New perspectives on pheochromocytoma and paraganglioma: toward a molecular classification

J Crona, D Taïeb, K Pacak - Endocrine reviews, 2017 - academic.oup.com
A molecular biology–based taxonomy has been proposed for pheochromocytoma and
paraganglioma (PPGL). Data from the Cancer Genome Atlas revealed clinically relevant …

Mitochondrial complex II: at the crossroads

A Bezawork-Geleta, J Rohlena, L Dong, K Pacak… - Trends in biochemical …, 2017 - cell.com
Mitochondrial complex II (CII), also called succinate dehydrogenase (SDH), is a central
purveyor of the reprogramming of metabolic and respiratory adaptation in response to …

Regulation of succinate dehydrogenase and role of succinate in cancer

E Dalla Pozza, I Dando, R Pacchiana, E Liboi… - Seminars in cell & …, 2020 - Elsevier
Succinate dehydrogenase (SDH) has been classically considered a mitochondrial enzyme
with the unique property to participate in both the citric acid cycle and the electron transport …

Succinate dehydrogenase (SDH)‐deficient neoplasia

AJ Gill - Histopathology, 2018 - Wiley Online Library
The succinate dehydrogenase (SDH) complex is a key respiratory enzyme composed of four
subunits: SDHA, SDHB, SDHC and SDHD. Remarkably, immunohistochemistry for SDHB …

Assembly of mitochondrial succinate dehydrogenase in human health and disease

K Cao, J Xu, W Cao, X Wang, W Lv, M Zeng… - Free Radical Biology …, 2023 - Elsevier
Mitochondrial succinate dehydrogenase (SDH), also known as electron transport chain
(ETC) Complex II, is the only enzyme complex engaged in both oxidative phosphorylation …

[HTML][HTML] Prognostic indicators for gastrointestinal stromal tumors: a review

H Zhang, Q Liu - Translational Oncology, 2020 - Elsevier
Gastrointestinal stromal tumors (GISTs) are potentially malignancies that can occur
anywhere in the digestive tract. Tyrosine kinase inhibitors (TKIs) such as imatinib have …

SDHB/SDHA immunohistochemistry in pheochromocytomas and paragangliomas: a multicenter interobserver variation analysis using virtual microscopy: a …

TG Papathomas, L Oudijk, A Persu, AJ Gill… - Modern …, 2015 - nature.com
Despite the established role of SDHB/SDHA immunohistochemistry as a valuable tool to
identify patients at risk for familial succinate dehydrogenase-related pheochromocytoma …

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 …

Paragangliomas of the head and neck: an overview from diagnosis to genetics

MD Williams - Head and Neck Pathology, 2017 - Springer
Paragangliomas (PGL) develop from the parasympathetic system in the head and neck (HN)
and arise primarily in four distinct areas: Carotid body, vagal, middle ear, and larynx …

Gastrointestinal stromal tumors

M von Mehren, BP Rubin, DB Flieder… - … of Uncommon Cancer, 2017 - Wiley Online Library
Gastrointestinal stromal tumors are rare malignancies involving the intestinal tract. They are
now easily recognized using standard immunohistochemistry. Management in the past was …