期刊文献+

HOXA13在非小细胞肺癌组织中的表达及其对A549细胞和移植瘤生长的影响 被引量:1

Expression of HOXA13 in non-small cell lung cancer tissues and its effect on growth of xenograft in nude mice
下载PDF
导出
摘要 目的:探讨HOXA13在非小细胞肺癌(non-small cell lung cancer,NSCLC)组织中的表达及沉默HOXA13基因表达对A549细胞和移植瘤生长的影响。方法:收集2014年3月至2016年4月在焦作煤业集团有限责任公司中央医院胸外科接受手术切除治疗的112例NSCLC癌组织和相对应的癌旁组织。q PCR实验检测NSCLC癌和癌旁组织中HOXA13表达。培养A549细胞并分为siRNA-HOXA13组、阴性对照组和对照组,q PCR实验检测A549细胞中HOXA13表达,CCK-8法检测细胞增殖能力,Transwell法检测细胞侵袭能力。建立裸鼠移植瘤模型,观察裸鼠生长情况,5周后处死,称瘤体质量并计算抑瘤率;qPCR实验检测瘤体组织中HOXA13表达水平。结果:NSCLC癌组织中HOXA13 mRNA相对表达量明显高于癌旁组织(1.83±0.13 vs 1.12±0.10,t=47.008,P=0.000),其相对表达量与TNM分期、分化程度和淋巴结转移相关(P<0.05)。siRNA-HOXA13组细胞中HOXA13 mRNA相对表达量低于阴性对照组和对照组(均P<0.05);siRNA-HOXA13组24、48、72、96 h时细胞增殖水平(D值)明显低于阴性对照组和对照组(F=30.727、5.427、13.816和24.454,均P<0.05或P<0.01);siRNA-HOXA13组侵袭细胞数低于阴性对照组和对照组(均P<0.05);siRNA-HOXA13组裸鼠移植瘤5周时瘤体质量小于阴性对照组和对照组,而抑瘤率高于阴性对照组(均P<0.05);siRNA-HOXA13组裸鼠移植瘤组织中HOXA13 m RNA相对表达量低于阴性对照组和对照组(均P<0.01)。结论:NSCLC癌组织中HOXA13呈高表达,且与肿瘤发生、进展及转移有关;特异性沉默HOXA13基因表达可抑制细胞增殖和侵袭力,并抑制裸鼠移植瘤生长。 Objective: To investigate the expression of HOXA13 in non-small cell lung cancer(NSCLC) tissues, and to explore the effect of silencing HOXA13 gene on the growth of A549 cells in vitro and xenograft in nude mice. Methods: A total of 112 pairs of NSCLC tissues and corresponding adjacent normal tissues from patients, who underwent surgical resection at the Department of Thoracic surgery, Central Hospital of Jiaozuo Coal Industry Group from March 2014 to April 2016, were selected for this study. Real-time fluorescence quantitative PCR was used to detect the expressions of HOXA13 in NSCLC tissues and adjacent tissues. A549 cells were cultured and divided into siRNA-HOXA13 group, negative control group and control group. Real-time quantitative PCR was used to detect the expression of HOXA13 in cells, CCK-8 was used to detect cell proliferation, and Transwell assay was used to detect cell invasion. Xenograft model in nude mice was constructed, and the growth of nude mice was observed. After 5 weeks, the mice was sacrificed and weighed, and the tumor-inhibition rate was calculated. Real-time fluorescence quantitative PCR(qPCR) was used to detect the expression of HOXA13 in xenograft tissues. Results: The relative expression level of HOXA13 mRNA in NSCLC tissues was significantly higher than that in the adjacent tissues(1.83±0.13 vs 1.12±0.10, t=47.008, P=0.000), and its expression was correlated to TNM staging, differentiation and lymph node metastasis(all P<0.05). The relative expression level of HOXA13 mRNA in cells of siRNAHOXA13 group was lower than that in the negative control group and the control group(P<0.05). The cell proliferation level(D values) at 24, 48, 72 and 96 h in the siRNA-HOXA13 group were significantly lower than those in the negative control group and control group(F=30.727, 5.427, 13.816 and 24.454, all P<0.05 or P<0.01);the number of invasive cells in the siRNA-HOXA13 group was lower than that in the negative control group and the control group(all P<0.05). The mass of xenograft in nude mice at week 5 in the siRNA-HOXA13 group was smaller than that in the negative control group and control group, while the tumor-inhibition rate was higher than the negative control group(all P<0.05). The relative mRNA expression level of HOXA13 in xenograft tumor tissue in the siRNA-HOXA13 group was lower than that in the negative control group and the control group(all P<0.01). Conclusion: HOXA13 was highly expressed in the non-small cell lung cancer tissues, and was related to oncogenesis, progression and metastasis of cancer. Specific silencing of HOXA13 gene expression could inhibit the proliferation and invasion of tumor cells and suppress the growth of xenograft in nude mice.
作者 刘玉玲 黄宝和 LIU Yuling;HUANG Baohe(Department of Respiratory,Central Hospital of Jiaozuo Coal Industry Group Co.,Ltd. of Jiaozuo City,Jiaozuo 454000,Henan,China)
出处 《中国肿瘤生物治疗杂志》 CAS CSCD 北大核心 2019年第6期689-694,共6页 Chinese Journal of Cancer Biotherapy
基金 河南省科技发展计划资助项目(No.152300410158)~~
关键词 非小细胞肺癌 HOXA13基因 小分子RNA干扰 移植瘤 non-small cell lung cancer HOXA13 gene small RNA interference xenograft
  • 相关文献

参考文献10

二级参考文献31

  • 1Ohgo S, Itoh A, Suzuki M,et al. Analysis of hoxall and hoxal3 ex- pression during patternless limb regeneration in Xenopus[ J]. Dev Bi- ol,2010,338(2) :148-157. DOI: 10. 1016/j. ydbio. 2009.11. 026.
  • 2Chew KY, Yu H, ]?ask AJ,et al. HOXA13 and HOXD13 expression during development of the syndactylous digits in the marsupial Macro- puseugenii [J]. BMC Dev Bio1,2012,12:2. DOI : 10.1186/1471. 213X-12-2.
  • 3Zhang Y, Thornburg CK, Stadler HS, et al. 1 H, 15N, and 13C chemi- cal shift assignments of mouse HOXA13 DNA binding domain [J]. Biomol NMR Assign ,2009,3 ( 2 ) : 199-201. DOI 10. 1007/s12104-009-9174-4.
  • 4Yamamoto-Shiraishi Y, Kuroiwa A. Wnt and BMP signaling cooperate with Hox in the control of Six2 expression in limb tendon precursor [J]. Dev Biol,2013,377(2) :363-374. DOI : 10.1016/j. ydbio. 2013.02. 023.
  • 5Zhang Y, Thornburg CK, Stadler HS, et al. Backbone chemical shift assignments of mouse HOXA13 DNA binding domain bound to duplex DNA[ J]. Biomol NMR Assign,2010,4( 1 ) :97-99. DOI : 10. 1007/s12104-010-9216-y.
  • 6Gu ZD, Shen LY, Wang H, et al. HOXA13 promotes cancer cell growth and predicts poor survival of patients with esophageal squa- mous cell carcinoma[ J]. Cancer Res ,2009,69( 12 ) :4969-4973. DOI: 10.1158/0008-5472.
  • 7CAN-08-4546. Di Giacomo D, Pierini V, Barba G, et al. Blast crisis Ph + chronic myeloid leukemia with NUP98/HOXA13 up-regulating MSI2 [ J ]. Mo- lecular Cytogeneties ,2014,7:42. DOI : 10.1186/1755-8166-7-42.
  • 8Guo B, Che T, Shi B, et al. Screening and identification of specific markers for bladder transitional cell carcinoma from urine urothelial cells with suppressive subtractive hybridization and eDNA mieroarray [J]. Can Urol Assoe J,2011,5(6) :E129-E137. DOI : 10. 5489/euaj. 09118.
  • 9Ma RL, Shen LY, Chen KN. Coexpression of ANXA2, SOD2 and HOXA13 predicts poor prognosis of esophageal squamous cell carci- noma[ J]. Oncol Rep,2014,31 (5) :2157-2164. DOI : 10. 3892/0r. 2014. 3088.
  • 10Kang JU. Characterization of amplification patterns and target genes on the short arm of chromosome 7 in early-stage lung adenocarcinoma [J]. Mol Med Rep,2013,8(5) :1373-1378. DOI : 10. 3892/mmr. 2013. 1686.

共引文献122

同被引文献3

引证文献1

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部