Fatty acid synthase expression and its association with clinicohistopathological features in triple-negative breast cancer

44Citations
Citations of this article
50Readers
Mendeley users who have this article in their library.

Abstract

Triple-Negative Breast Cancer (TNBC) has poor prognosis and no approved targeted therapy. We previously showed that the enzyme fatty acid synthase (FASN) was largely expressed in a small TNBC patients' cohort and its inhibition synergized with cetuximab in TNBC preclinical mouse models. Here, we evaluated FASN and EGFR expression in a cohort of TNBC patients and we study their prognostic role and their association with clinico-histopathological features, intrinsic TNBC subtypes and survival. FASN, EGFR, CK5/6 and vimentin expression were retrospective evaluated by Immunohistochemistry in 100 primary TNBC tumors. FASN expression was classified into high and low FASN groups. EGFR, CK5/6 and vimentin expression were used in TNBC intrinsic subtypes classification. FASN was expressed in most of the TNBC patients but did not correlate with overall survival or disease-free survival in this cohort. High FASN group was significantly associated with positive node status. FASN expression was significantly higher in Basal-Like patients than in Mesenchymal-Like ones. EGFR expression was positive in 50% of the tumors, and those patients showed poorer DFS. Altogether, our findings provide a rationale for further investigation the prognostic role of FASN and EGFR expression in a larger cohort of TNBC patients.

Author supplied keywords

Cite

CITATION STYLE

APA

Giró-Perafita, A., Sarrats, A., Pérez-Bueno, F., Oliveras, G., Buxó, M., Brunet, J., … Miquel, T. P. (2017). Fatty acid synthase expression and its association with clinicohistopathological features in triple-negative breast cancer. Oncotarget, 8(43), 74391–74405. https://doi.org/10.18632/oncotarget.20152

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free