文章摘要
Long Qin,Jing Ge. Expression of PinX1 and hTERT in basal cell carcinoma and their implications. Oncol Transl Med, 2015, 1: 140-143.
Pinx l和hTERT在基底细胞癌组织中的表达及意义
Expression of PinX1 and hTERT in basal cell carcinoma and their implications
Received:January 24, 2015  Revised:June 02, 2015
DOI:10.1007/s10330-015-0065-0
中文关键词: Pinxl,hTERT,基底细胞癌,实时定量PCR
英文关键词: telomerase inhibitor 1 (PinX1); human telomerase reverse transcriptase (hTERT); basal cell carcinoma; real-time polymerase chain reaction; immunohistochemistry
基金项目:
Author NameAffiliationE-mail
Long Qin Qingdao University qinlongliqian@163.com 
Jing Ge* Qingdao University gjing0310@163.com 
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中文摘要:
  摘要: 目的探讨内源性端粒酶抑制基因PinX1和端粒酶逆转录酶hTERT在基底细胞癌组织中的表达及其意义。方法采用实时定量PCR方法检测30例基底细胞癌组织中内源性端粒酶抑制基因PinXl和端粒酶逆转录酶hTERT的mRNA表达水平,并设15例正常人皮肤组织作为对照组。结果实验组PinXl基因的mRNA表达水平(2.75±1.07)低于对照组(4.33±2.92),两者差异具有统计学意义(t=4.128,P<0.05);hTERT基因的mRNA表达水平(5.64±2.37)明显高于对照组(1.55±0.58),两者差异具有统计学意义(t=5.413,P<0.05);Pinxl的表达水平与hTERT表达的相关性无统计学意义(P>0.05 )。结论:PinXl的下调及hTERT上调可能与基底细胞癌发生过程中端粒酶激活及维持机制有关。
英文摘要:
    Objective This study aimed to investigate the expression and significance of PIN2/TERF1 interacting, telomerase inhibitor 1 (PinX1) and human telomerase reverse transcriptase (hTERT) in basal cell carcinoma (BCC). Methods Real-time polymerase chain reaction and immunohistochemistry were performed to quantify the mRNA expressions and integrated optical density (IOD), respectively, of PinX1 and hTERT in BCC specimens (n = 30), as well as in normal skin specimens (n = 15). Results The mRNA expression level and IOD of PinX1 in the BCC samples were both significantly lower than those in the control specimens (P < 0.05). Conversely, the mRNA expression level and IOD of hTERT in BCC were both significantly higher than that in the control samples (P < 0.05). The correlation between the expression levels of PinX1 and hTERT showed no statistical significance (P > 0.05). Conclusion Downregulation of PinX1 and upregulation of hTERT expression may be associated with the activation and maintenance of telomerases in the induction of BCC.
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