miR-193a-5p promotes pancreatic cancer cell metastasis through SRSF6-mediated alternative splicing of OGDHL and ECM1

被引:12
作者
Li, Manman [1 ]
Wu, Pandi [1 ]
Yang, Zhaocong [2 ]
Deng, Siwei [1 ]
Ni, Lingyu [1 ]
Zhang, Yanfeng [1 ]
Jin, Liang [1 ]
Pan, Yi [1 ]
机构
[1] China Pharmaceut Univ, Sch Life Sci & Technol, Jiangsu Key Lab Druggabil Biopharmaceut, State Key Lab Nat Med, 24 Tongjiaxiang Ave, Nanjing, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Childrens Hosp, Dept Cardiothorac Surg, Nanjing 21008, Peoples R China
基金
中国国家自然科学基金;
关键词
Pancreatic cancer; miR-193a-5p; SRSF6; alternative splicing invasion; migration; OGDHL; ECM1; MICRORNA EXPRESSION PROFILES; DUCTAL ADENOCARCINOMA; FACTOR SRSF6; PROLIFERATION; INVASION;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNAs) are short and non-coding RNAs binding to 3'UTR of target mRNAs to downregulate their expression. Recent studies have shown that miRNAs indirectly regulated alternative splicing (AS) by targeting splicing factors and caused shifts in splicing patterns of target genes. However, the roles of miRNA-regulating splicing factors in pancreatic cancer progression remain unknown. Herein, we reported that miR-193a-5p was markedly upregulated in pancreatic cancer tissues and cells and correlated with clinical outcomes of pancreatic cancer patients. Overexpression of miR-193a-5p contributed to the metastasis of pancreatic cancer cells both in vitro and in vivo. The mechanistic investigation suggested that miR-193a-5p modulated oxoglutarate dehydrogenase-like (OGDHL) and extracellular matrix protein 1 (ECM1) AS by targeting serine/arginine-rich splicing factor 6 (SRSF6), leading to the activation of the epithelial-to-mesenchymal transition (EMT) process. Together, our findings highlighted the role of miR-193a-5p-targeting SRSF6 in pancreatic cancer metastasis, which may serve as a novel target for pancreatic cancer diagnosis and therapy.
引用
收藏
页码:38 / +
页数:29
相关论文
共 57 条
[1]   Regulation of gene expression programmes by serine-arginine rich splicing factors [J].
Aenkoe, Minna-Liisa .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2014, 32 :11-21
[2]   SRSF1-Regulated Alternative Splicing in Breast Cancer [J].
Anczukow, Olga ;
Akerman, Martin ;
Clery, Antoine ;
Wu, Jie ;
Shen, Chen ;
Shirole, Nitin H. ;
Raimer, Amanda ;
Sun, Shuying ;
Jensen, Mads A. ;
Hua, Yimin ;
Allain, Frederic H. -T. ;
Krainer, Adrian R. .
MOLECULAR CELL, 2015, 60 (01) :105-117
[3]  
[Anonymous], FASEB J
[4]   microRNAs target SRSF7 splicing factor to modulate the expression of osteopontin splice variants in renal cancer cells [J].
Boguslawska, Joanna ;
Sokol, Elzbieta ;
Rybicka, Beata ;
Czubaty, Alicja ;
Rodzik, Katarzyna ;
Piekielko-Witkowska, Agnieszka .
GENE, 2016, 595 (02) :142-149
[5]   A protocol for imaging alternative splicing regulation in vivo using fluorescence reporters in transgenic mice [J].
Bonano, Vivian I. ;
Oltean, Sebastian ;
Garcia-Blanco, Mariano A. .
NATURE PROTOCOLS, 2007, 2 (09) :2166-2181
[6]   MicroRNAs regulate the expression of the alternative splicing factor nPTB during muscle development [J].
Boutz, Paul L. ;
Chawla, Geetanjali ;
Stoilov, Peter ;
Black, Douglas L. .
GENES & DEVELOPMENT, 2007, 21 (01) :71-84
[7]   The RNA-binding protein Rbfox2: an essential regulator of EMT-driven alternative splicing and a mediator of cellular invasion [J].
Braeutigam, C. ;
Rago, L. ;
Rolke, A. ;
Waldmeier, L. ;
Christofori, G. ;
Winter, J. .
ONCOGENE, 2014, 33 (09) :1082-1092
[8]  
Bray F, 2018, CA-CANCER J CLIN, V68, P394, DOI [10.3322/caac.21492, 10.3322/caac.21609]
[9]   A specific subset of SR proteins shuttles continuously between the nucleus and the cytoplasm [J].
Cáceres, JF ;
Screaton, GR ;
Krainer, AR .
GENES & DEVELOPMENT, 1998, 12 (01) :55-66
[10]   MicroRNA-222 regulates muscle alternative splicing through Rbm24 during differentiation of skeletal muscle cells [J].
Cardinali, B. ;
Cappella, M. ;
Provenzano, C. ;
Garcia-Manteiga, J. M. ;
Lazarevic, D. ;
Cittaro, D. ;
Martelli, F. ;
Falcone, G. .
CELL DEATH & DISEASE, 2016, 7 :e2086-e2086