癌细胞
线粒体分裂
线粒体
DNM1L型
癌症
线粒体融合
癌症研究
程序性细胞死亡
背景(考古学)
细胞生物学
生物
转移
细胞凋亡
化学
生物化学
线粒体DNA
古生物学
基因
遗传学
作者
Samar Sami Alkafaas,Omar K. Obeid,Mustafa Ali Radwan,Mohamed I. Elsalahaty,Sara Samy Elkafas,Wael Hafez,Nenad Janković,Mohamed Hessien
标识
DOI:10.1016/j.bioorg.2024.107574
摘要
Mitochondrial dynamics have pillar roles in several diseases including cancer. Cancer cell survival is monitored by mitochondria which impacts several cellular functions such as cell metabolism, calcium signaling, and ROS production. The equilibrium of death and survival rate of mitochondria is important for healthy cellular processes. Whereas inhibition of mitochondrial metabolism and dynamics can have crucial regulatory decisions between cell survival and death. The steady rate of physiological flux of both mitochondrial fission and fusion is strongly related to the preservation of cellular bioenergetics. Dysregulation of mitochondrial dynamics including fission and fusion is a critical machinery in cells accompanied by crosstalk in cancer progression and resistance. Many cancer cells express high levels of Drp-1 to induce cancer cell invasion, metastasis and chemoresistance including breast cancer, liver cancer, pancreatic cancer, and colon cancer. Targeting Drp-1 by inhibitors such as Midivi-1 helps to enhance the responsiveness of cancer cells towards chemotherapy. The review showed Drp-1 linked processes such as mitochondrial dynamics and relationship with cancer, invasion, and chemoresistance along with computational assessing of all publicly available Drp-1 inhibitors. Drp1-IN-1 Dynole 34–2, Trimethyloctadecylammonium bromide, and Schaftoside showed potential inhibitory effects on Drp-1 as compared to standard Mdivi- 1. This emerging approach may have extensive strength in the context of cancer development and chemoresistance and further work is needed to aid in more effective cancer management.
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