老药出新招:瞄准泌尿生殖系统癌症的抗药性。

Karina Aguilar, Anuj K Sharma, Tianyu Yang, Dipen Mehta, Chandramukhi S Panda, Vinata B Lokeshwar
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引用次数: 0

摘要

在改善包括转移性肾细胞癌(mRCC)在内的转移性泌尿生殖系统癌症患者临床疗效的过程中,重点往往是寻找新的靶向疗法。然而,Jordan 等人(《Oncogenesis》,2020 年)和 Wang 等人(《Cancer Cell Int》,2022 年)的两项研究证明,通过攻击 RCC 细胞劫持的一种使 Sorafenib 失活的机制,可以提高疗效一般的药物 Sorafenib 对 mRCC 的疗效。研究还发现,透明质酸合成酶-3(HAS3)是索拉非尼在RCC细胞中的真正靶点。研究表明,一种非处方药物Hymecromone(4-甲基伞形酮)可通过抑制HAS3的表达和HA信号转导,阻止索拉非尼在RCC细胞中的失活,并提高其对mRCC的疗效。从更广泛的意义上讲,改善安全性良好的 "老药和失败药物 "的疗效,应能为晚期癌症患者提供更多有效的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Teaching an Old Drug a New Trick: Targeting Treatment Resistance in Genitourinary Cancers.

In the quest for improving the clinical outcome of patients with metastatic genitourinary cancers, including metastatic renal cell carcinoma (mRCC), the emphasis often is on finding new targeted therapies. However, two studies by Jordan et al. (Oncogenesis 2020) and Wang et al. (Cancer Cell Int 2022) demonstrate the feasibility of improving the efficacy of a modestly effective drug Sorafenib against mRCC by attacking a mechanism hijacked by RCC cells for inactivating Sorafenib. The studies also identified hyaluronic acid synthase -3 (HAS3) as a bonafide target of Sorafenib in RCC cells. The studies demonstrate that an over-the-counter drug Hymecromone (4-methylumbelliferone) blocks inactivation of Sorafenib in RCC cells and improves its efficacy against mRCC through the inhibition of HAS3 expression and HA signaling. In the broader context, improving the efficacy of "old and failed drugs" that have favorable safety profiles should increase the availability of effective treatments for patients with advanced cancers.

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