Role of Urokinase Plasminogen Activator and Plasminogen Activator Inhibitor MRNA Expression As Prognostic Factors in Molecular Subtypes of Breast Cancer
Overview
Authors
Affiliations
Background: Protein levels of urokinase plasminogen activator (uPA) and its inhibitor (PAI-1) determined by enzyme-linked immunosorbent assay from fresh-frozen tumor tissue have been evaluated as prognostic factors in prospectively randomized trials in breast cancer. However, the role of uPA and PAI-1 in the context of breast cancer subtypes and for mRNA expression of these factors is less clear.
Methods: We evaluated uPA and PAI-1 mRNA expression using the Affymetrix HG-U 133A array within molecular subgroups of breast cancer in cohorts of patients with systemic treatment (cohort A, n=362) and without systemic treatment (cohort B, n=200). We validated mRNA expression in a cohort of HER2-positive breast cancer patients (cohort C, n=290). Luminal, triple-negative, and HER2-positive subcohorts were defined by ESR1 and ERBB2 mRNA expression using predefined cutoffs.
Results: In the entire cohort A, elevated PAI-1 but not uPA mRNA expression was associated with shorter disease-free survival (P=0.007 for PAI and 0.069 for uPA). Regarding different molecular subgroups, 67% (n=244) of tumors were luminal, 14% (n=49) were HER2-positive, and 19% (n=69) were triple-negative. Elevated PAI-1 mRNA expression was associated with shorter disease-free survival only in the HER2-positive subgroup (P=0.031). The same disease-free survival results were found for uPA in HER2-positive patients (P=0.011). In contrast, no association between either marker and survival was observed in the luminal or triple-negative subgroups. In the HER2-positive validation cohort C, elevated uPA and PAI-1 mRNA expression also showed strong associations with shorter disease-free survival (P=0.014 for PAI-1, P<0.001 for uPA).
Conclusion: In this study, the prognostic impact of uPA and PAI-1 expression was mainly observed in patients with HER2-positive tumors.
Poskus M, McDonald J, Laird M, Li R, Norcoss K, Zervantonakis I Cell Mol Bioeng. 2024; 17(5):491-506.
PMID: 39513002 PMC: 11538110. DOI: 10.1007/s12195-024-00823-0.
Exploring the multifaceted role of obesity in breast cancer progression.
Kakkat S, Suman P, Turbat-Herrera E, Singh S, Chakroborty D, Sarkar C Front Cell Dev Biol. 2024; 12():1408844.
PMID: 39040042 PMC: 11260727. DOI: 10.3389/fcell.2024.1408844.
Hurtado M, Tama E, DAndre S, Shufelt C Crit Rev Oncol Hematol. 2023; 193:104213.
PMID: 38008197 PMC: 10843740. DOI: 10.1016/j.critrevonc.2023.104213.
Zhang W, Yang S, Chen D, Yuwen D, Zhang J, Wei X Cell Mol Life Sci. 2022; 79(1):59.
PMID: 34997317 PMC: 11072091. DOI: 10.1007/s00018-021-04120-1.
The Importance of Breast Adipose Tissue in Breast Cancer.
Kothari C, Diorio C, Durocher F Int J Mol Sci. 2020; 21(16).
PMID: 32796696 PMC: 7460846. DOI: 10.3390/ijms21165760.