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) ›› 2016, Vol. 54 ›› Issue (7): 69-74.doi: 10.6040/j.issn.1671-7554.0.2015.1146

• • 上一篇    下一篇

IRX5 mRNA在结直肠癌诊断及预后中的价值

刘童,张欣,王传新   

  1. 山东大学齐鲁医院检验医学中心, 山东 济南 250012
  • 收稿日期:2015-11-23 出版日期:2016-07-10 发布日期:2016-07-10
  • 通讯作者: 王传新. E-mail:cxwang@sdu.edu.cn E-mail:cxwang@sdu.edu.cn
  • 基金资助:
    国家自然科学基金(81301506,81472025);山东省科技发展基金(2014GSF118016)

Significance of IRX5 mRNA in the diagnosis and prognosis of colorectal cancer

LIU Tong, ZHANG Xin, WANG Chuanxin   

  1. Department of Clinical Laboratory, Qilu Hospital of Shandong University, Jinan 250012, Shandong, China
  • Received:2015-11-23 Online:2016-07-10 Published:2016-07-10

摘要: 目的 探讨易洛魁家族同源盒基因(IRX5)mRNA在结直肠癌组织中的表达与临床病理及预后的关系。 方法 收集17例炎症性肠病、48例增生性息肉、54例腺瘤、142例结直肠癌及癌旁正常组织手术切除标本,提取组织标本的总RNA,用实时定量PCR(RT-qPCR)方法测定IRX5 mRNA的表达水平,结合临床资料,对IRX5 mRNA的差异表达与结直肠癌患者临床病理信息和预后的相关性进行分析。 结果 在结直肠癌组织中IRX5 mRNA表达量明显高于其他各组。IRX5 mRNA的表达量与肿瘤大小、淋巴结转移和远处转移密切相关(P<0.05)。此外,IRX5 mRNA高表达组的无病生存率(DFS)和总生存率(OS)明显低于低表达组(P<0.001),并且高表达IRX5 mRNA为结直肠癌预后的独立危险因素(P=0.020, HR=1.863; 95%CI=1.101~3.152)。 结论 IRX5 mRNA在结直肠癌组织中表达升高,并且其表达量与肿瘤的恶性程度及预后相关,提示IRX5 mRNA可作为结直肠癌诊断及预后的标志物。

关键词: mRNA, 结直肠肿瘤, 预后, 实时定量PCR, 易洛魁族同源盒基因

Abstract: Objective To investigate the expression and clinical significance of iroquois homeobox(IRX5)mRNA in colorectal cancer(CRC). Methods Expressions of IRX5 mRNA were analyzed in 17 cases of inflammatory bowel diseases, 48 cases of hyperplastic polyp, 54 cases of colorectal adenoma, 142 CRC cases and 142 paired adjacent non-tumorous tissues by quantitative real-time polymerase chain reaction(RT-qPCR). The correlation between IRX5 mRNA expression and prognosis was analyzed. Results IRX5 mRNA expression was significantly elevated in the CRC group when compared with other groups(all P<0.001). In CRC, up-regulation of IRX5 mRNA expression was significantly correlated with tumor size, lymph node metastasis, and distant metastasis(all P<0.05). CRC patients with high IRX5 mRNA expression had poorer disease-free survival(DFS)and overall survival(OS)than those with low IRX5 mRNA expression(log-rank test, P<0.001). Further multivariable Cox regression analysis suggested that increased expression of IRX5 mRNA was an independent prognostic indicator for CRC(P=0.020, HR=1.863, 95%CI=1.101-3.152). Conclusion IRX5 mRNA expression is elevated in CRC, and associated with malignancy and prognosis of CRC, indicating that it may serve as a useful diagnostic and prognostic predictor.

Key words: Iroquois homeobox 5, Colorectal neoplasms, mRNA, RT-qPCR, Prognosis

中图分类号: 

  • R574
[1] 陈琼, 刘志才, 程兰平, 等. 2003~2007年中国结直肠癌发病与死亡分析[J]. 中国肿瘤, 2012, 21(3): 179-182. CHEN Qiong, LIU Zhicai, CHENG Lanping, et al. An analysis of incidence and mortality of colorectal cancer in China, 2003-2007[J]. China Cancer, 2012, 21(3): 179-182.
[2] Edwards BK, Noone AM, Mariotto AB, et al. Annual report to the nation on the status of cancer, 1975-2010, featuring prevalence of comorbidity and impact on survival among persons with lung, colorectal, breast, or prostate cancer[J]. Cancer, 2014, 120(9): 1290-1314.
[3] Cheng CW, Chow RL, Lebel M, et al. The iroquois homeobox gene, Irx5, is required for retinal cone bipolar cell development[J]. Dev Biol, 2005, 287(1): 48-60.
[4] Bonnard C, Strobl AC, Shboul M, et al. Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1[J]. Nat Genet, 2012, 44(6): 709-713.
[5] 杨惠洁, 余爽, 王静, 等. IRX1基因在肝癌中的表达及其临床意义[J]. 中国生物制品学杂志, 2012, 25(10): 1354-1357. YANG Huijie, YU Shuang, WANG Jing, et al. Expression and clinical significance of iroquois homebox gene IRX1 in human hepatocellular carcinoma cells[J]. Chin J Biologicals, 2012, 25(10): 1354-1357.
[6] 潘玉申, 于颖彦, 计骏, 等. 胃癌中IRX1的表达与启动子区甲基化的相关性[J]. 上海交通大学学报(医学版), 2007, 27(5): 524-527. PAN Yushen, YU Yingyan, JI Jun, et al. Correlation between expression of IRX1 gene and promoter sitem ethylation status in gastric cancer[J]. Journal of Shanghai Jiaotong University(Medical Science), 2007, 27(5): 524-527.
[7] Bosse A, Stoykova A, Nieselt-Struwe K, et al. Identification of a novel mouse iroquois homeobox gene, Irx5, and chromosomal localisation of all members of the mouse Iroquois gene family[J]. Dev Dyn, 2000, 218(1): 160-174.
[8] Schmutz J, Martin J, Terry A, et al. The DNA sequence and comparative analysis of human chromosome 5[J]. Nature, 2004, 431(7006): 268-274.
[9] Martin J, Han C, Gordon LA, et al. The sequence and analysis of duplication-rich human chromosome 16[J]. Nature, 2004, 432(7020): 988-994.
[10] Bruneau BG. Irx5: a transcription factor that regulates the cardiac repolarization gradient[J]. Med Sci(Paris), 2006, 22(3): 231-232.
[11] Myrthue A, Rademacher BL, Pittsenbarger J, et al. The iroquois homeobox gene 5 is regulated by 1,25-dihydroxyvitamin D3 in human prostate cancer and regulates apoptosis and the cell cycle in LNCaP prostate cancer cells[J]. Clin Cancer Res, 2008, 14(11): 3562-3570.
[12] Gartel AL, Tyner AL. Transcriptional regulation of the p21(WAF1/CIP1)gene[J]. Exp Cell Res, 1999, 246(2): 280-289.
[13] Gartel AL, Tyner AL. The role of the cyclin-dependent kinase inhibitor p21 in apoptosis[J]. Mol Cancer Ther, 2002, 1(8): 639-649.
[14] 郝艳萍, 胡顺明, 张世栋, 等. 干细胞标记物LGR5在结直肠癌发生发展中的表达及意义[J]. 山东大学学报(医学版), 2009, 47(8): 85-89. HAO Yanping, HU Shunming, ZHANG Shidong, et al. Expression and significance of stem cell marker LGR5 proteins in the development and progression of human colorectal carcinoma[J]. Journal of Shandong University(Health Sciences), 2009, 47(8): 85-89.
[15] Loomans HA, Andl CD. Intertwining of activin a and TGFbeta signaling: dual roles in cancer progression and cancer cell invasion[J]. Cancers, 2014, 7(1): 70-91.
[16] Martorell O, Barriga FM, Merlos-Suarez A, et al. Iro/IRX transcription factors negatively regulate Dpp/TGF-beta pathway activity during intestinal tumorigenesis[J]. EMBO Rep, 2014, 15(11): 1210-1218.
[1] 栗英林,宋道庆,徐忠华. 应用生物信息学方法分析肾透明细胞癌中FKBP11的表达[J]. 山东大学学报 (医学版), 2020, 1(9): 45-51.
[2] 史爽,李娟,米琦,王允山,杜鲁涛,王传新. 胃癌miRNAs预后风险评分模型的构建与应用[J]. 山东大学学报 (医学版), 2020, 1(7): 47-52.
[3] 路璐,孙志钢,张楠. 继发性嗜血细胞综合征1例[J]. 山东大学学报 (医学版), 2020, 1(7): 122-124.
[4] 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.
[5] 宗帅,肖东杰,刘华,郏雁飞,马晓丽,李焕杰,黎娉,郑燕,汪运山. CSN5在胃癌中的表达及与患者预后的相关性[J]. 山东大学学报(医学版), 2017, 55(7): 12-16.
[6] 李雁翔,张温花,杨飞龙,方量,徐忠华. 尿路上皮癌BRCA1基因与蛋白表达的相关性[J]. 山东大学学报(医学版), 2017, 55(5): 91-94.
[7] 孙启晶,陈方方,李春晓,张才擎. PNI及HGB评估中晚期非小细胞肺癌患者预后的临床价值[J]. 山东大学学报(医学版), 2017, 55(4): 55-59.
[8] 董尧,宋亚林,田涛,高建国. 确诊8年未经治疗却无明显进展的阴茎恶性黑色素瘤1例报道[J]. 山东大学学报(医学版), 2017, 55(3): 125-126.
[9] 林家香,郭子嘉,苏鹏,王晓,郭雅欣,吴晓娟,相磊,周志强, 王妍,崔秀杰,潘爱凤,郭成浩. 致癌蛋白CIP2A在乳腺导管上皮恶变中的作用及预测浸润性导管癌患者预后的能力[J]. 山东大学学报(医学版), 2017, 55(3): 100-106.
[10] 周兰兰,潘学谊,郭煜. 48例急性混合细胞表型白血病患者的临床特征及预后[J]. 山东大学学报(医学版), 2017, 55(2): 79-83.
[11] 张希英,翟春颜,李劲松,韩博. 中国尤文肉瘤患者EZH2蛋白表达与临床病理学参数及预后的关系[J]. 山东大学学报(医学版), 2017, 55(2): 84-91.
[12] 刘惠苓,王兴文,冯少滨,冯虹,韩俊庆. B类I型清道夫受体的高表达与结肠癌患者预后的相关性[J]. 山东大学学报(医学版), 2017, 55(10): 84-89.
[13] 李晓宁,崔连群. 急性心肌梗死合并多支血管病变患者非梗死相关动脉处理的时机[J]. 山东大学学报(医学版), 2016, 54(8): 50-54.
[14] 王雯,刘尧,龙飞,马卫霞,苏莉莉. 外周血淋巴细胞/单核细胞比值与恶性胸膜间皮瘤患者预后的关系[J]. 山东大学学报(医学版), 2016, 54(8): 72-77.
[15] 于斐,刘少壮,仲明惟,黄鑫,焦杰,胡三元,于文滨. 基于GC-TOF-MS的结直肠癌代谢组学差异分析[J]. 山东大学学报(医学版), 2016, 54(7): 60-68.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!