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用于癌症治疗的线粒体毒性化合物。

Mitochondriotoxic compounds for cancer therapy.

作者信息

Fantin V R, Leder P

机构信息

Merck & Co. Inc., Boston, MA, USA.

出版信息

Oncogene. 2006 Aug 7;25(34):4787-97. doi: 10.1038/sj.onc.1209599.

Abstract

One of the hallmarks of cancer cells is their increased resistance to apoptosis induction. Alterations in many apoptosis regulators belonging to the intrinsic pathway confer emerging neoplastic cells with a selective growth advantage in the hostile tumor microenvironment. The realization that those same defects contribute to resistance to radiation and chemotherapeutic agents have prompted the unrelenting search for mitochondria-targeted compounds for the treatment of cancer. Mitochondria play a central role in the process of cell death. They serve as integrators of upstream effector mechanisms. Most importantly, mitochondrial outer membrane permeabilization becomes a commitment point during cell death. Thus, strategies aimed at directly triggering this event by either blocking the activity of antiapoptotic factors or by interfering with vital mitochondrial functions may help to overcome resistance to standard cancer therapy.

摘要

癌细胞的一个标志是它们对凋亡诱导的抗性增加。许多属于内在途径的凋亡调节因子的改变赋予新兴肿瘤细胞在恶劣的肿瘤微环境中具有选择性生长优势。认识到这些相同的缺陷导致对放疗和化疗药物的抗性,促使人们不懈地寻找用于治疗癌症的线粒体靶向化合物。线粒体在细胞死亡过程中起核心作用。它们作为上游效应机制的整合者。最重要的是,线粒体外膜通透性改变成为细胞死亡过程中的一个关键节点。因此,旨在通过阻断抗凋亡因子的活性或干扰重要的线粒体功能来直接触发这一事件的策略可能有助于克服对标准癌症治疗的抗性。

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