Literature DB >> 21789102

Atypical early onset of diabetes, deafness and lung cancer in a male patient with mitochondrial mutations in peripheral mononuclear cells.

Satoru Suzuki1, Masahiro Takei, Takashi Ehara, Shin-Ichi Nishio, Hidefumi Inaba, Kiyoshi Hashizume.   

Abstract

As mitochondria play a major role in the conversion of dietary calories into usable energy, generating reactive oxygen species as a toxic byproduct, mitochondrial dysfunction plays a role in a wide range of age-related disorders and various forms of cancer. The present report concerns a heavy smoker who died of lung cancer at age 40. He also developed progressive diabetes and sensory hearing loss. Mitochondrial DNA sequence analysis revealed four mutations in peripheral mononuclear cells. Three were novel point mutations, including a mutation in ATP synthase F0 subunit 6 (ATP6). Mitochondrial mutations and smoking may have contributed to the development of atypical early onset of senescence-related diseases in this case.

Entities:  

Year:  2009        PMID: 21789102      PMCID: PMC3029046          DOI: 10.1136/bcr.03.2009.1648

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  9 in total

Review 1.  Pathogenesis of primary defects in mitochondrial ATP synthesis.

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Journal:  Semin Cell Dev Biol       Date:  2001-12       Impact factor: 7.727

Review 2.  Modulation of cigarette smoke-related end-points in mutagenesis and carcinogenesis.

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Journal:  Mutat Res       Date:  2003 Feb-Mar       Impact factor: 2.433

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Journal:  Science       Date:  1988-12-09       Impact factor: 47.728

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Journal:  Eur J Hum Genet       Date:  1999-01       Impact factor: 4.246

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Authors:  J P Jenuth; A C Peterson; E A Shoubridge
Journal:  Nat Genet       Date:  1997-05       Impact factor: 38.330

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Authors:  M B Graeber; U Müller
Journal:  J Neurol Sci       Date:  1998-01-08       Impact factor: 3.181

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Journal:  Science       Date:  2000-03-17       Impact factor: 47.728

8.  Mutation in mitochondrial tRNA(Leu)(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness.

Authors:  J M van den Ouweland; H H Lemkes; W Ruitenbeek; L A Sandkuijl; M F de Vijlder; P A Struyvenberg; J J van de Kamp; J A Maassen
Journal:  Nat Genet       Date:  1992-08       Impact factor: 38.330

9.  Diabetes with mitochondrial gene tRNALYS mutation.

Authors:  S Suzuki; Y Hinokio; S Hirai; M Onoda; M Matsumoto; M Ohtomo; H Kawasaki; Y Satoh; H Akai; K Abe
Journal:  Diabetes Care       Date:  1994-12       Impact factor: 19.112

  9 in total
  1 in total

Review 1.  The emergence of the mitochondrial genome as a partial regulator of nuclear function is providing new insights into the genetic mechanisms underlying age-related complex disease.

Authors:  Martin P Horan; David N Cooper
Journal:  Hum Genet       Date:  2013-12-04       Impact factor: 4.132

  1 in total

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