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Acute and long-term effects of hyperthermia in B16-F10 melanoma cells
Hyperthermia uses exogenous heat induction as a cancer therapy. This work addresses the acute and long-term effects of hyperthermia in the highly metastatic melanoma cell line B16-F10. Melanoma cells were submitted to one heat treatment, 45°C for 30 min, and thereafter were kept at 37°C for an addit...
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Published in: | PloS one 2012-04, Vol.7 (4), p.e35489-e35489 |
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description | Hyperthermia uses exogenous heat induction as a cancer therapy. This work addresses the acute and long-term effects of hyperthermia in the highly metastatic melanoma cell line B16-F10.
Melanoma cells were submitted to one heat treatment, 45°C for 30 min, and thereafter were kept at 37°C for an additional period of 14 days. Cultures maintained at 37°C were used as control. Cultures were assessed for the heat shock reaction.
Immediately after the heat shock, cells began a process of fast degradation, and, in the first 24 h, cultures showed decreased viability, alterations in cell morphology and F-actin cytoskeleton organization, significant reduction in the number of adherent cells, most of them in a process of late apoptosis, and an altered gene expression profile. A follow-up of two weeks after heat exposure showed that viability and number of adherent cells remained very low, with a high percentage of early apoptotic cells. Still, heat-treated cultures maintained a low but relatively constant population of cells in S and G(2)/M phases for a long period after heat exposure, evidencing the presence of metabolically active cells.
The melanoma cell line B16-F10 is susceptible to one hyperthermia treatment at 45°C, with significant induced acute and long-term effects. However, a low but apparently stable percentage of metabolically active cells survived long after heat exposure. |
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Melanoma cells were submitted to one heat treatment, 45°C for 30 min, and thereafter were kept at 37°C for an additional period of 14 days. Cultures maintained at 37°C were used as control. Cultures were assessed for the heat shock reaction.
Immediately after the heat shock, cells began a process of fast degradation, and, in the first 24 h, cultures showed decreased viability, alterations in cell morphology and F-actin cytoskeleton organization, significant reduction in the number of adherent cells, most of them in a process of late apoptosis, and an altered gene expression profile. A follow-up of two weeks after heat exposure showed that viability and number of adherent cells remained very low, with a high percentage of early apoptotic cells. Still, heat-treated cultures maintained a low but relatively constant population of cells in S and G(2)/M phases for a long period after heat exposure, evidencing the presence of metabolically active cells.
The melanoma cell line B16-F10 is susceptible to one hyperthermia treatment at 45°C, with significant induced acute and long-term effects. However, a low but apparently stable percentage of metabolically active cells survived long after heat exposure.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0035489</identifier><identifier>PMID: 22532856</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Actin ; Adherent cells ; Analysis ; Animals ; Antigens ; Apoptosis ; Apoptosis - physiology ; Biology ; Cancer ; Cancer metastasis ; Cancer therapies ; Cancer treatment ; Cell cycle ; Cell Cycle - physiology ; Cell Line, Tumor ; Cell morphology ; Cell Proliferation ; Cell Shape - physiology ; Cell Survival - physiology ; Cytology ; Cytoskeleton ; Dehydrogenases ; Exposure ; Fever ; Gene Expression ; Genes ; Health aspects ; Heat ; Heat shock ; Heat shock proteins ; Heat treatment ; Hot Temperature ; Hyperthermia ; Hyperthermia, Induced ; Immunotherapy ; Long-term effects ; Medicine ; Melanoma ; Melanoma, Experimental - therapy ; Metastases ; Mice ; Muscle proteins ; Studies ; Time ; Tumor Cells, Cultured ; Viability</subject><ispartof>PloS one, 2012-04, Vol.7 (4), p.e35489-e35489</ispartof><rights>COPYRIGHT 2012 Public Library of Science</rights><rights>2012 Garcia et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Garcia et al. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-49b5cdfd04a87f5c6bb847fdd41b434ce77765549fcbbaaeac2e6642627033713</citedby><cites>FETCH-LOGICAL-c692t-49b5cdfd04a87f5c6bb847fdd41b434ce77765549fcbbaaeac2e6642627033713</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1324573961/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1324573961?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25752,27923,27924,37011,37012,44589,53790,53792,74997</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22532856$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Slominski, Andrzej T.</contributor><creatorcontrib>Garcia, Mónica Pereira</creatorcontrib><creatorcontrib>Cavalheiro, José Roberto Tinoco</creatorcontrib><creatorcontrib>Fernandes, Maria Helena</creatorcontrib><title>Acute and long-term effects of hyperthermia in B16-F10 melanoma cells</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Hyperthermia uses exogenous heat induction as a cancer therapy. This work addresses the acute and long-term effects of hyperthermia in the highly metastatic melanoma cell line B16-F10.
Melanoma cells were submitted to one heat treatment, 45°C for 30 min, and thereafter were kept at 37°C for an additional period of 14 days. Cultures maintained at 37°C were used as control. Cultures were assessed for the heat shock reaction.
Immediately after the heat shock, cells began a process of fast degradation, and, in the first 24 h, cultures showed decreased viability, alterations in cell morphology and F-actin cytoskeleton organization, significant reduction in the number of adherent cells, most of them in a process of late apoptosis, and an altered gene expression profile. A follow-up of two weeks after heat exposure showed that viability and number of adherent cells remained very low, with a high percentage of early apoptotic cells. Still, heat-treated cultures maintained a low but relatively constant population of cells in S and G(2)/M phases for a long period after heat exposure, evidencing the presence of metabolically active cells.
The melanoma cell line B16-F10 is susceptible to one hyperthermia treatment at 45°C, with significant induced acute and long-term effects. However, a low but apparently stable percentage of metabolically active cells survived long after heat exposure.</description><subject>Actin</subject><subject>Adherent cells</subject><subject>Analysis</subject><subject>Animals</subject><subject>Antigens</subject><subject>Apoptosis</subject><subject>Apoptosis - physiology</subject><subject>Biology</subject><subject>Cancer</subject><subject>Cancer metastasis</subject><subject>Cancer therapies</subject><subject>Cancer treatment</subject><subject>Cell cycle</subject><subject>Cell Cycle - physiology</subject><subject>Cell Line, Tumor</subject><subject>Cell morphology</subject><subject>Cell Proliferation</subject><subject>Cell Shape - physiology</subject><subject>Cell Survival - physiology</subject><subject>Cytology</subject><subject>Cytoskeleton</subject><subject>Dehydrogenases</subject><subject>Exposure</subject><subject>Fever</subject><subject>Gene Expression</subject><subject>Genes</subject><subject>Health aspects</subject><subject>Heat</subject><subject>Heat shock</subject><subject>Heat shock proteins</subject><subject>Heat treatment</subject><subject>Hot Temperature</subject><subject>Hyperthermia</subject><subject>Hyperthermia, Induced</subject><subject>Immunotherapy</subject><subject>Long-term effects</subject><subject>Medicine</subject><subject>Melanoma</subject><subject>Melanoma, Experimental - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Garcia, Mónica Pereira</au><au>Cavalheiro, José Roberto Tinoco</au><au>Fernandes, Maria Helena</au><au>Slominski, Andrzej T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Acute and long-term effects of hyperthermia in B16-F10 melanoma cells</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2012-04-20</date><risdate>2012</risdate><volume>7</volume><issue>4</issue><spage>e35489</spage><epage>e35489</epage><pages>e35489-e35489</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Hyperthermia uses exogenous heat induction as a cancer therapy. This work addresses the acute and long-term effects of hyperthermia in the highly metastatic melanoma cell line B16-F10.
Melanoma cells were submitted to one heat treatment, 45°C for 30 min, and thereafter were kept at 37°C for an additional period of 14 days. Cultures maintained at 37°C were used as control. Cultures were assessed for the heat shock reaction.
Immediately after the heat shock, cells began a process of fast degradation, and, in the first 24 h, cultures showed decreased viability, alterations in cell morphology and F-actin cytoskeleton organization, significant reduction in the number of adherent cells, most of them in a process of late apoptosis, and an altered gene expression profile. A follow-up of two weeks after heat exposure showed that viability and number of adherent cells remained very low, with a high percentage of early apoptotic cells. Still, heat-treated cultures maintained a low but relatively constant population of cells in S and G(2)/M phases for a long period after heat exposure, evidencing the presence of metabolically active cells.
The melanoma cell line B16-F10 is susceptible to one hyperthermia treatment at 45°C, with significant induced acute and long-term effects. However, a low but apparently stable percentage of metabolically active cells survived long after heat exposure.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>22532856</pmid><doi>10.1371/journal.pone.0035489</doi><tpages>e35489</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Actin Adherent cells Analysis Animals Antigens Apoptosis Apoptosis - physiology Biology Cancer Cancer metastasis Cancer therapies Cancer treatment Cell cycle Cell Cycle - physiology Cell Line, Tumor Cell morphology Cell Proliferation Cell Shape - physiology Cell Survival - physiology Cytology Cytoskeleton Dehydrogenases Exposure Fever Gene Expression Genes Health aspects Heat Heat shock Heat shock proteins Heat treatment Hot Temperature Hyperthermia Hyperthermia, Induced Immunotherapy Long-term effects Medicine Melanoma Melanoma, Experimental - therapy Metastases Mice Muscle proteins Studies Time Tumor Cells, Cultured Viability |
title | Acute and long-term effects of hyperthermia in B16-F10 melanoma cells |
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