Pheochromocytomas and Paragangliomas, Genetically Diverse and Minimalist, All at Once!

Research output: Contribution to journalShort survey

7 Scopus citations

Abstract

Pheochromocytomas and paragangliomas are infrequent, genetically heterogeneous neuroendocrine tumors. In this issue of Cancer Cell, Fishbein et al. report novel driver genes, pathogenic mechanisms, and markers of malignancy. Notably, the new findings support the long-held view that these tumors distinctively arise from a single driver event, either inherited or acquired.

Original languageEnglish (US)
Pages (from-to)159-161
Number of pages3
JournalCancer Cell
Volume31
Issue number2
DOIs
StatePublished - Feb 13 2017

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ASJC Scopus subject areas

  • Oncology
  • Cell Biology
  • Cancer Research

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