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Epigenetic regulation of tumor cell invasiveness induced by irradiation

https://repo.qst.go.jp/records/70413
https://repo.qst.go.jp/records/70413
847814e7-8ac2-4098-8f2e-fed8f39c80cf
Item type 会議発表用資料 / Presentation(1)
公開日 2011-03-10
タイトル
タイトル Epigenetic regulation of tumor cell invasiveness induced by irradiation
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 691402

Ishikawa, Kenichi

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Fujita, Mayumi

× Fujita, Mayumi

WEKO 691403

Fujita, Mayumi

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Iizuka, Daisuke

× Iizuka, Daisuke

WEKO 691404

Iizuka, Daisuke

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Imai, Takashi

× Imai, Takashi

WEKO 691405

Imai, Takashi

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石川 顕一

× 石川 顕一

WEKO 691406

en 石川 顕一

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藤田 真由美

× 藤田 真由美

WEKO 691407

en 藤田 真由美

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飯塚 大輔

× 飯塚 大輔

WEKO 691408

en 飯塚 大輔

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今井 高志

× 今井 高志

WEKO 691409

en 今井 高志

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抄録
内容記述タイプ Abstract
内容記述 Identifying and characterizing regulators of cancer metastasis is important for cancer therapy. We recently investigated the induction of cellular invasiveness after X-ray irradiation in the MIAPaCa-2 cell line derived from human pancreatic cancer. Transcription levels of metalloproteinase 2 (MMP2) were increased drastically after X-ray irradiation. MMPs have been implicated in increased invasive and metastatic potential of tumors, possibly via interactions with the extracellular matrix. This radiation-induced invasiveness was different in irradiated PANC-1 cells that are also derived from human pancreatic cancer. Furthermore, this response in MIAPaCa-2 cells irradiated by X-ray was different from that in the same cells irradiated by carbon ion beam.
DNA methylation is an epigenetic modification that occurs in mammals to ensure the proper regulation of gene expression in response to environmental stimuli and stable gene silencing. However, the source of variation in DNA methylation itself remains poorly understood. We hypothesized that tumor cells can change their invasiveness after irradiation via epigenetic processes such as DNA methylation.
In this study, we measured DNA methylation at 27,578 CpG islands in MIAPaCa-2 and PANC-1 at 48 h after irradiation with either X-rays at 4 Gy or a carbon ion beam at 2 Gy using the HumanMethylation27 BeadChip. Many CpG islands in MIAPaCa-2 showed higher DNA methylation status compared with those in PANC-1 cells. Some CpG islands changed DNA methylation status after irradiation, but the MMP2 locus exhibited an almost completely methylated status both before and after X-ray irradiation in MIAPaCa-2 cells. It is possible that the MMP2 locus designed for the BeadChip probes used here represent discrete regions of the MMP2 locus recognized by X-ray-responsive transcription factors in MIAPaCa-2. We have now designed an experiment to measure DNA methylation status at high density using next generation sequencing technology. A methylated DNA enriched sample and an unmethylated DNA enriched sample are being analyzing in ongoing work to compare the methylation status of the radiation-responsive genes including MMP2.
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 1st RIRBM International Symposium
発表年月日
日付 2011-03-04
日付タイプ Issued
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