Myocardial Infarction-Induced INSL6 Decrease Contributes to Breast Cancer Progression

乳腺癌 医学 生物标志物 肿瘤科 内科学 肿瘤进展 癌症 免疫系统 心肌梗塞 癌症研究 生物 免疫学 生物化学
作者
Yue Zheng,Wenqing Gao,Song Wang,Bingcai Qi,Zhenchang Qi,Xiaomin Hu,Qiang Zhang,Yuheng Lang,Menɡ Ninɡ,Zhiqiang Luo,Tong Li
出处
期刊:Disease Markers [Hindawi Publishing Corporation]
卷期号:2023: 1-33 被引量:3
标识
DOI:10.1155/2023/8702914
摘要

Myocardial infarction (MI) induces early-stage breast cancer progression and increases breast cancer patients’ mortality and morbidity. Insulin-like peptide 6 (INSL6) overexpression can impede cardiotoxin-induced injury through myofiber regeneration, playing a significant role in MI progression. To investigate the diverse significance of INSL6 in a variety of malignant tumors, we explored INSL6 through MI GEO dataset and multiple omics data integrative analysis, such as gene expression level, enriched pathway analysis, protein-protein interaction (PPI) analysis, and immune subtypes as well as diagnostic value and prognostic value in pancancer. INSL6 expression was downregulated in the MI group, and overall survival analysis demonstrated that INSL6 could be the prognostic biomarkers in the overall survival of breast cancer (BRCA). INSL6 expression differs significantly not only in most cancers but also in different molecular and immune subtypes of cancers. INSL6 might be a potential diagnostic and prognostic biomarker of cancers due to the high accuracy in diagnostic and prognostic value. Furthermore, we focused on BRCA and further investigated INSL6 from the perspective of the correlations with clinical characteristics, prognosis in different clinical subgroups, coexpression genes, and differentially expressed genes (DEGs) and PPI analysis. Overall survival and disease-specific survival analysis of subgroups in BRCA demonstrated that lower INSL6 expression had a worse prognosis. Therefore, INSL6 aberrant expression is associated with the progression and immune cell infiltration of the tumor, especially in KIRP and BRCA. Therefore, INSL6 may serve as a potential prognostic biomarker and the crosstalk between MI and tumor progression.
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