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Pancreatic cancer chemo-resistance is driven by tumor phenotype rather than tumor genotype

机译:胰腺癌的化学耐药性是由肿瘤表型而非肿瘤基因型驱动的

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摘要

Pancreatic Ductal Adenocarcinoma (PDAC) is one of the deadliest forms of cancer. A major reason for this situation is the fact that these tumors are already resistant or become rapidly resistant to all conventional therapies. Like any transformation process, initiation and development of PDCA are driven by a well known panel of genetic alterations, few of them are shared with most cancers, but many mutations are specific to PDAC and are partially responsible for the great inter-tumor heterogeneity. Importantly, this knowledge has been inefficient in predicting response to anticancer therapy, or in establishing diagnosis and prognosis. Hence, the pre-existing or rapidly acquired resistance of pancreatic cancer cells to therapeutic drugs rely on other parameters and features developed by the cells and/or the micro-environment, that are independent of their genetic profiles. This review sheds light on all major phenotypic, non genetic, alterations known to play important roles in PDAC cells resistance to treatments and therapeutic escape.
机译:胰腺导管腺癌(PDAC)是最致命的癌症之一。造成这种情况的主要原因是这些肿瘤已经对所有常规疗法产生耐药性或变得迅速耐药。像任何转化过程一样,PDCA的启动和发育是由众所周知的遗传改变驱动的,其中很少与大多数癌症共享,但是许多突变是PDAC特有的,部分原因是巨大的肿瘤间异质性。重要的是,该知识在预测对抗癌疗法的反应或建立诊断和预后方面一直无效。因此,胰腺癌细胞对治疗药物的先前存在的或迅速获得的抗药性依赖于细胞和/或微环境产生的其他参数和特征,而这些参数和特征与它们的遗传特征无关。这篇综述揭示了所有主要的表型,非遗传性改变,这些改变在PDAC细胞对治疗和治疗逃逸的抵抗中起着重要作用。

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