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环状HIPK3通过吸附miR-330-5p促进胰腺癌细胞对吉西他滨(GEM)的耐药性并靶向RASSF1。

CircHIPK3 Promotes Gemcitabine (GEM) Resistance in Pancreatic Cancer Cells by Sponging miR-330-5p and Targets RASSF1.

作者信息

Liu Yunfei, Xia Li, Dong Luo, Wang Jiale, Xiao Qiangsheng, Yu Xiao, Zhu Hongwei

机构信息

Department of Hepatobiliary and Pancreatic Surgery‖, Third Xiangya Hospital, Central South University, Changsha 410006, People's Republic of China.

Department of Endocrinology, Third Xiangya Hospital, Central South University, Changsha, 410006, People's Republic of China.

出版信息

Cancer Manag Res. 2020 Feb 11;12:921-929. doi: 10.2147/CMAR.S239326. eCollection 2020.

Abstract

BACKGROUND

Pancreatic cancer is one of the most common malignant diseases in the world. Gemcitabine chemotherapy remains the most important clinical treatment. However, research found that pancreatic cancer cells have chemoresistance to gemcitabine and the effect is not satisfactory. Therefore, it is urgent to find an effective early diagnosis and treatment strategy. Circular RNA is one of the most popular prognostic biomarkers in GEM-resistant PC.

MATERIALS AND METHODS

The present study was designed to evaluate the role of circHIPK3 in PC. The expression of circHIPK3 in PC tissues and cells and its effect on proliferation, migration, invasion, EMT, and apoptosis were investigated in vitro; its effect on tumor xenografts was assessed in vivo. Used bioinformation analysis to predict which miRNAs could potentially interact with circHIPK3, mRNA, and miR-330-5p.

RESULTS

RT-PCR showed that the level of circHIPK3 was increased in PC tumor tissues; moreover, circHIPK3 was also increased in GEM-resistant PC tumors tissues and GEM-resistant PC cells. Sh-circHIPK3 could knockdown circHIPK3 in PANC-1-GEM and SW-1990-GEM and could significantly inhibit cell proliferation, invasion, migration, EMT and enhance cell apoptosis, compare with control group, the tumor xenografts of circHIPK3 knockdown group were significantly smaller. CircHIPK3 served as a sponge for miR-330-5p, and miR-330-5p directly bound to the 3' UTR of RASSF1 were revealed by dual luciferase assay and RIP in PC cells. CircHIPK3 knockdown of RASSF1 expression could neutralize the cytological function of PC cells by miR-330-5p inhibitor mediated GEM-resistance.

CONCLUSION

CircHIPK3 promotes gemcitabine (GEM) resistance in pancreatic cancer cells by targeting RASSF1 via miR-330-5p and regulates proliferation, invasive, migration, EMT, and apoptosis. Our research revealed that circHIPK3 may be a novel biomarker in GEM-resistant PC and could be used as a prognostic target.

摘要

背景

胰腺癌是世界上最常见的恶性疾病之一。吉西他滨化疗仍然是最重要的临床治疗方法。然而,研究发现胰腺癌细胞对吉西他滨具有化疗抗性,且效果并不理想。因此,迫切需要找到一种有效的早期诊断和治疗策略。环状RNA是吉西他滨耐药性胰腺癌中最受欢迎的预后生物标志物之一。

材料与方法

本研究旨在评估circHIPK3在胰腺癌中的作用。体外研究circHIPK3在胰腺癌组织和细胞中的表达及其对增殖、迁移、侵袭、上皮-间质转化和凋亡的影响;体内评估其对肿瘤异种移植的影响。利用生物信息学分析预测哪些miRNA可能与circHIPK3、mRNA和miR-330-5p潜在相互作用。

结果

RT-PCR显示circHIPK3在胰腺癌肿瘤组织中的水平升高;此外,circHIPK3在吉西他滨耐药性胰腺癌肿瘤组织和吉西他滨耐药性胰腺癌细胞中也升高。与对照组相比,sh-circHIPK3可敲低PANC-1-GEM和SW-1990-GEM中的circHIPK3,并可显著抑制细胞增殖、侵袭、迁移、上皮-间质转化并增强细胞凋亡,circHIPK3敲低组的肿瘤异种移植明显更小。双荧光素酶报告基因检测和RNA免疫沉淀显示,circHIPK3作为miR-330-5p的海绵,且miR-330-5p直接与胰腺癌细胞中RASSF1的3'UTR结合。circHIPK3敲低RASSF1表达可通过miR-330-5p抑制剂介导的吉西他滨耐药性来中和胰腺癌细胞的细胞学功能。

结论

circHIPK3通过miR-330-5p靶向RASSF1促进胰腺癌细胞对吉西他滨(GEM)的耐药性,并调节增殖、侵袭、迁移、上皮-间质转化和凋亡。我们的研究表明,circHIPK3可能是吉西他滨耐药性胰腺癌中的一种新型生物标志物,可作为预后靶点。

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