Back to Search
Start Over
Succinate Dehydrogenase (SDH)-Deficient Pancreatic Neuroendocrine Tumor Expands the SDH-Related Tumor Spectrum
- Source :
- Journal of Clinical Endocrinology and Metabolism, 100(10), E1386-E1393. Endocrine Society, Journal of Clinical Endocrinology and Metabolism, 100(10), E1386-E1393, Journal of Clinical Endocrinology and Metabolism, 100(10), E1386. The Endocrine Society
- Publication Year :
- 2015
- Publisher :
- The Endocrine Society, 2015.
-
Abstract
- Context: Mutations in genes encoding the subunits of succinate dehydrogenase (SDH) can lead to pheochromocytoma/paraganglioma formation. However, SDH mutations have also been linked to nonparaganglionic tumors. Objective: The objective was to investigate which nonparaganglionic tumors belong to the SDH-associated tumor spectrum. Design: This was a retrospective cohort study. Setting: The setting was a tertiary referral center. Patients: Patients included all consecutive SDHA/SDHB/SDHC and SDHD mutation carriers followed at the Department of Endocrinology of the Leiden University Medical Center who were affected by non-pheochromocytoma/paraganglioma solid tumors. Main Outcome Measures: Main outcome measures were SDHA/SDHB immunohistochemistry, mutation analysis, and loss of heterozygosity analysis of the involved SDH-encoding genes. Results: Twenty-five of 35 tumors (from 26 patients) showed positive staining on SDHB and SDHA immunohistochemistry. Eight tumors showed negative staining for SDHB and positive staining for SDHA: a pancreatic neuroendocrine tumor, a macroprolactinoma, two gastric gastrointestinal stromal tumors, an abdominal ganglioneuroma, and three renal cell carcinomas. With the exception of the abdominal ganglioneuroma, loss of heterozygosity was detected in all tumors. A prolactinoma in a patient with a germline SDHA mutation was the only tumor immunonegative for both SDHA and SDHB. Sanger sequencing of this tumor revealed a somatic mutation (p.D38V) as a likely second hit leading to biallelic inactivation of SDHA. One tumor (breast cancer) showed heterogeneous SDHB staining, positive SDHA staining, and retention of heterozygosity. Conclusions: This study strengthens the etiological association of SDH genes with pituitary neoplasia, renal tumorigenesis, and gastric gastrointestinal stromal tumors. Furthermore, our results indicate that pancreatic neuroendocrine tumor also falls within the SDH-related tumor spectrum.
- Subjects :
- Adult
Male
medicine.medical_specialty
Pathology
SDHB
Endocrinology, Diabetes and Metabolism
Clinical Biochemistry
DNA Mutational Analysis
SDHA
Context (language use)
macromolecular substances
Pituitary neoplasm
Neuroendocrine tumors
Biology
medical
Biochemistry
Pheochromocytoma
Endocrinology
SDG 3 - Good Health and Well-being
Succinate Dehydrogenase/genetics
Paraganglioma
Internal medicine
medicine
Humans
Pituitary Neoplasms
Aged
Retrospective Studies
Biochemistry, medical
Medicine(all)
Biochemistry (medical)
Middle Aged
Neuroendocrine Tumors/genetics
medicine.disease
Pancreatic Neoplasms/genetics
Pituitary Neoplasms/genetics
Pedigree
Diabetes and Metabolism
Pancreatic Neoplasms
Succinate Dehydrogenase
Neuroendocrine Tumors
Female
loss of heterozygosity
SDHD
mutation
Subjects
Details
- Language :
- English
- ISSN :
- 0021972X
- Database :
- OpenAIRE
- Journal :
- Journal of Clinical Endocrinology and Metabolism, 100(10), E1386-E1393. Endocrine Society, Journal of Clinical Endocrinology and Metabolism, 100(10), E1386-E1393, Journal of Clinical Endocrinology and Metabolism, 100(10), E1386. The Endocrine Society
- Accession number :
- edsair.doi.dedup.....de440fea29614a26f474aeb20da7cf68