» Articles » PMID: 25265904

Nuclear Ep-ICD Accumulation Predicts Aggressive Clinical Course in Early Stage Breast Cancer Patients

Overview
Journal BMC Cancer
Publisher Biomed Central
Specialty Oncology
Date 2014 Oct 1
PMID 25265904
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Regulated intramembrane proteolysis of Epithelial cell adhesion molecule (EpCAM) results in release of its intracellular domain (Ep-ICD) which triggers oncogenic signalling. The clinical significance of Ep-ICD in breast cancer remains to be determined. Herein, we examined the expression of nuclear and cytoplasmic Ep-ICD, and membranous extracellular domain of EpCAM (EpEx) in breast cancer patients, to determine its potential utility in predicting aggressive clinical course of the disease.

Methods: In this retrospective study, 266 breast cancers and 45 normal breast tissues were immunohistochemically analyzed to determine the expression patterns of nuclear and cytoplasmic Ep-ICD and membranous EpEx and correlated with clinicopathological parameters and follow up. Disease-free survival was determined by Kaplan-Meier method and multivariate Cox regression analysis.

Results: Nuclear Ep-ICD was more frequently expressed in breast cancers compared to normal tissues. Significant association was observed between increased nuclear Ep-ICD expression and reduced disease-free survival in patients with ductal carcinoma in situ (DCIS) and invasive ductal carcinoma (IDC) (p < 0.001). Nuclear Ep-ICD was positive in all the 13 DCIS and 25 IDC patients who had reduced disease-free survival, while none of the nuclear Ep-ICD negative DCIS or IDC patients had recurrence during the follow up period. Notably, majority of IDC patients who had recurrence had early stage tumors. Multivariate Cox regression analysis identified nuclear Ep-ICD as the most significant predictive factor for reduced disease-free survival in IDC patients (p = 0.011, Hazard ratio = 80.18).

Conclusion: Patients with nuclear Ep-ICD positive breast cancers had poor prognosis. The high recurrence of disease in nuclear Ep-ICD positive patients, especially those with early tumor stage suggests that nuclear Ep-ICD accumulation holds the promise of identifying early stage patients with aggressive disease who are likely to be in need of more rigorous post-operative surveillance and/or treatment.

Citing Articles

Functional Implications of the Dynamic Regulation of EpCAM during Epithelial-to-Mesenchymal Transition.

Brown T, Sankpal N, Gillanders W Biomolecules. 2021; 11(7).

PMID: 34209658 PMC: 8301972. DOI: 10.3390/biom11070956.


Identification of Potential Phosphorylation in the Cytoplasmic Domain of Epithelial Cell Adhesion Molecule.

Mal A, Dey P, Hayes R, McCarthy J, Ray A, De A ACS Omega. 2020; 5(48):30808-30816.

PMID: 33324790 PMC: 7726786. DOI: 10.1021/acsomega.0c02113.


Epithelial Cell Adhesion Molecule: An Anchor to Isolate Clinically Relevant Circulating Tumor Cells.

Eslami-S Z, Cortes-Hernandez L, Alix-Panabieres C Cells. 2020; 9(8).

PMID: 32764280 PMC: 7464831. DOI: 10.3390/cells9081836.


Biology and clinical relevance of EpCAM.

Keller L, Werner S, Pantel K Cell Stress. 2019; 3(6):165-180.

PMID: 31225512 PMC: 6558934. DOI: 10.15698/cst2019.06.188.


Subcellular differential expression of Ep-ICD in oral dysplasia and cancer is associated with disease progression and prognosis.

Somasundaram R, Kaur J, Leong I, MacMillan C, Witterick I, Walfish P BMC Cancer. 2016; 16:486.

PMID: 27421772 PMC: 4947324. DOI: 10.1186/s12885-016-2507-7.

References
1.
Zahl P, Gotzsche P, Maehlen J . Natural history of breast cancers detected in the Swedish mammography screening programme: a cohort study. Lancet Oncol. 2011; 12(12):1118-24. DOI: 10.1016/S1470-2045(11)70250-9. View

2.
Carpenter G, Brewer M . EpCAM: another surface-to-nucleus missile. Cancer Cell. 2009; 15(3):165-6. DOI: 10.1016/j.ccr.2009.02.005. View

3.
Arriagada R, Le M, Dunant A, Tubiana M, Contesso G . Twenty-five years of follow-up in patients with operable breast carcinoma: correlation between clinicopathologic factors and the risk of death in each 5-year period. Cancer. 2006; 106(4):743-50. DOI: 10.1002/cncr.21659. View

4.
Siegel R, Naishadham D, Jemal A . Cancer statistics, 2012. CA Cancer J Clin. 2012; 62(1):10-29. DOI: 10.3322/caac.20138. View

5.
Chaudry M, Sales K, Ruf P, Lindhofer H, Winslet M . EpCAM an immunotherapeutic target for gastrointestinal malignancy: current experience and future challenges. Br J Cancer. 2007; 96(7):1013-9. PMC: 2360124. DOI: 10.1038/sj.bjc.6603505. View