Manier S, Sacco A, Leleu X, Ghobrial I M, Roccaro A M
Dana-Farber Cancer Institute, Department of Medical Oncology, Harvard Medical School, 450 Brookline Avnue, HIM 246, Boston, MA 02215, USA.
J Biomed Biotechnol. 2012;2012:157496. doi: 10.1155/2012/157496. Epub 2012 Oct 3.
Substantial advances have been made in understanding the biology of multiple myeloma (MM) through the study of the bone marrow (BM) microenvironment. Indeed, the BM niche appears to play an important role in differentiation, migration, proliferation, survival, and drug resistance of the malignant plasma cells. The BM niche is composed of a cellular compartment (stromal cells, osteoblasts, osteoclasts, endothelial cells, and immune cells) and a noncellular compartment including the extracellular matrix (ECM) and the liquid milieu (cytokines, growth factors, and chemokines). In this paper we discuss how the interaction between the malignant plasma cell and the BM microenvironment allowed myeloma progression through cell homing and the new concept of premetastatic niche.
通过对骨髓(BM)微环境的研究,在理解多发性骨髓瘤(MM)生物学方面取得了重大进展。事实上,骨髓生态位似乎在恶性浆细胞的分化、迁移、增殖、存活和耐药性中发挥着重要作用。骨髓生态位由细胞成分(基质细胞、成骨细胞、破骨细胞、内皮细胞和免疫细胞)和非细胞成分组成,包括细胞外基质(ECM)和液体环境(细胞因子、生长因子和趋化因子)。在本文中,我们讨论了恶性浆细胞与骨髓微环境之间的相互作用如何通过细胞归巢和转移前生态位的新概念促进骨髓瘤进展。