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Versican Promotes Tumor Progression, Metastasis and Predicts Poor Prognosis in Renal Carcinoma

机译:versican促进肿瘤进展,转移和预测肾癌的预后差

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摘要

The proteoglycan versican (VCAN) promotes tumor progression and enhances metastasis in several cancers; however, its role in clear cell renal cell carcinoma (ccRCC) remains unknown. Recent evidence suggests that VCAN is an important target of chromosomal 5q gain, one of the most prevalent genetic abnormalities in ccRCC. Thus, we investigated whether VCAN expression is associated with the pathogenesis of ccRCC. VCAN expression was analyzed using three RCC and normal kidney cell lines as well as a clinical cohort of 84 matched ccRCC and normal renal tissues. Functional analyses on growth and progression properties were performed using VCAN-depleted ccRCC cells. Microarray expression profiling was employed to investigate the target genes and biologic pathways involved in VCAN-mediated ccRCC carcinogenesis. ccRCC had elevated VCAN expression in comparison with normal kidney in both cell lines and clinical specimens. The elevated expression of VCAN was significantly correlated with metastasis (P < 0.001) and worse 5year overall survival after radical nephrectomy (P = 0.014). In vitro, VCAN knockdown significantly decreased cell proliferation and increased apoptosis in Caki-2 and 786-O cells, and this was associated with alteration of several TNF signalingrelated genes such as TNF alpha, BID, and BAK. Furthermore, VCAN depletion markedly decreased cell migration and invasion which correlated with reduction of MMP7 and CXCR4. These results demonstrate that VCAN promotes ccRCC tumorigenesis and metastasis and thus is an attractive target for novel diagnostic, prognostic, and therapeutic strategies.
机译:蛋白质聚糖versican(vcan)促进肿瘤进展,并增强几种癌症中的转移;然而,它在透明细胞肾细胞癌(CCRCC)中的作用仍然未知。最近的证据表明,VCAN是染色体5Q增益的重要目标,CCRCC中最普遍的遗传异常之一。因此,我们研究了VCAN表达是否与CCRCC的发病机制有关。使用三种RCC和正常的肾细胞系以及临床队列的84种匹配的CCRCC和正常肾组织分析VCAN表达。使用VCAN耗尽的CCRCC细胞进行生长和进展性能的功能分析。使用微阵列表达分析来研究VCAN介导的CCRCC癌中涉及的靶基因和生物学途径。与细胞系和临床标本中的正常肾脏相比,CCRCC升高了VCAN表达。 VCAN的升高表达与转移显着相关(P <0.001),并且在激进的肾切除术后,5年总生存率更差(P = 0.014)。体外,VCAN敲低明显降低细胞增殖和CAKI-2和786-O细胞的细胞凋亡增加,这与几种TNF信号传递基因如TNFα,出价和Bak的改变相关。此外,VCAN耗竭明显降低细胞迁移和侵袭,其与MMP7和CXCR4的减少相关。这些结果表明,VCAN促进了CCRCC肿瘤发生和转移,因此是一种有吸引力的新诊断,预后和治疗策略。

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  • 来源
    《Molecular cancer research: MCR》 |2017年第7期|共12页
  • 作者单位

    Shimane Univ Fac Med Dept Urol 89-1 Enya Cho Izumo Shimane 6938501 Japan;

    Shimane Univ Fac Med Dept Urol 89-1 Enya Cho Izumo Shimane 6938501 Japan;

    Univ Calif San Francisco Vet Affairs Med Ctr Dept Urol San Francisco CA 94121 USA;

    Univ Calif San Francisco Vet Affairs Med Ctr Dept Urol San Francisco CA 94121 USA;

    Univ Calif San Francisco Vet Affairs Med Ctr Dept Urol San Francisco CA 94121 USA;

    Univ Calif San Francisco Vet Affairs Med Ctr Dept Urol San Francisco CA 94121 USA;

    Univ Calif San Francisco Vet Affairs Med Ctr Dept Urol San Francisco CA 94121 USA;

    Univ Calif San Francisco Vet Affairs Med Ctr Dept Urol San Francisco CA 94121 USA;

    Univ Calif San Francisco Vet Affairs Med Ctr Dept Urol San Francisco CA 94121 USA;

    Univ Calif San Francisco Vet Affairs Med Ctr Dept Urol San Francisco CA 94121 USA;

    Shimane Univ Fac Med Dept Urol 89-1 Enya Cho Izumo Shimane 6938501 Japan;

    Shimane Univ Fac Med Dept Urol 89-1 Enya Cho Izumo Shimane 6938501 Japan;

    Osaka Univ Grad Sch Med Dept Urol Suita Osaka Japan;

    Univ Calif San Francisco Vet Affairs Med Ctr Dept Urol San Francisco CA 94121 USA;

    Univ Calif San Francisco Vet Affairs Med Ctr Dept Urol San Francisco CA 94121 USA;

    Univ Calif San Francisco Vet Affairs Med Ctr Dept Urol San Francisco CA 94121 USA;

    Univ Calif San Francisco Vet Affairs Med Ctr Dept Urol San Francisco CA 94121 USA;

    Univ Calif San Francisco Vet Affairs Med Ctr Dept Urol San Francisco CA 94121 USA;

    Toho Univ Fac Med Dept Urol Tokyo Japan;

    Univ Calif San Francisco Vet Affairs Med Ctr Dept Urol San Francisco CA 94121 USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 肿瘤学;
  • 关键词

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