您的位置:山东大学 -> 科技期刊社 -> 《山东大学学报(医学版)》

山东大学学报(医学版) ›› 2014, Vol. 52 ›› Issue (8): 57-62.doi: 10.6040/j.issn.1671-7554.0.2013.773

• 临床医学 • 上一篇    下一篇

循环miR-128在结直肠癌患者血清中的表达及其对细胞迁移侵袭能力的影响

张艳丽1, 刘新风1, 张欣2, 王海燕2, 杨咏梅2, 杜鲁涛2, 王丽丽2, 李培龙2, 王传新2   

  1. 1. 山东省交通医院检验科, 山东 济南 250031;
    2. 山东大学齐鲁医院检验科, 山东 济南 250012
  • 收稿日期:2013-12-27 修回日期:2014-07-02 出版日期:2014-08-10 发布日期:2014-08-10
  • 通讯作者: 王传新。E-mail:wcx6601@126.com E-mail:wcx6601@126.com
  • 基金资助:
    国家自然科学基金(81271916,81301506);高等学校博士学科点专项科研基金(20130131120067);山东省自然科学基金(ZR2013HQ063)

Expression of circulating miR-128 in serum of colorectal cancer and its effect on migration and invasion of colorectal cancer cells

ZHANG Yanli1, LIU Xinfeng1, ZHANG Xin2, WANG Haiyan2, YANG Yongmei2, DU Lutao2, WANG Lili2, LI Peilong2, WANG Chuanxin2   

  1. 1. Department of Clinical Laboratory, Traffic Hospital of Shandong Province, Jinan 250031, Shandong, China;
    2. Department of Clinical Laboratory, Qilu Hospital of Shandong University, Jinan 250012, Shandong, China
  • Received:2013-12-27 Revised:2014-07-02 Online:2014-08-10 Published:2014-08-10

摘要: 目的 检测循环miR-128在结直肠癌患者血清中的表达,观察其对结直肠癌细胞迁移侵袭能力的影响。 方法 实时荧光定量PCR检测57例结直肠癌组和20例健康对照组血清中miR-128的表达,分析其与结直肠癌转移的关系。体外实验观察过表达miR-128对HT-29细胞迁移侵袭能力的影响。结果 结直肠癌组血清miR-128水平明显低于健康对照组(P<0.001),其中转移组水平明显低于未转移组(P=0.014)。ROC曲线分析显示,血清miR-128对诊断结直肠癌和转移鉴别诊断的效能分别为0.85、0.71(P均<0.05)。与阴性对照组和空白对照组比较,转染组的细胞迁移愈合率以及迁移、侵袭细胞数明显减少(P均<0.05)。结论 循环miR-128在结直肠癌患者血清中表达明显下调,并且与转移密切相关,为结直肠癌转移诊断和治疗提供了新思路。

关键词: 结直肠癌, MiR-128, 转移, 侵袭, 迁移

Abstract: Objective To detect the expression of miR-128 in the serum of patients with colorectal cancer and to observe its effect on the migration and invasion of colorectal cancer cells. Methods The serum miR-128 levels were detected by quantitative real-time PCR in 57 cases of colorectal cancer and 20 healthy controls. The correlation between miR-182 expression and colorectal cancer metastasis was analyzed. The migration and invasion ability were observed by vitro experiments in HT-29 cells transfected with miR-128 mimics. Results The miR-128 expression in colorectal cancer was significantly lower than that in healthy controls (P<0.001), and it markedly decreased in the colorectal cancer metastasis group compared with non-metastasis group (P=0.014). The diagnosis and metastasis differential diagnosis capability of serum miR-128 for colorectal cancer was 0.85 and 0.71 (both P<0.05). Compared with the negative control group and blank control group, the migration healing rates and number of migration and invasion cells in the transfection group were significantly decreased (all P<0.05). Conclusion Circulating miR-128 is significantly decreased in serum of colorectal cancer and closely associated with colorectal cancer metastasis, which may provide a new idea for the diagnosis and therapy of colorectal cancer.

Key words: Metastasis, Invasion, Migration, Colorectal cancer, MiR-128

中图分类号: 

  • R735.3+4
[1] Nicoloso M, Spizzo R, Shimizu M, et al. MicroRNAs-the micro steering wheel of tumour metastases [J]. Nat Rev Cancer, 2009, 9(4):293-302.
[2] Turchinovich A, Weiz L, Langheinz A, et al. Characterization of extracellular circulating microRNA [J]. Nucleic Acids Res, 2011, 39(16):7223-7233.
[3] Li M, Fu W, Wo L, et al. miR-128 and its target genes in tumorigenesis and metastasis [J]. Exp Cell Res, 2013, 319(20):3059-3064.
[4] 王传新, 张欣, 王海燕. 检测结直肠癌血清miR-128的专用引物、试剂盒及方法:中国, ZL201310012196 [P]. 2013-12-11.
[5] Zheng G, Wang H, Zhang X, et al. Identification and validation of reference genes for qPCR detection of serum microRNAs in colorectal adenocarcinoma patients [J]. PLoS One, 2013, 8(12): e83025. doi: 10.1371/journal.pone.0083025.
[6] Brismar T B, Kartalis N, Kylander C, et al. MRI of colorectal cancer liver metastases: comparison of orally administered manganese with intravenously administered gadobenate dimeglumine [J]. Eur radiol, 2012, 22(3): 633-641.
[7] Feng B, Dong T, Wang L, et al. Colorectal cancer migration and invasion initiated by microrna-106a [J]. PloS one, 2012, 7(8): e43452. doi: 10.1371/journal.pone.0043452.
[8] Xu Q, Liu L, Qian X, et al. miR-145 directly targets p70s6k1 in cancer cells to inhibit tumor growth and angiogenesis [J]. Nucleic Acids Res, 2012, 40(2):761-774.
[9] Hur K, Toiyama Y, Takahashi M, et al. MicroRNA-200c modulates epithelial-to-mesenchymal transition (EMT) in human colorectal cancer metastasis[J]. Gut, 2012, 62(9):1315-1326.
[10] Li J, Du L, Yang Y, et al. MiR-429 is an independent prognostic factor in colorectal cancer and exerts its anti-apoptotic function by targeting SOX2 [J]. Cancer lett, 2013, 329(1):84-90.
[11] 刘慧, 杜鲁涛, 杨咏梅, 等. MiR-182在结直肠癌中的表达及其对结直肠癌细胞迁移能力的影响 [J]. 山东大学学报: 医学版, 2013, 51(12):70-74.
[12] 李墨林, 沃璐璐, 付红勇, 等. miR-128与恶性肿瘤关系的研究进展[J]. 生命科学, 2013, 25(5):484-489.
[13] Khan A P, Poisson L M, Bhat V B, et al. Quantitative proteomic profiling of prostate cancer reveals a role for miR-128 in prostate cancer [J]. Mol Cell Proteomics, 2010, 9(2):298-312.
[14] Woo H H, Laszlo C F, Greco S, et al. Regulation of colony stimulating factor-1 expression and ovarian cancer cell behavior in vitro by miR-128 and miR-152 [J]. Mol Cancer, 2012, 11: 58. doi: 10.1186/1476-4598-11-58.
[15] Shi Z M, Wang J, Yan Z, et al. MiR-128 inhibits tumor growth and angiogenesis by targeting p70S6K1 [J]. PLoS One, 2012, 7(3):e32709.
[16] Qian P X, Banerjee A, Wu Z S, et al. Loss of SNAIL regulated miR-128-2 on chromosome 3p22.3 targets multiple stem cell factors to promote transformation of mammary epithelial cells [J]. Cancer Res, 2012, 72(22):6036-6050.
[1] 孙薏丰,高玉,梁永媛,高杨. CPLX2在30例肝癌组织的表达及其对体外细胞增殖与侵袭的影响[J]. 山东大学学报 (医学版), 2020, 1(9): 34-39.
[2] 马青源,蒲沛东,韩飞,王超,朱洲均,王维山,史晨辉. miR-27b-3p调控SMAD1对骨肉瘤细胞增殖、迁移和侵袭作用的影响[J]. 山东大学学报 (医学版), 2020, 1(7): 32-37.
[3] 李宁,李娟,谢艳,李培龙,王允山,杜鲁涛,王传新. 长链非编码RNA AL109955.1在80例结直肠癌组织中的表达及对细胞增殖与迁移侵袭的影响[J]. 山东大学学报 (医学版), 2020, 1(7): 38-46.
[4] 底学敏,牛书雷,赵静,杜随,于慧敏,张宏涛,王娟. CT引导下125I粒子植入治疗晚期胃癌淋巴结转移[J]. 山东大学学报(医学版), 2017, 55(9): 79-84.
[5] 李星凯,刘战业,姜运峰,李军. 原发性中央型和周围型肺鳞癌临床病理学及预后差异[J]. 山东大学学报(医学版), 2017, 55(9): 73-78.
[6] 林琦,张颖,袁苑,戴建建,徐瑞彩,杨琦,耿宝成,韩明勇. 肾上腺转移瘤放射性125I粒子植入治疗后胃穿孔1例[J]. 山东大学学报(医学版), 2017, 55(7): 124-129.
[7] 曾海燕,李睿,孙新东,谢鹏,孟雪,范秉杰,李万龙,袁双虎. 局限期小细胞肺癌患者预防性脑照射后脑转移的关联分析:双中心研究[J]. 山东大学学报(医学版), 2017, 55(7): 61-66.
[8] 林琦,张颖,戴建建,徐瑞彩,杨琦,耿宝成,韩明勇. CT引导放射性125I粒子植入治疗23例浅表淋巴结转移瘤[J]. 山东大学学报(医学版), 2017, 55(2): 38-44.
[9] 李扬,何闯,陈玉潇,杨丽,李良山,李廷源,黄学全. 放射性125I粒子植入近距离治疗长骨转移瘤的临床疗效[J]. 山东大学学报(医学版), 2017, 55(2): 50-54.
[10] 袁苑,张颖,林琦,戴建建,李冉冉,徐瑞彩,杨琦,耿宝成,韩猛,韩明勇. 125I粒子植入术后应用透明质酸钠凝胶皮下注射保护皮肤1例[J]. 山东大学学报(医学版), 2017, 55(11): 89-92.
[11] 王贲士, 单军奇,侯庆生,公为鹏,朱振宇,郭洪亮. CD11b+/CD66b-表型髓系细胞在结肠癌进展和肝转移中的作用[J]. 山东大学学报(医学版), 2017, 55(10): 41-45.
[12] 王甜甜,陈洁. EFEMP2在子宫内膜癌组织及细胞中的表达及其临床意义[J]. 山东大学学报(医学版), 2017, 55(10): 52-58.
[13] 陆衡,刘延国,李曙光,陈晓康,田琦,衣翠华,王秀问. YKL-40对卵巢癌SKOV-3细胞迁移能力的影响[J]. 山东大学学报(医学版), 2017, 55(1): 33-38.
[14] 王伟,曹煜姗,孙达权,黄小琼,徐国强. 人TIMP-2蛋白在肝癌细胞迁移与侵袭中的作用[J]. 山东大学学报(医学版), 2016, 54(7): 11-17.
[15] 贺武斌,苏荣健. 白头翁皂苷D联合索拉非尼对人肝癌细胞侵袭与转移的影响[J]. 山东大学学报(医学版), 2016, 54(7): 18-22.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!