Journal Article

Identification of <i>MEN1</i> Gene Mutations in Sporadic Carcinoid Tumors of the Lung

Larisa V. Debelenko, Elisabeth Brambilla, Sunita K. Agarwal, Jennifer I. Swalwell, Mary B. Kester, Irina A. Lubensky, Zhengping Zhuang, Siradanahalli C. Guru, Pachiappan Manickam, Shodimu-Emmanuel Olufemi, Settara C. Chandrasekharappa, Judy S. Crabtree, Young S. Kim, Christina Heppner, A. Lee Burns, Allen M. Spiegel, Stephen J. Marx, Lance A. Liotta, Francis S. Collins, William D. Travis and Michael R. Emmert-Buck

in Human Molecular Genetics

Volume 6, issue 13, pages 2285-2290
Published in print December 1997 | ISSN: 0964-6906
Published online December 1997 | e-ISSN: 1460-2083 | DOI:
Identification of MEN1 Gene Mutations in Sporadic Carcinoid Tumors of the Lung

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Lung carcinoids occur sporadically and rarely in association with multiple endocrine neoplasia type 1 (MEN1). There are no well defined genetic abnormalities known to occur in these tumors. We studied 11 sporadic lung carcinoids for loss of heterozygosity (LOH) at the locus of the MEN1 gene on chromosome 11q13, and for mutations of the MEN1 gene using dideoxy fingerprinting. Additionally, a lung carcinoid from a MEN1 patient was studied. In four of 11 (36%) sporadic tumors, both copies of the MEN1 gene were inactivated. All four tumors showed the presence of a MEN1 gene mutation and loss of the other allele. Observed mutations included a 1 bp insertion, a 1 bp deletion, a 13 bp deletion and a single nucleotide substitution affecting a donor splice site. Each mutation predicts truncation or potentially complete loss of menin. The remaining seven tumors showed neither the presence of a MEN1 gene mutation nor 11q13 LOH. The tumor from the MEN1 patient showed LOH at chromosome 11q13 and a complex germline MEN1 gene mutation. The data implicate the MEN1 gene in the pathogenesis of sporadic lung carcinoids, representing the first defined genetic alteration in these tumors.

Journal Article.  4159 words.  Illustrated.

Subjects: Genetics and Genomics

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