High LET Heavy Ion Radiation Induces p53-Independent Apoptosis
Conventional clinical treatments with X-rays provide an effective modality for widely various human cancers, however, therapeutic results are sometimes poor. Many mutations have been reported to be in the p53 gene in advanced human cancers. The p53 plays a pivotal role in the pathway which controls...
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Veröffentlicht in: | JOURNAL OF RADIATION RESEARCH 2009-01, Vol.50 (1), p.37-42 |
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creator | Mori, Eiichiro Takahashi, Akihisa Yamakawa, Nobuhiro Kirita, Tadaaki Ohnishi, Takeo |
description | Conventional clinical treatments with X-rays provide an effective modality for widely various human cancers, however, therapeutic results are sometimes poor. Many mutations have been reported to be in the p53 gene in advanced human cancers. The p53 plays a pivotal role in the pathway which controls apoptosis, cell growth and cell proliferation, and mutations or deletions in the p53 gene lead to resistance to cancer therapy. The involvement of the p53 gene in determining the sensitivity of many cell types toward low linear energy transfer(LET)radiation is now well established. In contrast to low LET radiation, high LET radiation has several potential advantages over X-rays, one of which is the fact that its effects may be independent of cellular p53 gene status. It is conceivable that effective future therapeutic strategies may be designed on the basis of genetic and biochemical events involved in cell death. Therefore, the accurate characterization and quantification of the mode of cell death, such as apoptosis and necrosis, has become increasingly important for the further understanding of the biological effectiveness of high LET radiation. This review discusses the mechanisms of p53-independent apoptosis by high LET radiation. |
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Many mutations have been reported to be in the p53 gene in advanced human cancers. The p53 plays a pivotal role in the pathway which controls apoptosis, cell growth and cell proliferation, and mutations or deletions in the p53 gene lead to resistance to cancer therapy. The involvement of the p53 gene in determining the sensitivity of many cell types toward low linear energy transfer(LET)radiation is now well established. In contrast to low LET radiation, high LET radiation has several potential advantages over X-rays, one of which is the fact that its effects may be independent of cellular p53 gene status. It is conceivable that effective future therapeutic strategies may be designed on the basis of genetic and biochemical events involved in cell death. Therefore, the accurate characterization and quantification of the mode of cell death, such as apoptosis and necrosis, has become increasingly important for the further understanding of the biological effectiveness of high LET radiation. This review discusses the mechanisms of p53-independent apoptosis by high LET radiation.</description><identifier>ISSN: 0449-3060</identifier><identifier>ISSN: 1349-9157</identifier><identifier>EISSN: 1349-9157</identifier><identifier>DOI: 10.1269/jrr.08075</identifier><identifier>PMID: 18957831</identifier><language>eng</language><publisher>England: THE JAPAN RADIATION RESEARCH SOCIETY</publisher><subject>Animals ; Apoptosis ; Apoptosis - physiology ; Apoptosis - radiation effects ; Cancer ; Cancer genetics ; Cancer treatment ; Caspase 9 - metabolism ; Cell proliferation ; DNA Damage - physiology ; DNA Repair - physiology ; DNA Repair - radiation effects ; Gene deletion ; Genetic aspects ; Health aspects ; Heavy ion radiation ; Heavy Ions ; Humans ; Ionizing radiation ; Linear Energy Transfer - physiology ; Linear Energy Transfer - radiation effects ; Mutation ; Necrosis ; p53 protein ; Radiation (Physics) ; Radiation Tolerance - physiology ; Radiation Tolerance - radiation effects ; Tumor proteins ; Tumor Suppressor Protein p53 - metabolism</subject><ispartof>JOURNAL OF RADIATION RESEARCH, 2009-01, Vol.50 (1), p.37-42</ispartof><rights>COPYRIGHT 2009 Oxford University Press</rights><rights>Copyright Japan Science and Technology Agency 2009</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c727t-c8e26bd22043ac91ad7ec193b76e8717d008d06e6f2fcfedcfb96cbf1c3112883</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,860,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18957831$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mori, Eiichiro</creatorcontrib><creatorcontrib>Takahashi, Akihisa</creatorcontrib><creatorcontrib>Yamakawa, Nobuhiro</creatorcontrib><creatorcontrib>Kirita, Tadaaki</creatorcontrib><creatorcontrib>Ohnishi, Takeo</creatorcontrib><creatorcontrib>School of Medicine</creatorcontrib><creatorcontrib>Departments of Oral and Maxillofacial Surgery</creatorcontrib><creatorcontrib>Departments of Biology</creatorcontrib><creatorcontrib>Nara Medical University</creatorcontrib><title>High LET Heavy Ion Radiation Induces p53-Independent Apoptosis</title><title>JOURNAL OF RADIATION RESEARCH</title><addtitle>J Radiat Res</addtitle><description>Conventional clinical treatments with X-rays provide an effective modality for widely various human cancers, however, therapeutic results are sometimes poor. Many mutations have been reported to be in the p53 gene in advanced human cancers. The p53 plays a pivotal role in the pathway which controls apoptosis, cell growth and cell proliferation, and mutations or deletions in the p53 gene lead to resistance to cancer therapy. The involvement of the p53 gene in determining the sensitivity of many cell types toward low linear energy transfer(LET)radiation is now well established. In contrast to low LET radiation, high LET radiation has several potential advantages over X-rays, one of which is the fact that its effects may be independent of cellular p53 gene status. It is conceivable that effective future therapeutic strategies may be designed on the basis of genetic and biochemical events involved in cell death. Therefore, the accurate characterization and quantification of the mode of cell death, such as apoptosis and necrosis, has become increasingly important for the further understanding of the biological effectiveness of high LET radiation. This review discusses the mechanisms of p53-independent apoptosis by high LET radiation.</description><subject>Animals</subject><subject>Apoptosis</subject><subject>Apoptosis - physiology</subject><subject>Apoptosis - radiation effects</subject><subject>Cancer</subject><subject>Cancer genetics</subject><subject>Cancer treatment</subject><subject>Caspase 9 - metabolism</subject><subject>Cell proliferation</subject><subject>DNA Damage - physiology</subject><subject>DNA Repair - physiology</subject><subject>DNA Repair - radiation effects</subject><subject>Gene deletion</subject><subject>Genetic aspects</subject><subject>Health aspects</subject><subject>Heavy ion radiation</subject><subject>Heavy Ions</subject><subject>Humans</subject><subject>Ionizing radiation</subject><subject>Linear Energy Transfer - physiology</subject><subject>Linear Energy Transfer - radiation effects</subject><subject>Mutation</subject><subject>Necrosis</subject><subject>p53 protein</subject><subject>Radiation (Physics)</subject><subject>Radiation Tolerance - physiology</subject><subject>Radiation Tolerance - radiation effects</subject><subject>Tumor proteins</subject><subject>Tumor Suppressor Protein p53 - metabolism</subject><issn>0449-3060</issn><issn>1349-9157</issn><issn>1349-9157</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkVGL1DAQx4Mo3nLeg19ACoLiQ9eZpkmaF2E57tyFBUHO55Cm6Zm129SkFe7bO-cuHPighMwMyW-Gmfkz9hphjZXUHw8praEBJZ6xFfJalxqFes5WUFPMQcIFu8o5tIBCAjSIL9kFNlqohuOKfdqG--_F_uau2Hr766HYxbH4artg50DRbuwW53MxCV5S7CdPZpyLzRSnOeaQX7EXvR2yvzr7S_bt9ubuelvuv3zeXW_2pVOVmkvX-Eq2XVVBza3TaDvlHWreKukbhaqjxjqQXvZV73rfub7V0rU9Oo5YNQ2_ZO9PdacUfy4-z-YYsvPDYEcfl2w0KBQNCCTy3T9JKXUltIb_ghVw2hLWBL79CzzEJY00rsGallxrKTRR6xN1bwdvwtjHOVlHp_PH4OLo-0DvG8ElippmpoQPpwSXYs7J92ZK4WjTg0Ewj8oaUtb8UZbYN-cWlvbouyfyrCMBtyeAfoOzQxyHMPqnRt0PeYgpeZoKtAEQAPjo6HJFpq60RuTAfwOVzbEo</recordid><startdate>20090101</startdate><enddate>20090101</enddate><creator>Mori, Eiichiro</creator><creator>Takahashi, Akihisa</creator><creator>Yamakawa, Nobuhiro</creator><creator>Kirita, Tadaaki</creator><creator>Ohnishi, Takeo</creator><general>THE JAPAN RADIATION RESEARCH SOCIETY</general><general>Oxford University Press</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>K9.</scope><scope>7TO</scope><scope>7U7</scope><scope>C1K</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20090101</creationdate><title>High LET Heavy Ion Radiation Induces p53-Independent Apoptosis</title><author>Mori, Eiichiro ; 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subjects | Animals Apoptosis Apoptosis - physiology Apoptosis - radiation effects Cancer Cancer genetics Cancer treatment Caspase 9 - metabolism Cell proliferation DNA Damage - physiology DNA Repair - physiology DNA Repair - radiation effects Gene deletion Genetic aspects Health aspects Heavy ion radiation Heavy Ions Humans Ionizing radiation Linear Energy Transfer - physiology Linear Energy Transfer - radiation effects Mutation Necrosis p53 protein Radiation (Physics) Radiation Tolerance - physiology Radiation Tolerance - radiation effects Tumor proteins Tumor Suppressor Protein p53 - metabolism |
title | High LET Heavy Ion Radiation Induces p53-Independent Apoptosis |
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