Zaher Dana M, Ramadan Wafaa S, El-Awady Raafat, Omar Hany A, Hersi Fatema, Srinivasulu Vunnam, Hachim Ibrahim Y, Al-Marzooq Farah I, Vazhappilly Cijo G, Merali Salim, Merali Carmen, Soares Nelson C, Schilf Paul, Ibrahim Saleh M, Al-Tel Taleb H
Sharjah Institute for Medical Researches, University of Sharjah, Sharjah 27272, United Arab Emirates.
College of Medicine, University of Sharjah, Sharjah 27272, United Arab Emirates.
Cancers (Basel). 2021 Jun 7;13(11):2840. doi: 10.3390/cancers13112840.
(1) Background: Today, the discovery of novel anticancer agents with multitarget effects and high safety margins represents a high challenge. Drug discovery efforts indicated that benzopyrane scaffolds possess a wide range of pharmacological activities. This spurs on building a skeletally diverse library of benzopyranes to identify an anticancer lead drug candidate. Here, we aim to characterize the anticancer effect of a novel benzopyrane derivative, aiming to develop a promising clinical anticancer candidate. (2) Methods: The anticancer effect of SIMR1281 against a panel of cancer cell lines was tested. In vitro assays were performed to determine the effect of SIMR1281 on GSHR, TrxR, mitochondrial metabolism, DNA damage, cell cycle progression, and the induction of apoptosis. Additionally, SIMR1281 was evaluated in vivo for its safety and in a xenograft mice model. (3) Results: SIMR1281 strongly inhibits GSHR while it moderately inhibits TrxR and modulates the mitochondrial metabolism. SIMR1281 inhibits the cell proliferation of various cancers. The antiproliferative activity of SIMR1281 was mediated through the induction of DNA damage, perturbations in the cell cycle, and the inactivation of Ras/ERK and PI3K/Akt pathways. Furthermore, SIMR1281 induced apoptosis and attenuated cell survival machinery. In addition, SIMR1281 reduced the tumor volume in a xenograft model while maintaining a high in vivo safety profile at a high dose. (4) Conclusions: Our findings demonstrate the anticancer multitarget effect of SIMR1281, including the dual inhibition of glutathione and thioredoxin reductases. These findings support the development of SIMR1281 in preclinical and clinical settings, as it represents a potential lead compound for the treatment of cancer.
(1)背景:如今,发现具有多靶点效应和高安全边际的新型抗癌药物是一项巨大挑战。药物研发工作表明,苯并吡喃支架具有广泛的药理活性。这促使构建一个骨架多样的苯并吡喃文库,以鉴定出一种抗癌先导药物候选物。在此,我们旨在表征一种新型苯并吡喃衍生物的抗癌作用,以期开发出一种有前景的临床抗癌候选药物。(2)方法:测试了SIMR1281对一组癌细胞系的抗癌作用。进行体外试验以确定SIMR1281对谷胱甘肽还原酶(GSHR)、硫氧还蛋白还原酶(TrxR)、线粒体代谢、DNA损伤、细胞周期进程及凋亡诱导的影响。此外,在体内评估了SIMR1281的安全性,并在异种移植小鼠模型中进行了评估。(3)结果:SIMR1281强烈抑制GSHR,同时适度抑制TrxR并调节线粒体代谢。SIMR1281抑制多种癌症的细胞增殖。SIMR1281的抗增殖活性是通过诱导DNA损伤、扰乱细胞周期以及使Ras/ERK和PI3K/Akt通路失活介导的。此外,SIMR1281诱导凋亡并削弱细胞存活机制。另外,SIMR1281在异种移植模型中减小了肿瘤体积,同时在高剂量时保持了较高的体内安全性。(4)结论:我们的研究结果证明了SIMR1281的抗癌多靶点效应,包括对谷胱甘肽和硫氧还蛋白还原酶的双重抑制。这些发现支持在临床前和临床环境中开发SIMR1281,因为它代表了一种治疗癌症的潜在先导化合物。