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紫檀芪:其作为细胞模型和体内研究中的肿瘤抑制因子的作用机制。

Pterostilbene: Mechanisms of its action as oncostatic agent in cell models and in vivo studies.

机构信息

Department of Thoracic Surgery, Tangdu Hospital, The Fourth Military Medical University, 1 Xinsi Road, Xi'an, 710038, China.

Department of Thoracic Surgery, Tangdu Hospital, The Fourth Military Medical University, 1 Xinsi Road, Xi'an, 710038, China; Battalion 5, The First Brigade of Cadets, The Fourth Military Medical University, Xi'an 710032, China; Department of Clinical Oncology, Xijing Hospital, The Fourth Military Medical University, Xi'an 710032, China.

出版信息

Pharmacol Res. 2019 Jul;145:104265. doi: 10.1016/j.phrs.2019.104265. Epub 2019 May 9.

Abstract

Pterostilbene, a natural dimethylated analog of resveratrol, exerts pleiotropic anticancer effects against a variety of cancer types. Due to the better lipophilic and oral absorption, higher cellular uptake and a longer half-life than resveratrol, pterostilbene may have a good prospect in the future clinic application. In this review, we summarize the previous in vitro and in vivo studies about the anticancer actions of pterostilbene on malignances, and we also evaluate the evidence related to the effects of pterostilbene on blocking normal cell carcinogenesis. Special focus is placed on the oncostatic effects of pterostilbene, including inhibition of tumor growth, metastasis, angiogenesis and cancer stem cells, activation of apoptosis, and enhancement of immunotherapy. We then clarify the emerging investigations about pterostilbene and chemotherapy and radiotherapy. Taken together, the information complied herein may serve as a comprehensive reference for the anticancer mechanisms of pterostilbene and may advance it as a future adjuvant therapeutic agent for cancer.

摘要

紫檀芪是白藜芦醇的一种天然二甲基化类似物,对多种癌症类型具有多种抗癌作用。由于紫檀芪比白藜芦醇具有更好的亲脂性和口服吸收性、更高的细胞摄取率和更长的半衰期,因此在未来的临床应用中可能具有良好的前景。在这篇综述中,我们总结了紫檀芪在恶性肿瘤方面的抗癌作用的先前体外和体内研究,并评估了与紫檀芪阻断正常细胞癌变作用相关的证据。特别关注紫檀芪的抗肿瘤作用,包括抑制肿瘤生长、转移、血管生成和癌症干细胞、促进细胞凋亡以及增强免疫治疗。然后,我们阐明了关于紫檀芪与化疗和放疗的新研究。总之,本文中的信息可以作为紫檀芪抗癌机制的综合参考,并可能将其作为癌症的未来辅助治疗剂。

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