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Current molecular targets for urological cancer

机译:当前的泌尿外科分子靶标

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Clinically advanced stages of urological cancers are currently treated with conventional surgery, radiation, and chemotherapy. As for molecular targets, multiple kinase inhibitors (MKIs) and mammalian target of rapamycin (mTOR) inhibitors have already been introduced to treat advanced metastatic renal cell carcinoma, which is refractory to cytokine therapies such as interferon-a and interleukin-2. In recent trends in cancer research, the translation of basic science into clinical application has been accelerated. In this review, new molecular targets, such as MKIs, mTOR inhibitors, along with the phosphatidylinositol 3-kinase (PI3K)/ Akt signaling pathway, vascular endothelial growth factor (VEGF), and NF-κB, as well as conventional COX inhibitors, are overviewed. As the putative source of cancer oncogenesis, cancer stem cells (CSCs) have been highlighted in recent research. Current understandings of CSCs in urologic oncology are also discussed.
机译:泌尿外科癌症的临床晚期阶段目前接受了常规手术,放射和化学疗法的治疗。 至于分子靶标,已经引入了多种激酶抑制剂(MKI)和雷帕霉素(MTOR)抑制剂的哺乳动物靶标,以治疗晚期转移性肾细胞癌,这是对细胞因子疗法(例如Interferon-A和interleuukin-a和interleulikin-2)的难治性。 在癌症研究的最新趋势中,将基础科学转化为临床应用。 在这篇综述中,新的分子靶标,例如MKI,MTOR抑制剂,以及磷脂酰肌醇3-激酶(PI3K)/ AKT信号途径,血管内皮生长因子(VEGF)和NF-κB以及常规COX抑制剂,血管内皮生长因子(VEGF)和NF-κB 被概述。 作为癌症发生的推定来源,最近的研究中强调了癌症干细胞(CSC)。 还讨论了当前对泌尿外科肿瘤学中CSC的理解。

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