Cell cycle dysregulation in cancer

癌症 癌症研究 细胞周期 医学 化学 内科学
作者
Antonino Glaviano,Samarendra Kumar Singh,E. Hui Clarissa Lee,Elena Okina,Hiu Yan Lam,Daniela Carbone,E. Premkumar Reddy,Mark J. O’Connor,Andrew Koff,Garima Singh,Justin Stebbing,Gautam Sethi,Karen Crasta,Patrizia Diana,Khandan Keyomarsi,Michael B. Yaffe,Seth A. Wander,Aditya Bardia,Alan Prem Kumar
出处
期刊:Pharmacological Reviews [American Society for Pharmacology & Experimental Therapeutics]
卷期号:77 (2): 100030-100030 被引量:26
标识
DOI:10.1016/j.pharmr.2024.100030
摘要

Cancer is a systemic manifestation of aberrant cell cycle activity and dysregulated cell growth. Genetic mutations can determine tumor onset by either augmenting cell division rates or restraining normal controls such as cell cycle arrest or apoptosis. As a result, tumor cells not only undergo uncontrolled cell division but also become compromised in their ability to exit the cell cycle accurately. Regulation of cell cycle progression is enabled by specific surveillance mechanisms known as cell cycle checkpoints, and aberrations in these signaling pathways often culminate in cancer. For instance, DNA damage checkpoints, which preclude the generation and augmentation of DNA damage in the G1, S, and G2 cell cycle phases, are often defective in cancer cells, allowing cell division in spite of the accumulation of genetic errors. Notably, tumors have evolved to become dependent on checkpoints for their survival. For example, checkpoint pathways such as the DNA replication stress checkpoint and the mitotic checkpoint rarely undergo mutations and remain intact because any aberrant activity could result in irreparable damage or catastrophic chromosomal missegregation leading to cell death. In this review, we initially focus on cell cycle control pathways and specific functions of checkpoint signaling involved in normal and cancer cells and then proceed to examine how cell cycle control and checkpoint mechanisms can provide new therapeutic windows that can be exploited for cancer therapy. SIGNIFICANCE STATEMENT: DNA damage checkpoints are often defective in cancer cells, allowing cell division in spite of the accumulation of genetic errors. Conversely, DNA replication stress and mitotic checkpoints rarely undergo mutations because any aberrant activity could result in irreparable damage or catastrophic chromosomal missegregation, leading to cancer cell death. This review focuses on the checkpoint signaling mechanisms involved in cancer cells and how an emerging understanding of these pathways can provide new therapeutic opportunities for cancer therapy.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
建议保存本图,每天支付宝扫一扫(相册选取)领红包
实时播报
1秒前
1秒前
2秒前
坚强的阳光菇完成签到 ,获得积分10
2秒前
2秒前
pluto应助majf采纳,获得10
2秒前
orixero应助zhao采纳,获得10
3秒前
Ther1111发布了新的文献求助10
5秒前
hiccup发布了新的文献求助10
6秒前
6秒前
早春完成签到 ,获得积分10
7秒前
8秒前
8秒前
dabai完成签到 ,获得积分10
9秒前
9秒前
bubble发布了新的文献求助10
10秒前
11秒前
11秒前
12秒前
13秒前
13秒前
彭于晏应助hiccup采纳,获得10
13秒前
Parsec完成签到 ,获得积分10
14秒前
英姑应助Yu采纳,获得10
15秒前
英俊的铭应助小米采纳,获得10
15秒前
irisjlj发布了新的文献求助10
16秒前
17秒前
前行的灿完成签到 ,获得积分10
18秒前
18秒前
19秒前
xiaoyao发布了新的文献求助10
19秒前
科研通AI6应助yx采纳,获得10
20秒前
23秒前
zhao发布了新的文献求助10
24秒前
qt发布了新的文献求助10
25秒前
安静行天关注了科研通微信公众号
27秒前
人间烟火发布了新的文献求助10
28秒前
勤恳幻柏完成签到,获得积分10
30秒前
量子星尘发布了新的文献求助10
30秒前
上官若男应助foxpeanut采纳,获得10
30秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Mentoring for Wellbeing in Schools 1200
List of 1,091 Public Pension Profiles by Region 1061
Binary Alloy Phase Diagrams, 2nd Edition 600
Atlas of Liver Pathology: A Pattern-Based Approach 500
A Technologist’s Guide to Performing Sleep Studies 500
EEG in Childhood Epilepsy: Initial Presentation & Long-Term Follow-Up 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 纳米技术 计算机科学 内科学 化学工程 复合材料 物理化学 基因 遗传学 催化作用 冶金 量子力学 光电子学
热门帖子
关注 科研通微信公众号,转发送积分 5496516
求助须知:如何正确求助?哪些是违规求助? 4594139
关于积分的说明 14443740
捐赠科研通 4526740
什么是DOI,文献DOI怎么找? 2480401
邀请新用户注册赠送积分活动 1464976
关于科研通互助平台的介绍 1437722