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内皮素-1及其在癌症中的作用和潜在治疗机会。

Endothelin-1 and Its Role in Cancer and Potential Therapeutic Opportunities.

作者信息

Harrison Madeline, Zinovkin Dmitry, Pranjol Md Zahidul Islam

机构信息

Department of Biochemistry, School of Life Sciences, University of Sussex, Brighton BN1 9QU, UK.

Department of Pathology, Gomel State Medical University, 246000 Gomel, Belarus.

出版信息

Biomedicines. 2024 Feb 23;12(3):511. doi: 10.3390/biomedicines12030511.

Abstract

Endothelin-1 (ET-1) plays a physiological role as a potent vasoconstrictor. It is implicated in an array of diseases, and its signalling is often found to be overactivated within cancers. ET-1 has been found to potentiate hallmarks of cancer progression such as cell proliferation, invasion and metastasis, as well as angiogenesis. ET-1 has also been implicated in inducing the epithelial-mesenchymal transition (EMT) and promoting resistance to anticancer drugs. Many preclinical efforts have been made to target ET-1 expression within cancer, such as by using ET-1 receptor antagonists, many of which have been approved for treating pulmonary hypertension. Targeting ET-1 has been shown to improve the response to various other cancer therapeutics, highlighting the potential benefits targeting this peptide may exert. Drug repurposing is an attractive strategy, and exploration of this avenue may be promising for targeting ET-1 in cancer. There are many clinical trials which have been completed and are currently undergoing involving the repurposing of ET-1 receptor antagonists for cancer treatment. In this review, the pathways through which ET-1 potentiates cancer will be discussed, as well as where the opportunity for therapeutic intervention lies in relation to cancer.

摘要

内皮素-1(ET-1)作为一种强效血管收缩剂发挥着生理作用。它与一系列疾病有关,并且在癌症中其信号传导常常被发现过度激活。已发现ET-1可增强癌症进展的特征,如细胞增殖、侵袭和转移以及血管生成。ET-1还与诱导上皮-间质转化(EMT)和促进抗癌药物耐药性有关。已经进行了许多临床前研究来针对癌症中的ET-1表达,例如使用ET-1受体拮抗剂,其中许多已被批准用于治疗肺动脉高压。靶向ET-1已被证明可改善对各种其他癌症治疗方法的反应,突出了靶向这种肽可能带来的潜在益处。药物重新利用是一种有吸引力的策略,探索这条途径可能有望用于癌症中ET-1的靶向治疗。有许多临床试验已经完成,并且目前正在进行将ET-1受体拮抗剂重新用于癌症治疗的研究。在这篇综述中,将讨论ET-1增强癌症的途径,以及与癌症相关的治疗干预机会所在。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b3d/10967712/999dfa0c25c1/biomedicines-12-00511-g001.jpg

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