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Prognostic Significance of Activated Leukocyte Cell Adhesion Molecule (ALCAM) in Association with Promoter Methylation of the ALCAM Gene in Breast Cancer. | LitMetric

AI Article Synopsis

  • ALCAM is a gene thought to play a role in tumor development, and this study analyzed its DNA methylation in breast cancer tissues to understand its impact on gene expression.
  • The researchers found that while the methylation status of ALCAM did not significantly differ between tumor and normal tissues, its expression correlated with inflammatory markers like TNFα and IL-4.
  • Ultimately, the study suggests that ALCAM's methylation may lead to lower expression levels, tying it to both inflammation and breast cancer characteristics.

Article Abstract

Activated leukocyte cell adhesion molecule (ALCAM) has been implicated in tumorigenesis. In this study, we studied DNA methylation status of the gene using pyrosequencing in breast cancer tissues. We analyzed the association between the methylation status of the gene and its expression. Also, the effects of inflammation on the gene methylation and its expression were investigated. The gene methylation was associated with the transcripts in tumor tissues. The methylation status of the gene was not significantly different between tumor and normal tissues. The level of transcripts was associated with the expression of TNFα, NF-κB p50, IL-4, and intratumoral inflammation. The IHC expression of ALCAM was associated with histologic grade, HER2 overexpression and molecular subtype. The expression of TNFα, NF-κB p50, and IL-4 showed significant association with the clinicopathologic characteristics. In conclusion, the gene methylation was related to the level of transcripts. Also, the level of transcripts was associated with the inflammatory markers in breast cancer. Our results suggest that the methylation of the gene contributes to the decreased expression of ALCAM. Also, ALCAM is linked to the inflammatory response in breast cancer.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017653PMC
http://dx.doi.org/10.3390/molecules23010131DOI Listing

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