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Hyperthermia induces cytoskeletal alterations and mitotic catastrophe in p53-deficient H1299 lung cancer cells
Hyperthermia is used in cancer therapy, however much remains to be discovered regarding its mechanisms of action at the cellular level. In this study, the effects of hyperthermia on cell death, survival, morphology and the cytoskeleton were investigated in a non-small cell lung cancer cell line, H12...
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Published in: | Acta histochemica 2013-01, Vol.115 (1), p.8-15 |
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description | Hyperthermia is used in cancer therapy, however much remains to be discovered regarding its mechanisms of action at the cellular level. In this study, the effects of hyperthermia on cell death, survival, morphology and the cytoskeleton were investigated in a non-small cell lung cancer cell line, H1299. Despite the fact that this cell line is widely used in research, it has not yet been tested for heat shock sensitivity. Cells were given a 30-min heat shock at 43.5°C and 45°C and left to recover at 37°C for 24 and 48h. 24h after heat shock treatment, we monitored changes in the organization of the cytoskeleton using immunofluorescence microscopy. The number of actin stress fibers was significantly reduced, microtubules formed a looser meshwork, a portion of the cells possessed multipolar mitotic spindles, whereas vimentin filaments collapsed into perinuclear complexes. 48h following heat stress, most of the cells showed recovery of the cytoskeleton, however we observed a considerable number of giant cells that were multinucleated or contained one enlarged nucleus. The data obtained by MTT assay showed a dose-dependent decrease of cell viability, while flow cytometric analysis revealed an increase in the number of cells with externalized phosphatidylserine. The results suggest that one of the modes of heat-induced cell death in H1299 cells is mitotic catastrophe, which probably ends in apoptosis. |
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In this study, the effects of hyperthermia on cell death, survival, morphology and the cytoskeleton were investigated in a non-small cell lung cancer cell line, H1299. Despite the fact that this cell line is widely used in research, it has not yet been tested for heat shock sensitivity. Cells were given a 30-min heat shock at 43.5°C and 45°C and left to recover at 37°C for 24 and 48h. 24h after heat shock treatment, we monitored changes in the organization of the cytoskeleton using immunofluorescence microscopy. The number of actin stress fibers was significantly reduced, microtubules formed a looser meshwork, a portion of the cells possessed multipolar mitotic spindles, whereas vimentin filaments collapsed into perinuclear complexes. 48h following heat stress, most of the cells showed recovery of the cytoskeleton, however we observed a considerable number of giant cells that were multinucleated or contained one enlarged nucleus. The data obtained by MTT assay showed a dose-dependent decrease of cell viability, while flow cytometric analysis revealed an increase in the number of cells with externalized phosphatidylserine. The results suggest that one of the modes of heat-induced cell death in H1299 cells is mitotic catastrophe, which probably ends in apoptosis.</description><identifier>ISSN: 0065-1281</identifier><identifier>EISSN: 1618-0372</identifier><identifier>DOI: 10.1016/j.acthis.2012.02.006</identifier><identifier>PMID: 22483983</identifier><language>eng</language><publisher>Germany: Elsevier GmbH</publisher><subject>Actin ; Actins - analysis ; Actins - metabolism ; Cell Death ; Cell Survival ; Cytoskeleton ; Cytoskeleton - metabolism ; Cytoskeleton - pathology ; Fluorescent Antibody Technique ; H1299 cells ; Hot Temperature ; Humans ; Hyperthermia ; Hyperthermia, Induced ; Mitosis ; Mitotic catastrophe ; Stress Fibers - chemistry ; Stress Fibers - metabolism ; Stress Fibers - pathology ; Tubulin - analysis ; Tumor Cells, Cultured ; Tumor Suppressor Protein p53 - deficiency ; Tumor Suppressor Protein p53 - genetics ; Tumor Suppressor Protein p53 - metabolism ; Vimentin - analysis</subject><ispartof>Acta histochemica, 2013-01, Vol.115 (1), p.8-15</ispartof><rights>2012 Elsevier GmbH</rights><rights>Copyright © 2012 Elsevier GmbH. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c461t-e4c8a4d232ec06c0f617f829ff8e6b0f3e5e548cab8f803cefb67a7543c065ce3</citedby><cites>FETCH-LOGICAL-c461t-e4c8a4d232ec06c0f617f829ff8e6b0f3e5e548cab8f803cefb67a7543c065ce3</cites></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/22483983$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pawlik, Andrzej</creatorcontrib><creatorcontrib>Nowak, Jakub Marcin</creatorcontrib><creatorcontrib>Grzanka, Dariusz</creatorcontrib><creatorcontrib>Gackowska, Lidia</creatorcontrib><creatorcontrib>Michalkiewicz, Jacek</creatorcontrib><creatorcontrib>Grzanka, Alina</creatorcontrib><title>Hyperthermia induces cytoskeletal alterations and mitotic catastrophe in p53-deficient H1299 lung cancer cells</title><title>Acta histochemica</title><addtitle>Acta Histochem</addtitle><description>Hyperthermia is used in cancer therapy, however much remains to be discovered regarding its mechanisms of action at the cellular level. In this study, the effects of hyperthermia on cell death, survival, morphology and the cytoskeleton were investigated in a non-small cell lung cancer cell line, H1299. Despite the fact that this cell line is widely used in research, it has not yet been tested for heat shock sensitivity. Cells were given a 30-min heat shock at 43.5°C and 45°C and left to recover at 37°C for 24 and 48h. 24h after heat shock treatment, we monitored changes in the organization of the cytoskeleton using immunofluorescence microscopy. The number of actin stress fibers was significantly reduced, microtubules formed a looser meshwork, a portion of the cells possessed multipolar mitotic spindles, whereas vimentin filaments collapsed into perinuclear complexes. 48h following heat stress, most of the cells showed recovery of the cytoskeleton, however we observed a considerable number of giant cells that were multinucleated or contained one enlarged nucleus. The data obtained by MTT assay showed a dose-dependent decrease of cell viability, while flow cytometric analysis revealed an increase in the number of cells with externalized phosphatidylserine. The results suggest that one of the modes of heat-induced cell death in H1299 cells is mitotic catastrophe, which probably ends in apoptosis.</description><subject>Actin</subject><subject>Actins - analysis</subject><subject>Actins - metabolism</subject><subject>Cell Death</subject><subject>Cell Survival</subject><subject>Cytoskeleton</subject><subject>Cytoskeleton - metabolism</subject><subject>Cytoskeleton - pathology</subject><subject>Fluorescent Antibody Technique</subject><subject>H1299 cells</subject><subject>Hot Temperature</subject><subject>Humans</subject><subject>Hyperthermia</subject><subject>Hyperthermia, Induced</subject><subject>Mitosis</subject><subject>Mitotic catastrophe</subject><subject>Stress Fibers - chemistry</subject><subject>Stress Fibers - metabolism</subject><subject>Stress Fibers - pathology</subject><subject>Tubulin - analysis</subject><subject>Tumor Cells, Cultured</subject><subject>Tumor Suppressor Protein p53 - deficiency</subject><subject>Tumor Suppressor Protein p53 - genetics</subject><subject>Tumor Suppressor Protein p53 - metabolism</subject><subject>Vimentin - analysis</subject><issn>0065-1281</issn><issn>1618-0372</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqFkU-LFDEQxYO4uOPufgORHL30WEk63emLIMvqCAte1nPIVFecjP3PJC3MtzfDrB4VCgqK36sq3mPsjYCtANG8P24d5kNIWwlCbqEUNC_YRjTCVKBa-ZJtykRXQhpxzV6ndASADpR8xa6lrI3qjNqwaXdaKOYDxTE4HqZ-RUocT3lOP2ig7AbuhkzR5TBPibup52PIcw7I0WWXcpyXAxUhX7SqevIBA02Z74TsOj6s0_fCTUiRIw1DumVX3g2J7p77Dfv26eHpflc9fv385f7jY4V1I3JFNRpX91JJQmgQfCNab2TnvaFmD16RJl0bdHvjDSgkv29a1-paFVwjqRv27rJ3ifPPlVK2Y0jnD9xE85psMUVDp0Hr_6Oia2tT_FIFrS8oxjmlSN4uMYwunqwAew7FHu0lFHsOxUIpaIrs7fOFdT9S_1f0J4UCfLgAVCz5FSjadHYRqQ-RMNt-Dv--8Bu7K6B5</recordid><startdate>201301</startdate><enddate>201301</enddate><creator>Pawlik, Andrzej</creator><creator>Nowak, Jakub Marcin</creator><creator>Grzanka, Dariusz</creator><creator>Gackowska, Lidia</creator><creator>Michalkiewicz, Jacek</creator><creator>Grzanka, Alina</creator><general>Elsevier GmbH</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>7X8</scope><scope>7TO</scope><scope>H94</scope></search><sort><creationdate>201301</creationdate><title>Hyperthermia induces cytoskeletal alterations and mitotic catastrophe in p53-deficient H1299 lung cancer cells</title><author>Pawlik, Andrzej ; 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In this study, the effects of hyperthermia on cell death, survival, morphology and the cytoskeleton were investigated in a non-small cell lung cancer cell line, H1299. Despite the fact that this cell line is widely used in research, it has not yet been tested for heat shock sensitivity. Cells were given a 30-min heat shock at 43.5°C and 45°C and left to recover at 37°C for 24 and 48h. 24h after heat shock treatment, we monitored changes in the organization of the cytoskeleton using immunofluorescence microscopy. The number of actin stress fibers was significantly reduced, microtubules formed a looser meshwork, a portion of the cells possessed multipolar mitotic spindles, whereas vimentin filaments collapsed into perinuclear complexes. 48h following heat stress, most of the cells showed recovery of the cytoskeleton, however we observed a considerable number of giant cells that were multinucleated or contained one enlarged nucleus. The data obtained by MTT assay showed a dose-dependent decrease of cell viability, while flow cytometric analysis revealed an increase in the number of cells with externalized phosphatidylserine. The results suggest that one of the modes of heat-induced cell death in H1299 cells is mitotic catastrophe, which probably ends in apoptosis.</abstract><cop>Germany</cop><pub>Elsevier GmbH</pub><pmid>22483983</pmid><doi>10.1016/j.acthis.2012.02.006</doi><tpages>8</tpages></addata></record> |
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subjects | Actin Actins - analysis Actins - metabolism Cell Death Cell Survival Cytoskeleton Cytoskeleton - metabolism Cytoskeleton - pathology Fluorescent Antibody Technique H1299 cells Hot Temperature Humans Hyperthermia Hyperthermia, Induced Mitosis Mitotic catastrophe Stress Fibers - chemistry Stress Fibers - metabolism Stress Fibers - pathology Tubulin - analysis Tumor Cells, Cultured Tumor Suppressor Protein p53 - deficiency Tumor Suppressor Protein p53 - genetics Tumor Suppressor Protein p53 - metabolism Vimentin - analysis |
title | Hyperthermia induces cytoskeletal alterations and mitotic catastrophe in p53-deficient H1299 lung cancer cells |
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