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.

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.

Related Concept Videos

Skin Cancer01:30

Skin Cancer

Skin cancer is a type of cancer that occurs when there is an abnormal growth of skin cells, usually triggered by damage to the DNA within the skin cells. It is primarily caused by exposure to ultraviolet (UV) radiation from the sun or artificial sources like tanning beds. Skin cancer is the most common type of cancer worldwide, and its incidence continues to rise.
Basal Cell Carcinoma (BCC): BCC is the most common type of skin cancer, accounting for about 80% of cases. It typically develops in...
6.6K
Tumor Immunotherapy01:27

Tumor Immunotherapy

Immunotherapy is a treatment that boosts or manipulates the immune system to fight diseases, including cancer. For instance, by stimulating an immune response through vaccinations against viruses that cause cancers, like hepatitis B virus and human papillomavirus, these diseases can be prevented. Nonetheless, some cancer cells can avoid the immune system due to their rapid mutation and division. The immune response to many cancers involves three phases: elimination, equilibrium, and escape.
2.2K
Tumor Progression02:07

Tumor Progression

Tumor progression is a phenomenon where the pre-formed tumor acquires successive mutations to become clinically more aggressive and malignant. In the 1950s, Foulds first described the stepwise progression of cancer cells through successive stages.
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...
7.8K
Tumor Progression02:07

Tumor Progression

3.5K
Immunoglobulin-like Cell Adhesion Molecules01:31

Immunoglobulin-like Cell Adhesion Molecules

Immunoglobulin-like cell adhesion molecules or Ig-CAMs are a versatile group of cell surface glycoproteins belonging to the immunoglobulin protein superfamily. Ig-CAMs possess the characteristic immunoglobulin protein domains and other domains such as the fibronectin type III domain. The Ig domains are glycosylated to varying degrees in different Ig-CAMs.
Ig-CAMs exhibit either homophilic binding (to other Ig-CAMs) or heterophilic binding (to other ligands such as integrins). While most Ig-CAMs...
4.6K