Dr. Rafiq Zakaria Campus, Y. B. Chavan College of Pharmacy, Aurangabad-431001, Maharashtra, India.
Curr Drug Discov Technol. 2020;17(5):585-615. doi: 10.2174/1570163816666190808120843.
Cancer is a complex disease involving genetic and epigenetic alteration that allows cells to escape normal homeostasis. Kinases play a crucial role in signaling pathways that regulate cell functions. Deregulation of kinases leads to a variety of pathological changes, activating cancer cell proliferation and metastases. The molecular mechanism of cancer is complex and the dysregulation of tyrosine kinases like Anaplastic Lymphoma Kinase (ALK), Bcr-Abl (Fusion gene found in patient with Chronic Myelogenous Leukemia (CML), JAK (Janus Activated Kinase), Src Family Kinases (SFKs), ALK (Anaplastic lymphoma Kinase), c-MET (Mesenchymal- Epithelial Transition), EGFR (Epidermal Growth Factor receptor), PDGFR (Platelet-Derived Growth Factor Receptor), RET (Rearranged during Transfection) and VEGFR (Vascular Endothelial Growth Factor Receptor) plays major role in the process of carcinogenesis. Recently, kinase inhibitors have overcome many problems of traditional cancer chemotherapy as they effectively separate out normal, non-cancer cells as well as rapidly multiplying cancer cells.
Electronic databases were searched to explore the small molecule tyrosine kinases by polyphenols with the help of docking study (Glide-7.6 program interfaced with Maestro-v11.3 of Schrödinger 2017) to show the binding energies of polyphenols inhibitor with different tyrosine kinases in order to differentiate between the targets.
From the literature survey, it was observed that the number of polyphenols derived from natural sources alters the expression and signaling cascade of tyrosine kinase in various tumor models. Therefore, the development of polyphenols as a tyrosine kinase inhibitor against targeted proteins is regarded as an upcoming trend for chemoprevention.
In this review, we have discussed the role of polyphenols as chemoreceptive which will help in future for the development and discovery of novel semisynthetic anticancer agents coupled with polyphenols.
癌症是一种涉及遗传和表观遗传改变的复杂疾病,使细胞能够逃脱正常的体内平衡。激酶在调节细胞功能的信号通路中起着至关重要的作用。激酶的失调导致各种病理变化,激活癌细胞的增殖和转移。癌症的分子机制复杂,原癌基因酪氨酸激酶(如间变性淋巴瘤激酶(ALK)、Bcr-Abl(慢性粒细胞白血病患者中发现的融合基因)、JAK(Janus 激活激酶)、Src 家族激酶(SFKs)、ALK(间变性淋巴瘤激酶)、c-MET(间质-上皮转化)、EGFR(表皮生长因子受体)、PDGFR(血小板衍生生长因子受体)、RET(转染过程中重排)和 VEGFR(血管内皮生长因子受体)的失调在致癌过程中起着重要作用。最近,激酶抑制剂克服了传统癌症化疗的许多问题,因为它们有效地将正常的非癌细胞与快速增殖的癌细胞区分开来。
通过对接研究(Glide-7.6 程序与 Schrödinger 2017 年的 Maestro-v11.3 接口),利用电子数据库搜索探讨了多酚类小分子酪氨酸激酶,以显示多酚类抑制剂与不同酪氨酸激酶的结合能,从而区分靶点。
从文献调查中可以看出,天然来源的多酚数量改变了各种肿瘤模型中酪氨酸激酶的表达和信号级联。因此,将多酚类物质开发为针对靶蛋白的酪氨酸激酶抑制剂被认为是化学预防的一个新趋势。
在这篇综述中,我们讨论了多酚类物质作为化学感受剂的作用,这将有助于未来开发和发现与多酚类物质偶联的新型半合成抗癌药物。