Expression and significance of transforming growth factor-β receptor type II and DPC4/Smad4 in non-small cell lung cancer

被引:19
|
作者
Chen, Hong [1 ]
Wang, Jing-Wei [2 ]
Liu, Li-Xin [2 ]
Yan, Ji-Dong [2 ]
Ren, Shu-Hua [2 ]
Li, Yan [2 ]
Lu, Zheng [2 ]
机构
[1] Tangshan Gongren Hosp, Dept Radiotherapy & Chemotherapy, Tangshan 063000, Hebei, Peoples R China
[2] Tangshan Gongren Hosp, Dept Thorac Surg, Tangshan 063000, Hebei, Peoples R China
关键词
transforming growth factor- receptor type II; DPC4; Smad4; non-small cell lung cancer; TGF-BETA; DPC4; INACTIVATION; POOR-PROGNOSIS; PROGRESSION; CARCINOMA; ADENOCARCINOMA; GENE;
D O I
10.3892/etm.2014.2065
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The aim of the present study was to investigate the expression levels of transforming growth factor- (TGF-) receptor type II (TRII) and DPC4/Smad4 in the TGF- signaling pathway and the importance of these expression levels in non-small cell lung cancer (NSCLC). The mRNA and protein expression levels of TRII and DPC4/Smad4 were detected by reverse transcription-quantitative polymerase chain reaction and western blotting, respectively, in NSCLC and control nonlesional lung tissues of 60 patients. The protein expression levels of DPC4/Smad4 were detected by immunohistochemistry in paraffin-embedded samples of NSCLC. In addition, the correlations among the expression levels of TRII and DPC4/Smad4 and their association with the clinical and pathological features of NSCLC were analyzed. The expression levels of TRII and DPC4/Smad4 in NSCLC tissues were significantly lower when compared with the control nonlesional lung tissues (P<0.05). In addition, the expression of TRII and DPC4/Smad4 in poorly-differentiated NSCLC tissues was significantly lower compared with moderately- or well-differentiated NSCLC tissues (P<0.05). The expression levels of TRII and DPC4/Smad4 were significantly lower in NSCLC tissues with metastatic lymph nodes compared with tissue without metastatic lymph nodes (P<0.05). Thus, the expression levels were demonstrated to significantly correlate with the clinical and pathological stages, and subsequently were shown to be associated with the occurrence and progression of NSCLC. In conclusion, TRII and DPC4/Smad4 may play an important role in the tumorigenesis, differentiation and progression of NSCLC via the TGF- signaling pathway.
引用
收藏
页码:227 / 231
页数:5
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