Gan Xia, Liu Yonghong, Wang Xueni
Guangxi Zhuang Yao Medicine Center of Engineering and Technology, Guangxi University of Chinese Medicine, 13 Wuhe Road, Qingxiu District, Nanning 530200, China.
Institute of Marine Drugs, Guangxi University of Chinese Medicine, 13 Wuhe Road, Qingxiu District, Nanning 530200, China.
Pharmaceuticals (Basel). 2022 Aug 21;15(8):1029. doi: 10.3390/ph15081029.
Death receptor 5 (DR5) is a membrane protein that mediates exogenous apoptosis. Based on its function, it is considered to be a target for the treatment of cancers including prostate cancer. It is encouraging to note that a number of drugs targeting DR5 are now progressing to different stages of clinical trial studies. We collected 38 active compounds that could produce anti-prostate-cancer effects by modulating DR5, 28 of which were natural compounds and 10 of which were synthetic compounds. In addition, 6 clinically used chemotherapeutic agents have also been shown to promote DR5 expression and thus exert apoptosis-inducing effects in prostate cancer cells. These compounds promote the expression of DR5, thereby enhancing its function in inducing apoptosis. When these compounds were used in combination with the natural ligand of DR5, the number of apoptotic cells was significantly increased. These compounds are all promising for development as anti-prostate-cancer drugs, while most of these compounds are currently being evaluated for their anti-prostate-cancer effects at the cellular level and in animal studies. A great deal of more in-depth research is needed to evaluate whether they can be developed as drugs. We collected literature reports on small molecules against prostate cancer through modulation of DR5 to understand the current dynamics in this field and to evaluate the prospects of small molecules against prostate cancer through modulation of DR5.
死亡受体5(DR5)是一种介导外源性细胞凋亡的膜蛋白。基于其功能,它被认为是包括前列腺癌在内的癌症治疗靶点。值得欣慰的是,目前一些靶向DR5的药物正处于临床试验研究的不同阶段。我们收集了38种可通过调节DR5产生抗前列腺癌作用的活性化合物,其中28种为天然化合物,10种为合成化合物。此外,6种临床常用的化疗药物也已被证明可促进DR5表达,从而在前列腺癌细胞中发挥诱导凋亡的作用。这些化合物促进DR5的表达,从而增强其诱导凋亡的功能。当这些化合物与DR5的天然配体联合使用时,凋亡细胞数量显著增加。这些化合物都有望开发成为抗前列腺癌药物,而目前大多数化合物正在细胞水平和动物研究中评估其抗前列腺癌作用。还需要大量更深入的研究来评估它们是否能够开发成药物。我们收集了通过调节DR5来抗前列腺癌的小分子的文献报道,以了解该领域的当前动态,并评估通过调节DR5来抗前列腺癌的小分子的前景。