Application values of miR-194 and miR-29 in the diagnosis and prognosis of gastric cancer

被引:32
作者
Zhao, Xin [1 ]
Hou, Yunxia [2 ]
Tuo, Zhongzhen [2 ]
Wei, Fangmeng [3 ]
机构
[1] Shandong Univ, Jinan Cent Hosp, Med Res & Lab Diagnost Ctr, Jinan 250013, Shandong, Peoples R China
[2] Weifang Yidu Cent Hosp, Dept Clin Lab, Weifang 262500, Shandong, Peoples R China
[3] Weifang Peoples Hosp, Dept Clin Lab, 151 Guangwen St, Weifang 261041, Shandong, Peoples R China
关键词
miR-194; miR-29; RT-PCR; gastric cancer; RENAL-CELL CARCINOMA; BLADDER-CANCER; BREAST-CANCER; LUNG-CANCER; INVASION; EXPRESSION; MIGRATION; MICRORNA; PATHWAY; PROTEIN;
D O I
10.3892/etm.2018.5931
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The object of this study was to analyzethe expression of miR-194 and miR-29 in gastric cancer and their roles in the regulation of malignant phenotype of gastric cancer cells, and to explore the application value of miR-194 and miR-29 in diagnosis and prognosis of gastric cancer. Tumor tissue and adjacent healthy tissue of 165 gastric cancer patients diagnosed by pathologic examinations were collected. Expression of miR-194 and miR-29 in the tissues was detected by RT-PCR. The relationship between miR-194 and miR-29 expression and clinical data was analyzed. SGC7901 cells were treated with miR-194 and miR-29 mimics, respectively. Effects of miR-194 and miR-29 on proliferation and invasion of SGC7901 cells were investigated. Expression levels of miR-194 and miR-29 in tumor tissue were lower than those in adjacent tissues (P < 0.001). There was no significant difference in expression level of miR-194 and miR-29 in cancer tissues derived from gastric cancer patients in different age and gender groups (P > 0.05). Expression of miR-194 and miR-29 in tumor tissue was closely related to TNM stage, differentiation degree of cancer cells and lymph node metastasis (P < 0.05). Proliferation and migration of SGC7901 cells were significantly inhibited by miR-194 mimic and miR-29 mimic transfection (P < 0.05). miR-194 and miR-29 are downregulated in gastric cancer, and the expression levels of miR-194 and miR-29 were closely related to tumor differentiation and metastasis. Overexpression of miR-194 and miR-29 significantly inhibited the proliferation and migration of gastric cancer. The detection of the expression of miR-194 and miR-29 can provide basis for the diagnosis and prognosis of gastric cancer.
引用
收藏
页码:4179 / 4184
页数:6
相关论文
共 30 条
[1]   MicroRNAs: Target Recognition and Regulatory Functions [J].
Bartel, David P. .
CELL, 2009, 136 (02) :215-233
[2]   MicroRNAs in liver cancer: a model for investigating pathogenesis and novel therapeutic approaches [J].
Callegari, E. ;
Gramantieri, L. ;
Domenicali, M. ;
D'Abundo, L. ;
Sabbioni, S. ;
Negrini, M. .
CELL DEATH AND DIFFERENTIATION, 2015, 22 (01) :46-57
[3]   Antisense inhibition of human miRNAs and indications for an involvement of miRNA in cell growth and apoptosis [J].
Cheng, AM ;
Byrom, MW ;
Shelton, J ;
Ford, LP .
NUCLEIC ACIDS RESEARCH, 2005, 33 (04) :1290-1297
[4]   miRNAs Are Essential for the Regulation of the PI3K/AKT/FOXO Pathway and Receptor Editing during B Cell Maturation [J].
Coffre, Maryaline ;
Benhamou, David ;
Riess, David ;
Blumenberg, Lili ;
Snetkova, Valentina ;
Hines, Marcus J. ;
Chakraborty, Tirtha ;
Bajwa, Sofia ;
Jensen, Kari ;
Chong, Mark M. W. ;
Getu, Lelise ;
Silverman, Gregg J. ;
Blelloch, Robert ;
Littman, Dan R. ;
Calado, Dinis ;
Melamed, Doron ;
Skok, Jane A. ;
Rajewsky, Klaus ;
Koralov, Sergei B. .
CELL REPORTS, 2016, 17 (09) :2271-2285
[5]   miRBase: tools for microRNA genomics [J].
Griffiths-Jones, Sam ;
Saini, Harpreet Kaur ;
van Dongen, Stijn ;
Enright, Anton J. .
NUCLEIC ACIDS RESEARCH, 2008, 36 :D154-D158
[6]   miR-194 is a negative regulator of GEF-H1 pathway in melanoma [J].
Guo, Bingyu ;
Hui, Qiang ;
Zhang, Yu ;
Chang, Peng ;
Tao, Kai .
ONCOLOGY REPORTS, 2016, 36 (04) :2412-2420
[7]   MicroRNA gene expression deregulation in human breast cancer [J].
Iorio, MV ;
Ferracin, M ;
Liu, CG ;
Veronese, A ;
Spizzo, R ;
Sabbioni, S ;
Magri, E ;
Pedriali, M ;
Fabbri, M ;
Campiglio, M ;
Ménard, S ;
Palazzo, JP ;
Rosenberg, A ;
Musiani, P ;
Volinia, S ;
Nenci, I ;
Calin, GA ;
Querzoli, P ;
Negrini, M ;
Croce, CM .
CANCER RESEARCH, 2005, 65 (16) :7065-7070
[8]   Serum microRNA expression signatures identified from genome-wide microRNA profiling serve as novel noninvasive biomarkers for diagnosis and recurrence of bladder cancer [J].
Jiang, Xiumei ;
Du, Lutao ;
Wang, Lili ;
Li, Juan ;
Liu, Yimin ;
Zheng, Guixi ;
Qu, Ailin ;
Zhang, Xin ;
Pan, Hongwei ;
Yang, Yongmei ;
Wang, Chuanxin .
INTERNATIONAL JOURNAL OF CANCER, 2015, 136 (04) :854-862
[9]   Tumour-suppressive microRNA-29s inhibit cancer cell migration and invasion by targeting laminin-integrin signalling in head and neck squamous cell carcinoma [J].
Kinoshita, T. ;
Nohata, N. ;
Hanazawa, T. ;
Kikkawa, N. ;
Yamamoto, N. ;
Yoshino, H. ;
Itesako, T. ;
Enokida, H. ;
Nakagawa, M. ;
Okamoto, Y. ;
Seki, N. .
BRITISH JOURNAL OF CANCER, 2013, 109 (10) :2636-2645
[10]   Restoration of MYC-repressed miR-29 in pancreatic cancer cells leads to increased reactive oxygen species and gemcitabine sensitization [J].
Kwon, Jason J. ;
Quirin, Kayla ;
Aljoufi, Arafat ;
Nafiseh, Amira ;
Kota, Janaiah .
CANCER RESEARCH, 2017, 77