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强调 Sonic hedgehog 通路。

A highlight on Sonic hedgehog pathway.

机构信息

Laboratorio de Biomedicina do Cérebro, Instituto Estadual do Cérebro Paulo Niemeyer (IECPN), Secretaria de Estado de Saúde, Rua do Rezende 156, Centro, Rio de Janeiro, CEP: 20230-024, Brazil.

Programa de Pós-Gradução em Anatomia Patológica, Hospital Universitário Clementino Fraga Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.

出版信息

Cell Commun Signal. 2018 Mar 20;16(1):11. doi: 10.1186/s12964-018-0220-7.

Abstract

Hedgehog (Hh) signaling pathway plays an essential role during vertebrate embryonic development and tumorigenesis. It is already known that Sonic hedgehog (Shh) pathway is important for the evolution of radio and chemo-resistance of several types of tumors. Most of the brain tumors are resistant to chemotherapeutic drugs, consequently, they have a poor prognosis. So, a better knowledge of the Shh pathway opens an opportunity for targeted therapies against brain tumors considering a multi-factorial molecular overview. Therefore, emerging studies are being conducted in order to find new inhibitors for Shh signaling pathway, which could be safely used in clinical trials. Shh can signal through a canonical and non-canonical way, and it also has important points of interaction with other pathways during brain tumorigenesis. So, a better knowledge of Shh signaling pathway opens an avenue of possibilities for the treatment of not only for brain tumors but also for other types of cancers. In this review, we will also highlight some clinical trials that use the Shh pathway as a target for treating brain cancer.

摘要

刺猬(Hh)信号通路在脊椎动物胚胎发育和肿瘤发生中起着至关重要的作用。已知 Sonic hedgehog(Shh)通路对几种类型肿瘤的放射和化学耐药性的进化很重要。大多数脑肿瘤对化疗药物有抵抗力,因此预后较差。因此,更好地了解 Shh 通路为针对脑肿瘤的靶向治疗提供了机会,考虑到多因素的分子概述。因此,正在进行新的研究以寻找 Shh 信号通路的新抑制剂,这些抑制剂可以安全地用于临床试验。Shh 可以通过经典和非经典途径发出信号,并且在脑肿瘤发生过程中与其他途径也有重要的相互作用点。因此,更好地了解 Shh 信号通路为不仅治疗脑肿瘤而且为治疗其他类型的癌症开辟了可能性。在这篇综述中,我们还将重点介绍一些临床试验,这些试验将 Shh 通路作为治疗脑癌的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b1e/5861627/e7e8ab99082c/12964_2018_220_Fig1_HTML.jpg

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