Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/126811
Title: A Catalog of Genes Homozygously Deleted in Human Lung Cancer and the Candidacy of PTPRD as a Tumor Suppressor Gene
Author: Kohno, Takashi
Otsuka, Ayaka
Girard, Luc
Sato, Masanori
Iwakawa, Reika
Ogiwara, Hideaki
Sánchez Céspedes, Montserrat
Minna, John D.
Yokota, Jun
Keywords: Càncer de pulmó
Antioncogens
Lung cancer
Antioncogenes
Issue Date: Apr-2010
Publisher: Wiley
Abstract: A total of 176 genes homozygously deleted in human lung cancer were identified by DNA array-based whole genome scanning of 52 lung cancer cell lines and subsequent genomic PCR in 74 cell lines, including the 52 cell lines scanned. One or more exons of these genes were homozygously deleted in one (1%) to 20 (27%) cell lines. These genes included known tumor suppressor genes, e.g., CDKN2A/p16, RB1, and SMAD4, and candidate tumor suppressor genes whose hemizygous or homozygous deletions were reported in several types of human cancers, such as FHIT KEAP1, and LRP1B/LRP-DIP CDKN2A/p16 and p14ARF located in 9p21 were most frequently deleted (20/74, 27%). The PTPRD gene was most frequently deleted (8/74, 1 1%) among genes mapping to regions other than 9p21. Somatic mutations, including a nonsense mutation, of the PTPRD gene were detected in 8/74 (11%) of cell lines and 4/95 (4%) of surgical specimens of lung cancer. Reduced PTPRD expression was observed in the majority (>80%) of cell lines and surgical specimens of lung cancer. Therefore, PTPRD is a candidate tumor suppressor gene in lung cancer. Microarray-based expression profiling of 19 lung cancer cell lines also indicated that some of the 176 genes, such as KANK and ADAMTS1, are preferentially inactivated by epigenetic alterations. Genetic/epigenetic as well as functional studies of these 176 genes will increase our understanding of molecular mechanisms behind lung carcinogenesis. (C) 2010 Wiley-Liss, Inc.
Note: Versió postprint del document publicat a: https://doi.org/10.1002/gcc.20746
It is part of: Genes Chromosomes & Cancer, 2010, vol. 49, num. 4, p. 342-352
URI: http://hdl.handle.net/2445/126811
Related resource: https://doi.org/10.1002/gcc.20746
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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