Department of Biological Science and Technology, College of Biological Science and Technology, National Chiao Tung University, Hsinchu, Taiwan.
Division of Gastroenterology and Hepatology, Department of Internal Medicine, Chung Shan Medical University Hospital, Taichung, Taiwan.
Sci Rep. 2017 May 19;7(1):2172. doi: 10.1038/s41598-017-02057-9.
Colorectal cancers (CRCs) are a critical health issue worldwide. Cancer stem cell (CSC) lineages are associated with tumour transformation, progression, and malignant transformation. However, how lineages are transformed and how chemoresistance is acquired by CRCs remain largely unknown. In this report, we demonstrated that the RNA-binding protein Musashi-1 enhanced the development of CD44 colorectal CSCs and triggered the formation of anti-apoptotic stress granules (SGs). Our results indicated that CD44 CSC lineage-specific induction of tumour malignancies was controlled by Musashi-1. In addition, Musashi-1 formed SGs when CRC cell lines were treated with 5-fluorouracil. The C-terminal domain of Musashi-1 was critical for recruitment of Musashi-1 into SGs. Intracellular Musashi-1 SGs enhanced the chemoresistance of CRCs. Analysis of clinical CRC samples indicated that Musashi-1 expression was prominent in CRC stage IIA and IIB. In summary, we demonstrated that Musashi-1, a stemness gene, is a critical modulator that promotes the development of CD44 colorectal CSCs and also enhances CRC chemoresistance via formation of SGs. Our findings elucidated a novel mechanism of CRC chemoresistance through increased anti-apoptotic effects via Musashi-1-associated SGs.
结直肠癌(CRC)是全球范围内的一个重大健康问题。癌症干细胞(CSC)谱系与肿瘤转化、进展和恶性转化有关。然而,CRC 如何发生谱系转化以及如何获得化疗耐药性在很大程度上仍不清楚。在本报告中,我们证明了 RNA 结合蛋白 Musashi-1 增强了 CD44 结直肠 CSC 的发育,并触发了抗细胞凋亡应激颗粒(SG)的形成。我们的结果表明,Musashi-1 控制着 CD44 CSC 谱系特异性诱导的肿瘤恶性程度。此外,当 CRC 细胞系用 5-氟尿嘧啶处理时,Musashi-1 会形成 SG。Musashi-1 的 C 端结构域对于 Musashi-1 招募到 SG 中至关重要。细胞内 Musashi-1 SG 增强了 CRC 的化疗耐药性。对临床 CRC 样本的分析表明,Musashi-1 在 CRC ⅡA 和ⅡB 期表达明显。总之,我们证明了干性基因 Musashi-1 是一个关键的调节剂,它通过形成 SG 促进 CD44 结直肠 CSC 的发展,并增强 CRC 的化疗耐药性。我们的研究结果阐明了通过 Musashi-1 相关 SG 增加抗细胞凋亡作用导致 CRC 化疗耐药性的新机制。