International consensus on initial screening and follow-up of asymptomatic SDHx mutation carriers

L Amar, K Pacak, O Steichen, SA Akker… - Nature Reviews …, 2021 - nature.com
Approximately 20% of patients diagnosed with a phaeochromocytoma or paraganglioma
carry a germline mutation in one of the succinate dehydrogenase (SDHx) genes (SDHA …

[HTML][HTML] Succinate, an intermediate in metabolism, signal transduction, ROS, hypoxia, and tumorigenesis

L Tretter, A Patocs, C Chinopoulos - Biochimica et Biophysica Acta (BBA) …, 2016 - Elsevier
Succinate is an important metabolite at the cross-road of several metabolic pathways, also
involved in the formation and elimination of reactive oxygen species. However, it is …

Succinate dehydrogenase (SDH)-deficient renal carcinoma: a morphologically distinct entity: a clinicopathologic series of 36 tumors from 27 patients

AJ Gill, O Hes, T Papathomas… - The American journal …, 2014 - journals.lww.com
Succinate dehydrogenase (SDH)-deficient renal carcinoma has been accepted as a
provisional entity in the 2013 International Society of Urological Pathology Vancouver …

[HTML][HTML] SDH mutations in cancer

C Bardella, PJ Pollard, I Tomlinson - Biochimica et Biophysica Acta (BBA) …, 2011 - Elsevier
The SDHA, SDHB, SDHC, SDHD genes encode the four subunits of succinate
dehydrogenase (SDH; mitochondrial complex II), a mitochondrial enzyme involved in two …

Succinate dehydrogenase–assembly, regulation and role in human disease

J Rutter, DR Winge, JD Schiffman - Mitochondrion, 2010 - Elsevier
Succinate dehydrogenase (or Electron Transport Chain Complex II) has been the subject of
a focused but significant renaissance. This complex, which has been the least studied of the …

Glutamine metabolism in cancer

T Li, A Le - The Heterogeneity of Cancer Metabolism, 2018 - Springer
Metabolism is the fundamental process for all cellular functions. For decades, there has
been growing evidence with regard to the relationship between metabolism and malignant …

15 Years of paraganglioma: clinical manifestations of paraganglioma syndromes types 1–5

DE Benn, BG Robinson… - Endocrine-related …, 2015 - erc.bioscientifica.com
The paraganglioma (PGL) syndromes types 1–5 are autosomal dominant disorders
characterized by familial predisposition to PGLs, phaeochromocytomas (PCs), renal cell …

Tumor risks and genotype–phenotype–proteotype analysis in 358 patients with germline mutations in SDHB and SDHD

CJ Ricketts, JR Forman, E Rattenberry… - Human …, 2010 - Wiley Online Library
Succinate dehydrogenase B (SDHB) and D (SDHD) subunit gene mutations predispose to
adrenal and extraadrenal pheochromocytomas, head and neck paragangliomas (HNPGL) …

The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas

N Burnichon, V Rohmer, L Amar… - The Journal of …, 2009 - academic.oup.com
Context: Germline mutations in SDHx genes cause hereditary paraganglioma. Objective:
The aim of the study was to assess the indications for succinate dehydrogenase (SDH) …

SDH mutations in tumorigenesis and inherited endocrine tumours: lesson from the phaeochromocytoma–paraganglioma syndromes

B Pasini, CA Stratakis - Journal of internal medicine, 2009 - Wiley Online Library
A genetic predisposition for paragangliomas and adrenal or extra‐adrenal
phaeochromocytomas was recognized years ago. Beside the well‐known syndromes …