MitoLab Team, MitoVasc Institut, CNRS UMR6015, INSERM U1083, Angers University, 49000 Angers, France.
Department of Internal Medicine and Clinical Immunology, Angers University Hospital, 49000 Angers, France.
Nutrients. 2022 May 14;14(10):2058. doi: 10.3390/nu14102058.
Cobalamin or vitamin B12 (B12) is a cofactor for methionine synthase and methylmalonyl-CoA mutase, two enzymes implicated in key pathways for cell proliferation: methylation, purine synthesis, succinylation and ATP production. Ensuring these functions in cancer cells therefore requires important cobalamin needs and its uptake through the transcobalamin II receptor (TCII-R). Thus, both the TCII-R and the cobalamin-dependent metabolic pathways constitute promising therapeutic targets to inhibit cancer development. However, the link between cobalamin and solid cancers is not limited to cellular metabolism, as it also involves the circulating transcobalamins I and II (TCI or haptocorrin and TCII) carrier proteins, encoded by and , respectively. In this respect, elevations of B12, TCI and TCII concentrations in plasma are associated with cancer onset and relapse, and with the presence of metastases and worse prognosis. In addition, and overexpressions are associated with chemoresistance and a proliferative phenotype, respectively. Here we review the involvement of cobalamin and transcobalamins in cancer diagnosis and prognosis, and as potential therapeutic targets. We further detail the relationship between cobalamin-dependent metabolic pathways in cancer cells and the transcobalamins' abundancies in plasma and tumors, to ultimately hypothesize screening and therapeutic strategies linking these aspects.
钴胺素或维生素 B12(B12)是蛋氨酸合成酶和甲基丙二酰辅酶 A 变位酶的辅助因子,这两种酶参与细胞增殖的关键途径:甲基化、嘌呤合成、琥珀酰化和 ATP 产生。因此,确保癌细胞具有这些功能需要重要的钴胺素需求及其通过转钴胺素 II 受体(TCII-R)摄取。因此,TCII-R 和依赖钴胺素的代谢途径共同构成了抑制癌症发展的有前途的治疗靶点。然而,钴胺素与实体瘤之间的联系不仅限于细胞代谢,因为它还涉及循环转钴胺素 I 和 II(TCI 或触珠蛋白和 TCII)载体蛋白,分别由 和 编码。在这方面,血浆中 B12、TCI 和 TCII 浓度的升高与癌症的发生和复发以及转移的存在和预后较差相关。此外, 和 的过度表达分别与化疗耐药性和增殖表型相关。在这里,我们综述了钴胺素和转钴胺素在癌症诊断和预后中的作用,以及作为潜在的治疗靶点。我们进一步详细说明了癌细胞中依赖钴胺素的代谢途径与血浆和肿瘤中转钴胺素的丰度之间的关系,最终假设将这些方面联系起来的筛选和治疗策略。