文章摘要
王 科,王应强,叶 静,张 雪,钟 玲,杨 力,马世丽.LncRNA RP11-316M1.12在甲状腺乳头状癌中的表达及对细胞侵袭、迁移的影响[J].,2020,(14):2646-2650
LncRNA RP11-316M1.12在甲状腺乳头状癌中的表达及对细胞侵袭、迁移的影响
Expression of LncRNA RP11-316M1.12 in Papillary Thyroid Carcinoma and Its Effects on Cell Invasion and Migration
投稿时间:2020-03-23  修订日期:2020-04-18
DOI:10.13241/j.cnki.pmb.2020.14.009
中文关键词: 长链非编码RNA  RP11-316M1.12  甲状腺乳头状癌  增殖  侵袭  迁移
英文关键词: Long non-coding RNA  RP11-316M1.12  Papillary thyroid carcinoma  Proliferation  Invasion  Migration
基金项目:四川省卫计委基金项目(19PJ141)
作者单位E-mail
王 科 西南医科大学附属成都三六三医院耳鼻喉头颈外科 四川 成都 610041 ym423yu@163.com 
王应强 西南医科大学附属成都三六三医院耳鼻喉头颈外科 四川 成都 610041  
叶 静 西南医科大学附属成都三六三医院耳鼻喉头颈外科 四川 成都 610041  
张 雪 西南医科大学附属成都三六三医院耳鼻喉头颈外科 四川 成都 610041  
钟 玲 西南医科大学附属成都三六三医院耳鼻喉头颈外科 四川 成都 610041  
杨 力 西南医科大学附属成都三六三医院耳鼻喉头颈外科 四川 成都 610041  
马世丽 成都市第一人民医院耳鼻喉科 四川 成都 610016  
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中文摘要:
      摘要 目的:探讨长链非编码RNA(LncRNA)RP11-316M1.12在甲状腺乳头状癌(PTC)中的表达及对细胞侵袭、迁移的影响。方法:采用荧光定量PCR(qRT-PCR)法检测42例PTC组织及其相应癌旁组织中LncRNA RP11-316M1.12表达水平。体外培养TPC-1细胞,将TPC-1细胞分为LncRNA RP11-316M1.12-siRNA组(敲低组)、阴性对照组(NC组)、空白对照组(NG组),qRT-PCR法检测各组TPC-1细胞中LncRNA RP11-316M1.12表达水平,CCK-8法检测各组TPC-1细胞增殖能力,Transwell实验检测各组TPC-1细胞迁移、侵袭能力,Western blot法检测各组TPC-1细胞中上皮-间充质转化(EMT)相关蛋白表达水平。结果:与癌旁组织相比,PTC癌组织中LncRNA RP11-316M1.12相对表达量明显升高(P<0.05)。与NC组、NG组比较,转染24、48、72 h敲低组TPC-1细胞增殖能力受到抑制(P<0.05)。与NC组、NG组比较,敲低组迁移细胞数、侵袭细胞数、间质细胞标志物波形蛋白(vimentin)、N-钙粘附蛋白(N-cadherin)蛋白相对表达量均显著降低(P<0.05),上皮细胞标志物E-钙粘附蛋白(E-cadherin)相对表达量显著升高(P<0.05)。结论:LncRNA RP11-316M1.12在PTC癌组织中呈高表达,沉默LncRNA RP11-316M1.12可抑制TPC-1细胞增殖、迁移、侵袭能力,其机制可能与PTC肿瘤细胞EMT过程有关。
英文摘要:
      ABSTRACT Objective: To investigate the expression of long non-coding RNA (LncRNA) RP11-316M1.12 in papillary thyroid carcinoma (PTC) and its effects on cell invasion and migration. Methods: The expression levels of LncRNA RP11-316M1.12 in PTC tissues and its corresponding paracancerous tissues of 42 cases were detected by fluorescence quantitative PCR (qRT-PCR). TPC-1 cells were cultured in vitro and divided into LncRNA RP11-316M1.12-siRNA group (Knockdown group), negative control group (NC group), blank control group (NG group), the expression of LncRNA RP11-316M1.12 in each group of TPC-1 cells was detected by qRT-PCR, CCK-8 method was used to detect the proliferation of each group of TPC-1 cells, the cell migration and invasion of each group of TPC-1 cells was detected by Transwell test, Western blot method was used to detect the expression levels of epithelial-mesenchymal transition (EMT) related proteins in each group of TPC-1 cells. Results: Compared with the paracancerous tissues, the relative expression of LncRNA RP11-316M1.12 was significantly higher in PTC tissues(P<0.05). Compared with NC group and NG group, the proliferation of TPC-1 cells was inhibited in knockdown group after transfection for 24, 48, 72 h(P<0.05). Compared with NC group and NG group, the number of migrating cells, invasive cells, the relative expressions of stromal cell markers vimentin(vimentin) and N-epithelial cadherin (N-cadherin) decreased significantly(P<0.05), the relative expression of epithelial cell marker E-epithelial cadherin(E-cadherin) increased significantly (P<0.05). Conclusion: LncRNA RP11-316M1.12 is highly expressed in PTC tissues, silent LncRNA RP11-316M1.12 can inhibit the proliferation, migration and invasion of TPC-1 cells and its mechanism may be related to the EMT processes of PTC tumor cells.
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