National Center for Cancer Care and Research, Hamad Medical Corporation, Doha, Qatar; Translational Cancer Research Facility and Clinical Trial Unit, Translational Research Institute, Hamad Medical Corporation, Doha, Qatar.
Translational Research Institute, Hamad Medical Corporation, Doha, Qatar.
Biomed Pharmacother. 2021 Sep;141:111844. doi: 10.1016/j.biopha.2021.111844. Epub 2021 Jun 24.
Tranilast (TRN) or (N-3,4 -dimethoxy cinnamoyl]-anthranilic acid) is an analog of a tryptophan metabolite and is identified mainly as an anti-allergic agent with limited side effects. The anti-cancer effects of tranilast either alone or in combination with chemotherapeutic drugs have been evidenced in several pre-clinical studies. The main mechanism of action of tranilast includes targeting and modulation of various signaling and immune regulatory pathways including Transforming growth factor-beta (TGF-β), nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB), phosphatidylinositol 3-kinase (PI3K), MAP-Kinase (MAPK), Protein kinase B (Akt/PKB), c-Jun N-terminal kinase, modulation of cancer stem cells, etc. Most of these pathways are involved in tumor proliferation, invasion, and metastasis and it is postulated that tranilast, with its low toxicity profile and high anti-carcinogenic abilities, can serve as a potential anti-tumorigenic agent. The main aim of this review is to provide updated information on the anti-cancer effects of tranilast and its significance as a therapeutic agent.
曲尼司特(TRN)或(N-3,4 -二甲氧基肉桂酰基)-邻氨基苯甲酸)是色氨酸代谢物的类似物,主要被鉴定为具有有限副作用的抗过敏剂。曲尼司特单独或与化疗药物联合使用的抗癌作用已在几项临床前研究中得到证实。曲尼司特的主要作用机制包括靶向和调节各种信号转导和免疫调节途径,包括转化生长因子-β(TGF-β)、核因子κB 轻链增强子的激活 B 细胞(NF-κB)、磷脂酰肌醇 3-激酶(PI3K)、MAP-激酶(MAPK)、蛋白激酶 B(Akt/PKB)、c-Jun N-末端激酶、调节癌症干细胞等。这些途径大多参与肿瘤的增殖、浸润和转移,据推测,曲尼司特具有低毒性和高抗癌能力,可用作潜在的抗肿瘤药物。本文的主要目的是提供曲尼司特的抗癌作用及其作为治疗剂的意义的最新信息。