Pezzotta Alex, Mazzola Mara, Spreafico Marco, Marozzi Anna, Pistocchi Anna
Dipartimento di Biotecnologie Mediche e Medicina Traslazionale, Università degli Studi di Milano, Milan, Italy.
Front Cell Dev Biol. 2019 Feb 27;7:21. doi: 10.3389/fcell.2019.00021. eCollection 2019.
The genes of the cohesin complex exert different functions, ranging from the adhesion of sister chromatids during the cell cycle, DNA repair, gene expression and chromatin architecture remodeling. In recent years, the improvement of DNA sequencing technologies allows the identification of cohesin mutations in different tumors such as acute myeloid leukemia (AML), acute megakaryoblastic leukemia (AMKL), and myelodysplastic syndromes (MDS). However, the role of cohesin dysfunction in cancer insurgence remains elusive. In this regard, cells harboring cohesin mutations do not show any increase in aneuploidy that might explain their oncogenic activity, nor cohesin mutations are sufficient to induce myeloid neoplasms as they have to co-occur with other causative mutations such as , , and . Several works, also using animal models for cohesin haploinsufficiency, correlate cohesin activity with dysregulated expression of genes involved in myeloid development and differentiation. These evidences support the involvement of cohesin mutations in myeloid neoplasms.
黏连蛋白复合体的基因发挥着不同的功能,从细胞周期中姐妹染色单体的黏附、DNA修复、基因表达到染色质结构重塑。近年来,DNA测序技术的进步使得在不同肿瘤中鉴定黏连蛋白突变成为可能,如急性髓系白血病(AML)、急性巨核细胞白血病(AMKL)和骨髓增生异常综合征(MDS)。然而,黏连蛋白功能障碍在癌症发生中的作用仍不清楚。在这方面,携带黏连蛋白突变的细胞并未显示出可能解释其致癌活性的非整倍体增加,黏连蛋白突变也不足以诱导髓系肿瘤,因为它们必须与其他致病突变如 、 和 共同发生。几项研究,也使用黏连蛋白单倍体不足的动物模型,将黏连蛋白活性与参与髓系发育和分化的基因表达失调联系起来。这些证据支持黏连蛋白突变参与髓系肿瘤的发生。