Department of Neurosurgery, Zhejiang Provincial Tongde Hospital, Hangzhou, China.
Department of Oncology, Zhejiang Hospital, Hangzhou, China.
Cancer Sci. 2023 Jan;114(1):129-141. doi: 10.1111/cas.15578. Epub 2022 Oct 27.
Vasculogenic mimicry (VM) has been reported to accelerate angiogenesis in malignant tumors, yet the mechanism underlying VM has not been fully elucidated. N6-methyladenosine (m6A) mainly modulates mRNA fate and affects multiple tumorigenesis. Here, we aimed to investigate m6A-modified HOXA transcript antisense RNA myeloid-specific 1 (HOTAIRM1) in the regulation of glioma-associated VM formation. Gene expression was analyzed by quantitative RT-PCR. Cell viability, metastases, and VM formation capacity were determined by CCK-8, migration and invasion, as well as tube formation assays, respectively. The function and mechanisms of m6A-modified HOTAIRM1 were defined through liquid chromatography-tandem mass spectrometry m6A quantification, methylated RNA immunoprecipitation sequencing, RNA stability assays, and RNA pull-down experiments. A glioma xenograft mouse model was further established for VM evaluation in vivo. The results showed that HOTAIRM1, methyltransferase-like 3 (METTL3), and insulin-like growth factor binding protein 2 (IGFBP2) were upregulated in glioma tissues and cell lines. HOTAIRM1 functions as an oncogene in glioma progression; however, knockdown of HOTAIRM1 significantly reduced cell viability, migration, invasion, and VM formation. Notably, METTL3-dependent m6A modification enhanced HOTAIRM1 mRNA stability, whereas knockdown of METTL3 deficiency significantly suppressed VM in glioma. Moreover, HOTAIRM1 was found to bind IGFBP2, and HOTAIRM1 deficiency blocked glioma progression and VM formation in vivo. Our results indicated that METTL3-dependent m6A-modified HOTAIRM1 promoted VM formation in glioma.
血管生成拟态 (VM) 已被报道可加速恶性肿瘤中的血管生成,但 VM 的机制尚未完全阐明。N6-甲基腺苷 (m6A) 主要调节 mRNA 命运,并影响多种肿瘤发生。在这里,我们旨在研究 m6A 修饰的 HOXA 转录物反义 RNA 髓系特异性 1 (HOTAIRM1) 在调节胶质瘤相关 VM 形成中的作用。通过定量 RT-PCR 分析基因表达。通过 CCK-8 测定细胞活力、转移和 VM 形成能力,分别通过迁移和侵袭以及管形成测定来测定。通过液相色谱-串联质谱 m6A 定量、甲基化 RNA 免疫沉淀测序、RNA 稳定性测定和 RNA 下拉实验定义 m6A 修饰的 HOTAIRM1 的功能和机制。进一步建立了胶质瘤异种移植小鼠模型,用于体内评估 VM。结果表明,HOTAIRM1、甲基转移酶样 3 (METTL3) 和胰岛素样生长因子结合蛋白 2 (IGFBP2) 在胶质瘤组织和细胞系中上调。HOTAIRM1 在胶质瘤进展中起癌基因作用;然而,HOTAIRM1 的敲低显着降低了细胞活力、迁移、侵袭和 VM 形成。值得注意的是,METTL3 依赖性 m6A 修饰增强了 HOTAIRM1 mRNA 的稳定性,而 METTL3 缺陷的敲低显着抑制了胶质瘤中的 VM。此外,发现 HOTAIRM1 与 IGFBP2 结合,HOTAIRM1 缺陷阻断了体内胶质瘤的进展和 VM 形成。我们的结果表明,METTL3 依赖性 m6A 修饰的 HOTAIRM1 促进了胶质瘤中的 VM 形成。