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Emerging Roles of NDUFS8 Located in Mitochondrial Complex I in Different Diseases.
Wang, Sifan; Kang, Yuanbo; Wang, Ruifeng; Deng, Junqi; Yu, Yupei; Yu, Jun; Wang, Junpu.
Afiliação
  • Wang S; Department of Pathology, Xiangya Hospital, Central South University, Changsha 410008, China.
  • Kang Y; Department of Pathology, School of Basic Medicine, Central South University, Changsha 410008, China.
  • Wang R; Xiangya School of Medicine, Central South University, Changsha 410013, China.
  • Deng J; National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha 410008, China.
  • Yu Y; Department of Dermatology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China.
  • Yu J; Department of Pathology, Xiangya Hospital, Central South University, Changsha 410008, China.
  • Wang J; Department of Pathology, School of Basic Medicine, Central South University, Changsha 410008, China.
Molecules ; 27(24)2022 Dec 09.
Article em En | MEDLINE | ID: mdl-36557887
ABSTRACT
NADHubiquinone oxidoreductase core subunit S8 (NDUFS8) is an essential core subunit and component of the iron-sulfur (FeS) fragment of mitochondrial complex I directly involved in the electron transfer process and energy metabolism. Pathogenic variants of the NDUFS8 are relevant to infantile-onset and severe diseases, including Leigh syndrome, cancer, and diabetes mellitus. With over 1000 nuclear genes potentially causing a mitochondrial disorder, the current diagnostic approach requires targeted molecular analysis, guided by a combination of clinical and biochemical features. Currently, there are only several studies on pathogenic variants of the NDUFS8 in Leigh syndrome, and a lack of literature on its precise mechanism in cancer and diabetes mellitus exists. Therefore, NDUFS8-related diseases should be extensively explored and precisely diagnosed at the molecular level with the application of next-generation sequencing technologies. A more distinct comprehension will be needed to shed light on NDUFS8 and its related diseases for further research. In this review, a comprehensive summary of the current knowledge about NDUFS8 structural function, its pathogenic mutations in Leigh syndrome, as well as its underlying roles in cancer and diabetes mellitus is provided, offering potential pathogenesis, progress, and therapeutic target of different diseases. We also put forward some problems and solutions for the following investigations.
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Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Assunto principal: Doença de Leigh Limite: Humans Idioma: En Revista: Molecules Assunto da revista: BIOLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Assunto principal: Doença de Leigh Limite: Humans Idioma: En Revista: Molecules Assunto da revista: BIOLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China