Nuffield Dept. of Surgical Sciences, University of Oxford, Oxford, UK.
Nuffield Dept. of Orthopaedics, Rheumatology & Musculoskeletal Sciences, University of Oxford, Oxford, UK.
Curr Osteoporos Rep. 2021 Oct;19(5):494-499. doi: 10.1007/s11914-021-00695-7. Epub 2021 Jul 28.
For solid tumours such as breast and prostate cancer, and haematological malignancies such as myeloma, bone represents a supportive home, where the cellular crosstalk is known to underlie both tumour growth and survival, and the development of the associated bone disease. The importance of metabolic reprogramming is becoming increasingly recognised, particularly within cancer biology, enabling tumours to adapt to changing environments and pressures. This review will discuss our current understanding of metabolic requirements and adaptations within the tumour-bone microenvironment.
The bone provides a unique metabolic microenvironment, home to highly energy-intensive processes such as bone resorption and bone formation, both of which are dysregulated in the presence of cancer. Approaches such as metabolomics demonstrate metabolic plasticity in patients with advanced disease. Metabolic crosstalk between tumour cells and surrounding stroma supports disease pathogenesis. There is increasing evidence for a key role for metabolic reprogramming within the tumour-bone microenvironment to drive disease progression. As such, understanding these metabolic adaptations should reveal new therapeutic targets and approaches.
对于乳腺癌和前列腺癌等实体瘤,以及骨髓瘤等血液系统恶性肿瘤,骨骼是一个支持性的家,细胞串扰已知是肿瘤生长和存活以及相关骨骼疾病发展的基础。代谢重编程的重要性日益得到认识,特别是在癌症生物学中,使肿瘤能够适应不断变化的环境和压力。这篇综述将讨论我们目前对肿瘤-骨骼微环境中代谢需求和适应的理解。
骨骼提供了一个独特的代谢微环境,是高能量密集型过程的所在地,如骨吸收和骨形成,在癌症存在的情况下,这两种过程都失调了。代谢组学等方法在晚期疾病患者中显示出代谢可塑性。肿瘤细胞和周围基质之间的代谢串扰支持疾病发病机制。越来越多的证据表明,代谢重编程在肿瘤-骨骼微环境中对于驱动疾病进展起着关键作用。因此,了解这些代谢适应应该揭示新的治疗靶点和方法。