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Different status of extracellular components associated with cellular radioresistance

https://repo.qst.go.jp/records/69189
https://repo.qst.go.jp/records/69189
9ac7e576-c720-4cc1-bde2-6d1b619c0782
Item type 会議発表用資料 / Presentation(1)
公開日 2007-11-22
タイトル
タイトル Different status of extracellular components associated with cellular radioresistance
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 Ishikawa, Kenichi

× Ishikawa, Kenichi

WEKO 678938

Ishikawa, Kenichi

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Ishikawa, Atsuko

× Ishikawa, Atsuko

WEKO 678939

Ishikawa, Atsuko

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Iwakawa, Mayumi

× Iwakawa, Mayumi

WEKO 678940

Iwakawa, Mayumi

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Imai, Takashi

× Imai, Takashi

WEKO 678941

Imai, Takashi

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石川 顕一

× 石川 顕一

WEKO 678942

en 石川 顕一

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石川 敦子

× 石川 敦子

WEKO 678943

en 石川 敦子

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岩川 眞由美

× 岩川 眞由美

WEKO 678944

en 岩川 眞由美

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今井 高志

× 今井 高志

WEKO 678945

en 今井 高志

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抄録
内容記述タイプ Abstract
内容記述 Radioresistance varies significantly in human tumor cells, thereby impacting the efficacy of radiotherapy. The pursuit of the idea that gene expression profiles could be used to identify radioresistant cell lines from others formed the basis of this study. Global gene expression profiles of 15 human tumor and normal fibroblast cell lines were analyzed using DNA microarrays. To begin, 6 of the cell lines were categorized into radioresistant (RG) or non-resistant (NRG) groups according to the radiation dose required to reduce their survival to 10% (D10). Genes whose expression was specific to each group at 1 or 3 hr after irradiation were isolated by ANOVA and a two-dimensional hierarchical clustering method. Then, the remaining 9 cell lines were subjected to k-nearest neighbor pattern classification. Classifying the 9 test-cell lines reasonably related to the cellular D10 value was effective for a set of 46 genes at 1 hour and for another set of 44 genes at 3 hours after irradiation, respectively. Of these genes, 25 showed altered expression at both time points in the NRG or RG, but independently were unable to classify the test cell lines. In general, genes that inhibited apoptosis and promoted proliferation were upregulated in the RG, while pro-apoptotic genes tend to be activated in the NRG. Interestingly, genes that localized in extracellular matrix were downregulated in the RG. Different status of the extracellular microenvironment may be a cause of different mobility of tumor cells following invasive or metastatic activity. These results suggest that certain gene categories may be useful not only for predicting the radioresistance of human tumor cells but also for gaining a better understanding of the relationship between tumorigenesis and radioresistance. In conclusions, radioresistant cell lines analyzed in this study showed certain radiation-induced changes in gene expression profiles that are different from the profile changes of the more-sensitive cell lines.
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 10th Anniversary of Kazusa Arc International Symposium on Advanced Functional Genomics
発表年月日
日付 2007-10-12
日付タイプ Issued
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