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hedgehog 信号通路抑制剂:更新的专利审查(2015 年至今)。

Hedgehog signaling pathway inhibitors: an updated patent review (2015-present).

机构信息

Department of Chemistry and Technology of Drugs, Department of Excellence 2018-2022, Sapienza University of Rome, Rome, Italy.

Center for Life Nano Science@Sapienza, Istituto Italiano di Tecnologia, Rome, Italy.

出版信息

Expert Opin Ther Pat. 2020 Apr;30(4):235-250. doi: 10.1080/13543776.2020.1730327. Epub 2020 Feb 19.

Abstract

: Hedgehog (Hh) signaling plays a pivotal role in tissue development and stemness, and its deregulation is found in many different tumors. Several efforts have been devoted to discovery of Hh inhibitors, including three drugs approved by the Food and Drug Administration (FDA), targeting the upstream receptor smoothened (SMO). However, SMO mutations or SMO-independent Hh pathway activation raise the need for novel Hh inhibitors.: This review describes Hh inhibitors with anticancer potential patented in the period 2015-present.: Despite the initial enthusiasm in SMO antagonists, drug-resistant mutations, and SMO-independent Hh activation limited their clinical application. A growing number of therapeutic strategies are currently focusing on downstream Hh effectors (i.e. glioma-associate oncogenes (GLI) proteins) or other signaling pathways related to Hh, in addition to drug repositioning. Given the heterogenic nature of cancers, a terrific clinical impact is expected by multi-targeting approaches able to modulate simultaneously SMO and GLI, and/or additional targets that act as regulators of Hh signaling. It is expected that these alternative strategies might be investigated in clinical trials in the next years against a wide variety of tumor types, and that they provide improved outcomes compared to current SMO antagonists or other single-agent anticancer drugs.

摘要

Hedgehog (Hh) 信号通路在组织发育和干细胞特性中起着关键作用,其失调存在于许多不同的肿瘤中。人们已经做出了许多努力来发现 Hh 抑制剂,包括三种已被美国食品和药物管理局 (FDA) 批准的针对上游受体 smoothened (SMO) 的药物。然而,SMO 突变或非 SMO 依赖的 Hh 信号通路激活,需要新型的 Hh 抑制剂。

本文综述了 2015 年至今已获得专利的具有抗癌潜力的 Hh 抑制剂。

尽管 SMO 拮抗剂最初受到了极大的关注,但耐药性突变和非 SMO 依赖的 Hh 激活限制了它们的临床应用。目前,越来越多的治疗策略将重点放在下游的 Hh 效应物(即神经胶质瘤相关致癌基因 (GLI) 蛋白)或与 Hh 相关的其他信号通路,除了药物再定位。鉴于癌症的异质性,预计能够同时调节 SMO 和 GLI 的多靶向方法,以及作为 Hh 信号调节剂的其他靶点,将产生巨大的临床影响。预计这些替代策略可能会在未来几年内针对多种肿瘤类型进行临床试验,并提供比目前的 SMO 拮抗剂或其他单药抗癌药物更好的疗效。

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