|本期目录/Table of Contents|

[1]姜波,文进,刘全新,等.血清miRNA let-7e和miRNA-375表达在食管腺癌早期诊断中的临床意义[J].慢性病学杂志,2018,(03):254-258.
 JIANGBo *,WENJin,LIUQuan-xin,et al.Clinical significance of serum miRNA let-7e and miRNA-375expression in the early diagnosis of esophageal adenocarcinoma[J].,2018,(03):254-258.
点击复制

血清miRNA let-7e和miRNA-375表达在食管腺癌早期诊断中的临床意义(PDF)

《慢性病学杂志》[ISSN:1674-8166/CN:11-5900/R]

卷:
期数:
2018年03期
页码:
254-258
栏目:
论著
出版日期:
2018-03-28

文章信息/Info

Title:
Clinical significance of serum miRNA let-7e and miRNA-375expression in the early diagnosis of esophageal adenocarcinoma
作者:
姜波1文进1刘全新1高爱民1赖建明1毛仁贤1赵胜乾2盛莹1
解放军第159医院(1.病理科;2.消化内科),河南 驻马店 463000
Author(s):
JIANGBo * WENJinLIUQuan-xinGAOAi-minLAIJian-mingMAORen-xianZHAOSheng-qianSHENGYing
*Departmentof Pathology, People'sLiberationArmy159Hospital,Zhumadian, Henan463000,China Correspondingauthor:SHENGYing,E-mail:jiang8848@163.com
关键词:
miRNA let-7emiRNA-375食管腺癌早期诊断癌基因
Keywords:
miRNA let-7e miRNA-375 Esophageal adenocarcinoma Early diagnosis Oncogene
分类号:
R735.1
DOI:
-
摘要:
目的 观察食管腺癌患者血清miRNA let-7e和miRNA-375表达及其临床意义。方法 选取2014年 1月—2017年3月来解放军第159医院就诊的食管腺癌患者65例作为食管腺癌组;选择同期行胃镜检查诊断为 Barrett食管的患者30例和健康体检者30例分别为Barrett食管组和健康对照组。用实时PCR的方法检测并比较各 组血清miRNA let-7e和miRNA-375表达,并观察食管癌患者血清miRNA let-7e和miRNA-375表达水平与 临床病理特征的关系。结果 食管腺癌组患者血清miRNA let-7e表达量明显高于Barrett食管组和健康对照组 (P<0.01),Barrett食管组高于健康对照组(P<0.01),手术后15d血清miRNA let-7e表达水平明显低于治疗前 (P<0.01)。食管腺癌组血清miRNA-375表达量明显低于Barrett食管组和健康对照组(P<0.01),而Barrett食 管组低于健康对照组(P<0.01),治疗后血清miRNA-375水平较治疗前明显升高(P<0.01)。食管腺癌组血清 miRNA let-7e和miRNA-375表达与性别、年龄、肿瘤部位、肿瘤大小和肿瘤浸润深度无明显相关性(P> 0.05),而与分化程度、淋巴转移和肿瘤分期具有明显相关性(P<0.01)。血清miRNA let-7e与miRNA-375表 达呈明显的负相关(r=-0.759,P<0.01)。结论 miRNA let-7e和miRNA-375基因参与了食管腺癌的发生 发展,miRNA let-7e促进肿瘤生长,miRNA-375抑制肿瘤生长,两组存在某种平衡,可能成为早期诊断食管 腺癌的生物标记物。
Abstract:
Objective To observe the expression of serum miRNA let-7e and miRNA-375 in patients with esophageal adenocarcinoma and its clinical significance.Methods Totally65 patients with esopha-geal adenocarcinoma, from January 2014 to March 2017, were selected as esophageal adenocarcinoma group; 30 patients with Barrett’s esophagus were selected for endoscopy as Barrett’s esophagus group; 30 healthy people were selected as healthy control group. The expression of serum miRNA let-7e and miR-NA-375was detected by real-time PCR. The levels of serum miRNA let-7e and miRNA-375were ob-served and compared in three groups, and the relationship between serum miRNA let-7e and miRNA-375 in esophageal adenocarcinoma patients and clinicopathological parameters were also observed. Results The level of serum miRNA let-7e in esophageal adenocarcinoma group was significantly higher than that in Barrett’s esophagus group and healthy control group(P<0.01), and Barrett’s esophagus group was significantly higher than control group(P<0.01). Serum miRNA let-7e was significantly decreased after treatment(P<0.01). The expression of miRNA-375 in esophageal adenocarcinoma group was significant-ly lower than that in Barrett’s esophagus group and healthy control group(P<0.01), and the expressionof Barrett’s esophagus was significantly lower than that of healthy control group(P<0.01). After treat-ment, the serum miRNA-375 level was significantly higher than that before treatment (P<0.01). The expressions of serum miRNA let-7e and miRNA-375 in esophageal adenocarcinoma patients were not significantly correlated with gender, age, tumor location, tumor size and tumor depth(P>0.05), but they were significantly correlated with the degree of differentiation, lymphatic metastasis and tumor stag-ing (P<0.01). The expression of serum miRNA let-7e in patients with esophageal adenocarcinoma was negatively correlated with the expression of serum miRNA-375(r=-0.759, P<0.01). Conclusion The miRNA let-7e and miRNA-375 are involved in the development of esophageal carcinoma. miRNA let-7e promotes tumor growth and miRNA-375 inhibits tumor growth. There is some balance between the two makers, which may become biomarkers of early diagnosis of esophageal adenocarcinoma.

参考文献/References:

[1] Vrana D, Matzenauer M, Aujesky R,et al. Potential Pre-dictive Role of MicroRNAs in the Neoadjuvant Treatment of Esophageal Cancer [J]. Anticancer Res, 2017,37(2):403-412.
[2] Zheng R, Liu Y, Zhang X,et al. miRNA-200c enhances radiosensitivity of esophageal cancer by cell cycle arrest and targeting P21 [J]. Biomed Pharmacother, 2017,90(6): 517-523.
[3] Zang Y, Tai Y, Wan B, et al. miR-200a-3p promotes the proliferation of human esophageal cancer cells by post-transcriptionally regulating cytoplasmic collapsin response mediator protein-1 [J]. Int J Mol Med, 2016,38(5):1558-1564.
[4] Melnik BC, Kakulas F, Geddes DT,et al. Milk miR-NAs: simple nutrients or systemic functional regulators [J]. Nutr Metab (Lond),2016,13(6):42.
[5] Malik R, Mushtaque RS, Siddiqui UA,et al. Association Between Coronary Artery Disease and MicroRNA: Litera-ture Review and Clinical Perspective [J]. Cureus, 2017,9 (4):e1188.
[6] Yan H, Ma F, Zhang Y,et al. miRNAs as biomarkers for diagnosis of heart failure: A systematic review and me-ta-analysis [J]. Medicine (Baltimore), 2017,96(22):e6825.
[7] Perdas E, Stawski R, Nowak D,et al. The Role of miR-NA in Papillary Thyroid Cancer in the Context of miRNA Let-7 Family [J]. Int J Mol Sci,2016,17(6):1-7.
[8] Ventayol M, Vinas JL, Sola A,et al. miRNA let-7e tar-geting MMP9 is involved in adipose-derived stem cell dif-ferentiation toward epithelia [J]. Cell Death Dis, 2014,5(2): e1048.
[9] Vinas JL, Ventayol M, Brune B,et al. miRNA let-7e modulates the Wnt pathway and early nephrogenic markers in mouse embryonic stem cell differentiation [J]. PLoS One,2013,8(4):e60937.
[10] 肖海静,王观宇,董庆华.人肝细胞肝癌和癌旁正常组织microR-NA表达差异的分析[J].肿瘤防治研究,2012,39(8):947-949.
[11] 许一鸣,肖平,仲崇俊,等.食管癌组织中miRNA let-7e的表达 [J].江苏医药,2014,40(21):2582-2584.
[12] Yabushita S, Fukamachi K, Tanaka H,et al. Circulating microRNAs in serum of human K-ras oncogene transgenic rats with pancreatic ductal adenocarcinomas [J]. Pancreas, 2012,41(7):1013-1018.
[13] Hlavna M, Raudenska M, Hudcova K,et al. MicroRNAs and zinc metabolism- related gene expression in prostate cancer cell lines treated with zinc(II) ions [J]. Int J Oncol, 2012,41(6):2237-2244.
[14] Shaker OG, Mohammed SR, Mohammed AM,et al. Im-pact of microRNA-375and its target gene SMAD-7 poly-morphism on susceptibility of colorectal cancer [J]. J Clin Lab Anal,2017.
[15] Zhou N, Qu Y, Xu C,et al. Upregulation of microRNA-375increases the cisplatin-sensitivity of human gastric can-cer cells by regulating ERBB2 [J]. Exp Ther Med, 2016, 11(2):625-630.

备注/Memo

备注/Memo:
作者简介:姜波,本科,主治医师,主要从事消化道肿瘤的病理学诊断及相关技术检查工作 通信作者:盛莹,E-mail:jiang8848@163.com
更新日期/Last Update: 2018-03-28