Organ-specific expression of the colon cancer antigen A33, a cell surface target for antibody-based therapy

P Garinchesa1, J Sakamoto, S Welt

  • 1MEM SLOAN KETTERING CANC CTR,DEPT PATHOL,NEW YORK,NY 10021. MEM SLOAN KETTERING CANC CTR,LUDWIG INST CANC RES,NEW YORK,NY 10021. MEM SLOAN KETTERING CANC CTR,DEPT MED,NEW YORK,NY 10021. MEM SLOAN KETTERING CANC CTR,PROGRAM IMMUNOL,NEW YORK,NY 10021. AICHI CANC CTR,DEPT SURG GASTROENTEROL,NAGOYA,AICHI 464,JAPAN. INST MUNICIPAL INVEST MED,E-08003 BARCELONA,SPAIN.

Insights

Monoclonal antibody mAbA33 targets the A33 antigen, a protein found primarily in colorectal cancers. This study confirms A33

Area of Science:

  • Oncology
  • Immunology
  • Molecular Biology

Background:

  • Monoclonal antibody mAbA33 targets the A33 antigen, a cell surface protein expressed in colorectal cancer.
  • Previous studies indicated selective targeting of radio-labeled mAbA33 in metastatic colorectal cancer patients.
  • Understanding A33 antigen distribution is crucial for developing targeted A33-directed therapies.

Purpose of the Study:

  • To define the distribution of the A33 antigen in normal human organs.
  • To examine A33 antigen expression across a wide spectrum of tumor types.
  • To elucidate the basis for selective mAbA33 targeting in patients.

Main Methods:

  • Immunohistochemical analysis of normal tissues.
  • Evaluation of over 450 tumor samples for A33 antigen expression.
  • Assessment of expression patterns, including uniformity and heterogeneity.

Main Results:

  • The A33 antigen is primarily expressed in the large and small intestinal mucosa.
  • Tumors of the gastrointestinal tract, particularly colorectal cancers (95%), consistently show A33 positivity.
  • A33 expression was observed in subsets of gastric and pancreatic cancers, but generally absent in other tumor types.

Conclusions:

  • The A33 antigen is a highly specific, constitutively expressed, organ-specific epithelial membrane antigen.
  • Its restricted expression pattern makes it an ideal target for highly specific tumor targeting in colorectal cancer.
  • This finding supports the potential of A33-directed therapies for gastrointestinal malignancies.

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