Yoshida Mina, Yamauchi Hirofumi, Sakumoto Marimu, Yoshimi Akihide
Department of Hematology, Saitama Medical Center, Saitama Medical University.
Division of Cancer RNA Research, National Cancer Center Research Institute.
Rinsho Ketsueki. 2023;64(7):646-653. doi: 10.11406/rinketsu.64.646.
Recurrent mutations in genes encoding key splicing factors, SF3B1, SRSF2, U2AF1, and ZRSR2 have been found in a variety of cancers, particularly in hematologic malignancies, including myelodysplastic syndromes, chronic myelomonocytic leukemia, acute myeloid leukemia, and chronic lymphocytic leukemia. Global mis-splicing of mRNAs targeted by aberrant splicing factors partly contributes to leukemogenesis through decrease protein expression of tumor suppressors and epigenetic modifiers, caused by mRNAs degradation of aberrantly spliced. Some of the mis-spliced mRNAs influence intracellular oncogenic pathways and cellular processes through a dysregulated expression of associated proteins, whereas others influence the function of co-mutated genes such as aberrant transcriptional regulators. Spliceosomal disruption is common in many cancers, making spliceosome an appealing therapeutic target. The findings that spliceosomal mutant cells rely on wild-type splicing machinery for survival and that splicing factor mutations occur in a mutually exclusive manner strongly suggest that inhibiting wild-type splicing machinery causes synthetic lethality in cancer cells with these mutations. We discuss the characteristics and oncogenic mechanisms of splicing factor mutations, as well as the development of novel treatment strategies targeting aberrant splicing factors in hematologic malignancies.
在多种癌症中,尤其是在血液系统恶性肿瘤,包括骨髓增生异常综合征、慢性粒单核细胞白血病、急性髓系白血病和慢性淋巴细胞白血病中,已发现编码关键剪接因子SF3B1、SRSF2、U2AF1和ZRSR2的基因存在复发性突变。异常剪接因子靶向的mRNA的整体错配剪接,部分通过异常剪接的mRNA降解导致肿瘤抑制因子和表观遗传修饰因子的蛋白质表达降低,从而促进白血病发生。一些错配剪接的mRNA通过相关蛋白质的表达失调影响细胞内致癌途径和细胞过程,而其他一些则影响共突变基因的功能,如异常转录调节因子。剪接体破坏在许多癌症中很常见,这使得剪接体成为一个有吸引力的治疗靶点。剪接体突变细胞依赖野生型剪接机制生存以及剪接因子突变以互斥方式发生的发现,强烈表明抑制野生型剪接机制会在具有这些突变的癌细胞中导致合成致死。我们讨论了剪接因子突变的特征和致癌机制,以及针对血液系统恶性肿瘤中异常剪接因子的新型治疗策略的发展。