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MDM2 and prognosis.

机译:MDM2和预后。

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摘要

The cellular stress response pathway regulated by the p53 tumor suppressor is critical to the maintenance of genomic integrity and to the prevention of oncogenic transformation. Intracellular levels of p53 are tightly regulated by an autoregulatory feedback loop comprised of p53 and MDM2. It might be predicted that disruption of this loop, either through p53 mutation or overexpression of MDM2, would be a negative prognostic marker for cancer development, likelihood of relapse, or response to therapy. In fact, although MDM2 overexpression is common in cancer, it can be both a positive and a negative predictor of outcome in different tumors, and its significance as a biomarker remains controversial. Data from a number of different tumor types are reviewed for the predictive significance of MDM2 expression, along with evidence for different mechanisms of MDM2 overexpression in these different tumors. In light of the biological complexities underlying the p53-MDM2 loop, it is, perhaps, not surprising that no simple paradigm exists that is generally applicable. Much work remains to be done to elucidate the basic mechanisms underlying the physical interactions between the two proteins, the role of protein modifications in altering those interactions, and also the genetic and transcriptional deregulations by which protein levels are altered in human cancers. Only in this way will truly biologically relevant predictive factors emerge.
机译:由p53肿瘤抑制因子调节的细胞应激反应途径对于维持基因组完整性和预防致癌转化至关重要。 p53的细胞内水平由包含p53和MDM2的自调节反馈回路严格调节。可以预见,通过p53突变或MDM2的过度表达破坏该环,将成为癌症发展,复发或对治疗反应的阴性预后指标。实际上,尽管MDM2过表达在癌症中很常见,但它可以同时预测不同肿瘤的预后,其作为生物标志物的意义仍然存在争议。审查了来自许多不同肿瘤类型的数据对MDM2表达的预测意义,以及这些不同肿瘤中MDM2过表达的不同机制的证据。鉴于p53-MDM2回路的生物学复杂性,也许并不奇怪,没有普遍适用的简单范式存在。阐明这两种蛋白质之间的物理相互作用的基础机制,蛋白质修饰在改变这些相互作用中的作用以及改变人类癌症中蛋白质水平的遗传和转录失调,还有许多工作要做。只有这样,才会出现真正具有生物学意义的预测因素。

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