Department of Gastrointestinal Surgery, Minhang Hospital, Fudan University, Shanghai, China.
Institute of Fudan-Minhang Academic Health System, Minhang Hospital, Fudan University, Shanghai, China.
Mol Oncol. 2021 Apr;15(4):1234-1255. doi: 10.1002/1878-0261.12911. Epub 2021 Feb 13.
Long noncoding RNAs (lncRNAs) can compete with endogenous RNAs to modulate the gene expression and contribute to oncogenesis and tumor metastasis. lncRNA NKX2-1-AS1 (NKX2-1 antisense RNA 1) plays a pivotal role in cancer progression and metastasis; however, the contribution of aberrant expression of NKX2-1-AS1 and the mechanism by which it functions as a competing endogenous RNA (ceRNA) in gastric cancer (GC) remains elusive. NKX2-1-AS1 expression was detected in paired tumor and nontumor tissues of 178 GC patients by quantitative reverse transcription PCR (qRT-PCR). Using loss-of-function and gain-of-function experiments, the biological functions of NKX2-1-AS1 were evaluated both in vitro and in vivo. Further, to assess that NKX2-1-AS1 regulates angiogenic processes, tube formation and co-culture assays were performed. RNA binding protein immunoprecipitation (RIP) assay, a dual-luciferase reporter assay, quantitative PCR, Western blot, and fluorescence in situ hybridization (FISH) assays were performed to determine the potential molecular mechanism underlying this ceRNA. The results indicated that NKX2-1-AS1 expression was upregulated in GC cell lines and tumor tissues. Overexpression of NKX2-1-AS1 was significantly associated with tumor progression and enhanced angiogenesis. Functionally, NKX2-1-AS1 overexpression promoted GC cell proliferation, metastasis, invasion, and angiogenesis, while NKX2-1-AS1 knockdown restored these effects, both in vitro and in vivo. RIP and dual-luciferase assays revealed that the microRNA miR-145-5p is a direct target of NKX2-1-AS1 and that NKX2-1-AS1 serves as a ceRNA to sponge miRNA and regulate angiogenesis in GC. Moreover, serpin family E member 1 (SERPINE1) is an explicit target for miR-145-5p; besides, the NKX2-1-AS1/miR-145-5p axis induces the translation of SERPINE1, thus activating the VEGFR-2 signaling pathway to promote tumor progression and angiogenesis. NKX2-1-AS1 overexpression is associated with enhanced tumor cell proliferation, angiogenesis, and poor prognosis in GC. Collectively, NKX2-1-AS1 functions as a ceRNA to miR-145-5p and promotes tumor progression and angiogenesis by activating the VEGFR-2 signaling pathway via SERPINE1.
长链非编码 RNA(lncRNA)可以与内源性 RNA 竞争,调节基因表达,促进肿瘤发生和转移。 lncRNA NKX2-1-AS1(NKX2-1 反义 RNA 1)在癌症进展和转移中发挥关键作用;然而,NKX2-1-AS1 异常表达的贡献及其作为胃癌(GC)中的竞争内源性 RNA(ceRNA)的功能机制仍不清楚。通过定量逆转录 PCR(qRT-PCR)检测了 178 例 GC 患者配对肿瘤和非肿瘤组织中的 NKX2-1-AS1 表达。通过失活和功能获得实验,在体外和体内评估了 NKX2-1-AS1 的生物学功能。此外,为了评估 NKX2-1-AS1 是否调节血管生成过程,进行了管形成和共培养测定。RNA 结合蛋白免疫沉淀(RIP)测定、双荧光素酶报告基因测定、定量 PCR、Western blot 和荧光原位杂交(FISH)测定用于确定这种 ceRNA 潜在的分子机制。结果表明,NKX2-1-AS1 在 GC 细胞系和肿瘤组织中表达上调。NKX2-1-AS1 的过表达与肿瘤进展和增强的血管生成显著相关。功能上,NKX2-1-AS1 的过表达促进 GC 细胞的增殖、转移、侵袭和血管生成,而 NKX2-1-AS1 的敲低则在体外和体内均恢复了这些效应。RIP 和双荧光素酶测定表明,microRNA miR-145-5p 是 NKX2-1-AS1 的直接靶标,NKX2-1-AS1 作为 ceRNA 来吸收 miRNA 并调节 GC 中的血管生成。此外,丝氨酸蛋白酶抑制剂家族 E 成员 1(SERPINE1)是 miR-145-5p 的明确靶标;此外,NKX2-1-AS1/miR-145-5p 轴诱导 SERPINE1 的翻译,从而激活 VEGFR-2 信号通路,促进肿瘤进展和血管生成。NKX2-1-AS1 的过表达与 GC 中增强的肿瘤细胞增殖、血管生成和不良预后相关。总之,NKX2-1-AS1 作为 ceRNA 通过激活 VEGFR-2 信号通路通过 SERPINE1 促进肿瘤进展和血管生成。