Germline SDHA mutations in children and adults with cancer

Cold Spring Harb Mol Case Stud. 2018 Aug 1;4(4):a002584. doi: 10.1101/mcs.a002584. Print 2018 Aug.

Abstract

Mutations in succinate dehydrogenase complex genes predispose to familial paraganglioma-pheochromocytoma syndrome (FPG) and gastrointestinal stromal tumors (GIST). Here we describe cancer patients undergoing agnostic germline testing at Memorial Sloan Kettering Cancer Center and found to harbor germline SDHA mutations. Using targeted sequencing covering the cancer census genes, we identified 10 patients with SDHA germline mutations. Cancer diagnoses for these patients carrying SDHA germline mutations included neuroblastoma (n = 1), breast (n = 1), colon (n = 1), renal (n = 1), melanoma and uterine (n = 1), prostate (n = 1), endometrial (n = 1), bladder (n = 1), and gastrointestinal stromal tumor (GIST) (n = 2). Immunohistochemical staining and assessment of patient tumors for second hits and loss of heterozygosity in SDHA confirmed GIST as an SDHA-associated tumor and suggests SDHA germline mutations may be a driver in neuroblastoma tumorigenesis.

Keywords: clear cell renal cell carcinoma; gastrointestinal stroma tumor; neoplasm of the breast; neuroblastoma.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adolescent
  • Adult
  • Cell Line, Tumor
  • Child
  • Child, Preschool
  • Electron Transport Complex II / genetics*
  • Female
  • Gene Frequency
  • Germ-Line Mutation*
  • HEK293 Cells
  • Humans
  • Male
  • Middle Aged
  • Neoplasms / genetics*

Substances

  • Electron Transport Complex II
  • SDHA protein, human