ERBB3 methylation and immune infiltration in tumor microenvironment of cervical cancer

Xiaoyue Yang1,2, Ying Chen2, Mei Li3

  • 1Department of Obstetrics and Gynecology, Affiliated Hospital of Jiangsu University, Jiefang Road 438, Zhenjiang, 212001, Jiangsu, China.

Scientific Reports
|May 17, 2022
PubMed

Insights

ERBB3 gene alterations influence the cervical cancer microenvironment by suppressing immune cells. Methylation of ERBB3 shows potential as an immunotherapy target for cervical squamous cell carcinoma and endocervical adenocarcinoma.

Area of Science:

  • Oncology
  • Molecular Biology
  • Genetics

Background:

  • The ERBB3 gene, part of the ERBB receptor tyrosine kinase family, is implicated in various cancers.
  • Its specific role and mechanisms in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC) require further elucidation.

Purpose of the Study:

  • To investigate the role of ERBB3 gene mutations and methylation in the CESC tumor microenvironment.
  • To determine if ERBB3 is a carcinogenic factor or a prognostic marker in cervical cancer.

Main Methods:

  • Utilized multi-omics bioinformatics approaches to analyze ERBB3 alterations.
  • Examined the association between ERBB3 modifications, the tumor microenvironment, and immune cell infiltration.

Main Results:

  • ERBB3 gene mutations and methylation extensively regulate the CESC microenvironment.
  • ERBB3 is involved in cervical cancer development, primarily through immune system suppression and RNA methylation, rather than prognosis.
  • Specific DNA methylation modifications downstream of ERBB3 were identified as the most significant.

Conclusions:

  • ERBB3 acts as a carcinogenic factor in cervical cancer, not a prognostic one.
  • ERBB3 methylation presents a potential target for immune checkpoint immunotherapy in CESC.

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