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CASC15 Gene Polymorphisms and Glioma Susceptibility in Chinese Children

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Abstract

Objective

Gliomas are the most common tumors in the central nervous system. The cancer susceptibility candidate 15 (CASC15) gene has been reported to be a susceptibility gene for several types of cancer. No studies have been carried out on the predisposing effect of CASC15 gene single nucleotide polymorphisms (SNPs) on glioma risk.

Methods

In order to determine whether CASC15 gene SNPs are involved in glioma susceptibility, the first association study in a relatively large sample, which consisted of 171 patients and 228 healthy controls recruited from China, was performed. The contribution of SNPs (rs6939340 A>G, rs4712653 T>C and rs9295536 C>A) to the risk of glioma was evaluated by multinomial logistic regression, based on the calculation of the odds ratio (OR) and 95% confidence interval (CI).

Results

In the single locus and combined analysis, it was revealed that the genetic risk score had no significant associations between CASC15 gene SNPs and glioma risk. However, in the stratified analysis, a significant decrease in risk of glioma was observed in subjects of <60 months old with the rs4712653 TT genotype, when compared to those with the CC/CT genotype (OR=0.12, 95% CI=0.02–0.91, P=0.041).

Conclusion

The present study provides referential evidence on the association between the genetic predisposition of the CASC15 gene and glioma risk in Chinese children. However, more well-designed case-control studies and functional experiments are needed to further explore the role of CASC15 gene SNPs.

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References

  1. Ostrom QT, Gittleman H, Liao P, et al. Cbtrus statistical report: Primary brain and central nervous system tumors diagnosed in the united states in 2007–2011. Neuro Oncol, 2014,16 Suppl 4:iv1–63

    Article  Google Scholar 

  2. Neglia JP, Robison LL, Stovall M, et al. New primary neoplasms of the central nervous system in survivors of childhood cancer: A report from the childhood cancer survivor study. J Natl Cancer Inst, 2006,98(21):1528–1537

    Article  Google Scholar 

  3. Feng RM, Zong YN, Cao SM, et al. Current cancer situation in china: Good or bad news from the 2018 global cancer statistics? Cancer Commun (Lond), 2019,39(1):22

    Article  Google Scholar 

  4. Weller M, Wick W, Aldape K, et al. Glioma. Nat Rev Dis Primers, 2015,1:15017

    Article  Google Scholar 

  5. Udaka YT, Packer RJ. Pediatric brain tumors. Neurol Clin, 2018,36(3):533–556

    Article  Google Scholar 

  6. Louis DN, Perry A, Reifenberger G, et al. The 2016 world health organization classification of tumors of the central nervous system: A summary. Acta Neuropathol, 2016,131(6):803–820

    Article  Google Scholar 

  7. Bush NA, Chang SM, Berger MS. Current and future strategies for treatment of glioma. Neurosurg Rev, 2017,40(1):1–14

    Article  Google Scholar 

  8. Bondy ML, Scheurer ME, Malmer B, et al. Brain tumor epidemiology: Consensus from the brain tumor epidemiology consortium. Cancer, 2008,113(7 Suppl):1953–1968

    Article  Google Scholar 

  9. Vienne-Jumeau A, Tafani C, Ricard D. Environmental risk factors of primary brain tumors: A review. Rev Neurol (Paris), 2019,175(10):664–678

    Article  CAS  Google Scholar 

  10. Davis ME. Epidemiology and overview of gliomas. Semin Oncol Nurs, 2018,34(5):420–429

    Article  Google Scholar 

  11. Wrensch M, Jenkins RB, Chang JS, et al. Variants in the cdkn2b and rtel1 regions are associated with high-grade glioma susceptibility. Nat Genet, 2009,41(8):905–908

    Article  CAS  Google Scholar 

  12. Shete S, Hosking FJ, Robertson LB, et al. Genome-wide association study identifies five susceptibility loci for glioma. Nat Genet, 2009,41(8):899–904

    Article  CAS  Google Scholar 

  13. Melin BS, Barnholtz-Sloan JS, Wrensch MR, et al. Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors. Nat Genet, 2017,49(5):789–794

    Article  CAS  Google Scholar 

  14. Kinnersley B, Labussiere M, Holroyd A, et al. Genome-wide association study identifies multiple susceptibility loci for glioma. Nat Commun, 2015,6:8559

    Article  CAS  Google Scholar 

  15. Chen H, Chen G, Li G, et al. Two novel genetic variants in the stk38l and rab27a genes are associated with glioma susceptibility. Int J Cancer, 2019,145(9):2372–2382

    Article  CAS  Google Scholar 

  16. Bhan A, Soleimani M, Mandal SS. Long noncoding rna and cancer: A new paradigm. Cancer Res, 2017,77(15):3965–3981

    Article  CAS  Google Scholar 

  17. Huang T, Alvarez A, Hu B, et al. Noncoding rnas in cancer and cancer stem cells. Chin J Cancer, 2013,32(11):582–593

    Article  CAS  Google Scholar 

  18. Kang CM, Bai HL, Li XH, et al. The binding of lncrna rp11-732m18.3 with 14-3-3 beta/alpha accelerates p21 degradation and promotes glioma growth. EBioMedicine, 2019,45:58–69

    Article  Google Scholar 

  19. Wang J, Zhuo Z, Chen M, et al. Ran/ranbp2 polymorphisms and neuroblastoma risk in chinese children: A three-center case-control study. Aging (Albany NY), 2018,10(4):808–818

    Article  CAS  Google Scholar 

  20. Zhuo ZJ, Liu W, Zhang J, et al. Functional polymorphisms at ercc1/xpf genes confer neuroblastoma risk in chinese children. EBioMedicine, 2018,30:113–119

    Article  Google Scholar 

  21. Maris JM, Mosse YP, Bradfield JP, et al. Chromosome 6p22 locus associated with clinically aggressive neuroblastoma. N Engl J Med, 2008,358(24):2585–93

    Article  CAS  Google Scholar 

  22. Russell MR, Penikis A, Oldridge DA, et al. Casc15-s is a tumor suppressor lncrna at the 6p22 neuroblastoma susceptibility locus. Cancer Res, 2015,75(15):3155–3166

    Article  CAS  Google Scholar 

  23. Capasso M, Diskin SJ, Totaro F, et al. Replication of gwas-identified neuroblastoma risk loci strengthens the role of bard1 and affirms the cumulative effect of genetic variations on disease susceptibility. Carcinogenesis, 2013,34(3):605–611

    Article  CAS  Google Scholar 

  24. Latorre V, Diskin SJ, Diamond MA, et al. Replication of neuroblastoma snp association at the bard1 locus in african-americans. Cancer Epidemiol Biomarkers Prev, 2012,21(4):658–663

    Article  CAS  Google Scholar 

  25. Mondal T, Juvvuna PK, Kirkeby A, et al. Sense-antisense lncrna pair encoded by locus 6p22.3 determines neuroblastoma susceptibility via the usp36-chd7-sox9 regulatory axis. Cancer Cell, 2018,33(3):417–434 e7

    Article  CAS  Google Scholar 

  26. Gao Z, Xiong Z, Sun Y, et al. Casc15 polymorphisms are correlated with cervical cancer susceptibility in chinese women. Mol Genet Genomic Med, 2020,8(6):e1246

    CAS  PubMed  PubMed Central  Google Scholar 

  27. Xie Y, Cheng Y. Long noncoding rna casc15 is upregulated in glioma and facilitates cell proliferation and metastasis via targeting mir-130b-3p. Eur Rev Med Pharmacol Sci, 2019,23(17):7475–7481

    CAS  PubMed  Google Scholar 

  28. He J, Zou Y, Wang T, et al. Genetic variations of gwas-identified genes and neuroblastoma susceptibility: A replication study in southern chinese children. Transl Oncol, 2017,10(6):936–941

    Article  Google Scholar 

  29. Zhang J, Zhuo ZJ, Wang J, et al. Casc15 gene polymorphisms reduce neuroblastoma risk in chinese children. Oncotarget, 2017,8(53):91343–91349

    Article  Google Scholar 

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Correspondence to Li Yuan or Zhen-jian Zhuo.

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The authors declare that they have no conflict of interest.

Additional information

This work was funded by grants from the Natural Science Foundation of Guangdong Province (No. 2020A1515010188), the National Natural Science Foundation of China (Nos. 81802346 and 81672496), and the Science and Technology Project of Guangzhou (No. 201804010042).

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Lin, Hr., Chen, Yp., Chen, Ht. et al. CASC15 Gene Polymorphisms and Glioma Susceptibility in Chinese Children. CURR MED SCI 42, 797–802 (2022). https://doi.org/10.1007/s11596-022-2613-5

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  • DOI: https://doi.org/10.1007/s11596-022-2613-5

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