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Genetic Variation and Radiosensitivity : towards an Individualized Radiation Therapy

https://repo.qst.go.jp/records/62484
https://repo.qst.go.jp/records/62484
9d23ca47-b6cc-416a-861d-8171c43e0d1d
Item type 会議発表用資料 / Presentation(1)
公開日 2008-03-26
タイトル
タイトル Genetic Variation and Radiosensitivity : towards an Individualized Radiation Therapy
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_c94f
資源タイプ conference object
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Iwakawa, Mayumi

× Iwakawa, Mayumi

WEKO 617351

Iwakawa, Mayumi

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Imai, Takashi

× Imai, Takashi

WEKO 617352

Imai, Takashi

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岩川 眞由美

× 岩川 眞由美

WEKO 617353

en 岩川 眞由美

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今井 高志

× 今井 高志

WEKO 617354

en 今井 高志

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抄録
内容記述タイプ Abstract
内容記述 To determine the genetic characteristics of individual patients and their cancers for more effective radiotherapy, we have studied genetic variations associated with individual radiosensitivity and gene expression of tumors with different radiosensitivity. First, as an experimental model, we subjected 276 second filial generation (F2) mice descended from two inbred mouse strains, radiation-sensitive C57BL/6J (B6) and radiation-resistant C3H/HeMs (C3H), to whole-body irradiation of 2.5 Gy. The largest difference in jejunal crypt apoptosis values was observed between the B6 and C3H strains. ASI values in B6 and C3H mice were 97.7 +- 32.9 and 49.0 +- 24.9, respectively. We selected SNP markers, where alleles between B6 and C3H were different, at 20-Mb intervals on the chromosomes. Genome-wide analysis revealed 8 QTLs (2 on chromosome 9, 4 on 15, 1 on 17, and 1 on 18) with log odds (LOD) scores ranging from 2.11 to 3.91. We found a significant locus on chromosome 15. Second, in clinical setting, DNA was sampled from 399 Japanese breast cancer patients who qualified for breast-conserving radiotherapy. A total of 999 single nucleotide polymorphisms from 137 candidate genes for radiation susceptibility were genotyped, and the global haplotype association indicated that estimated haplotypes in five loci, RAD9A, PTTG1, LIG3, CD44, and MAD2L2 genes, were associated with early adverse skin reaction risk. In addition, to contribute to the fundamental knowledge for selection of treatment modalities to achieve personalized radiotherapy, data from a murine model for biological effectiveness specific to carbon-ion radiotherapy should be presented.
会議概要(会議名, 開催地, 会期, 主催者等)
内容記述タイプ Other
内容記述 NIRS-MD Anderson Symposium on Clinical Issues for Particle Therapy
発表年月日
日付 2008-03-22
日付タイプ Issued
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