TANG Xiaolong, CHEN Xufeng, ZHENG Yang, YANG Shenglan. Expressions of miR-125a-5p, signal transducer and activator of transcription 3 in gastric cancer and their biological functions[J]. Journal of Clinical Medicine in Practice, 2021, 25(20): 61-67. DOI: 10.7619/jcmp.20212363
Citation: TANG Xiaolong, CHEN Xufeng, ZHENG Yang, YANG Shenglan. Expressions of miR-125a-5p, signal transducer and activator of transcription 3 in gastric cancer and their biological functions[J]. Journal of Clinical Medicine in Practice, 2021, 25(20): 61-67. DOI: 10.7619/jcmp.20212363

Expressions of miR-125a-5p, signal transducer and activator of transcription 3 in gastric cancer and their biological functions

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  • Received Date: June 07, 2021
  • Available Online: November 15, 2021
  • Published Date: October 27, 2021
  •   Objective  To verify the expression of miR-125a-5p, signal transducer and activator of transcription 3 (STAT3) in gastric cancer and their biological functions.
      Methods  Gastric cancer tissues were isolated from 30 patients with gastric cancer, and real-time fluorescent quantitative PCR (qRT-PCR) and Western blot (WB) were used to detect expression of miR-125a-5p and STAT3 in gastric cancer tissue and non-cancerous gastric tissue. After cell transfection, Cell Counting Kit-8 (CCK-8) was used to detect cell viability, and flow cytometry was used to detect cell cycle and apoptosis. Transwell migration test was used to detect migrating cells. The target relationship between miR-125a-5p and STAT3 was verified by dual luciferase reporter gene detection. The tumor inhibitory effect of miR-125a-5p was verified by tumor formation experiment in nude mice in vivo.
      Results  The expression of miR-125a-5p in gastric cancer tissue was significantly lower than that in non-cancerous gastric tissue (P < 0.05). In gastric cancer cell lines, the expression of miR-125a-5p was also significantly lower than that in the normal epithelial cells (P < 0.05). In addition, authors transfected gastric cancer cells with miR-125a-5p mimics, and the results showed that the over-expression of miR-125a-5p was able to inhibit the proliferation, migration and invasion of gastric cancer cells by targeting STAT3. Tumor formation experiment in nude mice verified that over-expression of miR-125a-5p was able to inhibit tumor proliferation and promote tumor cell apoptosis.
      Conclusion  MiR-125a-5p can inhibit tumors by inhibiting the expression of STAT3, and these findings will provide reliable theoretical bases for clinical targeted therapy and early selection of biomarkers.
  • [1]
    殷玉敬, 高辉, 岳林, 等. miR-193a-5p靶向VASP干扰PI3K/AKT信号通路抑制胃癌细胞增殖和诱导细胞凋亡的机制研究[J]. 解放军医药杂志, 2021, 33(5): 35-42. doi: 10.3969/j.issn.2095-140X.2021.05.008
    [2]
    刘会缔, 李彦科, 苗鹏, 等. circZEB1通过竞争性结合hsa-miR-656调控胃癌细胞的增殖和凋亡[J]. 中国医科大学学报, 2021, 50(6): 516-520, 525. https://www.cnki.com.cn/Article/CJFDTOTAL-ZGYK202106008.htm
    [3]
    韩卓婷, 黄妹, 林小菊, 等. 血清蛋白酶原Ⅰ、胃泌素-17及PGR联合检测对早期胃癌的鉴别诊断价值[J]. 沈阳医学院学报, 2020, 22(6): 550-552. https://www.cnki.com.cn/Article/CJFDTOTAL-SYYX202006011.htm
    [4]
    LI S, SUN S J, SUN H M, et al. A risk signature with inflammatory and immune cells infiltration predicts survival and efficiency of chemotherapy in gastric cancer[J]. Int Immunopharmacol, 2021, 96: 107589. doi: 10.1016/j.intimp.2021.107589
    [5]
    刘加霏, 王明义. MicroRNA对胃癌调控作用的研究进展[J]. 生命的化学, 2021, 41(4): 775-782. https://www.cnki.com.cn/Article/CJFDTOTAL-SMHX202104021.htm
    [6]
    XU M M, ZHAN J D, XIE J X, et al. MiR-125a-5p inhibits cell proliferation, cell cycle progression, and migration while promoting apoptosis in head and neck cancers by targeting ERBB3[J]. Auris Nasus Larynx, 2021, 48(3): 477-486. doi: 10.1016/j.anl.2020.10.001
    [7]
    赵华洲, 陈凛. 胃癌相关MicroRNA的研究进展[J]. 实用临床医药杂志, 2017, 21(13): 232-234. doi: 10.7619/jcmp.201713085
    [8]
    CUI L, WANG P, NING D D, et al. Identification of a novel prognostic signature for gastric cancer based on multiple level integration and global network optimization[J]. Front Cell Dev Biol, 2021, 9: 631534. doi: 10.3389/fcell.2021.631534
    [9]
    YOKOTA H, SATO K, SAKAMOTO S, et al. Effects of STAT3 polymorphisms and pharmacokinetics on the clinical outcomes of gefitinib treatment in patients with EGFR-mutation positive non-small cell lung cancer[J]. J Clin Pharm Ther, 2020, 45(4): 652-659. doi: 10.1111/jcpt.13173
    [10]
    CHEN Y, SHAO Z, JIANG E H, et al. CCL21/CCR7 interaction promotes EMT and enhances the stemness of OSCC via a JAK2/STAT3 signaling pathway[J]. J Cell Physiol, 2020, 235(9): 5995-6009. doi: 10.1002/jcp.29525
    [11]
    LI W Z, OKABE A, USUI G, et al. Activation of EHF via STAT3 phosphorylation by LMP2A in Epstein-Barr virus-positive gastric cancer[J]. Cancer Sci, 2021, 112(8): 3349-3362. doi: 10.1111/cas.14978

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