Apoptosis induced by low‐dose and low‐dose‐rate radiation

BACKGROUND It has been claimed that external radiation, as a treatment modality for malignant diseases, partly induces apoptosis. It is not known, however, whether therapeutic low‐dose and low‐dose‐rate radiation are able to induce apoptosis. METHODS The effect of low‐dose radiation on apoptosis ind...

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Veröffentlicht in:Cancer 2002-02, Vol.94 (S4), p.1210-1214
Hauptverfasser: Mirzaie‐Joniani, Homa, Eriksson, David, Sheikholvaezin, Ali, Johansson, Amanda, Löfroth, Per‐Olov, Johansson, Lennart, Stigbrand, Torgny
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container_end_page 1214
container_issue S4
container_start_page 1210
container_title Cancer
container_volume 94
creator Mirzaie‐Joniani, Homa
Eriksson, David
Sheikholvaezin, Ali
Johansson, Amanda
Löfroth, Per‐Olov
Johansson, Lennart
Stigbrand, Torgny
description BACKGROUND It has been claimed that external radiation, as a treatment modality for malignant diseases, partly induces apoptosis. It is not known, however, whether therapeutic low‐dose and low‐dose‐rate radiation are able to induce apoptosis. METHODS The effect of low‐dose radiation on apoptosis induction in HeLa Hep2 cells was studied, and quantitation of the apoptotic cells was performed by immunocytochemistry using TdT‐mediated dUtp‐x Nick End Labeling (TUNEL) technology and the M30 CytoDEATH antibody method. RESULTS When TUNEL staining was used to quantify apoptosis in untreated HeLa Hep2 cells kept in culture, approximately 5 ± 3% of the cells showed positive staining without any treatment. In the first experiment, the HeLa Hep2 cells were exposed to gamma radiation (i.e., 0.5, 1, 2, 5, 10, and 15 grays [Gy]) from a cobalt‐60 radiation source delivering a dose rate of 0.80 Gy/min. The radiated cells were cultivated for 5, 10, 24, 48, 72 and 168 hours after irradiation. Radiation doses below 2 Gy did not cause any significant apoptosis, but between 5 and 15 Gy significant apoptosis was observed, with peak values at 5 Gy (P < 0.001). Up to 60% of the investigated cells were shown to display apoptosis. Time to this peak value was 168 hours after irradiation. The HeLa Hep2 cells were exposed to doses of 2, 5, and 10 Gy at a 10‐fold lower dose rate (0.072 Gy/min). The cells that achieved a dose below 2 Gy did not present increased apoptosis. At doses above 2 Gy, however, the cells again demonstrated significant apoptosis. Up to 24 hours following irradiation, no apoptosis could be documented, whereas beyond 24 and up to 168 hours a highly significant apoptosis induction was observed. Significant cytotoxicity was confirmed by chromium‐51 release from the cells at 5 Gy. CONCLUSIONS Low‐dose and low‐dose‐rate radiation are able to induce significant apoptosis, and apoptosis may be one of the mechanisms by which low‐dose radiation causes growth inhibition. Cancer 2002;94:1210–4. © 2002 American Cancer Society. DOI 10.1002/cncr.10287 Low‐dose (2–5 grays) and low‐dose‐rate radiation (0.072 grays per minute) are able to induce significant apoptosis, and apoptosis may be one of the mechanisms by which low‐dose radiation causes growth inhibition of experimental tumors.
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It is not known, however, whether therapeutic low‐dose and low‐dose‐rate radiation are able to induce apoptosis. METHODS The effect of low‐dose radiation on apoptosis induction in HeLa Hep2 cells was studied, and quantitation of the apoptotic cells was performed by immunocytochemistry using TdT‐mediated dUtp‐x Nick End Labeling (TUNEL) technology and the M30 CytoDEATH antibody method. RESULTS When TUNEL staining was used to quantify apoptosis in untreated HeLa Hep2 cells kept in culture, approximately 5 ± 3% of the cells showed positive staining without any treatment. In the first experiment, the HeLa Hep2 cells were exposed to gamma radiation (i.e., 0.5, 1, 2, 5, 10, and 15 grays [Gy]) from a cobalt‐60 radiation source delivering a dose rate of 0.80 Gy/min. The radiated cells were cultivated for 5, 10, 24, 48, 72 and 168 hours after irradiation. Radiation doses below 2 Gy did not cause any significant apoptosis, but between 5 and 15 Gy significant apoptosis was observed, with peak values at 5 Gy (P &lt; 0.001). Up to 60% of the investigated cells were shown to display apoptosis. Time to this peak value was 168 hours after irradiation. The HeLa Hep2 cells were exposed to doses of 2, 5, and 10 Gy at a 10‐fold lower dose rate (0.072 Gy/min). The cells that achieved a dose below 2 Gy did not present increased apoptosis. At doses above 2 Gy, however, the cells again demonstrated significant apoptosis. Up to 24 hours following irradiation, no apoptosis could be documented, whereas beyond 24 and up to 168 hours a highly significant apoptosis induction was observed. Significant cytotoxicity was confirmed by chromium‐51 release from the cells at 5 Gy. CONCLUSIONS Low‐dose and low‐dose‐rate radiation are able to induce significant apoptosis, and apoptosis may be one of the mechanisms by which low‐dose radiation causes growth inhibition. Cancer 2002;94:1210–4. © 2002 American Cancer Society. DOI 10.1002/cncr.10287 Low‐dose (2–5 grays) and low‐dose‐rate radiation (0.072 grays per minute) are able to induce significant apoptosis, and apoptosis may be one of the mechanisms by which low‐dose radiation causes growth inhibition of experimental tumors.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/cncr.10287</identifier><identifier>PMID: 11877747</identifier><identifier>CODEN: CANCAR</identifier><language>eng</language><publisher>New York: John Wiley &amp; Sons, Inc</publisher><subject>apoptosis ; Apoptosis - radiation effects ; Biological and medical sciences ; Cell Survival - drug effects ; Dose-Response Relationship, Radiation ; HeLa Cells ; Humans ; Medical sciences ; radiation ; Radiation Dosage ; Radiation therapy and radiosensitizing agent ; radioimmunotherapy ; Radioimmunotherapy - methods ; radiotherapy ; Treatment with physical agents ; Treatment. 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It is not known, however, whether therapeutic low‐dose and low‐dose‐rate radiation are able to induce apoptosis. METHODS The effect of low‐dose radiation on apoptosis induction in HeLa Hep2 cells was studied, and quantitation of the apoptotic cells was performed by immunocytochemistry using TdT‐mediated dUtp‐x Nick End Labeling (TUNEL) technology and the M30 CytoDEATH antibody method. RESULTS When TUNEL staining was used to quantify apoptosis in untreated HeLa Hep2 cells kept in culture, approximately 5 ± 3% of the cells showed positive staining without any treatment. In the first experiment, the HeLa Hep2 cells were exposed to gamma radiation (i.e., 0.5, 1, 2, 5, 10, and 15 grays [Gy]) from a cobalt‐60 radiation source delivering a dose rate of 0.80 Gy/min. The radiated cells were cultivated for 5, 10, 24, 48, 72 and 168 hours after irradiation. Radiation doses below 2 Gy did not cause any significant apoptosis, but between 5 and 15 Gy significant apoptosis was observed, with peak values at 5 Gy (P &lt; 0.001). Up to 60% of the investigated cells were shown to display apoptosis. Time to this peak value was 168 hours after irradiation. The HeLa Hep2 cells were exposed to doses of 2, 5, and 10 Gy at a 10‐fold lower dose rate (0.072 Gy/min). The cells that achieved a dose below 2 Gy did not present increased apoptosis. At doses above 2 Gy, however, the cells again demonstrated significant apoptosis. Up to 24 hours following irradiation, no apoptosis could be documented, whereas beyond 24 and up to 168 hours a highly significant apoptosis induction was observed. Significant cytotoxicity was confirmed by chromium‐51 release from the cells at 5 Gy. CONCLUSIONS Low‐dose and low‐dose‐rate radiation are able to induce significant apoptosis, and apoptosis may be one of the mechanisms by which low‐dose radiation causes growth inhibition. Cancer 2002;94:1210–4. © 2002 American Cancer Society. DOI 10.1002/cncr.10287 Low‐dose (2–5 grays) and low‐dose‐rate radiation (0.072 grays per minute) are able to induce significant apoptosis, and apoptosis may be one of the mechanisms by which low‐dose radiation causes growth inhibition of experimental tumors.</description><subject>apoptosis</subject><subject>Apoptosis - radiation effects</subject><subject>Biological and medical sciences</subject><subject>Cell Survival - drug effects</subject><subject>Dose-Response Relationship, Radiation</subject><subject>HeLa Cells</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>radiation</subject><subject>Radiation Dosage</subject><subject>Radiation therapy and radiosensitizing agent</subject><subject>radioimmunotherapy</subject><subject>Radioimmunotherapy - methods</subject><subject>radiotherapy</subject><subject>Treatment with physical agents</subject><subject>Treatment. 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General aspects</topic><topic>Tumor Cells, Cultured</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mirzaie‐Joniani, Homa</creatorcontrib><creatorcontrib>Eriksson, David</creatorcontrib><creatorcontrib>Sheikholvaezin, Ali</creatorcontrib><creatorcontrib>Johansson, Amanda</creatorcontrib><creatorcontrib>Löfroth, Per‐Olov</creatorcontrib><creatorcontrib>Johansson, Lennart</creatorcontrib><creatorcontrib>Stigbrand, Torgny</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mirzaie‐Joniani, Homa</au><au>Eriksson, David</au><au>Sheikholvaezin, Ali</au><au>Johansson, Amanda</au><au>Löfroth, Per‐Olov</au><au>Johansson, Lennart</au><au>Stigbrand, Torgny</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Apoptosis induced by low‐dose and low‐dose‐rate radiation</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>2002-02-15</date><risdate>2002</risdate><volume>94</volume><issue>S4</issue><spage>1210</spage><epage>1214</epage><pages>1210-1214</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><coden>CANCAR</coden><abstract>BACKGROUND It has been claimed that external radiation, as a treatment modality for malignant diseases, partly induces apoptosis. It is not known, however, whether therapeutic low‐dose and low‐dose‐rate radiation are able to induce apoptosis. METHODS The effect of low‐dose radiation on apoptosis induction in HeLa Hep2 cells was studied, and quantitation of the apoptotic cells was performed by immunocytochemistry using TdT‐mediated dUtp‐x Nick End Labeling (TUNEL) technology and the M30 CytoDEATH antibody method. RESULTS When TUNEL staining was used to quantify apoptosis in untreated HeLa Hep2 cells kept in culture, approximately 5 ± 3% of the cells showed positive staining without any treatment. In the first experiment, the HeLa Hep2 cells were exposed to gamma radiation (i.e., 0.5, 1, 2, 5, 10, and 15 grays [Gy]) from a cobalt‐60 radiation source delivering a dose rate of 0.80 Gy/min. The radiated cells were cultivated for 5, 10, 24, 48, 72 and 168 hours after irradiation. Radiation doses below 2 Gy did not cause any significant apoptosis, but between 5 and 15 Gy significant apoptosis was observed, with peak values at 5 Gy (P &lt; 0.001). Up to 60% of the investigated cells were shown to display apoptosis. Time to this peak value was 168 hours after irradiation. The HeLa Hep2 cells were exposed to doses of 2, 5, and 10 Gy at a 10‐fold lower dose rate (0.072 Gy/min). The cells that achieved a dose below 2 Gy did not present increased apoptosis. At doses above 2 Gy, however, the cells again demonstrated significant apoptosis. Up to 24 hours following irradiation, no apoptosis could be documented, whereas beyond 24 and up to 168 hours a highly significant apoptosis induction was observed. Significant cytotoxicity was confirmed by chromium‐51 release from the cells at 5 Gy. CONCLUSIONS Low‐dose and low‐dose‐rate radiation are able to induce significant apoptosis, and apoptosis may be one of the mechanisms by which low‐dose radiation causes growth inhibition. Cancer 2002;94:1210–4. © 2002 American Cancer Society. DOI 10.1002/cncr.10287 Low‐dose (2–5 grays) and low‐dose‐rate radiation (0.072 grays per minute) are able to induce significant apoptosis, and apoptosis may be one of the mechanisms by which low‐dose radiation causes growth inhibition of experimental tumors.</abstract><cop>New York</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>11877747</pmid><doi>10.1002/cncr.10287</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record>
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subjects apoptosis
Apoptosis - radiation effects
Biological and medical sciences
Cell Survival - drug effects
Dose-Response Relationship, Radiation
HeLa Cells
Humans
Medical sciences
radiation
Radiation Dosage
Radiation therapy and radiosensitizing agent
radioimmunotherapy
Radioimmunotherapy - methods
radiotherapy
Treatment with physical agents
Treatment. General aspects
Tumor Cells, Cultured
Tumors
title Apoptosis induced by low‐dose and low‐dose‐rate radiation
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