实用医学杂志
實用醫學雜誌
실용의학잡지
THE JOURNAL OF PRACTICAL MEDICINE
2014年
4期
560-562
,共3页
莫碧文%李劳冬%王昌明%曾锦荣%王绩英%韦江红%陈峰%黄剑伟%于会娜
莫碧文%李勞鼕%王昌明%曾錦榮%王績英%韋江紅%陳峰%黃劍偉%于會娜
막벽문%리로동%왕창명%증금영%왕적영%위강홍%진봉%황검위%우회나
肺肿瘤%Nanog%CD44%诊断标志物%治疗靶点
肺腫瘤%Nanog%CD44%診斷標誌物%治療靶點
폐종류%Nanog%CD44%진단표지물%치료파점
Lung neoplasms%Nanog%CD44%Diagnostic marker%Therapeutic target
目的:探讨Nanog 和CD44蛋白在肺癌中的表达及其临床意义。方法:采用免疫组化检测50例肺癌组织、32例良性病变肺组织和18例癌旁正常肺组织中Nanog和CD44蛋白的表达,并分析二者与肺癌临床病理因素的关系。结果:Nanog 在肺癌中的表达显著高于良性病变肺组织和正常肺组织(P<0.05);CD44在肺癌、良性病变肺组织和正常肺组织中的表达无统计学差异(P>0.05);Nanog 和CD44在肺鳞癌中的表达显著高于肺腺癌和小细胞肺癌(P<0.05);Nanog 和CD44在肺癌中的表达与淋巴结转移相关(P<0.05),与肺癌患者的性别、年龄、肿瘤大小、TNM分期和肿瘤分化无关(P>0.05)。 Nanog 和CD44在肺癌中的表达呈正相关(r=0.564,P<0.05)。结论:Nanog和CD44蛋白可能共同参与了肺癌的发生发展,Nanog蛋白是一潜在的肺癌诊断标志物及治疗靶点。
目的:探討Nanog 和CD44蛋白在肺癌中的錶達及其臨床意義。方法:採用免疫組化檢測50例肺癌組織、32例良性病變肺組織和18例癌徬正常肺組織中Nanog和CD44蛋白的錶達,併分析二者與肺癌臨床病理因素的關繫。結果:Nanog 在肺癌中的錶達顯著高于良性病變肺組織和正常肺組織(P<0.05);CD44在肺癌、良性病變肺組織和正常肺組織中的錶達無統計學差異(P>0.05);Nanog 和CD44在肺鱗癌中的錶達顯著高于肺腺癌和小細胞肺癌(P<0.05);Nanog 和CD44在肺癌中的錶達與淋巴結轉移相關(P<0.05),與肺癌患者的性彆、年齡、腫瘤大小、TNM分期和腫瘤分化無關(P>0.05)。 Nanog 和CD44在肺癌中的錶達呈正相關(r=0.564,P<0.05)。結論:Nanog和CD44蛋白可能共同參與瞭肺癌的髮生髮展,Nanog蛋白是一潛在的肺癌診斷標誌物及治療靶點。
목적:탐토Nanog 화CD44단백재폐암중적표체급기림상의의。방법:채용면역조화검측50례폐암조직、32례량성병변폐조직화18례암방정상폐조직중Nanog화CD44단백적표체,병분석이자여폐암림상병리인소적관계。결과:Nanog 재폐암중적표체현저고우량성병변폐조직화정상폐조직(P<0.05);CD44재폐암、량성병변폐조직화정상폐조직중적표체무통계학차이(P>0.05);Nanog 화CD44재폐린암중적표체현저고우폐선암화소세포폐암(P<0.05);Nanog 화CD44재폐암중적표체여림파결전이상관(P<0.05),여폐암환자적성별、년령、종류대소、TNM분기화종류분화무관(P>0.05)。 Nanog 화CD44재폐암중적표체정정상관(r=0.564,P<0.05)。결론:Nanog화CD44단백가능공동삼여료폐암적발생발전,Nanog단백시일잠재적폐암진단표지물급치료파점。
Objective To detect the expressions and clinical significance of Nanog and CD44 protein in lung cancer. Methods The expressions of Nanog and CD44 were detected by immunohistochemistry in 50 cases of lung cancer, 32 cases of benign lesion lung tissue and 18 cases of paraneoplastic normal lung tissue. Then their relationships with clinicopathological factors were analyzed. Results The expression of Nanog in lung cancer was significantly higher than those in benign lesion lung tissue and paraneoplastic normal lung tissue (P < 0.05). There was no significant difference of the expression of CD44 among the three groups (P > 0.05). The expressions of Nanog and CD44 in squamous cell carcinomas were higher than those in adenocarcinomas and small cell lung carcinomas (P < 0.05). The expressions of Nanog and CD44 were significantly correlated with lymph node metastasis (P < 0.05), but were not correlated with age, gender, tumour size, TNM stage and differentiation of lung cancer (P>0.05). The positive correlation was also noted between the expressions of Nanog and CD44 in lung cancer (r = 0.564, P < 0.05). Conclusion Nanog and CD44 proteins may participate in the genesis and progression of lung cancer. Nanog protein is a potential diagnostic marker and therapeutic target for lung cancer.