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TRAIL-Dependent Resolution of Pulmonary Fibrosis.TRAIL 依赖性肺纤维化消退。
Mediators Inflamm. 2018 Jan 24;2018:7934362. doi: 10.1155/2018/7934362. eCollection 2018.
3
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Sirolimus enhances remission induction in patients with high risk acute myeloid leukemia and mTORC1 target inhibition.西罗莫司增强高危急性髓系白血病患者的缓解诱导和 mTORC1 靶向抑制。
Invest New Drugs. 2018 Aug;36(4):657-666. doi: 10.1007/s10637-018-0585-x. Epub 2018 Apr 2.
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Gene Profiling in Patients with Systemic Sclerosis Reveals the Presence of Oncogenic Gene Signatures.系统性硬化症患者的基因谱分析揭示了致癌基因特征的存在。
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Oncotarget. 2018 Jan 23;9(13):11145-11158. doi: 10.18632/oncotarget.24298. eCollection 2018 Feb 16.
7
The Role of the Mammalian Target of Rapamycin (mTOR) in Pulmonary Fibrosis.雷帕霉素靶蛋白(mTOR)在肺纤维化中的作用。
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抗纤维化和抗癌双效药物。

Dually Efficacious Medicine Against Fibrosis and Cancer.

作者信息

Chen Daohong

机构信息

Research Institute of Biological Medicine, Yiling Pharmaceutical; Beijing 102600, China.

出版信息

Med Sci (Basel). 2019 Mar 4;7(3):41. doi: 10.3390/medsci7030041.

DOI:10.3390/medsci7030041
PMID:30836705
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6473536/
Abstract

Although there is a contemporary consensus of managing a severe disease with multi-targeted approach-based therapeutic combinations, it should not be ignored that certain patho-biological pathways are shared by distinct medical conditions and can be exploited to develop an exceptional type of medication conferring a dual efficacy. This article thus presents a spectrum of emerging molecular targets that substantially contribute to the pathogenesis of both fibrotic and neoplastic disorders, including kinase activities, cytokine cascades, and protein dynamics among others. Moreover, recently approved therapeutic agents in this regard have been sorted out to corroborate the drug's ability upon targeting each one of these molecular pathways to treat fibrosis and cancer simultaneously. It not only streamlines an overlapping mechanistic profile in the pathogenesis across these two medical conditions, but also inspires clinicians and pharmaceutical innovation to tackle concomitant diseases, such as fibrosis and cancer, with an optimally efficacious medication.

摘要

尽管目前对于采用基于多靶点方法的治疗组合来管理严重严重严重严重疾病已达成共识,但不应忽视的是,某些病理生物学途径在不同的医学病症中是共有的,并且可以利用这些途径来开发具有双重疗效的特殊类型药物。因此,本文介绍了一系列新出现的分子靶点,这些靶点在纤维化和肿瘤性疾病的发病机制中起着重要作用,包括激酶活性、细胞因子级联反应和蛋白质动态变化等。此外,还梳理了近期在这方面获批的治疗药物,以证实这些药物针对每一种分子途径治疗纤维化和癌症的能力。这不仅简化了这两种医学病症发病机制中的重叠机制,也激励临床医生和药物创新,以一种疗效最佳的药物来应对诸如纤维化和癌症等并发疾病。