Fighting Carcinogenesis with Plant Metabolites by Weakening Proliferative Signaling and Disabling Replicative Immortality Networks of Rapidly Dividing and Invading Cancerous Cells.

IF 2.8 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Atif Khurshid Wani, Nahid Akhtar, Arun Sharma, Sally A El-Zahaby
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引用次数: 6

Abstract

Background: Cancer, an uncontrolled multistage disease causing swift division of cells, is a leading disease with the highest mortality rate. Cellular heterogeneity, evading growth suppressors, resisting cell death, and replicative immortality drive the tumor progression by resisting the therapeutic action of existing anticancer drugs through a series of intrinsic and extrinsic cellular interactions. The innate cellular mechanisms also regulate the replication process as a fence against proliferative signaling, enabling replicative immortality through telomere dysfunction.

Area covered: The conventional genotoxic drugs have several off-target and collateral side effects associated with them. Thus, the need for the therapies targeting cyclin-dependent kinases or P13K signaling pathway to expose cancer cells to immune destruction, deactivation of invasion and metastasis, and maintaining cellular energetics is imperative. Compounds with anticancer attributes isolated from plants and rich in alkaloids, terpenes, and polyphenols have proven to be less toxic and highly targetspecific, making them biologically significant. This has opened a gateway for the exploration of more novel plant molecules by signifying their role as anticancer agents in synergy and alone, making them more effective than the existing cytotoxic regimens.

Expert opinion: In this context, the current review presented recent data on cancer cases around the globe, along with discussing the fundamentals of proliferative signaling and replicative immortality of cancer cells. Recent findings were also highlighted, including antiproliferative and antireplicative action of plant-derived compounds, besides explaining the need for improving drug delivery systems.

通过削弱增殖信号和破坏快速分裂和入侵癌细胞的复制不朽网络,用植物代谢物对抗癌变。
背景:癌症是一种不受控制的多阶段疾病,引起细胞快速分裂,是死亡率最高的主要疾病。细胞异质性、逃避生长抑制因子、抵抗细胞死亡和复制不朽通过一系列内在和外在的细胞相互作用来抵抗现有抗癌药物的治疗作用,从而驱动肿瘤的进展。先天细胞机制也调节复制过程,作为防止增殖信号的屏障,通过端粒功能障碍实现复制不朽。涉及领域:传统的基因毒性药物有几种脱靶和附带副作用。因此,需要针对周期蛋白依赖性激酶或P13K信号通路的治疗,使癌细胞暴露于免疫破坏,使其侵袭和转移失活,并维持细胞能量。从植物中分离出来的具有抗癌特性的化合物,富含生物碱、萜烯和多酚,已被证明毒性较低,具有高度的靶向性,具有重要的生物学意义。这为探索更多新的植物分子打开了大门,表明它们作为抗癌剂在协同作用和单独作用下的作用,使它们比现有的细胞毒性方案更有效。专家意见:在此背景下,当前的综述介绍了全球癌症病例的最新数据,并讨论了癌细胞增殖信号传导和复制不朽的基本原理。最近的发现也被强调,包括植物源化合物的抗增殖和抗复制作用,除了解释需要改善药物输送系统。
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来源期刊
Current drug delivery
Current drug delivery PHARMACOLOGY & PHARMACY-
CiteScore
5.10
自引率
4.20%
发文量
170
期刊介绍: Current Drug Delivery aims to publish peer-reviewed articles, research articles, short and in-depth reviews, and drug clinical trials studies in the rapidly developing field of drug delivery. Modern drug research aims to build delivery properties of a drug at the design phase, however in many cases this idea cannot be met and the development of delivery systems becomes as important as the development of the drugs themselves. The journal aims to cover the latest outstanding developments in drug and vaccine delivery employing physical, physico-chemical and chemical methods. The drugs include a wide range of bioactive compounds from simple pharmaceuticals to peptides, proteins, nucleotides, nucleosides and sugars. The journal will also report progress in the fields of transport routes and mechanisms including efflux proteins and multi-drug resistance. The journal is essential for all pharmaceutical scientists involved in drug design, development and delivery.
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