Literature DB >> 9187130

FHIT and FRA3B 3p14.2 allele loss are common in lung cancer and preneoplastic bronchial lesions and are associated with cancer-related FHIT cDNA splicing aberrations.

K M Fong1, E J Biesterveld, A Virmani, I Wistuba, Y Sekido, S A Bader, M Ahmadian, S T Ong, F V Rassool, P V Zimmerman, G Giaccone, A F Gazdar, J D Minna.   

Abstract

We evaluated primary lung cancers, tumor cell lines, and preneoplastic bronchial lesions for molecular genetic abnormalities in the candidate tumor suppressor gene FHIT, which spans the FRA3B fragile site at 3p14.2. 3p14.2 allele loss was very frequent in 32 lung cancer cell lines [100% of small cell lung cancer and 88% of non-small cell lung cancer (NSCLC)] and 108 primary NSCLC cancers (45%), with numerous breakpoints indicating involvement of several distinct regions in the FRA3B site. 3p14 allele loss was least frequent in the adenocarcinoma subtype and occurred at the relatively late carcinoma in situ stage of preneoplastic bronchial lesions found in NSCLC patients. Homozygous deletions within the FHIT/FRA3B region were found in 6 of 135 (4.4%) thoracic cancer cell lines. Northern blot showed low or absent FHIT expression in most thoracic cancer cell lines tested, whereas reverse transcription-PCR showed that 59-62% exhibited aberrant FHIT transcripts but nearly always (93-100%) also expressing the wild-type transcripts. Aberrant transcripts included precise deletions of FHIT exons, insertion of non-FHIT sequences between exons and insertions replacing exons. Complete open reading frame single-strand conformational polymorphism analysis of 102 lung cancer cDNAs revealed only one nonsplicing mutation. Normal cells including bronchial epithelium, lung, and trachea expressed wild-type FHIT transcript and a variant transcript deleted for exon 8 but not the other aberrant transcripts, arguing against exon 8-deleted FHIT transcripts being tumor specific. Our findings support the conclusion that FHIT/FRA3B abnormalities are associated with lung cancer pathogenesis but that FHIT abnormalities differ from the types of mutations and lack of wild-type transcript found in classic tumor suppressor genes, and functional studies are needed to define the role of FHIT in thoracic tumorigenesis.

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Year:  1997        PMID: 9187130

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  39 in total

Review 1.  Molecular genetic abnormalities in the pathogenesis of human lung cancer.

Authors:  E Forgacs; S Zöchbauer-Müller; E Oláh; J D Minna
Journal:  Pathol Oncol Res       Date:  2001       Impact factor: 3.201

2.  Deletion at fragile sites is a common and early event in Barrett's esophagus.

Authors:  Lisa A Lai; Rumen Kostadinov; Michael T Barrett; Daniel A Peiffer; Dimitry Pokholok; Robert Odze; Carissa A Sanchez; Carlo C Maley; Brian J Reid; Kevin L Gunderson; Peter S Rabinovitch
Journal:  Mol Cancer Res       Date:  2010-07-20       Impact factor: 5.852

3.  Lack of association of fragile histidine triad (FHIT) polymorphisms with lung cancer in the Korean population.

Authors:  Hae-Yun Jung; Jae Sook Sung; Young Mi Whang; Hyoung Doo Shin; Byung Lae Park; Jun Suk Kim; Sang Won Shin; Hee Yun Seo; Hwa Jung Sung; In Keun Choi; Sang Cheul Oh; Jae Hong Seo; Yeul Hong Kim
Journal:  J Hum Genet       Date:  2007-07-04       Impact factor: 3.172

Review 4.  Pulmonary preinvasive neoplasia.

Authors:  K M Kerr
Journal:  J Clin Pathol       Date:  2001-04       Impact factor: 3.411

5.  Control of 5',5'-dinucleoside triphosphate catabolism by APH1, a Saccharomyces cerevisiae analog of human FHIT.

Authors:  J Chen; A Brevet; S Blanquet; P Plateau
Journal:  J Bacteriol       Date:  1998-05       Impact factor: 3.490

6.  Usefulness of plasma epigenetic changes of five major genes involved in the pathogenesis of colorectal cancer.

Authors:  Seung-Chul Pack; Hye-Ran Kim; Sang-Woo Lim; Hwan-Young Kim; Jung-Yun Ko; Ki-Sang Lee; David Hwang; Seong-Il Park; Hoon Kang; Sang-Wook Park; Gun-Young Hong; Se-Min Hwang; Myung-Geun Shin; Soong Lee
Journal:  Int J Colorectal Dis       Date:  2012-09-19       Impact factor: 2.571

Review 7.  Lung cancer. 9: Molecular biology of lung cancer: clinical implications.

Authors:  K M Fong; Y Sekido; A F Gazdar; J D Minna
Journal:  Thorax       Date:  2003-10       Impact factor: 9.139

8.  Using next-generation sequencing for high resolution multiplex analysis of copy number variation from nanogram quantities of DNA from formalin-fixed paraffin-embedded specimens.

Authors:  Henry M Wood; Ornella Belvedere; Caroline Conway; Catherine Daly; Rebecca Chalkley; Melissa Bickerdike; Claire McKinley; Phil Egan; Lisa Ross; Bruce Hayward; Joanne Morgan; Leslie Davidson; Ken MacLennan; Thian K Ong; Kostas Papagiannopoulos; Ian Cook; David J Adams; Graham R Taylor; Pamela Rabbitts
Journal:  Nucleic Acids Res       Date:  2010-06-04       Impact factor: 16.971

9.  FHIT gene sequence variants and reduced Fhit protein expression in glioblastoma multiforme.

Authors:  Gulsah Cecener; Berrin Tunca; Unal Egeli; Ahmet Bekar; Gulnur Guler; Sahsine Tolunay; Kaya Aksoy
Journal:  Cell Mol Neurobiol       Date:  2009-09-17       Impact factor: 5.046

10.  The hereditary renal cell carcinoma 3;8 translocation fuses FHIT to a patched-related gene, TRC8.

Authors:  R M Gemmill; J D West; F Boldog; N Tanaka; L J Robinson; D I Smith; F Li; H A Drabkin
Journal:  Proc Natl Acad Sci U S A       Date:  1998-08-04       Impact factor: 11.205

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