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The c-MYC oncoprotein as a treatment target in cancer and other disorders of cell growth.

机译:c-MYC癌蛋白作为癌症和其他细胞生长疾病的治疗靶标。

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摘要

The c-MYC proto-oncogene is essential for cellular proliferation but, paradoxically, may also promote cell death. Deregulated expression of c-MYC is present in most, if not all, human cancers, and is associated with a poor prognosis. However, given that human tumours at diagnosis generally carry multiple genetic lesions that have accumulated during (although they are not necessarily essential for) tumour progression, it has proved difficult to attribute a specific role to any given single factor or indeed to explore the therapeutic potential of selectively mitigating their biological functions. Regulatable transgenic mouse models of oncogenesis have shed light on these issues, influenced our thinking about cancer and provided encouragement for the future development of cancer therapies based on targeting individual oncogenes such as c-MYC. Although still in its infancy, encouraging results have been reported using antisense oligodeoxynucleotide-based methods, as well as other approaches to interfere with MYC expression both in vitro and in vivo.
机译:c-MYC原癌基因对于细胞增殖至关重要,但自相矛盾的是,它也可能促进细胞死亡。 c-MYC的表达失调存在于大多数(如果不是全部)人类癌症中,并且与不良预后有关。但是,鉴于诊断时的人类肿瘤通常携带多种遗传病灶,这些遗传病灶在肿瘤发展过程中积累了(尽管不一定是必需的),因此已证明很难将任何特定的作用归因于任何给定的单一因素,或者难以探索其治疗潜力选择性减轻其生物学功能。可调节的致癌基因转基因小鼠模型阐明了这些问题,影响了我们对癌症的思考,并为基于靶向单个癌基因(例如c-MYC)的癌症疗法的未来发展提供了鼓励。尽管仍处于起步阶段,但已经报道了使用基于反义寡聚脱氧核苷酸的方法以及其他在体外和体内干扰MYC表达的方法的令人鼓舞的结果。

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