|本期目录/Table of Contents|

[1]王小东,马博昭,戚 峰.MiR-148a-3p通过靶向SRPK2抑制结肠癌细胞转移[J].天津医科大学学报,2019,25(02):99-104109.
 WANG Xiao-dong,MA Bo-zhao,QI Feng.MiR-148a-3p inhibits colon cancer cell metastasis by targeting SRPK2[J].Journal of Tianjin Medical University,2019,25(02):99-104109.
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MiR-148a-3p通过靶向SRPK2抑制结肠癌细胞转移(PDF)
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《天津医科大学学报》[ISSN:1006-8147/CN:12-1259/R]

卷:
25卷
期数:
2019年02期
页码:
99-104109
栏目:
基础医学
出版日期:
2019-03-20

文章信息/Info

Title:
MiR-148a-3p inhibits colon cancer cell metastasis by targeting SRPK2
文章编号:
1006-8147(2019)02-0099-06
作者:
王小东马博昭戚 峰
(天津医科大学总医院普通外科,天津 300052)
Author(s):
WANG Xiao-dong MA Bo-zhao QI Feng
(Department of General Surgery, General Hospital , Tianjin Medical University ,Tianjin 300052,China)
关键词:
miRNA结肠癌转移上皮-间质转化
Keywords:
miRNA colon cancer metastasis epithelial-mesenchymaltransition
分类号:
R735.3+5
DOI:
-
文献标志码:
A
摘要:
目的:MicroRNA (miRNA/miR)参与结肠癌各种生物学过程。目前,miR-148a-3p在结肠癌中的作用还不完全清楚。本研究旨在探讨miR-148a-3p对结肠癌细胞转移及侵袭能力的影响及机制。方法:实时定量PCR (qRT-PCR)检测结肠癌细胞系中miR-148a-3p及SRPK2 mRNA的表达,Western blot检测SRPK2 蛋白的表达。使用miR-148a-3p mimic, miR-148a-3p inhibitor调节HCT-116及SW480细胞中miR-148a-3p的水平。通过划痕及transwell实验检测miR-148a-3p对结肠癌细胞迁移及侵袭能力的影响。生物信息学分析预测miR-148a-3p的靶点,荧光素酶报告实验验证。Western blot及qRT-PCR检测miR-148a-3p对结肠癌细胞上皮-间质转化及SRPK2表达的影响。结果:与正常结直肠粘膜细胞FHC相比,结肠癌细胞系中miR-148a-3p水平降低(P<0.05)。结肠癌细胞中miR-148a-3p过表达可以明显抑制结肠癌细胞转移及侵袭能力(P<0.05)。相反的,敲低miR-148a-3p结肠癌细胞转移及侵袭能力增强(P<0.05)。荧光素酶报告系统结果提示SRPK2是miR-148a-3p的直接作用靶点。过表达miR-148a-3p可以抑制SRPK2在结肠癌中的表达(P<0.05),但是敲低miR-148a-3p时SRPK2表达明显增高(P<0.05)。结论:MiR-148a-3p可能通过靶向SRPK2抑制结肠癌细胞的转移及侵袭能力。MiR-148a-3p可能成为诊断和治疗结肠癌的靶点之一。
Abstract:
Objective: To investigate the effects of miR-148a-3p on colon cancer cell metastasis and invasion. Methods: The expressions of miR-148a-3p and SRPK2 mRNA in colon cancer cell lines were detected by quantitative real-time PCR (qRT-PCR). The expression of SRPK2 protein was detected by Western blot. MiR-148a-3p mimic, miR-148a-3p inhibitor was used to regulate the level of miR-148a-3p in HCT-116 and SW480 cells. The effects of miR-148a-3p on the migration and invasion of colon cancer cells were examined by wound-healing and transwellassay. The target of miR-148a-3p was predicted by bioinformatics analysis and was verified by luciferase reporter assay. The effects of miR-148a-3p on epithelial-mesenchymal transition and SRPK2 expression in colon cancer cells were detected by Western blot and qRT-PCR. Results: MiR-148a-3p levels were reduced in CRC cell lines as compared to normal colon cell FHC (P<0.05). Overexpression of miR-148a-3p in colon cancer cells significantly inhibited the metastasis and invasion of colon cancer cells (P<0.05). In contrast, knockdown of miR-148a-3p showed an increased metastasis and invasion of colon cancer cells (P<0.05). SRPK2 is a direct target of miR-148a-3p. Overexpression of miR-148a-3p inhibited the expression of SRPK2 in colon cancer (P<0.05), while the expression of SRPK2 was significantly increased in miR-148a-3p CRC cells (P<0.05). Conclusion: MiR-148a-3p can inhibit the metastasis and invasion of colon cancer cells by targeting SRPK2. MiR-148a-3pmight be one of the targets for the diagnosis and treatment of colon cancer.

参考文献/References:


[1] Siegel R L, Miller K D, Jemal A. Cancer statistics, 2018[J]. CA Cancer J Clin, 2018, 68(1): 7
[2] Garden O J, Rees M, Poston G J, et al. Guidelines for resection of colorectal cancer liver metastases[J]. Gut, 2006, 55(Suppl 3): 1
[3] Gallagher D J, Kemeny N. Metastatic colorectal cancer: from improved survival to potential cure[J]. Oncology, 2010, 78(3/4): 237
[4] Andre T, Bondi C, Navarro M, et al. Improved overall survival with oxaliplatin, fluorouracil, and leucovorin as adjuvant treatment in stage II or III colon cancer in the MOSAIC trial[J]. J Clin Oncol, 2009, 27(19): 3109
[5] Bartel D P. MicroRNAs: genomics, biogenesis, mechanism, and function [J]. Cell, 2004, 116(2): 281
[6] Yan W, Yang W, Liu Z, et al. Characterization of microRNA expression in primary human colon adenocarcinoma cells (SW480) and their lymph node metastatic derivatives(SW620)[J]. Onco Targets Ther, 2018, 11(47):4701
[7] Munkacsy G, Szasz M A, Menyhart O. Gene expression-based prognostic and predictive tools in breast cancer[J]. Breast Cancer, 2015, 22(3): 245
[8] Xu C, Zheng Y, Lian D, et al. Analysis of microRNA expression profile identifies novel biomarkers for non-small cell lung cancer[J]. Tumori, 2015, 101(1): 104
[9] Guo J, Miao Y, Xiao B, et al. Differential expression of microRNA species in human gastric cancer versus non-tumorous tissues[J]. J Gastroenterol Hepatol, 2009, 24(4): 652
[10] Baffa R, Fassan M, Volinia S, et al. MicroRNA expression profiling of human metastatic cancers identifies cancer gene targets[J]. J Pathol, 2009, 219(2): 214
[11] Katar S, Baran O, Evran S, et al. Expression of miRNA-21, miRNA-107, miRNA-137 and miRNA-29b in meningioma[J]. Clin Neurol Neurosurg, 2017, 156:66
[12] Akao Y, Nakagawa Y, Naoe T. MicroRNA-143 and -145 in colon cancer [J]. DNA Cell Biol, 2007, 26(5): 311
[13] Schlormann W, Naumann S, Renner C, et al. Influence of miRNA-106b and miRNA-135a on butyrate-regulated expression of p21 and Cyclin D2 in human colon adenoma cells[J]. Genes Nutr, 2015, 10(6): 50
[14] Borralho P M, Simoes A E, Gomes S E, et al. miR-143 overexpression impairs growth of human colon carcinoma xenografts in mice with induction of apoptosis and inhibition of proliferation[J]. PloS one, 2011, 6(8): e23787
[15] Liffers S T, Munding J B, Vogt M, et al. MicroRNA-148a is down-regulated in human pancreatic ductal adenocarcinomas and regulates cell survival by targeting CDC25B[J]. Lab Invest, 2011, 91(10): 1472
[16] Zheng B, Liang L, Wang C, et al. MicroRNA-148a suppresses tumor cell invasion and metastasis by downregulating ROCK1 in gastric cancer[J]. Clin Cancer Res, 2011, 17(24): 7574
[17] Wang S H, Li X, Zhou L S, et al. microRNA-148a suppresses human gastric cancer cell metastasis by reversing epithelial-to-mesenchymal transition [J]. Tumour Biol, 2013, 34(6): 3705
[18] Shi H, Chen X, Jiang H, et al. miR-148a suppresses cell invasion and migration in gastric cancer by targeting DNA methyltransferase 1 [J]. Oncol Lett, 2018, 15(4): 4944
[19] Chen Y, Min L, Zhang X, et al. Decreased miRNA-148a is associated with lymph node metastasis and poor clinical outcomes and functions as a suppressor of tumor metastasis in non-small cell lung cancer [J]. Oncol Rep, 2013, 30(4): 1832
[20] Xu Y, Chao L, Wang J, et al. miRNA-148a regulates the expression of the estrogen receptor through DNMT1-mediated DNA methylation in breast cancer cells [J]. Oncol Lett, 2017, 14(4): 4736
[21] Li H P, Huang H Y, Lai Y R, et al. Silencing of miRNA-148a by hypermethylation activates the integrin-mediated signaling pathway in nasopharyngeal carcinoma [J]. Oncotarget, 2014, 5(17): 7610
[22] Jang S W, Yang S J, Ehlen A, et al. Serine/arginine protein-specific kinase 2 promotes leukemia cell proliferation by phosphorylating acinus and regulating cyclin A1[J]. Cancer Res, 2008, 68(12): 4559
[23] Wang J, Wu H F, Shen W, et al. SRPK2 promotes the growth and migration of the colon cancer cells [J]. Gene, 2016, 586(1): 41
[24] Volinia S, Calin G A, Liu C G, et al. A microRNA expression signature of human solid tumors defines cancer gene targets [J]. Proceedings of the National Academy of Sciences of the United States of America, 2006, 103(7): 2257
[25] Schetter A J, Leung S Y, Sohn J J, et al. MicroRNA expression profiles associated with prognosis and therapeutic outcome in colon adenocarcinoma [J]. JAMA, 2008, 299(4): 425
[26] Lodes M J, Caraballo M, Suciu D, et al. Detection of cancer with serum miRNAs on an oligonucleotide microarray[J]. PloS One, 2009, 4(7): e6229
[27] Baltruskeviciene E, Schveigert D, Stankevicius V, et al. Down-regulation of miRNA-148a and miRNA-625-3p in colorectal cancer is associated with tumor budding [J]. BMC cancer, 2017, 17(1): 607
[28] Tsai H L, Yang I P, Huang C W, et al. Clinical significance of microRNA-148a in patients with early relapse of stage II stage and III colorectal cancer after curative resection [J]. Translational Research, 2013, 162(4): 258
[29] Li N, Mao D, Cao Y, et al. Downregulation of SIRT6 by miR-34c-5p is associated with poor prognosis and promotes colon cancer proliferation through inhibiting apoptosis via the JAK2/STAT3 signaling pathway [J]. Int J Oncol, 2018, doi:10.3892/ijO. 2018.4304
[30] Gong L, Ren M, Lv Z, et al. miR-92b-3p Promotes Colorectal Carcinoma Cell Proliferation, Invasion, and Migration by Inhibiting FBXW7 In Vitro and In Vivo [J]. DNA Cell Biol, 2018, 37(5): 501
[31] Wei L J, Li J A, Bai D M, et al. miR-223-RhoB signaling pathway regulates the proliferation and apoptosis of colon adenocarcinoma [J]. Chem Biol Interact, 2018, 289: 9
[32] Meng X, Fu R. miR-206 regulates 5-FU resistance by targeting Bcl-2 in colon cancer cells [J]. Onco Targets Ther, 2018, 11: 1757
[33] Meng Q, Chen Y, Lian B, et al. miR218 promotes apoptosis of SW1417 human colon cancer cells by targeting cFLIP [J]. Oncol Rep, 2018, 40(2): 916
[34] Wang H Y, Lin W, Dyck J A, et al. SRPK2: a differentially expressed SR protein-specific kinase involved in mediating the interaction and localization of pre-mRNA splicing factors in mammalian cells [J]. J Cell Biol, 1998, 140(4): 737
[35] Zhuo Y J, Liu Z Z, Wan S, et al. Enhanced expression of SRPK2 contributes to aggressive progression and metastasis in prostate cancer[J]. Biomed Pharmacother, 2018, 102(5): 31

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备注/Memo

备注/Memo:
基金项目 国家自然科学基金资助项目(81570375) 作者简介 王小东(1990-),男,博士在读,研究方向:普通外科;通信作者:戚峰,E-mail:qf@medmail.com.cn,qifengtmu2017@163.com。
更新日期/Last Update: 2019-04-25