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CKS1B as Drug Resistance-Inducing Gene-A Potential Target to Improve Cancer Therapy
Wenwen Shi1, Qiudi Huang1, Jiacui Xie1
1Key Laboratory of Molecular Target and Clinical Pharmacology, The State Key Laboratory of Respiratory Disease, School of Pharmaceutical Sciences and The Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
Abstract:
Cancer is a threat to human health and life. Although previously centered on chemical drug treatments, cancer treatment has entered an era of precision targeted therapy. Targeted therapy entails precise guidance, allowing the selective killing of cancer cells and thereby reducing damage to healthy tissues. Therefore, the need to explore potential targets for tumor treatment is vital. Cyclin-dependent kinase regulatory subunit 1B (CKS1B), a member of the conserved cyclin kinase subunit 1 (CKS1) protein family, plays an essential role in cell cycling. A large number of studies have shown that CKS1B is associated with the pathogenesis of many human cancers and closely related to drug resistance. Here, we describe the current understanding of the cellular functions of CKS1B and its underlying mechanisms, summarize a recent study of CKS1B as a target for cancer treatment and discuss the potential of CKS1B as a therapeutic target.
Insights
Targeted cancer therapy is advancing, with Cyclin-dependent kinase regulatory subunit 1B (CKS1B) emerging as a key target. Understanding CKS1B
Area of Science:
- Oncology
- Molecular Biology
- Cell Biology
Background:
- Cancer treatment is shifting towards precision targeted therapy.
- Targeted therapy selectively eliminates cancer cells, minimizing harm to healthy tissues.
- Identifying novel therapeutic targets is crucial for effective cancer treatment.
Purpose of the Study:
- To review the cellular functions and mechanisms of Cyclin-dependent kinase regulatory subunit 1B (CKS1B).
- To summarize recent research on CKS1B as a target for cancer therapy.
- To discuss the therapeutic potential of CKS1B in treating human cancers.
Main Methods:
- Literature review of CKS1B's role in cell cycling and cancer.
- Analysis of studies investigating CKS1B as a therapeutic target.
- Discussion of CKS1B's association with cancer pathogenesis and drug resistance.
Main Results:
- CKS1B is integral to cell cycle regulation.
- CKS1B is implicated in the development and progression of numerous human cancers.
- CKS1B is linked to cancer drug resistance.
Conclusions:
- CKS1B plays a significant role in cancer.
- CKS1B presents a promising therapeutic target for precision cancer treatment.
- Further research into CKS1B mechanisms can advance targeted cancer therapies.
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