Veisi Ali, Akbari Ghaidafeh, Mard Seyyed Ali, Badfar Gholamreza, Zarezade Vahid, Mirshekar Mohammad Ali
Behbahan Faculty of Medical Sciences, Behbahan, Iran.
Medicinal Plants Research Center, Yasuj University of Medical Sciences, Yasuj, Iran.
Iran J Basic Med Sci. 2020 Jan;23(1):3-12. doi: 10.22038/IJBMS.2019.37821.8995.
Cancer is a major public health problem worldwide. The most important considerable features of cancer cells are uncontrolled proliferation, up-regulated differentiation, and immortality. Crocin, as a bioactive compound of saffron and as a water-soluble carotenoid has radical scavenging, anti-hyperlipidemia, memory improving, and inhibition of tumor growth effects. The present review was designed to evaluate molecular mechanisms underlying crocin effects against cancer cell lines. Data of this review have been collected from the scientific articles published in databases such as Science Direct, Scopus, PubMed, and Scientific Information Database from 1982 to 2019. According to various literature, crocin inhibits tumor growth, and its spread in several types of cancer including colorectal, pancreatic, breast, and prostate, as well as chronic myelogenous and leukemia. It inhibits telomerase activity, microtubule polymerization, cyclin D1, nuclear factor kappa B (NF-kB), multidrug resistance-associated protein (MRP1), and MRP2 overexpression. Crocin can induce apoptosis through activation of caspase 8, up-regulation of p53 expression, Bax/Bcl-2 ratio, and down-regulation expression of Bcl-2, survivin, and cyclin D1. It also down-regulates matrix metalloproteinase 2 and 9 (MMP2 and MMP9), N-cadherin, and beta-catenin expression, which are involved in tumor invasion and metastasis. Tumor invasion was also inhibited by crocin through increasing E-cadherin expression, cell cycle suppression at G1, G0/G1, S, and G2/M phases. Crocin has therapeutic and preventive effects on cancer cells line. Therefore, it has been suggested that this agent can be administered in patients that suffer from this problem.
癌症是全球主要的公共卫生问题。癌细胞最重要的显著特征是不受控制的增殖、分化上调和永生。藏红花素作为藏红花的一种生物活性化合物,是一种水溶性类胡萝卜素,具有自由基清除、抗高血脂、改善记忆和抑制肿瘤生长的作用。本综述旨在评估藏红花素对癌细胞系作用的分子机制。本综述的数据收集自1982年至2019年发表在科学直投、Scopus、PubMed和科学信息数据库等数据库中的科学文章。根据各种文献,藏红花素可抑制肿瘤生长及其在几种癌症中的扩散,包括结直肠癌、胰腺癌、乳腺癌和前列腺癌,以及慢性粒细胞白血病和白血病。它抑制端粒酶活性、微管聚合、细胞周期蛋白D1、核因子κB(NF-κB)、多药耐药相关蛋白(MRP1)和MRP2的过表达。藏红花素可通过激活半胱天冬酶8、上调p53表达、Bax/Bcl-2比值以及下调Bcl-2、生存素和细胞周期蛋白D1的表达来诱导细胞凋亡。它还下调参与肿瘤侵袭和转移的基质金属蛋白酶2和9(MMP2和MMP9)、N-钙黏蛋白和β-连环蛋白的表达。藏红花素还通过增加E-钙黏蛋白表达、在G1、G0/G1、S和G2/M期抑制细胞周期来抑制肿瘤侵袭。藏红花素对癌细胞系具有治疗和预防作用。因此,有人建议可以将这种药物用于患有该疾病的患者。