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Chinese Journal of Brain Diseases and Rehabilitation(Electronic Edition) ›› 2021, Vol. 11 ›› Issue (03): 139-146. doi: 10.3877/cma.j.issn.2095-123X.2021.03.003

• Clinical Research • Previous Articles     Next Articles

Analysis of the expression and mutation of PARK2 in pan-cancer based on multiple databases

Ya’nan Dou1, Xiaowei Fei1, Jialiang Wei1, Zhou Fei1,()   

  1. 1. Department of Neurosurgery, The First Affiliated Hospital of Air Force Military Medical University, Xi’an 710032, China
  • Received:2021-05-18 Online:2021-06-15 Published:2021-11-26
  • Contact: Zhou Fei

Abstract:

Objective

To analyze the expression and mutation of PARK2 in pan-cancer.

Methods

The tumor immune database TIMER2.0 was used to analyze the mRNA expression level of PARK2 in 33 tumors, and to investigate the potential relationship between the level of cancer-related fibroblast infiltration and PARK2 gene expression in different cancer types of The Cancer Genome Atlas (TCGA); the GEPIA database was used to obtain the overall survival and disease-free survival of PARK2 in all TCGA tumors; the cBioportal database was used to summarize the mutations of pan-cancer genes and obtain the specific mutation site information on the PARK2 functional domain map; the STRING database was used to obtain the protein interaction network of PARK2.

Results

PARK2 is highly expressed in most cancers and has a significant correlation with the prognosis of tumor patients. The expression of PARK2 was correlated with the infiltration of tumor associated fibroblasts in cervical squamous cell carcinoma and endocervical adenocarcinoma, colon adenocarcinoma, esophageal carcinoma, head and neck squamous cell carcinoma. Mutations and/or deletions of PARK2 gene are also involved in the function of PARK2.

Conclusion

The pan-cancer analysis of PARK2 showed that PARK2 expression was statistically correlated with clinical prognosis, immune invasion, etc., which will help to understand the role of in tumorigenesis from the perspective of clinical tumor samples and provide a potential targeted therapeutic strategy for the treatment of multiple cancers.

Key words: PARK2, Pan-cancer, Prognosis, Gene mutation, Immune infiltration

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