The Difference in LET and Ion Species Dependence for Induction of Initially Measured and Non-rejoined Chromatin Breaks in Normal Human Fibroblasts

Tsuruoka, C., Suzuki, M., Hande, M. P., Furusawa, Y., Anzai, K. and Okayasu, R. The Difference in LET and Ion Species Dependence for Induction of Initially Measured and Non-rejoined Chromatin Breaks in Normal Human Fibroblasts. Radiat. Res. 170, 163–171 (2008). We studied the LET and ion species dep...

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Veröffentlicht in:Radiation research 2008-08, Vol.170 (2), p.163-171
Hauptverfasser: Tsuruoka, Chizuru, Suzuki, Masao, Hande, M. Prakash, Furusawa, Yoshiya, Anzai, Kazunori, Okayasu, Ryuichi
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container_issue 2
container_start_page 163
container_title Radiation research
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creator Tsuruoka, Chizuru
Suzuki, Masao
Hande, M. Prakash
Furusawa, Yoshiya
Anzai, Kazunori
Okayasu, Ryuichi
description Tsuruoka, C., Suzuki, M., Hande, M. P., Furusawa, Y., Anzai, K. and Okayasu, R. The Difference in LET and Ion Species Dependence for Induction of Initially Measured and Non-rejoined Chromatin Breaks in Normal Human Fibroblasts. Radiat. Res. 170, 163–171 (2008). We studied the LET and ion species dependence of the induction of chromatin breaks measured immediately after irradiation as initially measured breaks and after 24 h postirradiation incubation (37°C) as non-rejoined breaks in normal human fibroblasts with different heavy ions, such as carbon, neon, silicon and iron, generated by the Heavy Ion Medical Accelerator in Chiba (HIMAC) at the National Institute of Radiological Science (NIRS). Chromatin breaks were measured as an excess number of fragments of prematurely condensed chromosomes using premature chromosome condensation (PCC). The results showed that the number of excess fragments per cell per Gy for initially measured chromatin breaks was dependent on LET in the range from 13.3 to 113.1 keV/μm but was not dependent on ion species. On the other hand, the number of non-rejoined chromatin breaks detected after 24 h postirradiation incubation was clearly dependent on both LET and ion species. No significant difference was observed in the cross section for initially measured breaks, but a statistically significant difference was observed in the cross section for non-rejoined breaks among carbon, neon, silicon and iron ions. This suggests that the LET-dependent structure in the biological effects is reflected in biological consequences of repair processes.
doi_str_mv 10.1667/RR1279.1
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Chromatin breaks were measured as an excess number of fragments of prematurely condensed chromosomes using premature chromosome condensation (PCC). The results showed that the number of excess fragments per cell per Gy for initially measured chromatin breaks was dependent on LET in the range from 13.3 to 113.1 keV/μm but was not dependent on ion species. On the other hand, the number of non-rejoined chromatin breaks detected after 24 h postirradiation incubation was clearly dependent on both LET and ion species. No significant difference was observed in the cross section for initially measured breaks, but a statistically significant difference was observed in the cross section for non-rejoined breaks among carbon, neon, silicon and iron ions. 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We studied the LET and ion species dependence of the induction of chromatin breaks measured immediately after irradiation as initially measured breaks and after 24 h postirradiation incubation (37°C) as non-rejoined breaks in normal human fibroblasts with different heavy ions, such as carbon, neon, silicon and iron, generated by the Heavy Ion Medical Accelerator in Chiba (HIMAC) at the National Institute of Radiological Science (NIRS). Chromatin breaks were measured as an excess number of fragments of prematurely condensed chromosomes using premature chromosome condensation (PCC). The results showed that the number of excess fragments per cell per Gy for initially measured chromatin breaks was dependent on LET in the range from 13.3 to 113.1 keV/μm but was not dependent on ion species. On the other hand, the number of non-rejoined chromatin breaks detected after 24 h postirradiation incubation was clearly dependent on both LET and ion species. No significant difference was observed in the cross section for initially measured breaks, but a statistically significant difference was observed in the cross section for non-rejoined breaks among carbon, neon, silicon and iron ions. This suggests that the LET-dependent structure in the biological effects is reflected in biological consequences of repair processes.</description><subject>Cell Line</subject><subject>Cell lines</subject><subject>Chromatin</subject><subject>Chromatin - genetics</subject><subject>Chromatin - radiation effects</subject><subject>Chromosomes</subject><subject>DNA Breaks</subject><subject>DNA Repair - genetics</subject><subject>DNA Repair - radiation effects</subject><subject>Dose response relationship</subject><subject>Dose-Response Relationship, Radiation</subject><subject>Fibroblasts - physiology</subject><subject>Fibroblasts - radiation effects</subject><subject>Heavy Ions</subject><subject>Humans</subject><subject>Ion sources</subject><subject>Linear Energy Transfer - physiology</subject><subject>Linear Energy Transfer - radiation effects</subject><subject>Neon</subject><subject>Radiation Dosage</subject><subject>REGULAR ARTICLES</subject><subject>Silicon</subject><subject>Solar X rays</subject><subject>Tumor cell line</subject><issn>0033-7587</issn><issn>1938-5404</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kM9O3DAQxi3UCra0Ei8A8gn1EojjxH-OZYGy0hYkuj1HtjMWXhJ7sZMDr8ET18uuyqmn0cz85vtGH0InpLwgjPHLx0dScXlBDtCMSCqKpi7rT2hWlpQWvBH8CH1JaV3mnjB5iI6IYIwJ0szQ2-oJ8LWzFiJ4A9h5vLxZYeU7vAge_96AcZDwNWzAd--EDREvfDeZ0WUg2Ny40am-f8W_QKUpQvd-fh98EWEdnM-D-VMMgxqz-lUE9Zy2PvchDqrHd9OgPL51OgbdqzSmr-izVX2Cb_t6jP7c3qzmd8Xy4edi_mNZ6Jo3YyEMV0QzKrRUHe1oVTHFTC14KSy1Nc9BaMakENAwVVlDNe-spNLQerss6TE63-luYniZII3t4JKBvlcewpRaInlDqawz-H0HmhhSimDbTXSDiq8tKdtt_u0u_5Zk9GyvOekBug9wH3gGTnfAOo0h_ttXDWGcN_XHU9qF4OH_Tn8BnmGV_A</recordid><startdate>200808</startdate><enddate>200808</enddate><creator>Tsuruoka, Chizuru</creator><creator>Suzuki, Masao</creator><creator>Hande, M. 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Prakash ; Furusawa, Yoshiya ; Anzai, Kazunori ; Okayasu, Ryuichi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b475t-8c7a1b638b9ad3d3226a6c48708f3f47193b66988e56a2fc3b7df939c34471903</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Cell Line</topic><topic>Cell lines</topic><topic>Chromatin</topic><topic>Chromatin - genetics</topic><topic>Chromatin - radiation effects</topic><topic>Chromosomes</topic><topic>DNA Breaks</topic><topic>DNA Repair - genetics</topic><topic>DNA Repair - radiation effects</topic><topic>Dose response relationship</topic><topic>Dose-Response Relationship, Radiation</topic><topic>Fibroblasts - physiology</topic><topic>Fibroblasts - radiation effects</topic><topic>Heavy Ions</topic><topic>Humans</topic><topic>Ion sources</topic><topic>Linear Energy Transfer - physiology</topic><topic>Linear Energy Transfer - radiation effects</topic><topic>Neon</topic><topic>Radiation Dosage</topic><topic>REGULAR ARTICLES</topic><topic>Silicon</topic><topic>Solar X rays</topic><topic>Tumor cell line</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tsuruoka, Chizuru</creatorcontrib><creatorcontrib>Suzuki, Masao</creatorcontrib><creatorcontrib>Hande, M. 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We studied the LET and ion species dependence of the induction of chromatin breaks measured immediately after irradiation as initially measured breaks and after 24 h postirradiation incubation (37°C) as non-rejoined breaks in normal human fibroblasts with different heavy ions, such as carbon, neon, silicon and iron, generated by the Heavy Ion Medical Accelerator in Chiba (HIMAC) at the National Institute of Radiological Science (NIRS). Chromatin breaks were measured as an excess number of fragments of prematurely condensed chromosomes using premature chromosome condensation (PCC). The results showed that the number of excess fragments per cell per Gy for initially measured chromatin breaks was dependent on LET in the range from 13.3 to 113.1 keV/μm but was not dependent on ion species. On the other hand, the number of non-rejoined chromatin breaks detected after 24 h postirradiation incubation was clearly dependent on both LET and ion species. No significant difference was observed in the cross section for initially measured breaks, but a statistically significant difference was observed in the cross section for non-rejoined breaks among carbon, neon, silicon and iron ions. This suggests that the LET-dependent structure in the biological effects is reflected in biological consequences of repair processes.</abstract><cop>United States</cop><pub>Radiation Research Society</pub><pmid>18666815</pmid><doi>10.1667/RR1279.1</doi><tpages>9</tpages></addata></record>
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subjects Cell Line
Cell lines
Chromatin
Chromatin - genetics
Chromatin - radiation effects
Chromosomes
DNA Breaks
DNA Repair - genetics
DNA Repair - radiation effects
Dose response relationship
Dose-Response Relationship, Radiation
Fibroblasts - physiology
Fibroblasts - radiation effects
Heavy Ions
Humans
Ion sources
Linear Energy Transfer - physiology
Linear Energy Transfer - radiation effects
Neon
Radiation Dosage
REGULAR ARTICLES
Silicon
Solar X rays
Tumor cell line
title The Difference in LET and Ion Species Dependence for Induction of Initially Measured and Non-rejoined Chromatin Breaks in Normal Human Fibroblasts
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