[1] FENG RM, ZONG YN, CAO SM, et al.Current cancer situation in China:good or bad news from the 2018 Global Cancer Statistics[J].Cancer Commun (Lond), 2019, 39(1):22. [2] 黄英丹, 鹿全意. MicroRNA介导的急性髓系白血病化疗耐药机制研究进展[J]. 中国实验血液学杂志, 2017, 25(1):255-258. [3] 凌斌勋, 蔡云, 阿斯木古丽·阿不都克里木. 微小RNA-149靶向调控FOXM1的表达及其对非小细胞肺癌细胞A549增殖和凋亡的影响[J]. 临床肿瘤学杂志, 2017, 22(7):583-587. [4] 宋玮华, 刘月华, 关超, 等. miR-149基因对口腔鳞癌生长抑制的研究[J]. 河北医药, 2019, 41(4):520-523. [5] 张琪琪. MicroRNA-149通过拮抗STAT3途径抑制肝脏炎症[M]. 北京化工大学, 2017. [6] 耿亚军, 李树栋, 刘申政, 等. microRNA-149-5p过表达对肝癌细胞HepG2和Bel-7402增殖及迁移的抑制作用[J]. 临床肝胆病杂志, 2017, 33(6):1126-1130. [7] VASAIKAR SV, STRAUB P, WANG J, et al.LinkedOmics: analyzing multi-omics data within and across 32 cancer types[J]. Nucleic Acids Res, 2018, 46(D1):D956-956D963. [8] REN JM, WANG XL, GAO YM, et al.The expression of the nicotinic acetylcholine receptor α3 subunit in the brains of patients with Alzheimer's disease and its effects on α- and γ-secretases and Notch signal transduction in SH-SY5Y cells[J]. Int J Clin Exp Pathol, 2019, 12(9):3644-3652. [9] ASHRAFIZADEH M, ZARRABI A, HUSHMANDI K, et al.MicroRNAs in cancer therapy:Their involvement in oxaliplatin sensitivity/resistance of cancer cells with a focus on colorectal cancer[J]. Life Sci, 2020, 256(7):117973. [10] HE YJ, YU DD, ZHU LP, et al.miR-149 in Human Cancer: A Systemic Review[J]. J Cancer, 2018, 9(2):375-388. [11] TIAN P, YAN L.Inhibition of MicroRNA-149-5p Induces Apoptosis of Acute Myeloid Leukemia Cell Line THP-1 by Targeting Fas Ligand (FASLG)[J]. Med Sci Monit, 2016,22(12):5116-5123. [12] FAN SJ, LI HB, CUI G, et al.miRNA-149* promotes cell proliferation and suppresses apoptosis by mediating JunB in T-cell acute lymphoblastic leukemia[J]. Leuk Res, 2016, 41(2):62-70. [13] FUJII T, SHIMADA K, TATSUMI Y, et al.Syndecan-1 responsive microRNA-126 and 149 regulate cell proliferation in prostate cancer[J]. Biochem Biophys Res Commun, 2015, 456(1):183-189. [14] ZHANG GD, LIU XZ, LI YF, et al.EphB3-targeted regulation of miR-149 in the migration and invasion of human colonic carcinoma HCT116 and SW620 cells[J]. Cancer Sci, 2017, 108(3):408-418. [15] BISCHOFF A, HUCK B, KELLER B, et al.miR149 functions as a tumor suppressor by controlling breast epithelial cell migration and invasion[J]. Cancer Res, 2014, 74(18):5256-5265. [16] 谢顺明, 王文晓, 赵文武. miR-149-3p通过靶向S100A4抑制膀胱癌细胞的增殖、迁移和侵袭[J]. 现代肿瘤医学, 2019, 27(1):12-17. [17] TAO WC, MA CX, A BEMDEN M, et al. Mechanisms underlying the synaptic trafficking of the glutamate delta receptor GluD1[J]. Mol Psychiatry, 2019, 24(10):1451-1460. [18] BENAMER N, MARTI F, LUJAN R, et al.GluD1, linked to schizophrenia, controls the burst firing of dopamine neurons[J]. Mol Psychiatry, 2018, 23(3):691-700. [19] CRAZE ML, EL-ANSARI R, ALESKANDARANY MA, et al.Glutamate dehydrogenase (GLUD1) expression in breast cancer[J]. Breast Cancer Res Treat, 2019, 174(1):79-91. [20] 路欣. HSD17B4促进肝癌细胞增殖及其机制的研究[M]. 河北医科大学, 2015. |