PER1 Serves as a Tumor Suppressor in Breast Cancer by Regulating MEK5/ERK5 Signaling Pathway.

Background: Breast cancer (BC) is one of the most frequently diagnosed malignant tumors worldwide. Period circadian protein homolog 1 (PER1) is a primary component of the biorhythm molecular oscillation system. The objective of this study was to elucidate the association between PER1 and clinical BC outcomes and determine the potential effect of PER1 on BC tumor development. Methods: Immunohistochemical staining for PER1 was performed on 30 normal breast tissue and 172 BC samples. Those BC cases were categorized into two groups to analyze the prognostic significance of PER1 expression. The expression of key proteins in the MEK/ERK pathway (ERK1/2, ERK5, P38, JNK1/2/3) and their phosphorylation levels (p-ERK1/2, p-ERK5, p-P38, and p-JNK1/2/3) were elucidated by western blot test. XMD17-109, a specific ERK5 inhibitor, was used to treat BT-549 and MCF-7 BC cells with knockdown of PER1. Results: Increased PER1 expression was identified in 26 and 80 normal breast and BC tissues, respectively, whereas low expression was detected in 4 normal and 92 BC tissues. Although no differences were observed in the estrogen receptor (ER), menstrual cycle, TNM, progesterone receptor (PR), and HER-2 stages, age, and tumor size between the two cohorts, both the rate of axillary lymph node metastasis ( Conclusion: PER1 plays an anti-tumor role by regulating the MEK5/ERK5 pathway in BC.