» Articles » PMID: 26170987

Fascin Expression Predicts an Aggressive Clinical Course in Patients with Advanced Breast Cancer

Overview
Journal Oncol Lett
Specialty Oncology
Date 2015 Jul 15
PMID 26170987
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

Fascin is an actin cross-linking protein, which regulates actin dynamics and filopodia or spike formation, as well as the epithelial-mesenchymal transition, and has been implicated in cell motility. Although, fascin is pivotal in mediating the aggressive behaviour of various types of cancer, its prognostic significance according to tumour stage has yet to be evaluated. Therefore, the present study investigated fascin expression in 194 patients diagnosed with invasive ductal carcinoma of the breast between 2000 and 2005. Fascin protein expression levels were evaluated by immunostaining on a tissue microarray, and the association between fascin expression and various clinicopathological parameters was analysed. Fascin expression was significantly correlated with various clinicopathological parameters, including high histological grade, tumour necrosis, resistance to adjuvant therapy, high expression of p53 and Ki-67 and specific therapeutic markers (oestrogen and progesterone receptor negativity; all P<0.05). Furthermore, univariate and multivariate analyses identified a significant association between fascin expression, and poor disease-free and overall survival, in late-stage breast cancer (all P<0.05). Therefore, fascin may be crucial in predicting aggressive tumour behaviour, particularly in patients with advanced-stage disease that has acquired the properties of migration and invasion.

Citing Articles

Comparative Analysis of Breast Cancer Metabolomes Highlights Fascin's Central Role in Regulating Key Pathways Related to Disease Progression.

AlMalki R, Al-Nasrallah H, Aldossry A, Barnawi R, Al-Khaldi S, Almozyan S Int J Mol Sci. 2024; 25(14).

PMID: 39063133 PMC: 11277536. DOI: 10.3390/ijms25147891.


The association of FSCN1 (rs852479, rs1640233) and HOTAIR (rs920778) polymorphisms with the risk of breast cancer in Egyptian women.

Galal E, Abdelhakam D, Ahmed L, Elhusseny Y, Sayed S, Eltaweel N Mol Biol Rep. 2024; 51(1):495.

PMID: 38587571 PMC: 11001669. DOI: 10.1007/s11033-024-09459-9.


AEBP1 promotes papillary thyroid cancer progression by activating BMP4 signaling.

Ju G, Xing T, Xu M, Zhang X, Sun Y, Mu Z Neoplasia. 2024; 49:100972.

PMID: 38237535 PMC: 10828808. DOI: 10.1016/j.neo.2024.100972.


Fascin-1 in Cancer Cell Metastasis: Old Target-New Insights.

Sarantelli E, Mourkakis A, Zacharia L, Stylianou A, Gkretsi V Int J Mol Sci. 2023; 24(14).

PMID: 37511011 PMC: 10379093. DOI: 10.3390/ijms241411253.


Fascin-1: Updated biological functions and therapeutic implications in cancer biology.

Li C, Chan M, Liang S, Chang Y, Hsiao M BBA Adv. 2023; 2:100052.

PMID: 37082587 PMC: 10074911. DOI: 10.1016/j.bbadva.2022.100052.


References
1.
Ogston K, Miller I, Payne S, Hutcheon A, Sarkar T, Smith I . A new histological grading system to assess response of breast cancers to primary chemotherapy: prognostic significance and survival. Breast. 2003; 12(5):320-7. DOI: 10.1016/s0960-9776(03)00106-1. View

2.
Feeley L, Mulligan A, Pinnaduwage D, Bull S, Andrulis I . Distinguishing luminal breast cancer subtypes by Ki67, progesterone receptor or TP53 status provides prognostic information. Mod Pathol. 2013; 27(4):554-61. DOI: 10.1038/modpathol.2013.153. View

3.
Harris L, Fritsche H, Mennel R, Norton L, Ravdin P, Taube S . American Society of Clinical Oncology 2007 update of recommendations for the use of tumor markers in breast cancer. J Clin Oncol. 2007; 25(33):5287-312. DOI: 10.1200/JCO.2007.14.2364. View

4.
Jayo A, Parsons M . Fascin: a key regulator of cytoskeletal dynamics. Int J Biochem Cell Biol. 2010; 42(10):1614-7. DOI: 10.1016/j.biocel.2010.06.019. View

5.
Puppa G, Maisonneuve P, Sonzogni A, Masullo M, Chiappa A, Valerio M . Independent prognostic value of fascin immunoreactivity in stage III-IV colonic adenocarcinoma. Br J Cancer. 2007; 96(7):1118-26. PMC: 2360113. DOI: 10.1038/sj.bjc.6603690. View