TY - JOUR
T1 - An anti-adenoma antibody, Adnab-9, may reflect the risk for neoplastic progression in familial hamartomatous polyposis syndromes
AU - Tobi, Martin
AU - Kam, Michael
AU - Ullah, Nadeem
AU - Qureshi, Kashif
AU - Yordanova, Violeta
AU - Hatfield, James
AU - Fligiel, Suzanne E.G.
AU - Sochacki, Paula
AU - McGarrity, Thomas
AU - Cole, Carolyn
AU - Lawson, Michael
AU - Jacoby, Russell
N1 - Funding Information:
Acknowledgements The authors would like to express their gratitude to Susan Katz, BA, for assistance with specimen collection. The work was supported in part by a Department of Veterans Affairs (VAMC) grant awarded to Dr. Martin Tobi, a Kaiser Permanente Research Foundation grant to Dr. Michael Lawson, and a VAMC Merit Review Grant to Dr. Russell Jacoby. This paper is dedicated to the memory of Irwin Stein.
PY - 2008/3
Y1 - 2008/3
N2 - Patients with the hamartomatous polyposis Peutz-Jeghers and familial juvenile polyposis syndromes are predisposed to colorectal cancer but lack early genetic alterations found in adenomatous premalignant lesions. We studied hamartomatous polyps for the expression of an early preneoplastic colorectal neoplasia risk marker also found in familial adenomatous polyposis patients. Retrospective, genetic, and hospital archival tissue immunohistochemistry using Adnab-9, a premalignant marker often found in Paneth-like cells (PCs), was performed on sections of polyps from eight patients with Peutz-Jeghers syndrome, eight patients with familial juvenile polyposis, and 36 hyperplastic polyp control sections. Anti-α-defensin 5 (AD5), a universal PC marker, was also used to label a subgroup of sections. Hamartomatous polyposis patients also underwent specific genetic analysis. Eighty-nine percent of Peutz-Jeghers syndrome polyps labeled with Adnab-9 compared with 63% for AD5; 88% of familial juvenile polyposis sections also labeled with Adnab-9. Of the 36 hyperplastic polyp sections, only four (11%) labeled with Adnab-9 and one (3%) with AD5. Adnab-9 labeling of PCs in the epithelial elements of hamartomatous colonic lesions of hereditary hamartomatous syndrome patients reflects the predisposition to colorectal cancer, further justifying early intervention strategies.
AB - Patients with the hamartomatous polyposis Peutz-Jeghers and familial juvenile polyposis syndromes are predisposed to colorectal cancer but lack early genetic alterations found in adenomatous premalignant lesions. We studied hamartomatous polyps for the expression of an early preneoplastic colorectal neoplasia risk marker also found in familial adenomatous polyposis patients. Retrospective, genetic, and hospital archival tissue immunohistochemistry using Adnab-9, a premalignant marker often found in Paneth-like cells (PCs), was performed on sections of polyps from eight patients with Peutz-Jeghers syndrome, eight patients with familial juvenile polyposis, and 36 hyperplastic polyp control sections. Anti-α-defensin 5 (AD5), a universal PC marker, was also used to label a subgroup of sections. Hamartomatous polyposis patients also underwent specific genetic analysis. Eighty-nine percent of Peutz-Jeghers syndrome polyps labeled with Adnab-9 compared with 63% for AD5; 88% of familial juvenile polyposis sections also labeled with Adnab-9. Of the 36 hyperplastic polyp sections, only four (11%) labeled with Adnab-9 and one (3%) with AD5. Adnab-9 labeling of PCs in the epithelial elements of hamartomatous colonic lesions of hereditary hamartomatous syndrome patients reflects the predisposition to colorectal cancer, further justifying early intervention strategies.
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U2 - 10.1007/s10620-007-9947-5
DO - 10.1007/s10620-007-9947-5
M3 - Article
C2 - 17934846
AN - SCOPUS:39849105351
SN - 0163-2116
VL - 53
SP - 723
EP - 729
JO - Digestive Diseases and Sciences
JF - Digestive Diseases and Sciences
IS - 3
ER -