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KIF18B: an important role in signaling pathways and a potential resistant target in tumor development
Shicheng Chen1, Bo Yu1, Guo Tu DU2
1Department of Urology, The Second Affiliated Hospital of Zunyi Medical University, Zunyi, 563000, P. R. China.
Abstract:
KIF18B is a key member of the kinesin-8 family, involved in regulating various physiological processes such as microtubule length, spindle assembly, and chromosome alignment. This article briefly introduces the structure and physiological functions of KIF18B, examines its role in malignant tumors, and the associated carcinogenic signaling pathways such as PI3K/AKT, Wnt/β-catenin, and mTOR pathways. Research indicates that the upregulation of KIF18B enhances tumor malignancy and resistance to radiotherapy and chemotherapy. KIF18B could become a new target for anticancer drugs, offering significant potential for the treatment of malignant tumors and reducing chemotherapy resistance.
Insights
Kinesin family member KIF18B promotes tumor growth and resistance to cancer treatments. Targeting KIF18B offers a promising strategy for developing new anticancer drugs and overcoming therapeutic resistance in malignant tumors.
Area of Science:
- Molecular Biology
- Oncology
- Cell Biology
Background:
- KIF18B, a kinesin-8 family member, regulates microtubule dynamics, spindle assembly, and chromosome alignment.
- Dysregulation of KIF18B is implicated in various cellular processes and cancer development.
Purpose of the Study:
- To review the structure, physiological functions, and role of KIF18B in malignant tumors.
- To explore the association between KIF18B and key carcinogenic signaling pathways.
- To evaluate KIF18B as a potential therapeutic target for cancer treatment.
Main Methods:
- Literature review of studies on KIF18B structure, function, and cancer-related pathways.
- Analysis of research linking KIF18B expression to tumor malignancy and treatment resistance.
- Examination of signaling pathways including PI3K/AKT, Wnt/β-catenin, and mTOR in the context of KIF18B.
Main Results:
- KIF18B plays a crucial role in microtubule dynamics and chromosome segregation.
- Upregulation of KIF18B is associated with increased tumor malignancy and resistance to radiotherapy and chemotherapy.
- KIF18B interacts with signaling pathways like PI3K/AKT, Wnt/β-catenin, and mTOR, contributing to tumorigenesis.
Conclusions:
- KIF18B is a significant factor in promoting cancer progression and therapeutic resistance.
- Targeting KIF18B presents a novel therapeutic strategy for treating malignant tumors.
- Further research into KIF18B inhibition could lead to more effective anticancer drugs and overcome chemotherapy resistance.
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