The Expression of miR-34c-5p Induces G0/G1 Cell Cycle Arrest and Apoptosis in SW480 Colon Cancer Cell

被引:3
作者
Farzaneh, Shirin [1 ]
Bandad, Shabnam [1 ]
Shaban, Faezeh [1 ]
Heshmati, Masoumeh [2 ]
Barikrow, Nooshin [3 ]
Pashapour, Sanaz [4 ]
机构
[1] Islamic Azad Univ, Pharmaceut Sci Ctr, Tehran Med Sci, Tehran, Iran
[2] Islamic Azad Univ, Fac Adv Sci & Technol, Dept Cellular & Mol Biol, Tehran Med Sci, Tehran, Iran
[3] Islamic Azad Univ, Fac Adv Sci & Technol, Dept Genet, Tehran Med Sci, Tehran, Iran
[4] Islamic Azad Univ, Fac Pharm & Pharmaceut Sci, Dept Pharmacol & Toxicol, Tehran Med Sci, Tehran, Iran
来源
IRANIAN JOURNAL OF PHARMACEUTICAL RESEARCH | 2023年 / 22卷 / 01期
关键词
Micro RNAs; miR-34c-5p; Tumor Suppression; Colorectal Cancer; Cell Cycle; Apoptosis; MICRORNAS; INVASION;
D O I
10.5812/ijpr-135501
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Expression of the miR-34 family, including miR-34a/b/c, has been reported to inhibit the progression of several cancer types by inhibiting cell proliferation and inducing apoptosis.Objectives: We attempted to investigate the effect of SW480 cell transfection with miR-34c-5p mimics on cell proliferation.Methods: To do this, SW480 colon cancer cell line was transfected with miR-34c-5p mimics, scramble sequence, and the vehicle in PBS mock, and then cell proliferation was assessed by MTT assay. The population of cells in cell cycle phases, ROS generation, and apoptosis rate were evaluated by flow cytometry. Additionally, we determined the relative expression of apoptotic genes through real-time PCR technique.Results: We observed a reduced proliferation rate in cells transfected with miR-34c-5p compared to the control group (P <0.05). We also found that miR-34c-5p caused a significant increase in apoptosis rate (P < 0.001) and cell cycle arrest in the G0 and G1 phases (P < 0.05). Moreover, a significant increase was reported in the expression of pro-apoptotic genes, including BAK (P < 0.001), BAX and BAD (P < 0.0001), and Caspase 7/9 (P < 0.0001).Conclusions: However, no remarkable difference was seen in the expression of MCL1, BCL2, and CASPASE 3 genes. Our conclusion is that overexpression of miR-34c-5p could be considered a promising approach for colorectal cancer treatment.
引用
收藏
页数:9
相关论文
共 27 条
[1]   Expression of miR-34c induces G2/M cell cycle arrest in breast cancer cells [J].
Achari, Chandrani ;
Winslow, Sofia ;
Ceder, Yvonne ;
Larsson, Christer .
BMC CANCER, 2014, 14
[2]  
Ardekani Ali M., 2010, Avicenna Journal of Medical Biotechnology, V2, P161
[3]   miRNA control of tumor cell invasion and metastasis [J].
Baranwal, Somesh ;
Alahari, Suresh K. .
INTERNATIONAL JOURNAL OF CANCER, 2010, 126 (06) :1283-1290
[4]   Knockdown of the oncogene lncRNA NEAT1 restores the availability of miR-34c and improves the sensitivity to cisplatin in osteosarcoma [J].
Hu, Yuliang ;
Yang, Qiuyong ;
Wang, Long ;
Wang, Shuo ;
Sun, Fei ;
Xu, Dong ;
Jiang, Jian .
BIOSCIENCE REPORTS, 2018, 38
[5]   miR-34a and miR-34b/c Suppress Intestinal Tumorigenesis [J].
Jiang, Longchang ;
Hermeking, Heiko .
CANCER RESEARCH, 2017, 77 (10) :2746-2758
[6]   Role of miRNA-Regulated Cancer Stem Cells in the Pathogenesis of Human Malignancies [J].
Khan, Abdul Q. ;
Ahmed, Eiman, I ;
Elareer, Noor R. ;
Junejo, Kulsoom ;
Steinhoff, Martin ;
Uddin, Shahab .
CELLS, 2019, 8 (08)
[7]   Promising Therapeutic Strategies for Colorectal Cancer Treatment Based on Nanomaterials [J].
Krasteva, Natalia ;
Georgieva, Milena .
PHARMACEUTICS, 2022, 14 (06)
[8]   MiR-34c induces apoptosis and inhibits the viability of M4e cells by targeting BCL2 [J].
Li, Rui ;
Zhang, Hongxia ;
Zheng, Xiling .
ONCOLOGY LETTERS, 2018, 15 (03) :3357-3361
[9]   Transcriptional regulation of nuclear miRNAs in tumorigenesis [J].
Liu, Junjie ;
Yang, Tianhao ;
Huang, Zishen ;
Chen, Huifang ;
Bai, Yinshan .
INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2022, 50 (01)
[10]   Mir-34: A New Weapon Against Cancer? [J].
Misso, Gabriella ;
Di Martino, Maria Teresa ;
De Rosa, Giuseppe ;
Farooqi, Ammad Ahmad ;
Lombardi, Angela ;
Campani, Virginia ;
Zarone, Mayra Rachele ;
Gulla, Annamaria ;
Tagliaferri, Pierosandro ;
Tassone, Pierfrancesco ;
Caraglia, Michele .
MOLECULAR THERAPY-NUCLEIC ACIDS, 2014, 3 :e195