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Hedgehog 信号通路抑制剂的研究现状

Current Status of Hedgehog Signaling Inhibitors.

机构信息

Laboratory Animal Center, Shanxi Medical University, No 56, Xinjian South Rd, Taiyuan, 030001, China.

Department of Basic Medical Sciences, Shanxi Medical University, No 56, Xinjian South Rd, Taiyuan, 030001, China.

出版信息

Curr Top Med Chem. 2024;24(3):243-258. doi: 10.2174/0115680266280850231221074340.

Abstract

The Hedgehog (Hh) signaling pathway plays a crucial role in diverse biological processes such as cell differentiation, proliferation, senescence, tumorigenesis, malignant transformation, and drug resistance. Aberrant Hh signaling, resulting from mutations and excessive activation, can contribute to the development of various diseases during different stages of biogenesis and development. Moreover, it has been linked to unfavorable outcomes in several human cancers, including basal cell carcinoma (BCC), multiple myeloma (MM), melanoma, and breast cancer. Hence, the presence of mutations and excessive activation of the Hh pathway presents obstacles and constraints in the realm of cancer treatment. Extant research has demonstrated that small molecule inhibitors are regarded as the most effective therapeutic approaches for targeting the Hh pathway in contrast to traditional chemotherapy and radiotherapy. Consequently, this review focuses on the present repertoire of small molecule inhibitors that target various components of the Hh pathway, including Hh ligands, Ptch receptors, Smo transmembrane proteins, and Gli nuclear transcription factors. This study provides a comprehensive analysis of small molecules' structural and functional aspects in the preclinical and clinical management of cancer. Additionally, it elucidates the obstacles encountered in targeting the Hh pathway for human cancer therapy and proposes potential therapeutic approaches.

摘要

刺猬(Hh)信号通路在多种生物学过程中起着至关重要的作用,如细胞分化、增殖、衰老、肿瘤发生、恶性转化和耐药性。Hh 信号通路的异常,源于突变和过度激活,可能导致生物发生和发展的不同阶段多种疾病的发展。此外,它与几种人类癌症的不良结局有关,包括基底细胞癌(BCC)、多发性骨髓瘤(MM)、黑色素瘤和乳腺癌。因此,Hh 通路的突变和过度激活存在于癌症治疗的障碍和限制。现有研究表明,小分子抑制剂被认为是针对 Hh 通路最有效的治疗方法,与传统的化疗和放疗相比。因此,本综述重点介绍了针对 Hh 通路的各种成分的小分子抑制剂,包括 Hh 配体、Ptch 受体、Smo 跨膜蛋白和 Gli 核转录因子。本研究对小分子在癌症临床前和临床管理中的结构和功能方面进行了全面分析。此外,它阐明了针对人类癌症治疗的 Hh 通路的靶向治疗所遇到的障碍,并提出了潜在的治疗方法。

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