Oncotarget

Research Papers:

Target of obstructive sleep apnea syndrome merge lung cancer: based on big data platform

Lifeng Li, Jingli Lu, Wenhua Xue, Liping Wang, Yunkai Zhai, Zhirui Fan, Ge Wu, Feifei Fan, Jieyao Li, Chaoqi Zhang, Yi Zhang and Jie Zhao _

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Oncotarget. 2017; 8:21567-21578. https://doi.org/10.18632/oncotarget.15372

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Abstract

Lifeng Li1,2,3,*, Jingli Lu3,*, Wenhua Xue3,*, Liping Wang2, Yunkai Zhai4,5, Zhirui Fan2, Ge Wu4,5, Feifei Fan1,2,6, Jieyao Li1,2, Chaoqi Zhang1,2, Yi Zhang1,2, Jie Zhao3,4,5

1Biotherapy Center, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, Henan, China

2Department of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, Henan, China

3Department of Pharmacy, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, Henan, China

4Engineering Research Center of Digital Medicine, Zhengzhou 450052, Henan, China

5Engineering Laboratory for Digital Telemedicine Service, Zhengzhou 450052, Henan, China

6Department of Respiratoty and Sleep Disease, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, Henan, China

*These authors have contributed equally to this work

Correspondence to:

Jie Zhao, email: [email protected]

Yi Zhang, email: [email protected]

Keywords: obstructive sleep apnea syndrome, lung cancer, big data platform

Received: October 20, 2016    Accepted: January 16, 2017    Published: February 16, 2017

ABSTRACT

Based on our hospital database, the incidence of lung cancer diagnoses was similar in obstructive sleep apnea Syndrome (OSAS) and hospital general population; among individual with a diagnosis of lung cancer, the presence of OSAS was associated with an increased risk for mortality. In the gene expression and network-level information, we revealed significant alterations of molecules related to HIF1 and metabolic pathways in the hypoxic-conditioned lung cancer cells. We also observed that GBE1 and HK2 are downstream of HIF1 pathway important in hypoxia-conditioned lung cancer cell. Furthermore, we used publicly available datasets to validate that the late-stage lung adenocarcinoma patients showed higher expression HK2 and GBE1 than early-stage ones. In terms of prognostic features, a survival analysis revealed that the high GBE1 and HK2 expression group exhibited poorer survival in lung adenocarcinoma patients. By analyzing and integrating multiple datasets, we identify molecular convergence between hypoxia and lung cancer that reflects their clinical profiles and reveals molecular pathways involved in hypoxic-induced lung cancer progression. In conclusion, we show that OSAS severity appears to increase the risk of lung cancer mortality.


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