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细胞周期蛋白:连接细胞周期与肿瘤

Cell cycle proteins: Linking the cell cycle to tumors.

作者信息

Zhong Jie, Liu Jue, Tang Xing, Zhou Wenchao, Song Guangming, Zeng Yuhuan, Zhang Xiaodi, Zhou Jianbin, Cao L U, Zhang Qunfeng, Li Yukun

机构信息

Department of Obstetrics and Gynecology, The Second Affiliated Hospital, Hengyang Medical School, University of South China, Hengyang, 421001, China.

Department of Assisted Reproductive Centre, Zhuzhou Hospital Affiliated to Xiangya School of Medicine, Central South University, Zhuzhou, 412000, China.

出版信息

Oncol Res. 2025 May 29;33(6):1335-1346. doi: 10.32604/or.2025.058760. eCollection 2025.


DOI:10.32604/or.2025.058760
PMID:40486867
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12144634/
Abstract

The cell cycle is a tightly coupled series of events that enable cells to grow and proliferate. Cyclin-dependent kinases (CDKs) play crucial roles in the cell cycle by enabling cells to transition between different phases when they are activated. Cell cycle proteins enhance the activity of CDKs, while natural CDK inhibitors (CDKIs) suppress them. The cell cycle continues in cycles under normal conditions, but when conditions change, cells halt or terminate the cell cycle. Tumors are tissues that grow out of control, and the mechanisms of various types of tumors are different; however, almost all tumor cells share several common characteristics, including proliferation, prevention of apoptosis and genomic instability. Cellular division is essential in the progression of cancer. A key characteristic of cancer is the uncontrolled growth of tumor cells, which is due to the erratic behavior of several proteins during the cell cycle. Therefore, cell cycle regulators are considered attractive targets for the treatment of cancer. The present analysis highlights proteins that play a direct role in controlling the tumor cell cycle, such as CDKs, and provides a brief overview of checkpoint kinases. The present review also discusses how cell cycle proteins contribute to cancer and describes some of the antitumor drugs that are being researched.

摘要

细胞周期是一系列紧密相连的事件,使细胞能够生长和增殖。细胞周期蛋白依赖性激酶(CDK)在细胞周期中发挥关键作用,当它们被激活时,能使细胞在不同阶段之间转换。细胞周期蛋白增强CDK的活性,而天然CDK抑制剂(CDKI)则抑制其活性。在正常情况下,细胞周期循环进行,但当条件改变时,细胞会停止或终止细胞周期。肿瘤是失控生长的组织,各类肿瘤的机制各不相同;然而,几乎所有肿瘤细胞都有几个共同特征,包括增殖、抗凋亡和基因组不稳定。细胞分裂在癌症进展中至关重要。癌症的一个关键特征是肿瘤细胞的不受控制生长,这是由于细胞周期中几种蛋白质的异常行为所致。因此,细胞周期调节因子被认为是癌症治疗的有吸引力的靶点。本分析重点介绍了在控制肿瘤细胞周期中起直接作用的蛋白质,如CDK,并简要概述了检查点激酶。本综述还讨论了细胞周期蛋白如何促成癌症,并描述了一些正在研究的抗肿瘤药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/189e/12144634/6695365320a8/OncolRes-33-58760-f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/189e/12144634/d52ac7e35f67/OncolRes-33-58760-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/189e/12144634/bcef9a478e53/OncolRes-33-58760-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/189e/12144634/05e69c7736ba/OncolRes-33-58760-f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/189e/12144634/6695365320a8/OncolRes-33-58760-f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/189e/12144634/d52ac7e35f67/OncolRes-33-58760-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/189e/12144634/bcef9a478e53/OncolRes-33-58760-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/189e/12144634/05e69c7736ba/OncolRes-33-58760-f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/189e/12144634/6695365320a8/OncolRes-33-58760-f004.jpg

相似文献

[1]
Cell cycle proteins: Linking the cell cycle to tumors.

Oncol Res. 2025-5-29

[2]
Targeting Cyclin-Dependent Kinases and Cell Cycle Progression in Human Cancers.

Semin Oncol. 2015-12

[3]
Cyclin-dependent protein kinase inhibitors including palbociclib as anticancer drugs.

Pharmacol Res. 2016-3-16

[4]
Cyclin-dependent protein serine/threonine kinase inhibitors as anticancer drugs.

Pharmacol Res. 2018-11-30

[5]
Therapeutic targets in cancer treatment: Cell cycle proteins.

Adv Protein Chem Struct Biol. 2023

[6]
The roles and therapeutic potential of cyclin-dependent kinases (CDKs) in sarcoma.

Cancer Metastasis Rev. 2016-6

[7]
Early development of cyclin dependent kinase modulators.

Curr Pharm Des. 2001-11

[8]
Naturally Sourced CDK Inhibitors and Current Trends in Structure-Based Synthetic Anticancer Drug Design by Crystallography.

Anticancer Agents Med Chem. 2022

[9]
Cyclin-dependent kinase inhibition: an opportunity to target protein-protein interactions.

Adv Protein Chem Struct Biol. 2020

[10]
Histone acetylation and the cell-cycle in cancer.

Front Biosci. 2001-4-1

本文引用的文献

[1]
Autophagy in aging-related diseases and cancer: Principles, regulatory mechanisms and therapeutic potential.

Ageing Res Rev. 2024-9

[2]
Determinants of p53 DNA binding, gene regulation, and cell fate decisions.

Cell Death Differ. 2024-7

[3]
Therapeutic targeting of PLK1 in TERT promoter-mutant hepatocellular carcinoma.

Clin Transl Med. 2024-5

[4]
Understanding the complexity of p53 in a new era of tumor suppression.

Cancer Cell. 2024-6-10

[5]
CDK4/6 activity is required during G arrest to prevent stress-induced endoreplication.

Science. 2024-5-3

[6]
Ki-67 is necessary during DNA replication for fork protection and genome stability.

Genome Biol. 2024-4-22

[7]
Inhibition of cyclin-dependent kinase 7 mitigates doxorubicin cardiotoxicity and enhances anticancer efficacy.

Cardiovasc Res. 2024-7-31

[8]
CDK activity at the centrosome regulates the cell cycle.

Cell Rep. 2024-4-23

[9]
A fast-acting lipid checkpoint in G1 prevents mitotic defects.

Nat Commun. 2024-3-18

[10]
Ferroptosis in cancer: From molecular mechanisms to therapeutic strategies.

Signal Transduct Target Ther. 2024-3-8

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