Target intelligence / Profile preview

Carcinoembryonic antigen-related cell adhesion molecule 5 (CEACAM5), Carcinoembryonic antigen-related cell adhesion molecule 6 (CEACAM6) (CEACAM5, CEACAM6)

Target
CEACAM5, CEACAM6
Molecular classification
Cell adhesion molecule, GPI-anchored membrane glycoprotein, Tumor-associated antigen, Member of the immunoglobulin superfamily
01

Overview

Carcinoembryonic antigen-related cell adhesion molecule 5 (CEACAM5) and cell adhesion molecule 6 (CEACAM6) are glycosylphosphatidylinositol (GPI)-anchored cell surface glycoproteins and members of the immunoglobulin superfamily. Both function as adhesion molecules, facilitating homophilic and heterophilic cell-cell interactions and regulating differentiation, immune responses, and resistance to anoikis (cell death induced by detachment). CEACAM5 serves as a critical FDA-approved biomarker for colorectal cancer diagnosis and prognosis, while CEACAM6 is upregulated in various cancers and correlates with more aggressive phenotypes, including increased metastatic potential and chemoresistance. Their roles in promoting tumor progression are mediated through multiple signaling pathways, including ERK/MAPK, Src/FAK, and PI3K/AKT, and their expression is regulated at both the transcriptional and post-translational levels. Therapeutic targeting with monoclonal antibodies, siRNA, and other agents is under investigation, with the potential to modulate tumor cell adhesion, apoptosis, and drug sensitivity.

Other names
CEA (commonly for CEACAM5)CD66c (for CEACAM6)NCA-90 (for CEACAM6)Carcinoembryonic antigen (CEA; for CEACAM5 specifically)CEACAM5 is sometimes called tumor-associated antigen CEACEACAM6 is sometimes called NCA (non-specific cross-reacting antigen)
02

Mechanism of action

Antibodies: Block cell adhesion, disrupt signaling, and enhance apoptosis or anoikis sensitivity. siRNA: Knockdown of CEACAM6 reverses resistance to anoikis and promotes apoptosis. Chemotherapy: CEACAM5 and CEACAM6 overexpression mediates resistance to apoptosis induced by agents like 5-fluorouracil and gemcitabine; targeting these molecules enhances chemosensitivity. Oncolytic virus: CEACAM6 modulates adenovirus trafficking and antitumor efficacy via cytoskeletal interactions.

03

Biological functions

Cell adhesion (homophilic and heterophilic)Regulation of cell differentiationInhibition of anoikis (apoptosis induced by loss of adhesion)Immune modulationTumor invasion and metastasisSignal transduction (via Src, FAK, ERK/MAPK, PI3K/AKT pathways)Intercellular communication
04

Disease associations

Cancer (colon, pancreas, breast, lung, gallbladder, gastric, among others)Inflammatory bowel diseasePoor prognosis/relapse in several tumor typesChemoresistance and modulation of drug sensitivity
05

Safety considerations

Antibody-mediated targeting may affect normal cell adhesion, potentially leading to off-target effects on healthy tissues expressing CEACAM proteinsLoss of adhesion could theoretically trigger unwanted apoptosis in non-tumor tissuesGene silencing (e.g. siRNA) carries general risks of immune stimulation and off-target gene effectsOverexpression is associated with tumor progression, chemoresistance, and poor prognosis
06

Interacting drugs

Monoclonal antibodies targeting CEACAM5/CEACAM6 (e.g., anti-CEA antibody, anti-CEACAM6 antibody such as 8F5)

3 more in the full profile.

07

Biomarkers

CEACAM5 is FDA-approved as a diagnostic and prognostic marker for colon cancerCEACAM6 is considered an independent prognostic factor in colorectal cancer and other tumorsBoth are used clinically as indicators for tumor burden, progression, and relapse risk

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