Related Experiment Video
Updated: Mar 28, 2026

The In ovo CAM-assay as a Xenograft Model for Sarcoma
Published on: July 17, 2013
Serum CEACAM1 Elevation Correlates with Melanoma Progression and Failure to Respond to Adoptive Cell Transfer
R Ortenberg1, S Sapoznik1, D Zippel1
1The Ella Lemelbaum Institute for Melanoma, Sheba Medical Center, 52621 Tel Hashomer, Israel.
Abstract:
Malignant melanoma is a devastating disease whose incidences are continuously rising. The recently approved antimelanoma therapies carry new hope for metastatic patients for the first time in decades. However, the clinical management of melanoma is severely hampered by the absence of effective screening tools. The expression of the CEACAM1 adhesion molecule on melanoma cells is a strong predictor of poor prognosis. Interestingly, a melanoma-secreted form of CEACAM1 (sCEACAM1) has recently emerged as a potential tumor biomarker. Here we add novel evidences supporting the prognostic role of serum CEACAM1 by using a mice xenograft model of human melanoma and showing a correlation between serum CEACAM1 and tumor burden. Moreover, we demonstrate that serum CEACAM1 is elevated over time in progressive melanoma patients who fail to respond to immunotherapy as opposed to responders and stable disease patients, thus proving a correlation between sCEACAM1, response to treatment, and clinical deterioration.
Insights
Serum CEACAM1 shows promise as a biomarker for melanoma progression and treatment response. Elevated levels correlate with tumor burden and predict poor outcomes in immunotherapy-treated patients.
Area of Science:
- Oncology
- Molecular Biology
- Immunology
Background:
- Malignant melanoma incidence is rising, necessitating improved screening and prognostic tools.
- Current treatments offer hope for metastatic melanoma, but clinical management is challenged by a lack of effective screening.
- Carcinine antigen 1 (CEACAM1) expression on melanoma cells predicts poor prognosis, with a secreted form (sCEACAM1) emerging as a potential biomarker.
Purpose of the Study:
- To investigate the prognostic role of serum CEACAM1 in melanoma.
- To correlate serum CEACAM1 levels with tumor burden in a preclinical model.
- To assess the relationship between serum CEACAM1 and response to immunotherapy in melanoma patients.
Main Methods:
- Utilized a mice xenograft model of human melanoma to assess serum CEACAM1.
- Monitored serum CEACAM1 levels over time in melanoma patients undergoing immunotherapy.
- Correlated serum CEACAM1 levels with tumor burden and treatment response (progressive disease, stable disease, responders).
Main Results:
- Demonstrated a correlation between serum CEACAM1 levels and tumor burden in the mice xenograft model.
- Observed elevated serum CEACAM1 levels in melanoma patients with progressive disease who did not respond to immunotherapy.
- Showed significantly lower serum CEACAM1 levels in immunotherapy responders and patients with stable disease.
Conclusions:
- Serum CEACAM1 serves as a valuable prognostic biomarker in melanoma.
- Elevated sCEACAM1 levels are associated with clinical deterioration and lack of response to immunotherapy.
- sCEACAM1 holds potential for monitoring melanoma progression and treatment efficacy.
More Related Videos
06:25Author Spotlight: Assessing the Potential of Circulating Tumor Cells in Leptomeningeal Disease Research
Published on: March 29, 2024
07:47Author Spotlight: Unveiling Transmembrane Protein Family-Related Markers in Gastric Cancer and Implications for Targeted Therapies
Published on: September 15, 2023
Related Concept Videos
Skin Cancer
Basal Cell Carcinoma (BCC): BCC is the most common type of skin cancer, accounting for about 80% of cases. It typically develops in...
Tumor Immunotherapy
Tumor Progression
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...
Tumor Progression
Immunoglobulin-like Cell Adhesion Molecules
Ig-CAMs exhibit either homophilic binding (to other Ig-CAMs) or heterophilic binding (to other ligands such as integrins). While most Ig-CAMs...