Qiu Fuman, Yang Lei, Lu Xiaoxiao, Chen Jiansong, Wu Di, Wei Yongfang, Nong Qingqing, Zhang Lisha, Fang Wenxiang, Chen Xiaoliang, Ling Xiaoxuan, Yang Binyao, Zhang Xin, Zhou Yifeng, Lu Jiachun
The State Key Lab of Respiratory Disease, The Institute for Chemical Carcinogenesis, Collaborative Innovation Center for Environmental Toxicity, School of Public Health, Guangzhou Medical University, Guangzhou, People's Republic of China.
Biomedicine Research Center and Department of Surgery, The Third Affiliated Hospital of Guangzhou Medicine University, Guangzhou, People's Republic of China.
PLoS Genet. 2016 Mar 30;12(3):e1005955. doi: 10.1371/journal.pgen.1005955. eCollection 2016 Mar.
Accumulated evidence indicates that rare variants exert a vital role on predisposition and progression of human diseases, which provides neoteric insights into disease etiology. In the current study, based on three independently retrospective studies of 5,016 lung cancer patients and 5,181 controls, we analyzed the associations between five rare polymorphisms (i.e., p.Glu116Lys, p.Asn118Ser, p.Arg138Cys, p.Ala195Thr and p.Leu259Phe) in MKK7 and lung cancer risk and prognosis. To decipher the precise mechanisms of MKK7 rare variants on lung cancer, a series of biological experiments was further performed. We found that the MKK7 p.Glu116Lys rare polymorphism was significantly associated with lung cancer risk, progression and prognosis. Compared with Glu/Glu common genotype, the 116Lys rare variants (Lys/Glu/+ Lys/Lys) presented an adverse effect on lung cancer susceptibility (odds ratio [OR] = 3.29, 95% confidence interval [CI] = 2.70-4.01). These rare variants strengthened patients' clinical progression that patients with 116Lys variants had a significantly higher metastasis rate and advanced N, M stages at diagnosis. In addition, the patients with 116Lys variants also contributed to worse cancer prognosis than those carriers with Glu/Glu genotype (hazard ratio [HR] = 1.53, 95% CI = 1.32-1.78). Functional experiments further verified that the MKK7 p.116Lys variants altered the expression of several cancer-related genes and thus affected lung cancer cells proliferation, tumor growth and metastasis in vivo and in vitro. Taken together, our findings proposed that the MKK7 p.Glu116Lys rare polymorphism incurred a pernicious impact on lung cancer risk and prognosis through modulating expressions of a serial of cancer-related genes.
越来越多的证据表明,罕见变异在人类疾病的易感性和进展中起着至关重要的作用,这为疾病病因学提供了新的见解。在本研究中,基于对5016例肺癌患者和5181例对照的三项独立回顾性研究,我们分析了MKK7基因中五个罕见多态性(即p.Glu116Lys、p.Asn118Ser、p.Arg138Cys、p.Ala195Thr和p.Leu259Phe)与肺癌风险和预后之间的关联。为了阐明MKK7罕见变异影响肺癌的确切机制,我们进一步开展了一系列生物学实验。我们发现,MKK7基因的p.Glu116Lys罕见多态性与肺癌风险、进展及预后显著相关。与Glu/Glu常见基因型相比,116Lys罕见变异(Lys/Glu/+Lys/Lys)对肺癌易感性有不利影响(优势比[OR]=3.29,95%置信区间[CI]=2.70 - 4.01)。这些罕见变异加速了患者的临床进展,携带116Lys变异的患者转移率显著更高,诊断时N、M分期更晚。此外,与Glu/Glu基因型携带者相比,携带116Lys变异的患者癌症预后更差(风险比[HR]=1.53,95%CI=1.32 - 1.78)。功能实验进一步证实,MKK7基因的p.116Lys变异改变了多个癌症相关基因的表达,从而在体内外影响肺癌细胞的增殖、肿瘤生长和转移。综上所述,我们的研究结果表明,MKK7基因的p.Glu116Lys罕见多态性通过调节一系列癌症相关基因的表达,对肺癌风险和预后产生有害影响。