Birt-Hogg-Dubé renal tumors are genetically distinct from other renal neoplasias and are associated with up-regulation of mitochondrial gene expression. - Archive ouverte HAL Access content directly
Journal Articles BMC Medical Genomics Year : 2010

Birt-Hogg-Dubé renal tumors are genetically distinct from other renal neoplasias and are associated with up-regulation of mitochondrial gene expression.

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Jeff Klomp
  • Function : Author
  • PersonId : 918808
David Petillo
  • Function : Author
  • PersonId : 918809
Natalie Niemi
  • Function : Author
  • PersonId : 918810
Karl Dykema
  • Function : Author
  • PersonId : 918811
Jindong Chen
  • Function : Author
  • PersonId : 918812
Ximing Yang
  • Function : Author
  • PersonId : 909721
Peter Zickert
  • Function : Author
  • PersonId : 918814
Markus Aly
  • Function : Author
  • PersonId : 918815
Sophie Gad
  • Function : Author
  • PersonId : 918818
Yves Denoux
  • Function : Author
  • PersonId : 918819
Laurent Yonneau
  • Function : Author
  • PersonId : 918820
Jeffrey Mackeigan
  • Function : Author
  • PersonId : 918822

Abstract

BACKGROUND: Germline mutations in the folliculin (FLCN) gene are associated with the development of Birt-Hogg-Dubé syndrome (BHDS), a disease characterized by papular skin lesions, a high occurrence of spontaneous pneumothorax, and the development of renal neoplasias. The majority of renal tumors that arise in BHDS-affected individuals are histologically similar to sporadic chromophobe renal cell carcinoma (RCC) and sporadic renal oncocytoma. However, most sporadic tumors lack FLCN mutations and the extent to which the BHDS-derived renal tumors share genetic defects associated with the sporadic tumors has not been well studied. METHODS: BHDS individuals were identified symptomatically and FLCN mutations were confirmed by DNA sequencing. Comparative gene expression profiling analyses were carried out on renal tumors isolated from individuals afflicted with BHDS and a panel of sporadic renal tumors of different subtypes using discriminate and clustering approaches. qRT-PCR was used to confirm selected results of the gene expression analyses. We further analyzed differentially expressed genes using gene set enrichment analysis and pathway analysis approaches. Pathway analysis results were confirmed by generation of independent pathway signatures and application to additional datasets. RESULTS: Renal tumors isolated from individuals with BHDS showed distinct gene expression and cytogenetic characteristics from sporadic renal oncocytoma and chromophobe RCC. The most prominent molecular feature of BHDS-derived kidney tumors was high expression of mitochondria-and oxidative phosphorylation (OXPHOS)-associated genes. This mitochondria expression phenotype was associated with deregulation of the PGC-1α-TFAM signaling axis. Loss of FLCN expression across various tumor types is also associated with increased nuclear mitochondrial gene expression. CONCLUSIONS: Our results support a genetic distinction between BHDS-associated tumors and other renal neoplasias. In addition, deregulation of the PGC-1α-TFAM signaling axis is most pronounced in renal tumors that harbor FLCN mutations and in tumors from other organs that have relatively low expression of FLCN. These results are consistent with the recently discovered interaction between FLCN and AMPK and support a model in which FLCN is a regulator of mitochondrial function.
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Dates and versions

inserm-00663705 , version 1 (27-01-2012)

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Jeff Klomp, David Petillo, Natalie Niemi, Karl Dykema, Jindong Chen, et al.. Birt-Hogg-Dubé renal tumors are genetically distinct from other renal neoplasias and are associated with up-regulation of mitochondrial gene expression.. BMC Medical Genomics, 2010, 3 (1), pp.59. ⟨10.1186/1755-8794-3-59⟩. ⟨inserm-00663705⟩
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