Association between GLS Gene Polymorphisms and the Susceptibility to Lung Cancer in the Chinese Han Population

被引:2
作者
Wang, Yuhe [1 ,2 ,3 ]
Chen, Mingyue [2 ]
Yi, Faling [2 ]
Xu, Jinpeng [2 ]
Liu, Changchun [2 ]
Zhang, Ziyi [2 ]
Wang, Ping [4 ]
Jin, Tianbo [2 ]
Chen, Mingwei [1 ]
机构
[1] Xi An Jiao Tong Univ, Dept Resp Med, Affiliated Hosp 1, Xian 710061, Shaanxi, Peoples R China
[2] Xizang Minzu Univ, Sch Med, Key Lab Mol Mech & Intervent Res Plateau Dis Tibet, Xianyang 712082, Shaanxi, Peoples R China
[3] Xizang Minzu Univ, Dept Clin Lab, Affiliated Hosp, Xianyang 712082, Shaanxi, Peoples R China
[4] Shaanxi Inst Int Trade & Commerce, Sch Pharm, Xian 712046, Shaanxi, Peoples R China
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2023年 / 28卷 / 05期
关键词
lung cancer; susceptibility; GLS; SNPs; COLORECTAL-CANCER; GLUTAMINASE; EXPRESSION; RISK; EGFR; VARIANTS; GROWTH; TUMOR;
D O I
10.31083/j.fbl2805095
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Lung cancer is one of the most serious malignant tumors endangering human health and life. This study focused on evaluating the association between single nucleotide polymorphisms (SNPs) of the glutaminase (GLS) and lung cancer susceptibility in the Chinese Han population. Methods: A total of 684 lung cancer patients and 684 healthy individuals were enrolled. Five GLS SNPs (rs143584207 C/A, rs117985587 T/C, rs74271715 G/T, rs2355570 G/A, and rs6713444 A/G) were screened as candidate genetic loci. Odds ratios (ORs) and 95% confidence intervals (95% CIs) were calculated to assess the association between GLS SNPs and lung cancer susceptibility. False-positive report probability (FPRP) analysis further verified whether the positive results deserved attention. Finally, the multi-factor dimensionality reduction (MDR) method was applied to analyze the interactions between SNPs. Results: The overall analysis revealed that GLS rs143584207 and rs6713444 were significantly associated with lung cancer susceptibility. The subgroup and clinical information analyses further revealed that GLS rs143584207 and rs6713444 could remarkably reduce lung cancer susceptibility in different subgroups (age >60, females, body mass index (BMI) <24, and lung adenocarcinoma). Rs143584207 could significantly reduce lung cancer susceptibility in non-smokers. Additionally, rs6713444 also had a protective effect on patients with advanced lung cancer. Conclusions: Our study indicated that GLS rs143584207 and rs6713444 could strikingly reduce lung cancer susceptibility in the Chinese Han population, which will give a new direction for the timely treatment of lung cancer.
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页数:10
相关论文
共 35 条
[1]   Divergent trends in lung cancer incidence by gender, age and histological type in Estonia: a nationwide population-based study [J].
Aareleid, Tiiu ;
Zimmermann, Mari-Liis ;
Baburin, Aleksei ;
Innos, Kaire .
BMC CANCER, 2017, 17
[2]   Risk factors of Lung Cancer in nonsmoker [J].
Akhtar, Nahid ;
Bansal, Jeena Gupta .
CURRENT PROBLEMS IN CANCER, 2017, 41 (05) :328-339
[3]   Inhibition of Anaplerotic Glutaminolysis Underlies Selenite Toxicity in Human Lung Cancer [J].
Bruntz, Ronald C. ;
Belshoff, Alex C. ;
Zhang, Yan ;
Macedo, Jessica K. A. ;
Higashi, Richard M. ;
Lane, Andrew N. ;
Fan, Teresa W-M .
PROTEOMICS, 2019, 19 (21-22)
[4]   Expression of GLS1 in intrahepatic cholangiocarcinoma and its clinical significance [J].
Cao, Jun ;
Zhang, Chi ;
Jiang, Guo-Qing ;
Jin, Sheng-Jie ;
Gao, Zhi-Hui ;
Wang, Qian ;
Yu, De-Cai ;
Ke, Ai-Wu ;
Fan, Yi-Qun ;
Li, Da-Wei ;
Wang, Ao-Qing ;
Bai, Dou-Sheng .
MOLECULAR MEDICINE REPORTS, 2019, 20 (02) :1915-1924
[5]   EGFR polymorphisms, hormone replacement therapy and lung adenocarcinoma risk: analysis from a genome-wide association study in never-smoking women [J].
Chen, Kuan-Yu ;
Hsiao, Chin-Fu ;
Chang, Gee-Chen ;
Tsai, Ying-Huang ;
Su, Wu-Chou ;
Chen, Yuh-Min ;
Huang, Ming-Shyan ;
Hsiung, Chao A. ;
Chen, Chien-Jen ;
Yang, Pan-Chyr .
CARCINOGENESIS, 2013, 34 (03) :612-619
[6]   Cancer Statistics in China, 2015 [J].
Chen, Wanqing ;
Zheng, Rongshou ;
Baade, Peter D. ;
Zhang, Siwei ;
Zeng, Hongmei ;
Bray, Freddie ;
Jemal, Ahmedin ;
Yu, Xue Qin ;
He, Jie .
CA-A CANCER JOURNAL FOR CLINICIANS, 2016, 66 (02) :115-132
[7]   Impact of COL6A4P2 gene polymorphisms on the risk of lung cancer: A case-control study [J].
Dang, Xiaodong ;
Zhao, Wenhui ;
Li, Chen ;
Yang, Hua ;
Li, Dianzhen ;
Zhang, Shanshan ;
Jin, Tianbo .
PLOS ONE, 2021, 16 (05)
[8]   NF-kB2 Genetic Variations are Significantly Associated with Non-Small Cell Lung Cancer Risk and Overall Survival [J].
Dimitrakopoulos, Foteinos-Ioannis D. ;
Antonacopoulou, Anna G. ;
Kottorou, Anastasia E. ;
Maroussi, Stella ;
Panagopoulos, Nikolaos ;
Koukourikou, Ioulia ;
Scopa, Chrisoula ;
Kalofonou, Melpomeni ;
Koutras, Angelos ;
Makatsoris, Thomas ;
Papadaki, Helen ;
Dougenis, Dimitrios ;
Brock, Malcolm ;
Kalofonos, Haralabos P. .
SCIENTIFIC REPORTS, 2018, 8
[9]   LKB1 and KEAP1/NRF2 Pathways Cooperatively Promote Metabolic Reprogramming with Enhanced Glutamine Dependence in KRAS-Mutant Lung Adenocarcinoma [J].
Galan-Cobo, Ana ;
Sitthideatphaiboon, Piyada ;
Qu, Xiao ;
Poteete, Alissa ;
Pisegna, Marlese A. ;
Tong, Pan ;
Chen, Pei-Hsuan ;
Boroughs, Lindsey K. ;
Rodriguez, Mirna L. M. ;
Zhang, Winter ;
Parlati, Francesco ;
Wang, Jing ;
Gandhi, Varsha ;
Skoulidis, Ferdinandos ;
DeBerardinis, Ralph J. ;
Minna, John D. ;
Heymach, John, V .
CANCER RESEARCH, 2019, 79 (13) :3251-3267
[10]   Development of lung cancer before the age of 50: the role of xenobiotic metabolizing genes [J].
Gemignani, Federica ;
Landi, Stefano ;
Szeszenia-Dabrowska, Neonilia ;
Zaridze, David ;
Lissowska, Jolanta ;
Rudnai, Peter ;
Fabianova, Eleonora ;
Mates, Dana ;
Foretova, Lenka ;
Janoutl, Vladimir ;
Bencko, Vladimir ;
Gaborieau, Valerie ;
Gioia-Patricola, Lydie ;
Bellini, Ilaria ;
Barale, Roberto ;
Canzian, Federico ;
Hall, Janet ;
Boffetta, Paolo ;
Hung, Raviean J. ;
Brennan, Pul .
CARCINOGENESIS, 2007, 28 (06) :1287-1293