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Special Agents Hunting Down Women Silent Killer: The Emerging Role of the p38αKinase

机译:特工搜寻女性沉默杀手:p38α激酶的新兴作用

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Ovarian cancer is sensitive to chemotherapy with platinum compounds; however, the therapy success rate is significantly lowered by a high incidence of recurrence and by the acquisition of drug resistance. These negative outcomes mainly depend on altered apoptotic and drug resistance pathways, determining the need for the design of new therapeutic strategies to improve patient survival. This challenge has become even more critical because it has been recognized that hindering uncontrolled cell growth is not sufficient as the only curative approach. In fact, while current therapies are mostly conceived to impair survival of highly proliferating cells, several lines of research are now focusing on cancer-specific features to specifically target malignant cells with the aim of avoiding drug resistance and reducing adverse effects. Recently, great interest has been generated by the identification of metabolic reprogramming mechanisms occurring in cancer cells, such as the increase in glycolysis levels. In this light, pharmacologic manipulation of relevant pathways involved in cancer-specific metabolism and drug resistance could prove an effective approach to treat ovarian cancer patients.
机译:卵巢癌对铂类化合物的化学疗法敏感。然而,由于复发率高和获得耐药性,治疗成功率显着降低。这些负面结果主要取决于凋亡和耐药性途径的改变,从而确定了设计新治疗策略以提高患者生存率的需要。由于已经认识到,阻碍不受控制的细胞生长不足以作为唯一的治疗方法,因此这一挑战变得更加关键。实际上,虽然当前的疗法主要是考虑到损害高度增殖细胞的存活,但现在有几项研究集中在针对癌症的特征上,以特异性靶向恶性细胞,从而避免耐药性并减少不良反应。最近,通过鉴定癌细胞中发生的代谢重编程机制,例如糖酵解水平的增加,引起了极大的兴趣。有鉴于此,涉及癌症特异性代谢和耐药性的相关途径的药理学操纵可以证明是治疗卵巢癌患者的有效方法。

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