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Molecular determinants of ovarian cancer chemoresistance: new insights into an old conundrum

机译:卵巢癌化学的分子决定因素:新的谜语洞察力

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Ovarian cancer is the most lethal gynecological malignancy. Cisplatin and its derivatives are first-line chemotherapeutics, and their resistance is a major hurdle in successful ovarian cancer treatment. Understanding the molecular dysregulation underlying chemoresistance is important for enhancing therapeutic outcome. Here, we review two established pathways in cancer chemoresistance. p53 is a major tumor suppressor regulating proliferation and apoptosis, and its mutation is a frequent event in human malignancies. The PI3K/Akt axis is a key oncogenic pathway regulating survival and tumorigenesis by controlling several tumor suppressors, including p53. The interplay between these pathways is well established, although the oncogenic phosphatase PPM1D adds a new layer to this intricate relationship and provides new insights into the processes determining cell fate. Inhibition of the PI3K/Akt pathway by functional food compounds as an adjunct to chemotherapeutics may tip the balance in favor of apoptosis rather than survival, enhancing therapeutic efficacy, and reducing side effects.
机译:卵巢癌是最致命的妇科恶性肿瘤。顺铂及其衍生物是一线化学治疗剂,其抗性是成功卵巢癌治疗的主要障碍。理解潜在化学抑制的分子失调对于提高治疗结果是重要的。在这里,我们回顾了癌症化学抑制的两种已建立的途径。 P53是一种调节增殖和凋亡的主要肿瘤抑制作用,其突变是人类恶性肿瘤的频繁事件。 PI3K / AKT轴是通过控制几种肿瘤抑制剂(包括P53)调节存活率和肿瘤的关键致癌途径。尽管致癌磷酸酶PPM1D将新层添加到这种复杂的关系,但是在确定细胞命运的过程中提供了新的洞察,但这些途径之间的相互作用。抑制功能性食品化合物的PI3K / AKT途径作为化学治疗剂的辅助性能可以提高凋亡的平衡,而不是存活,增强治疗效果,降低副作用。

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