Aim: To explore the prognostic value of synaptonemal complex protein-2 (SYCP2) in different subtypes of breast cancer. Patients & materials: In silico bioinformatic analysis was conducted using large databases.
Results: SYCP2 was only significantly upregulated in luminal B tumors compared with the adjacent normal tissues. SYCP2 expression was an independent indicator of shorter overall survival in luminal A patients (hazard ratio: 2.269; 95% CI: 1.059-4.862; p = 0.035) and luminal B patients (hazard ratio: 2.546; 95% CI: 1.020-6.355; p = 0.045). Its expression was negatively correlated with the methylation status of multiple CpG sites (cg22214414, cg23241473 and cg07347645) in both luminal A and luminal B tumors.
Conclusion: Increased SYCP2 expression might be an independent indicator of shorter overall survival in both luminal A and luminal B patients.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.2217/fon-2018-0821 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!