Neural cell adhesion molecule (N-CAM) in gastrointestinal neoplasias. 1997

P Fogar, and D Basso, and C Pasquali, and M De Paoli, and C Sperti, and G Roveroni, and S Pedrazzoli, and M Plebani
Department of Laboratory Medicine, University of Padova, Italy.

BACKGROUND The neural adhesion molecule N-CAM, a membrane bound glycoprotein, seems to play an important role in the development of normal tissue architecture and in contact-dependent inhibition of cell growth. METHODS We evaluated the behaviour of circulating N-CAM in patients with pancreatic cancer (24 cases) and chronic pancreatitis (15 cases) and compared it with that of 20 controls, 6 patients with colon adenoma, 31 with colorectal cancer or 21 with gastric cancer and ascertained the influence of tumor stage and grade on the findings. RESULTS N-CAM levels were significantly lower in patients with pancreatic cancer and chronic pancreatitis than in the other groups studied. High levels were found only in few colorectal carcinoma patients (4/31). No correlation was found between tumor stage and N-CAM levels when pancreatic and colorectal cancer were considered. However, low N-CAM levels were found in 50% of advanced, but not in early gastric cancer. When pancreatic, colorectal and gastric cancer were considered, poorly differentiated (G3) had lower levels of N-CAM than well (G1) or moderately (G2) differentiated tumors. The variations found in circulating N-CAM were comparable to those in CEA but not to those in CA 19-9. CONCLUSIONS a) perhaps because of its higher aggressiveness, pancreatic cancer is associated with low serum N-CAM levels unlike other gastrointestinal neoplasias; b) the association between aggressiveness and reduced N-CAM levels is borne out by the correlation found with the grade of differentiation; c) the reduced levels found in chronic pancreatitis suggest that this molecule plays a role in stromaparenchymal interactions, which might be altered in the presence of fibrotic phenomena.

UI MeSH Term Description Entries
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D009367 Neoplasm Staging Methods which attempt to express in replicable terms the extent of the neoplasm in the patient. Cancer Staging,Staging, Neoplasm,Tumor Staging,TNM Classification,TNM Staging,TNM Staging System,Classification, TNM,Classifications, TNM,Staging System, TNM,Staging Systems, TNM,Staging, Cancer,Staging, TNM,Staging, Tumor,System, TNM Staging,Systems, TNM Staging,TNM Classifications,TNM Staging Systems
D005260 Female Females
D005770 Gastrointestinal Neoplasms Tumors or cancer of the GASTROINTESTINAL TRACT, from the MOUTH to the ANAL CANAL. Gastrointestinal Cancer,Cancer of Gastrointestinal Tract,Cancer of the Gastrointestinal Tract,Neoplasms, Gastrointestinal,Cancer, Gastrointestinal,Cancers, Gastrointestinal,Gastrointestinal Cancers,Gastrointestinal Neoplasm,Gastrointestinal Tract Cancer,Gastrointestinal Tract Cancers,Neoplasm, Gastrointestinal
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults
D000368 Aged A person 65 years of age or older. For a person older than 79 years, AGED, 80 AND OVER is available. Elderly
D000369 Aged, 80 and over Persons 80 years of age and older. Oldest Old
D019006 Neural Cell Adhesion Molecules Cell adhesion molecule involved in a diverse range of contact-mediated interactions among neurons, astrocytes, oligodendrocytes, and myotubes. It is widely but transiently expressed in many tissues early in embryogenesis. Four main isoforms exist, including CD56; (CD56 ANTIGEN); but there are many other variants resulting from alternative splicing and post-translational modifications. (From Pigott & Power, The Adhesion Molecule FactsBook, 1993, pp115-119) Cell Adhesion Molecule, Neural,NCAM,Neural Cell Adhesion Molecule,Cell Adhesion Molecules, Neural

Related Publications

P Fogar, and D Basso, and C Pasquali, and M De Paoli, and C Sperti, and G Roveroni, and S Pedrazzoli, and M Plebani
September 2014, Annals of medicine and surgery (2012),
P Fogar, and D Basso, and C Pasquali, and M De Paoli, and C Sperti, and G Roveroni, and S Pedrazzoli, and M Plebani
November 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience,
P Fogar, and D Basso, and C Pasquali, and M De Paoli, and C Sperti, and G Roveroni, and S Pedrazzoli, and M Plebani
January 1994, Cytobios,
P Fogar, and D Basso, and C Pasquali, and M De Paoli, and C Sperti, and G Roveroni, and S Pedrazzoli, and M Plebani
September 1984, Science (New York, N.Y.),
P Fogar, and D Basso, and C Pasquali, and M De Paoli, and C Sperti, and G Roveroni, and S Pedrazzoli, and M Plebani
July 1990, FEBS letters,
P Fogar, and D Basso, and C Pasquali, and M De Paoli, and C Sperti, and G Roveroni, and S Pedrazzoli, and M Plebani
January 1990, The Journal of cell biology,
P Fogar, and D Basso, and C Pasquali, and M De Paoli, and C Sperti, and G Roveroni, and S Pedrazzoli, and M Plebani
May 2002, Biotechnic & histochemistry : official publication of the Biological Stain Commission,
P Fogar, and D Basso, and C Pasquali, and M De Paoli, and C Sperti, and G Roveroni, and S Pedrazzoli, and M Plebani
July 1985, Proceedings of the National Academy of Sciences of the United States of America,
P Fogar, and D Basso, and C Pasquali, and M De Paoli, and C Sperti, and G Roveroni, and S Pedrazzoli, and M Plebani
March 1989, Brain research,
P Fogar, and D Basso, and C Pasquali, and M De Paoli, and C Sperti, and G Roveroni, and S Pedrazzoli, and M Plebani
March 1992, Developmental biology,
Copied contents to your clipboard!