Ping Wei, Jiang Wen-Yang, Chen Wen-Shu, Sun Wei, Fu Xiang-Ning
Department of Thoracic Surgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Asian Pac J Cancer Prev. 2013;14(6):3613-8. doi: 10.7314/apjcp.2013.14.6.3613.
To detect expression of hypoxia inducible factor-1α (HIF-1α) and lysyl oxidase (LOX) in non-small cell lung cancer (NSCLC) and explore their roles in prognosis.
The mRNA levels of HIF-1α and LOX were investigated by real-time reverse-transcriptase polymerase chain reaction in 40 cases of tumour and paired normal tissues. In addition, protein expression of HIF-1α and LOX was examined by immunohistochemistry in 82 cases of tumour and 45 paired normal tissues. The relationship between HIF-1α or LOX and clinicopathologic characteristics, as well as the correlation between HIF-1α and LOX, were also examined. Kaplan-Meier survival curves and the log-rank test were used to analyze progression-free survival.
HIF-1α or LOX mRNA levels in tumor tissues was significantly higher than those in paired normal tissues (p<0.01). Positive HIF-1α or LOX protein expression in tumor tissues was noted in 46/82 (56.1%) and 49/82 (59.8%) of the cases, respectively, being significantly higher than those in paired normal tissues (p<0.05). There was significant correlation between the expression of HIF-1α or LOX and tumor size, lymph node metastasis and pathological stage (p<0.05). The expression of HIF-1α and LOX had a significant inverse impact on survival of patients with NSCLC.
HIF-1α and LOX may play a pivotal role in the development of NSCLC, and may act in synergy to promote the progression of NSCLC.
检测非小细胞肺癌(NSCLC)中缺氧诱导因子-1α(HIF-1α)和赖氨酰氧化酶(LOX)的表达,并探讨它们在预后中的作用。
采用实时逆转录聚合酶链反应检测40例肿瘤组织及配对正常组织中HIF-1α和LOX的mRNA水平。此外,采用免疫组织化学法检测82例肿瘤组织及45例配对正常组织中HIF-1α和LOX的蛋白表达。还检测了HIF-1α或LOX与临床病理特征的关系,以及HIF-1α与LOX之间的相关性。采用Kaplan-Meier生存曲线和对数秩检验分析无进展生存期。
肿瘤组织中HIF-1α或LOX的mRNA水平显著高于配对的正常组织(p<0.01)。肿瘤组织中HIF-1α或LOX蛋白阳性表达分别为46/82例(56.1%)和49/82例(59.8%),显著高于配对正常组织(p<0.05)。HIF-1α或LOX的表达与肿瘤大小、淋巴结转移及病理分期之间存在显著相关性(p<0.05)。HIF-1α和LOX的表达对NSCLC患者的生存有显著的负面影响。
HIF-1α和LOX可能在NSCLC的发生发展中起关键作用,并可能协同作用促进NSCLC的进展。