibits A549 lung cancer cell lines via BCL2/STAT3 regulating pathways</title><title>World journal of microbiology & biotechnology</title><addtitle>World J Microbiol Biotechnol</addtitle><description>Biomolecules from
Streptomyces
spp. are emerging sources of natural drugs and have been focused on over the decade. The discovery of bioactive chemotherapeutic molecules from soil
Streptomyces
spp. has opened the medium for the search for natural drugs. In the current study, 8-HOQ was extracted and purified from soil
Streptomyces
spp. and was evaluated on A549 and BEAS cell lines. The apoptotic and caspase mediated pathways were evaluated using cell proliferation, dual fluorescent staining, migration, invasion and mRNA as well as protein quantification of apoptotic markers. In vitro cytotoxicity test revealed that 8-HOQ possesses potent cytotoxicity activities with IC
50
values of 26 µM, 5 µM, 7.2 µM at 24 h, 48 h, and 72 h respectively against A549 lung cancer cell lines. The result also demonstrated that 8-HOQ from
Streptomyces
spp significantly inhibited the A549 lung cancer cell lines and activated the intrinsic pathways of apoptosis. The caspase-3 and caspase-8 activities were potentially elevated in 8-HOQ treated A549 cell lines and confirmed that 8-HOQ mediated A549 cancer cell death through the intrinsic pathway. The results explored caspase-mediated apoptosis as a mechanism underlying the inhibition of cancer cell viability in a dose-dependent manner. The expression of P53, BCL2 and STAT3 were inhibited in A549 cell lines and confirmed the metastasis inhibitory potential of 8-HOQ by blocking migration and invasion in A549 cell lines. These results indicated that 8-HOQ from
Streptomyces
spp. potentially inhibited growth and migration of A549 lung cancer cell lines.</description><subject>8-Hydroxyquinoline</subject><subject>Apoptosis</subject><subject>Applied Microbiology</subject><subject>Biochemistry</subject><subject>Biocompatibility</subject><subject>Biomedical and Life Sciences</subject><subject>Biomolecules</subject><subject>Biotechnology</subject><subject>Caspase-3</subject><subject>Caspase-8</subject><subject>Cell death</subject><subject>Cell proliferation</subject><subject>Cell viability</subject><subject>Chelating agents</subject><subject>Chelation</subject><subject>Cytotoxicity</subject><subject>Drug development</subject><subject>Drugs</subject><subject>Environmental Engineering/Biotechnology</subject><subject>Fluorescence</subject><subject>Hydroxyquinoline</subject><subject>In vitro methods and tests</subject><subject>Life Sciences</subject><subject>Lung cancer</subject><subject>Metastases</subject><subject>Microbiology</subject><subject>mRNA</subject><subject>p53 Protein</subject><subject>Soils</subject><subject>Stat3 protein</subject><subject>Streptomyces</subject><subject>Toxicity testing</subject><subject>Tumor cell 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a natural chelating agent from Streptomyces spp. inhibits A549 lung cancer cell lines via BCL2/STAT3 regulating pathways</title><author>Balthazar, Joseph Devadass ; Soosaimanickam, Maria Packiam ; Emmanuel, C. ; Krishnaraj, Thirugnansambantham ; Sheikh, Abdullah ; Alghafis, Saleh Fahad ; Ibrahim, Hairul-Islam Mohamed</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c352t-8e3fc42ecdf40cef863d47a3d2669d5c9f9b909115a43290888c8dd7c7050c833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>8-Hydroxyquinoline</topic><topic>Apoptosis</topic><topic>Applied Microbiology</topic><topic>Biochemistry</topic><topic>Biocompatibility</topic><topic>Biomedical and Life Sciences</topic><topic>Biomolecules</topic><topic>Biotechnology</topic><topic>Caspase-3</topic><topic>Caspase-8</topic><topic>Cell death</topic><topic>Cell proliferation</topic><topic>Cell viability</topic><topic>Chelating 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Saleh Fahad</au><au>Ibrahim, Hairul-Islam Mohamed</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>8-Hydroxyquinoline a natural chelating agent from Streptomyces spp. inhibits A549 lung cancer cell lines via BCL2/STAT3 regulating pathways</atitle><jtitle>World journal of microbiology & biotechnology</jtitle><stitle>World J Microbiol Biotechnol</stitle><date>2022-10-01</date><risdate>2022</risdate><volume>38</volume><issue>10</issue><spage>182</spage><epage>182</epage><pages>182-182</pages><artnum>182</artnum><issn>0959-3993</issn><eissn>1573-0972</eissn><abstract>Biomolecules from
Streptomyces
spp. are emerging sources of natural drugs and have been focused on over the decade. The discovery of bioactive chemotherapeutic molecules from soil
Streptomyces
spp. has opened the medium for the search for natural drugs. In the current study, 8-HOQ was extracted and purified from soil
Streptomyces
spp. and was evaluated on A549 and BEAS cell lines. The apoptotic and caspase mediated pathways were evaluated using cell proliferation, dual fluorescent staining, migration, invasion and mRNA as well as protein quantification of apoptotic markers. In vitro cytotoxicity test revealed that 8-HOQ possesses potent cytotoxicity activities with IC
50
values of 26 µM, 5 µM, 7.2 µM at 24 h, 48 h, and 72 h respectively against A549 lung cancer cell lines. The result also demonstrated that 8-HOQ from
Streptomyces
spp significantly inhibited the A549 lung cancer cell lines and activated the intrinsic pathways of apoptosis. The caspase-3 and caspase-8 activities were potentially elevated in 8-HOQ treated A549 cell lines and confirmed that 8-HOQ mediated A549 cancer cell death through the intrinsic pathway. The results explored caspase-mediated apoptosis as a mechanism underlying the inhibition of cancer cell viability in a dose-dependent manner. The expression of P53, BCL2 and STAT3 were inhibited in A549 cell lines and confirmed the metastasis inhibitory potential of 8-HOQ by blocking migration and invasion in A549 cell lines. These results indicated that 8-HOQ from
Streptomyces
spp. potentially inhibited growth and migration of A549 lung cancer cell lines.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><doi>10.1007/s11274-022-03368-4</doi><tpages>1</tpages></addata></record> |
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subjects | 8-Hydroxyquinoline Apoptosis Applied Microbiology Biochemistry Biocompatibility Biomedical and Life Sciences Biomolecules Biotechnology Caspase-3 Caspase-8 Cell death Cell proliferation Cell viability Chelating agents Chelation Cytotoxicity Drug development Drugs Environmental Engineering/Biotechnology Fluorescence Hydroxyquinoline In vitro methods and tests Life Sciences Lung cancer Metastases Microbiology mRNA p53 Protein Soils Stat3 protein Streptomyces Toxicity testing Tumor cell lines |
title | 8-Hydroxyquinoline a natural chelating agent from Streptomyces spp. inhibits A549 lung cancer cell lines via BCL2/STAT3 regulating pathways |
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