Department of Cancer Biology, Vanderbilt University Medical Center, 771 Preston, Research Building, 2220 Pierce Avenue, Nashville, TN 37232, USA.
Department of Pediatrics-Nutrition, Baylor College of Medicine, BCM320, Huston, TX 77030, USA.
Semin Cancer Biol. 2015 Jun;32:18-31. doi: 10.1016/j.semcancer.2014.05.005. Epub 2014 Jun 2.
Mesenchymal stem cells (MSCs) originate from embryonic mesoderm and give rise to the multiple lineages of connective tissues. Transformed MSCs develop into aggressive sarcomas, some of which are initiated by specific chromosomal translocations that generate fusion proteins with potent oncogenic properties. The sarcoma oncogenes typically prime MSCs through aberrant reprogramming. They dictate commitment to a specific lineage but prevent mature differentiation, thus locking the cells in a state of proliferative precursors. Deregulated expression of lineage-specific transcription factors and controllers of chromatin structure play a central role in MSC reprogramming and sarcoma pathogenesis. This suggests that reversing the epigenetic aberrancies created by the sarcoma oncogenes with differentiation-related reagents holds great promise as a beneficial addition to sarcoma therapies.
间充质干细胞(MSCs)起源于胚胎中胚层,并分化为多种结缔组织谱系。转化的间充质干细胞发展为侵袭性肉瘤,其中一些是由特定的染色体易位引发的,这些易位产生具有潜在致癌特性的融合蛋白。肉瘤致癌基因通常通过异常重编程使间充质干细胞原癌化。它们决定了细胞向特定谱系的分化,但阻止了成熟分化,从而使细胞锁定在增殖前体细胞状态。谱系特异性转录因子和染色质结构控制器的失调表达在间充质干细胞重编程和肉瘤发病机制中起着核心作用。这表明,用与分化相关的试剂逆转肉瘤致癌基因引起的表观遗传异常,作为肉瘤治疗的有益补充,具有巨大的潜力。