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  1. 原著論文

Metabolic and physiologic imaging biomarkers of the tumor microenvironment predict treatment outcome with radiation or a hypoxia-activated prodrug in mice

https://repo.qst.go.jp/records/49392
https://repo.qst.go.jp/records/49392
2a45bf36-29cb-4e3e-b32a-6348d774235b
Item type 学術雑誌論文 / Journal Article(1)
公開日 2018-06-04
タイトル
タイトル Metabolic and physiologic imaging biomarkers of the tumor microenvironment predict treatment outcome with radiation or a hypoxia-activated prodrug in mice
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_6501
資源タイプ journal article
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 Matsumoto, Shingo

× Matsumoto, Shingo

WEKO 748058

Matsumoto, Shingo

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Kishimoto, Shun

× Kishimoto, Shun

WEKO 748059

Kishimoto, Shun

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Saito, Keita

× Saito, Keita

WEKO 748060

Saito, Keita

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Takakusagi, Yoichi

× Takakusagi, Yoichi

WEKO 748061

Takakusagi, Yoichi

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P. Munasinghe, Jeeva

× P. Munasinghe, Jeeva

WEKO 748062

P. Munasinghe, Jeeva

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Devasahayam, Nallathamby

× Devasahayam, Nallathamby

WEKO 748063

Devasahayam, Nallathamby

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P. Hart, Charles

× P. Hart, Charles

WEKO 748064

P. Hart, Charles

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J. Gillies, Robert

× J. Gillies, Robert

WEKO 748065

J. Gillies, Robert

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B. Mitchell, James

× B. Mitchell, James

WEKO 748066

B. Mitchell, James

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C. Krishna, Murali

× C. Krishna, Murali

WEKO 748067

C. Krishna, Murali

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Takakusagi, Yoichi

× Takakusagi, Yoichi

WEKO 748068

en Takakusagi, Yoichi

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抄録
内容記述タイプ Abstract
内容記述 Pancreatic ductal adenocarcinoma (PDAC) is characterized by hypoxic niches that lead to treatment resistance. Therefore, studies of tumor oxygenation and metabolic profiling should contribute to improved treatment strategies. Here we define two imaging biomarkers that predict differences in tumor response to therapy: 1) partial oxygen pressure (pO2), measured by EPR imaging; and 2) [1-13C] pyruvate metabolism rate, measured by hyperpolarized 13C MRI. Three human PDAC xenografts with varying treatment sensitivity (Hs766t, MiaPaCa-2, and Su.86.86) were grown in mice. The median pO2 of the mature Hs766t, MiaPaCa-2, and Su.86.86 tumors was 9.1±1.7, 11.1±2.2, and 17.6±2.6 mmHg, and the rate of pyruvate-to-lactate conversion was 2.72+/-0.48, 2.28+/-0.26, and 1.98+/-0.51 min-1, respectively (n=6, each). These results are in agreement with steady state data of matabolites quantified by mass spectroscopy and histological analysis indicating glycolytic and hypoxia profile in Hs766t, MiaPaca-2, and Su.86.86 tumors. Fractionated radiation therapy (3 Gy x 5) resulted in a tumor growth delay of 16.7±1.6 and 18.0±2.7 days in MiaPaca-2 and Su.86.86 tumors, respectively, compared to 6.3±2.7 days in hypoxic Hs766t tumors. Treatment with gemcitabine, a first-line chemotherapeutic agent, or the hypoxia-activated prodrug TH-302 was more effective against Hs766t tumors (20.0+/-3.5 and 25.0+/-7.7 days increase in survival time, respectively) than MiaPaCa-2 (2.7±0.4 and 6.7±0.7 days) and Su.86.86 (4.7±0.6 and 0.7±0.6 days) tumors. Collectively, these results demonstrate the ability of molecular imaging biomarkers to predict the response of PDAC to treatment with radiation therapy and TH-302.
書誌情報 Cancer Research

巻 78, 号 14, p. 3783-3792, 発行日 2018-05
出版者
出版者 AACR
ISSN
収録物識別子タイプ ISSN
収録物識別子 0008-5472
PubMed番号
識別子タイプ PMID
関連識別子 29792309
DOI
識別子タイプ DOI
関連識別子 10.1158/0008-5472.CAN-18-0491
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