文化大學機構典藏 CCUR:Item 987654321/39375
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    jsp.display-item.identifier=請使用永久網址來引用或連結此文件: https://irlib.pccu.edu.tw/handle/987654321/39375


    题名: Voltage-gated calcium channels: Novel targets for cancer therapy
    作者: Phan, NN (Nam Nhut Phan)
    Wang, CY (Wang, Chih-Yang)
    Chen, CF (Chen, Chien-Fu)
    Sun, ZD (Sun, Zhengda)
    Lai, MD (Lai, Ming-Derg)
    Lin, YC (Lin, Yen-Chang)
    贡献者: 生科所
    关键词: voltage-gated calcium channels
    cancer
    under-expression
    potential biomarker
    meta-analysis
    Oncomine
    日期: 2017-08
    上传时间: 2018-01-30 14:50:11 (UTC+8)
    摘要: Voltage-gated calcium channels (VGCCs) comprise five subtypes: The L-type; R-type; N-type; P/Q-type; and T-type, which are encoded by a1 subunit genes. Calcium ion channels also have confirmed roles in cellular functions, including mitogenesis, proliferation, differentiation, apoptosis and metastasis. An association between VGCCs, a reduction in proliferation and an increase in apoptosis in prostate cancer cells has also been reported. Therefore, in the present study, the online clinical database Oncomine was used to identify the alterations in the mRNA expression level of VGCCs in 19 cancer subtypes. Overall, VGCC family genes exhibited under-expression in numerous types of cancer, including brain, breast, kidney and lung cancers. Notably, the majority of VGCC family members (CACNA1C, CACNA1D, CACNA1A, CACNA1B, CACNA1E, CACNA1H and CACNA1I) exhibited low expression in brain tumors, with mRNA expression levels in the top 1-9% of downregulated gene rankings. A total of 5 VGCC family members (CACNA1A, CACNA1B, CACNA1E, CACNA1G and CACNA1I) were under-expressed in breast cancer, with a gene ranking in the top 1-10% of the low-expressed genes compared with normal tissue. In kidney and lung cancers, CACNA1S, CACNA1C, CACNA1D, CACNA1A and CACNA1H exhibited low expression, with gene rankings in the top 1-8% of downregulated genes. In conclusion, the present findings may contribute to the development of new cancer treatment approaches by identifying target genes involved in specific types of cancer.
    關聯: ONCOLOGY LETTERS 卷: 14 期: 2 頁碼: 2059-2074
    显示于类别:[生物科技研究所 ] 期刊論文

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