z-logo
open-access-imgOpen Access
High expression of cytokeratin CAM5.2 in esophageal squamous cell carcinoma is associated with poor prognosis
Author(s) -
Songbing He,
Jie Peng,
Lei Li,
Ying Xü,
Xiaoxiao Wu,
Juan Yu,
Jianli Liu,
Jinguo Zhang,
Renya Zhang,
Wei Wang
Publication year - 2019
Publication title -
medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.59
H-Index - 148
eISSN - 1536-5964
pISSN - 0025-7974
DOI - 10.1097/md.0000000000017104
Subject(s) - medicine , immunohistochemistry , oncology , esophageal cancer , cytokeratin , tissue microarray , pathological , esophageal squamous cell carcinoma , lymph node , carcinoma , metastasis , retrospective cohort study , population , pathology , cancer , environmental health
Abstract Esophageal cancer is a common human malignant tumor with high mortality. Glandular epithelial markers, such as CAM5.2, can be expressed in esophageal squamous cell carcinoma (ESCC), but the clinical significance of these cells in ESCC remains elusive. Immunohistochemical analysis of CAM5.2 was performed on 604 ESCC specimens using tissue microarray. Our study design and study population used retrospective cohorts based on the hospital information system and pathological information management system which included medical information, date of admission, procedures undergone, registration, examinations, and medication. In total, positive staining of CAM5.2 was 145 of 604 (24%). Statistical analysis showed that the expression of CAM5.2 had no relationship with sex, age, tumor differentiation, tumor size, tumor-node-metastasis (TNM) classification, and lymph node metastasis, but it was significantly associated with poor prognosis of overall survival ( P  = .0041) and disease-free survival ( P  = .0048) in ESCC patients. Herein, we report for the first time that the high expression of the CAM 5.2 is an independent predictor of poor prognosis in patients with ESCC.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here