Article Summary
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].现代生物医学进展英文版,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
Received:March 23, 2020  Revised:April 18, 2020
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)
Author NameAffiliationE-mail
WANG Ke Department of Otolaryngology Head and Neck Surgery,Chengdu 363 Hospital Affiliated to Southwest Medical University, Chengdu, Sichuan, 610041, China ym423yu@163.com 
WANG Ying-qiang Department of Otolaryngology Head and Neck Surgery,Chengdu 363 Hospital Affiliated to Southwest Medical University, Chengdu, Sichuan, 610041, China  
YE Jing Department of Otolaryngology Head and Neck Surgery,Chengdu 363 Hospital Affiliated to Southwest Medical University, Chengdu, Sichuan, 610041, China  
ZHANG Xue Department of Otolaryngology Head and Neck Surgery,Chengdu 363 Hospital Affiliated to Southwest Medical University, Chengdu, Sichuan, 610041, China  
ZHONG Ling Department of Otolaryngology Head and Neck Surgery,Chengdu 363 Hospital Affiliated to Southwest Medical University, Chengdu, Sichuan, 610041, China  
YANG Li Department of Otolaryngology Head and Neck Surgery,Chengdu 363 Hospital Affiliated to Southwest Medical University, Chengdu, Sichuan, 610041, China  
MA Shi-li Department of Otolaryngology, Chengdu First People's Hospital, Chengdu, Sichuan, 610016, China  
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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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