» Articles » PMID: 36309616

The Expression and Clinical Significance of STAMBP in Breast Cancer

Overview
Journal Mol Biol Rep
Specialty Molecular Biology
Date 2022 Oct 30
PMID 36309616
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Breast cancer is the leading cause of death from cancer in women worldwide. STAMBP functions as a JAMM family deubiquitinating enzyme that modulates the stability of substrate proteins in cells by cleaving ubiquitin moieties. The expression of STAMBP and its clinical significance in breast cancer remain unclear.

Methods And Results: The level of the STAMBP protein in noncancerous and tumor tissues of breast cancer patients was examined by immunohistochemical staining. The expression of STAMBP mRNA in tissues based on healthy individual and breast cancer patient data in the TCGA database was evaluated. The association between the expression of STAMBP mRNA and clinical features and prognosis was evaluated using TCGA database. Cell growth was assessed by Cell Counting Kit-8 (CCK-8) assay, and cell migration and invasion were assessed by wound healing and Transwell assays. Activation of the ERK signaling was detected by Western blotting. The expression of STAMBP was markedly upregulated in the cytoplasm of tumor cells from breast cancer patients. The level of STAMBP was closely associated with the tumor subtype and size and the TNM stage of the breast cancer patients. Importantly, high expression of STAMBP predicted poor overall survival (OS) for breast cancer patients. Furthermore, knockdown of STAMBP expression reduced cell mobility and invasion of breast cancer cells. Notably, the phosphorylation of EGFR and ERK was markedly reduced in STAMBP-knockdown cells.

Conclusion: STAMBP plays a critical role in the progression of breast cancer and may serve as a biomarker to monitor the progression of the disease.

Citing Articles

IL-20RA is Associated with the Risk of Diabetic Microangiopathy: A Bidirectional Mendelian Randomization Analysis and Clinical Validation.

Li J, Yang H, Wang T, Ruan N, Lin Y, Fang Z Diabetes Metab Syndr Obes. 2024; 17:4803-4816.

PMID: 39712242 PMC: 11663374. DOI: 10.2147/DMSO.S480366.


Identification of STAM-binding protein as a target for the treatment of gemcitabine resistance pancreatic cancer in a nutrient-poor microenvironment.

Zhang W, Xu Z, Du Y, Liu T, Xiong Z, Hu J Cell Death Dis. 2024; 15(9):657.

PMID: 39242557 PMC: 11379802. DOI: 10.1038/s41419-024-07048-z.