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Understanding the biology of urothelial cancer metastasis

机译:了解尿路上皮癌转移的生物学

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Management of unresectable urothelial cancer (UC) has been a clinical challenge for decades. While drug resistance is a key issue, precise understanding of biology of UC metastasis is another challenge for the improvement of treatment outcome of UC patients. Introduction of the cell biology concepts including epithelial-mesenchymal transition (EMT) and cancer stemness seems to explain UC metastasis. Molecular genetics based on gene expression profiling, next generation sequencing, and explosion of non-coding RNA world has opened the door to intrinsic molecular subtyping of UC. Next steps include, based on the recently accumulated understanding, the establishment of novel disease models representing UC metastasis in various experimental platforms, particularly in?vivo animal systems. Indeed, novel knowledge molecular genetics has not been fully linked to the modeling of UC metastasis. Further understanding of bladder carcinogenesis is needed particularly with regard to cell of origin related to tumor characteristics including driver gene alterations, pathological differentiations, and metastatic ability. Then we will be able to establish better disease models, which will consequently lead us to further understanding of biology and eventually the development of novel therapeutic strategies for UC metastasis.
机译:数十年来,不可切除的尿路上皮癌(UC)的管理一直是一项临床挑战。虽然耐药性是一个关键问题,但对UC转移生物学的准确了解是改善UC患者治疗结果的另一项挑战。引入细胞生物学概念(包括上皮-间质转化(EMT)和癌干)似乎可以解释UC转移。基于基因表达谱,下一代测序和非编码RNA世界的爆炸式发展的分子遗传学为UC的固有分子亚型化打开了大门。根据最近积累的理解,下一步包括在各种实验平台(尤其是体内动物系统)中建立代表UC转移的新型疾病模型。确实,新知识分子遗传学尚未与UC转移的建模完全相关联。需要进一步了解膀胱癌的发生,特别是对于与肿瘤特征相关的起源细胞,包括驱动基因改变,病理分化和转移能力。然后,我们将能够建立更好的疾病模型,从而使我们对生物学有进一步的了解,并最终为UC转移开发新的治疗策略。

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