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  1. 原著論文

Functional Biological Activity of Sorafenib as a Tumor-Treating Field Sensitizer for Glioblastoma Therapy.

https://repo.qst.go.jp/records/49571
https://repo.qst.go.jp/records/49571
3d10170b-a5bc-46ac-a29d-7abb74c49a26
Item type 学術雑誌論文 / Journal Article(1)
公開日 2019-02-07
タイトル
タイトル Functional Biological Activity of Sorafenib as a Tumor-Treating Field Sensitizer for Glioblastoma Therapy.
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 Jo, Yunhui

× Jo, Yunhui

WEKO 776628

Jo, Yunhui

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Ho Kim, Eun

× Ho Kim, Eun

WEKO 776629

Ho Kim, Eun

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Sai, Sei

× Sai, Sei

WEKO 776630

Sai, Sei

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Su Kim, Jin

× Su Kim, Jin

WEKO 776631

Su Kim, Jin

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Jae-Min, Cho

× Jae-Min, Cho

WEKO 776632

Jae-Min, Cho

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Kim, Hyeongi

× Kim, Hyeongi

WEKO 776633

Kim, Hyeongi

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Jeong-Hwa, Baek

× Jeong-Hwa, Baek

WEKO 776634

Jeong-Hwa, Baek

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Jeong-Yub, Kim

× Jeong-Yub, Kim

WEKO 776635

Jeong-Yub, Kim

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Sang-Gu, Hwang

× Sang-Gu, Hwang

WEKO 776636

Sang-Gu, Hwang

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Yoon, Myonggeun

× Yoon, Myonggeun

WEKO 776637

Yoon, Myonggeun

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Ho Kim, Eun

× Ho Kim, Eun

WEKO 776638

en Ho Kim, Eun

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Sai, Sei

× Sai, Sei

WEKO 776639

en Sai, Sei

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抄録
内容記述タイプ Abstract
内容記述 Glioblastoma, the most common primary brain tumor in adults, is an incurable malignancy with poor short-term survival and is typically treated with radiotherapy along with temozolomide. While the development of tumor-treating fields (TTFields), electric fields with alternating low and intermediate intensity has facilitated glioblastoma treatment, clinical outcomes of TTFields are reportedly inconsistent. However, combinatorial administration of chemotherapy with TTFields has proven effective for glioblastoma patients. Sorafenib, an anti-proliferative and apoptogenic agent, is used as first-line treatment for glioblastoma. This study aimed to investigate the effect of sorafenib on TTFields-induced anti-tumor and anti-angiogenesis responses in glioblastoma cells in vitro and in vivo. Sorafenib sensitized glioblastoma cells to TTFields, as evident from significantly decreased post-TTFields cell viability ( < 0.05), and combinatorial treatment with sorafenib and TTFields accelerated apoptosis via reactive oxygen species (ROS) generation, as evident from Poly (ADP-ribose) polymerase (PARP) cleavage. Furthermore, use of sorafenib plus TTFields increased autophagy, as evident from LC3 upregulation and autophagic vacuole formation. Cell cycle markers accumulated, and cells underwent a G2/M arrest, with an increased G0/G1 cell ratio. In addition, the combinatorial treatment significantly inhibited tumor cell motility and invasiveness, and angiogenesis. Our results suggest that combination therapy with sorafenib and TTFields is slightly better than each individual therapy and could potentially be used to treat glioblastoma in clinic, which requires further studies.
書誌情報 International journal of molecular sciences

巻 19, 号 11, p. 3684, 発行日 2018-11
出版者
出版者 MDPI
ISSN
収録物識別子タイプ ISSN
収録物識別子 1422-0067
PubMed番号
識別子タイプ PMID
関連識別子 30469352
DOI
識別子タイプ DOI
関連識別子 10.3390/ijms19113684
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