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FGF2 expression change as an acute radiotherapy responsive marker in sequential biopsy samples from cervical cancer patients during fractionated radiotherapy.

https://repo.qst.go.jp/records/54179
https://repo.qst.go.jp/records/54179
9ac5959e-e02e-450d-896d-8ca805631558
Item type 会議発表論文 / Conference Paper(1)
公開日 2009-11-11
タイトル
タイトル FGF2 expression change as an acute radiotherapy responsive marker in sequential biopsy samples from cervical cancer patients during fractionated radiotherapy.
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_5794
資源タイプ conference paper
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 553161

Iwakawa, Mayumi

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Nakawatari, Miyako

× Nakawatari, Miyako

WEKO 553162

Nakawatari, Miyako

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Imadome, Kaori

× Imadome, Kaori

WEKO 553163

Imadome, Kaori

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Ohno, Tatsuya

× Ohno, Tatsuya

WEKO 553164

Ohno, Tatsuya

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Kato, Shingo

× Kato, Shingo

WEKO 553165

Kato, Shingo

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Nakamura, Etsuko

× Nakamura, Etsuko

WEKO 553166

Nakamura, Etsuko

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Sakai, Minako

× Sakai, Minako

WEKO 553167

Sakai, Minako

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Ohkubo, Yu

× Ohkubo, Yu

WEKO 553168

Ohkubo, Yu

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Tamaki, Tomoaki

× Tamaki, Tomoaki

WEKO 553169

Tamaki, Tomoaki

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Imai, Takashi

× Imai, Takashi

WEKO 553170

Imai, Takashi

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岩川 眞由美

× 岩川 眞由美

WEKO 553171

en 岩川 眞由美

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中渡 美也子

× 中渡 美也子

WEKO 553172

en 中渡 美也子

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今留 香織

× 今留 香織

WEKO 553173

en 今留 香織

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大野 達也

× 大野 達也

WEKO 553174

en 大野 達也

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加藤 眞吾

× 加藤 眞吾

WEKO 553175

en 加藤 眞吾

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中村 悦子

× 中村 悦子

WEKO 553176

en 中村 悦子

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酒井 美奈子

× 酒井 美奈子

WEKO 553177

en 酒井 美奈子

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大久保 悠

× 大久保 悠

WEKO 553178

en 大久保 悠

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田巻 倫明

× 田巻 倫明

WEKO 553179

en 田巻 倫明

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今井 高志

× 今井 高志

WEKO 553180

en 今井 高志

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抄録
内容記述タイプ Abstract
内容記述 Purpose
Tumor microenvironment possesses extreamly important role for tumor progression and metastasis. Cytokines have autocrine and paracrine functions, and they are also secreted by normal and cancerous cells. Herewith we investigated an indicator for the efficacy of radiotherapy in cervical cancers (CC) using microarray analysis and immunohistochemical analysis.
Patients and methods
One hundred and four patients with CC were recruited and divided into two groups (research set: n =35, and validation set: n =69). Microarray analysis was performed in research set and further immunohistochemical analysis (IHA) was performed for all patients to detect candidate radioresponsive markers using pre-radiotherapy and mid-radiotherapy biopsy samples, which were taken one week after initiation of radiotherapy.
Results
FGF2 in tumor cells (FGF2–T) significantly increased in midtreatment samples compared with pretreatment samples in research set of patients, and the ratio change of FGF2-T was significantly related with better prognosis. This evidence was confirmed in validation set. Next using all 104 patimets we found IHA positive FGF2 in stromal cells (FGF2-S) in 85 patients, and the radiotherapy-induced increase of FGF-S in 23 patients. Though positive FGF2-S in pretreatment samples was significantly related with increased expression change of VEGF, it was not related with poor prognosis.
Conclusion
Radiation causes severing the normal or cancerous associations with adjacent cells and changes the extracellular matrix environment. Therefore, we need to investigate not only pretreatment status of tumors, but also modified tumor structures during fractionated radiotherapy. In this study, we found FGF2-T expression change as a monitoring marker for the effectiveness of radiotherapy, and found the relationship between FGF2-S in pretreatment status and VEGF expression change in a subgroup of patients.
書誌情報 Cancer Microenvironment

巻 2, 号 1, p. 116-116, 発行日 2009-09
ISSN
収録物識別子タイプ ISSN
収録物識別子 1875-2292
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