help button home button Am J Pathol International Conference on Pathology of Chest Diseases
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Purchase Article
Right arrow View Shopping Cart
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Finkelstein, S. D.
Right arrow Articles by Yousem, S. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Finkelstein, S. D.
Right arrow Articles by Yousem, S. A.
(American Journal of Pathology. 1999;155:633-640.)
© 1999 American Society for Investigative Pathology


Regular Articles

11q13 Allelic Imbalance Discriminates Pulmonary Carcinoids from Tumorlets

A Microdissection-Based Genotyping Approach Useful in ClinicalPractice

Sydney D. Finkelstein*, Tsuyoshi Hasegawa*, Thomas Colby{dagger} and Samuel A. Yousem*

From the Department of Pathology,*
University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania; and the Department of Pathology,{dagger}
Mayo Clinic, Scottsdale, Arizona

Pulmonary tumorlets are minute neuroendocrine cell proliferations believed to be precursor lesions to pulmonary carcinoids. Little is known of their molecular pathogenesis because of their small size. Using tissue microdissection, we evaluated 11q13 region allelic imbalance in the pathogenesis of pulmonary tumorlet/carcinoid lesions. The int-2 gene was selected because of its chromosomal location at 11q13 in close proximity to MEN1, a tumor suppressor gene frequently mutated in familial forms of neuroendocrine cancer. Three cohorts of patients were studied: subjects with typical carcinoid tumors and coexisting tumorlets (n = 5), typical carcinoids without tumorlets (n = 6), and tumorlets alone without carcinoid lesions (n = 5). A total of 11 carcinoids and 11 tumorlets were microdissected from 4-µm-thick histological sections. Genotyping was designed to detect allelic imbalance of the int-2 gene and involved DNA sequencing of two closely spaced deoxynucleotide polymorphisms. Subjects shown to be informative were evaluated for allelic imbalance in tumorlet/carcinoid tissue. Eight of 11 (73%) carcinoids manifested allelic, in contrast to only one of 11 (9%) of tumorlets. Int-2 allelic imbalance was significantly associated with carcinoid tumor formation (P < 0.01). In patients having both carcinoid tumors and tumorlets, the latter showed allelic balance and were thus discordant in genotype with coexisting carcinoid excluding pathogenesis of tumorlets from intramucosal spread from carcinoid tumors. Int-2 allelic imbalance was shown to be an early event in carcinoid tumor formation by virtue of the absence of allelic imbalance for other common cancer-related gene disturbances involving 11p13 (Wilms' tumor), 3p25 (von-Hippel-Lindau), and 17p13 (p53). Demonstration of 11q13 allelic imbalance by microdissection/genotyping may be a useful discriminatory marker for pulmonary neuroendocrine neoplasia.





This article has been cited by other articles:


Home page
Am. J. Roentgenol.Home page
M. S. Ginsberg, O. Akin, D. M. Berger, M. F. Zakowski, and D. M. Panicek
Pulmonary Tumorlets: CT Findings
Am. J. Roentgenol., August 1, 2004; 183(2): 293 - 296.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Microbiol.Home page
H. Takeuchi, H. Fujita, F. Iwasaki, T. Takeuchi, K.-I. Imadome, T. Okumiya, T. Matsui, and M. Takahashi
A Case of Epstein-Barr Virus (EBV)-Associated Thymic Carcinoid and Investigation of Existence of EBV-Infected Cells in Thymus and Thymic Tumors
J. Clin. Microbiol., June 1, 2004; 42(6): 2850 - 2854.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
B. Zhao, S. S. Chua, M. M. Burcin, S. D. Reynolds, B. R. Stripp, R. A. Edwards, M. J. Finegold, S. Y. Tsai, and F. J. DeMayo
Phenotypic consequences of lung-specific inducible expression of FGF-3
PNAS, April 25, 2001; (2001) 101116598.
[Abstract] [Full Text]


Home page
Proc. Natl. Acad. Sci. USAHome page
B. Zhao, S. S. Chua, M. M. Burcin, S. D. Reynolds, B. R. Stripp, R. A. Edwards, M. J. Finegold, S. Y. Tsai, and F. J. DeMayo
Phenotypic consequences of lung-specific inducible expression of FGF-3
PNAS, May 8, 2001; 98(10): 5898 - 5903.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1999 by the American Society for Investigative Pathology.