» Articles » PMID: 19701705

PIK3CA Expression in Invasive Breast Cancer: a Biomarker of Poor Prognosis

Overview
Specialty Oncology
Date 2009 Aug 25
PMID 19701705
Citations 41
Authors
Affiliations
Soon will be listed here.
Abstract

The implications of Phosphatidylinositol 3-kinase (PIK3CA) mutations and its aberrant protein expression in breast cancer (BC) different molecular subtypes and patients' outcome remain controversial. The aims of this study were to assess the prevalence and clinical significance of PIK3CA protein expression in BC and to determine its association with its different molecular classes. PIK3CA protein expression was assessed in a well-characterized series of early stage BC (n = 1,394) with long-term follow-up, using tissue microarrays and immunohistochemistry. Associations between PIK3CA expression and clinicopathological variables, molecular classes, and patients' outcome were investigated. Positive PIK3CA expression was associated with poor prognostic variables including higher grade, larger size, nodal involvement, vascular invasion, and higher proliferative fraction (P < 0.001). Increased PIK3CA expression was associated with the basal-like breast cancer (BLBC) and HER2-positive classes as well as triple negative non-basal (TNnon-B) tumors (P < 0.001). The luminal class showed reduced PIK3CA expression relative to other classes. Patients with PIK3CA positive tumors had shorter BC specific and disease free survival, independent of other prognostic factors except grade. Similar associations with outcome were found when the analysis was restricted to the large luminal class of tumors. PIK3CA is an oncogenic biomarker associated with poor prognosis in BC. Although, PIK3CA over-expression was more prevalent in BLBC and HER2-positive tumors it appeared to be a marker of poor differentiation rather than of a particular subtype. Thus, targeting of PIK3CA using specific inhibitors could potentially be beneficial, particularly for patients with more aggressive poorly differentiated tumors, irrespective of their molecular subtype.

Citing Articles

SLC1A5 is a key regulator of glutamine metabolism and a prognostic marker for aggressive luminal breast cancer.

Alfarsi L, Ansari R, Erkan B, Fakroun A, Craze M, Aleskandarany M Sci Rep. 2025; 15(1):2805.

PMID: 39843491 PMC: 11754656. DOI: 10.1038/s41598-025-87292-1.


Guidelines for diagnosis and treatment of advanced breast cancer in China (2022 edition).

J Natl Cancer Cent. 2024; 4(2):107-127.

PMID: 39282589 PMC: 11390704. DOI: 10.1016/j.jncc.2023.12.001.


PIK3CA mutational status in tissue and plasma as a prognostic biomarker in HR+/HER2- breast cancer.

Teran E, Lozano R, Rodriguez C, Abad M, Figuero L, Munoz J Cancer Med. 2024; 13(17):e70101.

PMID: 39235099 PMC: 11375731. DOI: 10.1002/cam4.70101.


Molecular signaling and clinical implications in the human aging-cancer cycle.

Rezaeian A, Wei W Semin Cancer Biol. 2024; 106-107:28-42.

PMID: 39197809 PMC: 11625621. DOI: 10.1016/j.semcancer.2024.08.003.


CD74-AKT Axis Is a Potential Therapeutic Target in Triple-Negative Breast Cancer.

Wang J, Huang D, Nguyen T, Phan L, Wei W, Rezaeian A Biology (Basel). 2024; 13(7).

PMID: 39056676 PMC: 11274071. DOI: 10.3390/biology13070481.