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Relationship between the expression of lncRNA ADPGK-AS1 and miR-1301-3p and the prognosis of gastric cancer#br# |
WEI Haofei SUN Haibin WANG Chuan LI Xinjiang#br# |
Department of General Surgery, the Second Hospital of Hebei Medical University, Hebei Province, Shijiazhuang 050000, China
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Abstract Objective To study the relationship between the expression of long non-coding RNA (lncRNA) ADPGK-AS1 and microRNA (miR)-1301-3p and the prognosis of gastric cancer. Methods One hundred and forty-two patients with gastric cancer treated in the Second Hospital of Hebei Medical University from May 2016 to May 2018 were selected. The expression levels of lncRNA ADPGK-AS1 and miR-1301-3p in cancer tissues and adjacent tissues were detected by real time quantitative PCR, according to the average value of the two groups, they were divided into lncRNA ADPGK-AS1 high expression group (69 cases), lncRNA ADPGK-AS1 low expression group (73 cases), miR-1301-3p high expression group (70 cases), and miR-1301-3p low expression group (72 cases). Pearson correlation was used to analyze the correlation between lncRNA ADPGK-AS1 and miR-1301-3p expression in cancer tissues. The binding sites between lncRNA ADPGK-AS1 and miR-1301-3p were predicted by online bioinformatics software. Kaplan-Meier survival was used to analyze the survival situation of patients with different lncRNA ADPGK-AS1 and miR-1301-3p expression levels. Results The expressions of lncRNA ADPGK-AS1 and miR-1301-3p in cancer tissues were higher than those in adjacent tissues (P < 0.05). LncRNA ADPGK-AS1 was positively correlated with miR-1301-3p (r = 0.601, P < 0.01). LncRNA ADPGK-AS1 had a binding site with miR-1301-3p at 2422-2443 bases. The median survival time of patients in lncRNA ADPGK-AS1 high expression group was 23.3 months (95%CI: 15.2-26.1), which was lower than that in lncRNA ADPGK-AS1 low expression group of 31.6 months (95%CI: 22.9-34.9) (P < 0.05). The median survival time of patients in miR-1301-3p high expression group was 24.2 months (95%CI: 17.6-28.5), which was lower than that in miR-1301-3p low expression group of 30.5 months (95%CI: 21.6-34.5) (P < 0.05). Conclusion The expressions of lncRNA ADPGK-AS1 and miR-1301-3p are increased in gastric cancer. There are binding sites between lncRNA ADPGK-AS1 and miR-1301-3p, they are potential molecular markers for predicting the prognosis of gastric cancer.
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[1] 蒋枋利,章程,高静,等.胃肠道肿瘤精准治疗一体化研究体系的建设[J].中国肿瘤临床,2021,48(17):865-869.
[2] 张宇飞,何亮,徐国栋,等.新辅助化疗后行腹腔镜胃切除术治疗局部晚期胃癌的疗效和安全性分析[J].中华保健医学杂志,2021,23(2):146-149.
[3] 吕元皓,季鸣,陈晓光.胃癌免疫治疗研究进展[J].中国生化药物杂志,2016,36(11):197-199.
[4] 肖钦晓,程宏宁,颜洪顺,等.lncRNA ADPGK-AS1通过调控miR-217表达对非小细胞肺癌细胞增殖和凋亡的影响[J].临床肺科杂志,2020,25(7):998-1004.
[5] 张俊,刘彩林,卜战云.lncRNA ADPGK-AS1对视网膜母细胞瘤细胞生物学行为的抑制作用及其调控机制[J].中华实验眼科杂志,2021,39(3):207-215.
[6] Song S,Yu W,Lin S,et al. LncRNA ADPGK-AS1 promotes pancreatic cancer progression through activating ZEB1-mediated epithelial-mesenchymal transition [J]. Cancer Biol Ther,2018,19(7):573-583.
[7] 杜泽森,罗何三,李绪渊,等.基于12个miRNAs表达信息学分析构建食管癌预后风险评分系统[J].中华肿瘤防治杂志,2019,26(12):842-848.
[8] 蔡茗,邵峰,林先盛,等.不同来源的胰腺星状细胞CircRNA表达谱差异分析[J].安徽医科大学学报,2020,55(8):1209-1214.
[9] Jiang HY,Wang ZJ. ADPGK-AS1 promotes the progression of colorectal cancer via sponging miR-525 to upregulate FUT1 [J]. Eur Rev Med Pharmacol Sci,2020,24(5):2380-2386.
[10] 檀碧波,李勇,赵群,等.胃癌组织中miR-218和凋亡相关蛋白Bcl-2、Bax、xIAP、SurvivinmRNA的表达观察[J].山东医药,2018,58(47):20-23.
[11] 郑晋,苏婷婷,李永盛,等.非编码RNA在胃癌中的作用机制研究进展[J].中国普通外科杂志,2021,30(4):471-481.
[12] 周迪,路明亮,蒋明茗.胃癌早期诊断的研究[J].胃肠病学和肝病学杂志,2021,30(6):606-611.
[13] 帕孜来提·亚森,袁浩,路红,等.胃癌靶向治疗药物临床实验研究进展[J].中国临床药理学与治疗学,2021, 26(4):454-461.
[14] 李翠霞,苏秀兰.长链非编码RNA(lncRNAs)参与肿瘤细胞免疫逃逸的研究进展[J].免疫学杂志,2019,35(9):817-822.
[15] 聂俊杰,陈小翔,刘翔翔,等.非编码RNA编码多肽的研究进展[J].中华检验医学杂志,2021,44(10):978-982.
[16] Zhong Q,Lu M,Yuan W,et al. Eight-lncRNA signature of cervical cancer were identified by integrating DNA methylation,copy number variation and transcriptome data [J]. J Transl Med,2021,19(1):58.
[17] Yang J,Wu W,Wu M,et al. Long noncoding RNA ADPGK-AS1 promotes cell proliferation,migration,and EMT process through regulating miR-3196/OTX1 axis in breast cancer [J]. In Vitro Cell Dev Biol Anim,2019,55(7):522-532.
[18] 高红叶,李莲,郑红.低表达miR-1301与卵巢癌患者不良预后的相关分析[J].天津医药,2017,45(3):258-262.
[19] Wang L,Zhao Y,Xu M,et al. Serum miR-1301-3p,miR-335-5p,miR-28-5p,and their target B7-H3 may serve as novel biomarkers for colorectal cancer [J]. J BUON,2019,24(3):1120-1127.
[20] 张飞,史成宇,杨世坤,等.miR-1301对肝细胞肝癌增殖的影响及机制研究[J].南京医科大学学报(自然科学版),2020,40(3):355-359.
[21] Wu Q,Chen Z,Zhang G,et al. EZH2 induces the expression of miR-1301 as a negative feedback control mechanism in triple negative breast cancer [J]. Acta Biochim Biophys Sin(Shanghai),2018,50(7):693-700.
[22] Peng X,Yan B,Shen Y. MiR-1301-3p inhibits human breast cancer cell proliferation by regulating cell cycle progression and apoptosis through directly targeting ICT1 [J]. Breast Cancer,2018,25(6):742-752.
[23] 周鉴基,王山,王太洪.ADPGK-AS1调控miR-1301-3p基因表达影响胃癌细胞增殖和凋亡的机制研究[J].河北医药,2021,43(9):1285-1290.
[24] Huang Z,Yang H. Upregulation of the long noncoding RNA ADPGK-AS1 promotes carcinogenesis and predicts poor prognosis in gastric cancer [J]. Biochem Biophys Res Commun,2019,513(1):127-134. |
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