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Article

A longitudinal study of CEACAM1 expression in melanoma disease progression

  • Authors:
    • Douglas Zippel
    • Hani Barlev
    • Rona Ortenberg
    • Iris Barshack
    • Jacob Schachter
    • Gal Markel
  • View Affiliations / Copyright

    Affiliations: Department of Surgery C, Chaim Sheba Medical Center, Tel Hashomer, Israel, Ella Institute of Melanoma, Chaim Sheba Medical Center, Tel Hashomer, Israel, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel
  • Pages: 1314-1318
    |
    Published online on: December 30, 2014
       https://doi.org/10.3892/or.2014.3703
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Abstract

The present study characterized the carcinoembryonic antigen-related cell adhesion molecule 1 (CEACAM1) expression profile in a longitudinal study during melanoma progression, in lesions obtained from the same patients: a primary skin lesion, a lymph node and a distant metastasis. The present study is expected to increase our understanding of the expression patterns of CEACAM1 in melanoma development. We identified 20 patients who could be analyzed for CEACAM1 expression over the course of disease progression. The pathology blocks were cut, and two slides were generated for each specimen. One underwent standard hematoxylin and eosin (H&E) staining and a corresponding slide underwent immunohistochemical staining for the detection of CEACAM1. For 13 patients who were able to be followed up serially from primary lesion, lymph node and distant metastasis, a borderline significant increase in the staining of the membrane was noted (P=0.06). In contrast, there was no equivalent increase in cytoplasmic CEACAM1 in the same group of patients. For the cohort of 20 patients with primary and distant metastasis, a significant increase in the membrane staining was noted (P=0.026) and again, no equivalent significant increase in cytoplasmic staining was observed. We report that CEACAM1 expression increases along the course of disease development and progression of a patient. CEACAM1 represents a novel area of research which may have profound influence in future methods of harnessing cellular immunity to combat this disease. The results of the present study confirm that CEACAM1 is potentially an extremely useful target in arresting melanoma progression.
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Copy and paste a formatted citation
Spandidos Publications style
Zippel D, Barlev H, Ortenberg R, Barshack I, Schachter J and Markel G: A longitudinal study of CEACAM1 expression in melanoma disease progression. Oncol Rep 33: 1314-1318, 2015.
APA
Zippel, D., Barlev, H., Ortenberg, R., Barshack, I., Schachter, J., & Markel, G. (2015). A longitudinal study of CEACAM1 expression in melanoma disease progression. Oncology Reports, 33, 1314-1318. https://doi.org/10.3892/or.2014.3703
MLA
Zippel, D., Barlev, H., Ortenberg, R., Barshack, I., Schachter, J., Markel, G."A longitudinal study of CEACAM1 expression in melanoma disease progression". Oncology Reports 33.3 (2015): 1314-1318.
Chicago
Zippel, D., Barlev, H., Ortenberg, R., Barshack, I., Schachter, J., Markel, G."A longitudinal study of CEACAM1 expression in melanoma disease progression". Oncology Reports 33, no. 3 (2015): 1314-1318. https://doi.org/10.3892/or.2014.3703
Copy and paste a formatted citation
x
Spandidos Publications style
Zippel D, Barlev H, Ortenberg R, Barshack I, Schachter J and Markel G: A longitudinal study of CEACAM1 expression in melanoma disease progression. Oncol Rep 33: 1314-1318, 2015.
APA
Zippel, D., Barlev, H., Ortenberg, R., Barshack, I., Schachter, J., & Markel, G. (2015). A longitudinal study of CEACAM1 expression in melanoma disease progression. Oncology Reports, 33, 1314-1318. https://doi.org/10.3892/or.2014.3703
MLA
Zippel, D., Barlev, H., Ortenberg, R., Barshack, I., Schachter, J., Markel, G."A longitudinal study of CEACAM1 expression in melanoma disease progression". Oncology Reports 33.3 (2015): 1314-1318.
Chicago
Zippel, D., Barlev, H., Ortenberg, R., Barshack, I., Schachter, J., Markel, G."A longitudinal study of CEACAM1 expression in melanoma disease progression". Oncology Reports 33, no. 3 (2015): 1314-1318. https://doi.org/10.3892/or.2014.3703
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