A HIf1α regulatory loop links hypoxia and mitochondrial signals in pheochromocytomas

Patricia L.M. Dahia, Ken N. Ross, Matthew E. Wright, César Y. Hayashida, Sandro Santagata, Marta Barontini, Andrew L. Kung, Gabriela Sanso, James F. Powers, Arthur S. Tischler, Richard Hodin, Shannon Heitritter, Francis Moore, Robert Dluhy, Julie Ann Sosa, I. Tolgay Ocal, Diana E. Benn, Deborah J. Marsh, Bruce G. Robinson, Katherine SchneiderJudy Garber, Seth M. Arum, Márta Korbonits, Ashley Grossman, Pascal Pigny, Sérgio P.A. Toledo, Vania Nose, Cheng Li, Charles D. Stiles

Producción científica: Articlerevisión exhaustiva

393 Citas (Scopus)

Resumen

Pheochromocytomas are neural crest-derived tumors that arise from inherited or sporadic mutations in at least six independent genes. The proteins encoded by these multiple genes regulate distinct functions. We show here a functional link between tumors with VHL mutations and those with disruption of the genes encoding for succinate dehydrogenase (SDH) subunits B (SDHB) and D (SDHD). A transcription profile of reduced oxidoreductase is detected in all three of these tumor types, together with an angiogenesis/hypoxia profile typical of VHL dysfunction. The oxidoreductase defect, not previously detected in VHL-null tumors, is explained by suppression of the SDHB protein, a component of mitochondrial complex II. The decrease in SDHB is also noted in tumors with SDHD mutations. Gain-of-function and loss-of-function analyses show that the link between hypoxia signals (via VHL) and mitochondrial signals (via SDH) is mediated by HIF1a. These findings explain the shared features of pheochromocytomas with VHL and SDH mutations and suggest an additional mechanism for increased HIF1a activity in tumors.

Idioma originalEnglish (US)
Páginas (desde-hasta)72-80
Número de páginas9
PublicaciónPLoS Genetics
Volumen1
N.º1
DOI
EstadoPublished - jul 2005
Publicado de forma externa

ASJC Scopus subject areas

  • Ecology, Evolution, Behavior and Systematics
  • Molecular Biology
  • Genetics
  • Genetics(clinical)
  • Cancer Research

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