Transient receptor potential (TRP) channels, promising potential diagnostic and therapeutic tools for cancer
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- Chen Jianpeng
- Department of Oncology, Provincial Hospital Affiliated with Shandong University
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- Luan Yi
- Center for Disease Control, Ji'nan Command of the People's Liberation Army
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- Yu Ruofei
- Department of Oncology, Nanfang Hospital, Southern Medical University
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- Zhang Zheng
- Department of Oncology, Provincial Hospital Affiliated with Shandong University
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- Zhang Jinbiao
- Department of Oncology, the 148th Hospital of the People's Liberation Army
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- Wang Weibo
- Department of Oncology, Provincial Hospital Affiliated with Shandong University
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Despite the advances in detection of and therapies for various tumors, high rates of treatment failure and mortality still exist throughout the world. These high rates are mainly due to the powerful capability of tumor cells to proliferate and migrate. Recent studies regarding the transient receptor potential (TRP) have indicated that TRP channels are associated with tumors and that TRP channels might represent potential targets for cancer treatment. TRP channels are important calcium-selective ion channels in many different tissues and cell types in mammals and are crucial regulators of calcium and sodium. TRP were first discovered in the photoreceptors of Drosophila with gene defects or mutations. TRP channels can be divided into seven subfamilies: TRPC (canonical), TRPV (vanilloid), TRPM (melastatin), TRPML (mucolipin), TRPP (polycystin), TRPA (ankyrin transmembrane protein), and TRPN (NomPC-like). TRPC proteins are conserved across organisms since they are most homologous to Drosophila TRP. TRP superfamilies have been linked to many physiological and pathological functions, including cell differentiation, proliferation, apoptosis, and ion homeostasis. This review focuses on the properties of TRP in oncogenesis, cancer proliferation, and cell migration.
収録刊行物
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- BioScience Trends
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BioScience Trends 8 (1), 1-10, 2014
特定非営利活動法人 バイオ&ソーシャル・サイエンス推進国際研究交流会
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詳細情報 詳細情報について
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- CRID
- 1390001205736696320
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- NII論文ID
- 130003397278
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- DOI
- 10.5582/bst.8.1
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- ISSN
- 18817823
- 18817815
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- PubMed
- 24647107
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- Crossref
- PubMed
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可