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Gene signatures in radiation-induced T cell lymphomas.

https://repo.qst.go.jp/records/71133
https://repo.qst.go.jp/records/71133
c857f9b2-86d3-4e95-a725-6e1b52880874
Item type 会議発表用資料 / Presentation(1)
公開日 2013-06-10
タイトル
タイトル Gene signatures in radiation-induced T cell lymphomas.
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 Blyth, Benjamin

× Blyth, Benjamin

WEKO 699243

Blyth, Benjamin

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Kakinuma, Shizuko

× Kakinuma, Shizuko

WEKO 699244

Kakinuma, Shizuko

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Amasaki, Yoshiko

× Amasaki, Yoshiko

WEKO 699245

Amasaki, Yoshiko

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Shang, Yi

× Shang, Yi

WEKO 699246

Shang, Yi

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Sawai, Tomoko

× Sawai, Tomoko

WEKO 699247

Sawai, Tomoko

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Hirano, Shinobu

× Hirano, Shinobu

WEKO 699248

Hirano, Shinobu

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Tsuruoka, Chizuru

× Tsuruoka, Chizuru

WEKO 699249

Tsuruoka, Chizuru

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Nishimura, Mayumi

× Nishimura, Mayumi

WEKO 699250

Nishimura, Mayumi

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Shimada, Yoshiya

× Shimada, Yoshiya

WEKO 699251

Shimada, Yoshiya

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et.al

× et.al

WEKO 699252

et.al

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Blyth Benjamin

× Blyth Benjamin

WEKO 699253

en Blyth Benjamin

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柿沼 志津子

× 柿沼 志津子

WEKO 699254

en 柿沼 志津子

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甘崎 佳子

× 甘崎 佳子

WEKO 699255

en 甘崎 佳子

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尚 奕

× 尚 奕

WEKO 699256

en 尚 奕

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澤井 知子

× 澤井 知子

WEKO 699257

en 澤井 知子

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坂入 しのぶ

× 坂入 しのぶ

WEKO 699258

en 坂入 しのぶ

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鶴岡 千鶴

× 鶴岡 千鶴

WEKO 699259

en 鶴岡 千鶴

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西村 まゆみ

× 西村 まゆみ

WEKO 699260

en 西村 まゆみ

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島田 義也

× 島田 義也

WEKO 699261

en 島田 義也

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抄録
内容記述タイプ Abstract
内容記述 T cell lymphomas in mice can overcome natural tumour barriers via several routes, including deregulation of Bcl11b, Notch, Pten or Ikaros via gene mutation, amplification or loss. Our research has shown that the etiology of T cell lymphomas (e.g. radiation or chemical mutagenesis) is correlated with a pattern in the disruption of the above pathways and how they are activated or inactivated. Carbon ion radiotherapy may be associated with different risks of secondary cancer than conventional photon therapies. A sub-cohort of mice irradiated with 4 or 4.8 Gy carbon ions starting at one week of age (either in a single exposure, or four weekly fractions), was selected for detailed genetic analysis of radiation-induced thymic lymphomas (n = 102 mice). Gross genomic changes at tumour suppressor loci including Pten, Bcl11b and Ikzf1 are being assessed by loss of heterozygosity (LOH) analysis and array-based comparative genome hybridisation. Smaller genetic alterations are being further assessed by exon sequencing of Pten, Bcl11b and Ikzf1 to identify small insertions/deletions and point-mutations. Preliminary results show that although the same pathways are involved in both carbon- and photon radiation-induced tumours, how these pathways are disrupted may be different between radiation types. Mechanistic insight into carbon ion-induced carcinogenesis will be vital in assessing the long-term safety of carbon ion radiotherapy for children.
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 The 6th International Workshop of the Kyoto T Cell Conference
発表年月日
日付 2013-06-07
日付タイプ Issued
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