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Updated: Oct 23, 2025

Fluorescence-based Monitoring of PAD4 Activity via a Pro-fluorescence Substrate Analog
Published on: November 5, 2014
Basic Pan-Cancer Analysis of the Carcinogenic Effects of Cyclin-Dependent Kinase 4 (CDK4) in Human Surface Tumors
Jingping Wu1, Tinghan Deng2, Yuanen Huang2
1Department of Medical Cosmetology, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu 610075, China.
Abstract:
Although the evidence based on current human, animal, or molecular biology can explain some of the relationships between CDK4 and cancer, there is no pan-cancer analysis of the gene CDK4 in human skin tumors. Therefore, the potential carcinogenic effects of CDK4 in 33 tumors were initially explored in the datasets of the GEO (Gene Expression Omnibus) and the CGA (Cancer Genome Atlas). We found that CDK4 was highly expressed in most cancers and that CDK4 performance levels significantly correlated with the prognosis of cancer patients. These were found in our preliminary exploration. In addition, we used the dataset in tumors such as cutaneous melanoma or lung adenocarcinoma and found increased levels of phosphorylation of r24 l/C/h/s. In addition, fibroblast infiltration associated with CDK4 cancer was observed in head and neck, sarcoma, and melanoma skin. Using this pan-cancer study, our group has provided a comprehensive preliminary demonstration of the oncogenic effects of the CDK4 gene on different human skin tumors.
Insights
This study explored the role of CDK4 in various human skin tumors. High CDK4 expression was linked to poorer cancer prognosis, suggesting its potential as a therapeutic target.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- The role of Cyclin-Dependent Kinase 4 (CDK4) in cancer is known, but a comprehensive pan-cancer analysis in human skin tumors is lacking.
- Previous research suggests potential links between CDK4 and carcinogenesis, necessitating further investigation.
Purpose of the Study:
- To conduct a pan-cancer analysis of CDK4 gene expression and its correlation with patient prognosis across 33 human tumors.
- To investigate the oncogenic effects of CDK4 in human skin tumors, including melanoma and lung adenocarcinoma.
Main Methods:
- Utilized datasets from Gene Expression Omnibus (GEO) and Cancer Genome Atlas (CGA) for pan-cancer analysis.
- Examined CDK4 expression levels, patient prognosis, and specific molecular alterations (e.g., r24l/C/h/s phosphorylation) in various tumor types.
- Assessed fibroblast infiltration associated with CDK4 in specific skin cancers.
Main Results:
- CDK4 was found to be highly expressed in the majority of analyzed cancers.
- Elevated CDK4 expression significantly correlated with poorer patient prognosis across multiple cancer types.
- Increased r24l/C/h/s phosphorylation and fibroblast infiltration were observed in CDK4-associated skin cancers like melanoma and head and neck tumors.
Conclusions:
- This pan-cancer study provides preliminary evidence for the oncogenic role of CDK4 in diverse human skin tumors.
- CDK4's high expression and association with poor prognosis highlight its potential as a therapeutic target in skin cancer treatment.
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