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Updated: Aug 17, 2026

A Method for Screening and Validation of Resistant Mutations Against Kinase Inhibitors
Published on: December 7, 2014
Roles and regulatory mechanisms of KIN17 in cancers (Review)
Xueran Huang1, Zichang Dai2, Qiuyan Li1,3
1Medical Laboratory, Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong 524000, P.R. China.
Abstract:
KIN17, which is known as a DNA and RNA binding protein, is highly expressed in numerous types of human cancers and was discovered to participate in several vital cell behaviors, including DNA replication, damage repair, regulation of cell cycle and RNA processing. Furthermore, KIN17 is associated with cancer cell proliferation, migration, invasion and cell cycle regulation by regulating pathways including the p38 MAPK, NF-κB-Snail and TGF-β/Smad2 signaling pathways. In addition, knockdown of KIN17 was found to enhance the sensitivity of tumor cells to chemotherapeutic agents. Immunohistochemical analysis revealed that there were significant differences in the expression of KIN17 between cancer tissues and adjacent tissues. Both the Kaplan-Meier survival analysis and multivariate Cox regression analysis indicated that KIN17 is aberrantly high expressed in various tumor tissues and is also associated with poor prognosis in patients with various tumor types. Taken together, KIN17 has key roles in tumorigenesis and cancer development. Investigating the relationship between KIN17 and neoplasms will provide a vital theoretical basis for KIN17 to serve as a diagnostic and prognostic biomarker for cancer patients and as a potential target for cancer therapy.
Insights
The DNA and RNA binding protein KIN17 is highly expressed in human cancers, promoting tumor growth and poor prognosis. Reducing KIN17 enhances chemotherapy sensitivity, suggesting its potential as a cancer biomarker and therapeutic target.
Area of Science:
- Molecular Biology
- Oncology
- Biochemistry
Background:
- KIN17 is a DNA and RNA binding protein implicated in essential cellular processes.
- High expression of KIN17 is observed across various human cancers.
- KIN17 plays a role in cell proliferation, migration, invasion, and cell cycle regulation.
Purpose of the Study:
- To investigate the role of KIN17 in tumorigenesis and cancer development.
- To evaluate KIN17 as a potential diagnostic and prognostic biomarker.
- To explore KIN17 as a therapeutic target in cancer treatment.
Main Methods:
- Immunohistochemical analysis to compare KIN17 expression in cancer and adjacent tissues.
- Kaplan-Meier survival analysis and multivariate Cox regression analysis.
- Assessment of KIN17 knockdown effects on tumor cell sensitivity to chemotherapeutic agents.
Main Results:
- KIN17 is aberrantly overexpressed in diverse tumor tissues compared to normal tissues.
- High KIN17 expression correlates with poor prognosis in cancer patients.
- Knockdown of KIN17 increases the sensitivity of tumor cells to chemotherapy.
Conclusions:
- KIN17 is a key driver in tumorigenesis and cancer progression.
- KIN17 serves as a potential diagnostic and prognostic biomarker for various cancers.
- Targeting KIN17 may offer a novel therapeutic strategy for cancer treatment.
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