einstein (São Paulo). 02/Oct/2020;18:eAO5447.

In silico investigation of heparanase-correlated genes in breast cancer subtypes

Carina Mucciolo Melo ORCID logo , Henrique Pereira Prado ORCID logo , Gabriela Araújo Attie ORCID logo , Daniel Lacaz Ruiz ORCID logo , Manoel João Batista Castello Girão ORCID logo , Maria Aparecida da Silva Pinhal ORCID logo

DOI: 10.31744/einstein_journal/2020AO5447

ABSTRACT

Objective

To investigate the possible genes that may be related to the mechanisms that modulate heparanase-1.

Methods

The analysis was conducted at Universidade Federal de São Paulo, on the data provided by: The Cancer Genome Atlas, University of California Santa Cruz Genome Browser, Kyoto Encyclopedia of Genes and Genomes Pathway Database, Database for Annotation, Visualization and Integrated Discovery Bioinformatics Database and the softwares cBioPortal and Ingenuity Pathway Analysis.

Results

Using messenger RNA expression pattern of different molecular subtypes of breast cancer, we proposed that heparinase-1 was co-related with its progression. In addition, genes that were analyzed presented co-expression with heparanase-1. The results that showed that heparanase-1 co-expressed with phosphoinositide 3-kinase adapter protein 1, sialic acid-binding immunoglobulin-like lectin 7, and leukocyte-associated immunoglobulin-like receptor 1 are directed related with immune system evasion during breast cancer progression. Furthermore, cathepsin L was co-expressed with heparanase-1 and transformed inactive heparanase-1 form into active heparanase-1, triggering extracellular matrix remodeling, which contributes to enhanced tumor-host interaction of the tumor.

Conclusion

The signaling pathway analysis using bioinformatics tools gives supporting evidence of possible mechanisms related to breast cancer development. Evasion genes of the immune system co-expressed with heparanase-1, a enzyme related with tumor progression.

In silico investigation of heparanase-correlated genes in breast cancer subtypes