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Review | Open Access

Cell cycle proteins: Linking the cell cycle to tumors

JIE ZHONG1JUE LIU1XING TANG2WENCHAO ZHOU2GUANGMING SONG1YUHUAN ZENG1XIAODI ZHANG1JIANBIN ZHOU1LU CAO1QUNFENG ZHANG1( )YUKUN LI2( )
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
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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.

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Oncology Research
Pages 1335-1346

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Cite this article:
ZHONG J, LIU J, TANG X, et al. Cell cycle proteins: Linking the cell cycle to tumors. Oncology Research, 2025, 33(6): 1335-1346. https://doi.org/10.32604/or.2025.058760

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Received: 20 September 2024
Accepted: 25 December 2024
Published: 29 May 2025
© The Author 2024.

This work is licensed under a Creative Commons Attribution 4.0 International License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.