Differential expressions of cancer-associated genes and their regulatory miRNAs in colorectal carcinoma

被引:171
作者
Kara, Murat [1 ]
Yumrutas, Onder [2 ]
Ozcan, Onder [3 ]
Celik, Ozgur Ilhan [4 ]
Bozgeyik, Esra [5 ]
Bozgeyik, Ibrahim [2 ]
Tasdemir, Sener [6 ]
机构
[1] Mugla Sitki Kocman Univ, Dept Med Genet, Fac Med, Mugla, Turkey
[2] Adiyaman Univ, Dept Med Biol, Fac Med, Adiyaman, Turkey
[3] Mugla Sitki Kocman Univ, Fac Med, Dept Gen Surg, Mugla, Turkey
[4] Mugla Sitki Kocman Univ, Fac Med, Dept Med Pathol, Mugla, Turkey
[5] Gaziantep Univ, Fac Med, Dept Med Biol & Genet, Gaziantep, Turkey
[6] Ataturk Univ, Fac Med, Dept Med Genet, Erzurum, Turkey
关键词
Colorectal cancer; miRNA; ADAMTS1; FHIT; RUNXs; SIRT1; WWOX; TUMOR-SUPPRESSOR; MICRORNAS; CELLS; PROLIFERATION; PROGRESSION; SIRTUINS; TARGET; RUNX3; SIRT1;
D O I
10.1016/j.gene.2015.04.065
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
Colorectal cancer is one of the frequently seen malignancies in the world. To date, several oncogenes and tumor suppressor genes have been identified and linked to colorectal cancer pathogenesis. Although recent advances in the diagnosis and therapy of colorectal cancer are promising, identifying novel genetic contributors is still high priority. In the present study, expression profile of some cancer-related genes and their regulatory miRNA molecules were evaluated by using a high-throughput real-time PCR method. For the study, a total of 54 patients diagnosed with CRC and normal colon tissue samples of 42 healthy controls were included. For the expression analysis, total RNA was extracted from FFPE tissue samples and converted to cDNA. All expression analyses were assessed by using Fluidigm Microfluidic Dynamic Array chips for 96 samples and the reactions were held in Fluidigm BioMark (TM) HD System Real-Time PCR. As a result of the study, expression of the ADAMTS1, FHIT, RUNX1, RUNX3 and WWOX genes was shown to be significantly altered in CRC tissues in contrast to normal tissue samples. Moreover, miR-378a-3p, miR-155-5p, miR-193b-3p, miR-96-5p, miR-17-5p, miR-27a-3p, miR-133b, miR-203a, miR-205-5p, miR-34c-5p, miR-130a-3p, miR-301a-3p, miR-132-3p, miR-222-3p, miR-34a-5p, miR-21-5p, miR-29a-3p and miR-29b-3p were found to be significantly deregulated in CRC. Consequently, results of the current study strongly suggest the involvement of novel cancer-related genes and their regulatory miRNAs in CRC physiopathology. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:81 / 86
页数:6
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