Department of Pathology and Microbiology, University of Nebraska Medical Center, 985900 Nebraska Medical Center, Omaha, NE, 68198-5900, USA.
Fred & Pamela Buffett Cancer Center, Omaha, NE, USA.
Cancer Metastasis Rev. 2021 Jun;40(2):413-425. doi: 10.1007/s10555-021-09965-3. Epub 2021 Apr 14.
Metastasis, especially bone metastasis, is a major cause of cancer-related deaths, which is associated with long-term pain due to skeletal-related events and poor quality of life. Tumor cells alter the bone microenvironment through aberrant activation of osteoclasts and osteoblasts which induces bone osteolysis and release of growth factors leading to cancer growth. Though this phenomenon has been well characterized, bone-targeted therapies have shown little improvement in patient survival. Recent evidence indicates a growing appreciation for the complex bone environment, in addition to bone-remodeling stromal cells, which includes an abundance of myeloid immune cells that can either protect against or contribute to the progression of the disease within the bone cavity. Additionally, myeloid cells are recruited into primary tumor sites, where they promote development of the pre-metastatic niche and also can regulate tumor progression within the tumor-bone microenvironment through a milieu of complex mechanisms and involving heterogeneous myeloid populations. In this review, we have highlighted the complex roles of myeloid immunity in bone metastasis and hope to bring attention to the potential of novel immunotherapeutic interventions for the elimination of bone metastasis.
转移,特别是骨转移,是癌症相关死亡的主要原因,与骨骼相关事件引起的长期疼痛和生活质量差有关。肿瘤细胞通过破骨细胞和成骨细胞的异常激活改变骨微环境,导致骨溶解和生长因子释放,从而促进癌症生长。尽管这种现象已经得到很好的描述,但针对骨骼的治疗方法在患者生存方面的改善甚微。最近的证据表明,人们越来越认识到复杂的骨环境,除了骨重塑基质细胞外,还包括大量的髓样免疫细胞,这些细胞可以防止或促进骨腔内疾病的进展。此外,髓样细胞被招募到原发性肿瘤部位,在那里它们促进转移前生态位的发展,也可以通过复杂的机制和涉及异质髓样细胞群体的微环境来调节肿瘤在肿瘤-骨微环境中的进展。在这篇综述中,我们强调了髓样免疫在骨转移中的复杂作用,并希望引起人们对新型免疫治疗干预措施消除骨转移的潜力的关注。