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揭示叶酸依赖性一碳代谢在癌症和神经退行性疾病中的治疗潜力。

Unveiling the Therapeutic Potential of Folate-Dependent One-Carbon Metabolism in Cancer and Neurodegeneration.

机构信息

Associate Laboratory i4HB-Institute for Health and Bioeconomy, University Institute of Health Sciences-CESPU, 4585-116 Gandra, Portugal.

UCIBIO-Applied Molecular Biosciences Unit, Toxicologic Pathology Research Laboratory, University Institute of Health Sciences (1H-TOXRUN, IUCS-CESPU), 4585-116 Gandra, Portugal.

出版信息

Int J Mol Sci. 2024 Aug 28;25(17):9339. doi: 10.3390/ijms25179339.

Abstract

Cellular metabolism is crucial for various physiological processes, with folate-dependent one-carbon (1C) metabolism playing a pivotal role. Folate, a B vitamin, is a key cofactor in this pathway, supporting DNA synthesis, methylation processes, and antioxidant defenses. In dividing cells, folate facilitates nucleotide biosynthesis, ensuring genomic stability and preventing carcinogenesis. Additionally, in neurodevelopment, folate is essential for neural tube closure and central nervous system formation. Thus, dysregulation of folate metabolism can contribute to pathologies such as cancer, severe birth defects, and neurodegenerative diseases. Epidemiological evidence highlights folate's impact on disease risk and its potential as a therapeutic target. In cancer, antifolate drugs that inhibit key enzymes of folate-dependent 1C metabolism and strategies targeting folate receptors are current therapeutic options. However, folate's impact on cancer risk is complex, varying among cancer types and dietary contexts. In neurodegenerative conditions, including Alzheimer's and Parkinson's diseases, folate deficiency exacerbates cognitive decline through elevated homocysteine levels, contributing to neuronal damage. Clinical trials of folic acid supplementation show mixed outcomes, underscoring the complexities of its neuroprotective effects. This review integrates current knowledge on folate metabolism in cancer and neurodegeneration, exploring molecular mechanisms, clinical implications, and therapeutic strategies, which can provide crucial information for advancing treatments.

摘要

细胞代谢对于各种生理过程至关重要,而叶酸依赖性一碳(1C)代谢则起着关键作用。叶酸作为一种 B 族维生素,是该途径的关键辅助因子,支持 DNA 合成、甲基化过程和抗氧化防御。在分裂细胞中,叶酸促进核苷酸的生物合成,确保基因组的稳定性并防止致癌作用。此外,在神经发育过程中,叶酸对于神经管闭合和中枢神经系统的形成至关重要。因此,叶酸代谢的失调可能导致癌症、严重的出生缺陷和神经退行性疾病等病理状态。流行病学证据强调了叶酸对疾病风险的影响及其作为治疗靶点的潜力。在癌症中,抑制叶酸依赖性 1C 代谢关键酶的抗叶酸药物和靶向叶酸受体的策略是当前的治疗选择。然而,叶酸对癌症风险的影响是复杂的,因癌症类型和饮食背景而异。在神经退行性疾病中,包括阿尔茨海默病和帕金森病,叶酸缺乏通过升高的同型半胱氨酸水平加剧认知能力下降,导致神经元损伤。叶酸补充的临床试验结果喜忧参半,突显了其神经保护作用的复杂性。本综述整合了关于癌症和神经退行性变中叶酸代谢的最新知识,探讨了分子机制、临床意义和治疗策略,为推进治疗提供了重要信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e8c/11395277/ccaafed96044/ijms-25-09339-g001.jpg

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