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Prognostic value of the immune target CEACAM6 in cancer: a meta-analysis

Authors :
Instituto de Salud Carlos III
Acepain Albacete
Diputación de Albacete
Centro de Investigación Biomédica en Red Cáncer (España)
Fundación CRIS contra el Cáncer
Universidad de Castilla La Mancha
Junta de Comunidades de Castilla-La Mancha
Burgos, Miguel
Cavero-Redondo, Iván
Álvarez-Bueno, Celia
Galán-Moya, Eva María
Pandiella, Atanasio
Amir, Eitan
Ocaña, Alberto
Instituto de Salud Carlos III
Acepain Albacete
Diputación de Albacete
Centro de Investigación Biomédica en Red Cáncer (España)
Fundación CRIS contra el Cáncer
Universidad de Castilla La Mancha
Junta de Comunidades de Castilla-La Mancha
Burgos, Miguel
Cavero-Redondo, Iván
Álvarez-Bueno, Celia
Galán-Moya, Eva María
Pandiella, Atanasio
Amir, Eitan
Ocaña, Alberto
Publication Year :
2022

Abstract

[Background]: Identification of membrane proteins differentially expressed on tumor cells is a key step in drug development. The carcinoembryonic antigen-related cell adhesion molecule 6 (CEACAM6) is a cell adhesion protein belonging to the immunoglobulin superfamily. Here, we explore the prognostic role CEACAM6 expression on patient outcome in cancer. [Methods]: A systematic search for studies evaluating the association between tumor expression of CEACAM6 and overall survival (OS) and disease-free survival (DFS) was performed. Hazard ratios (HR) were pooled in a meta-analysis using generic inverse variance and random effect modeling. Subgroup analyses were conducted based on tumor type and method of HR extraction. [Results]: Sixteen studies met the inclusion criteria. CEACAM6 expression was associated with worse OS [HR = 1.96, 95% confidence interval (CI) = 1.51–2.53], and DFS (HR = 2.49, 95% CI = 2.01–3.07) with subgroup analysis showing no significant differences between disease site subgroups. [Conclusions]: High expression of CEACAM6 is associated with worse OS and DFS in different malignancies. CEACAM6 is a target for the future development of novel therapeutics.

Details

Database :
OAIster
Publication Type :
Electronic Resource
Accession number :
edsoai.on1356199772
Document Type :
Electronic Resource