Zhou Xiaofeng, An Zheng, Lei Hao, Liao Hongyuan, Guo Xinjian
Pathology Department, Qinghai University Affiliated Hospital, Xining, Qinghai 810001, P.R. China.
Pathology Department, Qinghai Women and Children's Hospital, Xining, Qinghai 810007, P.R. China.
Oncol Lett. 2024 Dec 23;29(3):111. doi: 10.3892/ol.2024.14857. eCollection 2025 Mar.
The human cytochrome b561 (hCytb561) family consists of electron transfer transmembrane proteins characterized by six conserved α-helical transmembrane domains and two β-type heme cofactors. These proteins contribute to the regulation of iron metabolism and numerous different physiological and pathological processes by recycling ascorbic acid and maintaining iron reductase activity. Key members of this family include cytochrome b561 (CYB561), duodenal CYB561 (Dcytb), lysosomal CYB561 (LCytb), stromal cell-derived receptor 2 (SDR2) and 101F6, which are widely expressed in human tissues and participate in the pathogenesis of several diseases and tumors. They are associated with the promotion or inhibition of tumor growth and progression in various malignancies and are potential therapeutic targets for malignant tumors. The present review summarizes the existing literature regarding the structure of the Cytb561 family, the basic functional characteristics of hCytb561 family members, and the roles of the CYB561, Dcytb, LCytb, SDR2 and 101F6 in various diseases and tumors.
人类细胞色素b561(hCytb561)家族由电子传递跨膜蛋白组成,其特征是具有六个保守的α-螺旋跨膜结构域和两个β型血红素辅因子。这些蛋白质通过循环利用抗坏血酸和维持铁还原酶活性,有助于调节铁代谢以及许多不同的生理和病理过程。该家族的关键成员包括细胞色素b561(CYB561)、十二指肠CYB561(Dcytb)、溶酶体CYB561(LCytb)、基质细胞衍生受体2(SDR2)和101F6,它们在人体组织中广泛表达,并参与多种疾病和肿瘤的发病机制。它们与各种恶性肿瘤中肿瘤生长和进展的促进或抑制相关,是恶性肿瘤潜在的治疗靶点。本综述总结了关于Cytb561家族结构、hCytb561家族成员的基本功能特征以及CYB561、Dcytb、LCytb、SDR2和101F6在各种疾病和肿瘤中的作用的现有文献。