The copy number variation of GSTM1 as a promising prognostic factor of oral squamous cell carcinoma

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article
Data de publicação
2022
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ELSEVIER SCIENCE INC
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ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY, v.134, n.5, p.615-626, 2022
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Unidades Organizacionais
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Resumo
Objective. The aim of this study was to investigate whether the copy number variation (CNV) of GSTM1 and GSTT1 is related to the occurrence of oral squamous cell carcinoma (OSCC) relapses, along the overall and progression-free survival of patients. Study Design. A total of 234 OSCC patients were recruited from the Heliopolis hospital and they were distributed among 4 groups according to the occurrence of OSCC relapses. Fisher exact test, odds ratio (OR), and 95% CI were determined to investigate the chances of OSCC progression. The overall and progression-free survival were analyzed by the Kaplan-Meier and Cox regression methods. Results. The CNV of GSTM1 analysis showed that one copy of the gene was associated with reduced chances of OSCC recurrences (OR 0.45; 95% CI 0.25-0.81) and decreased the risk of tumor progression (HR 0.50; 95% CI 0.33-0.75). Furthermore, one copy of GSTM1 was related to a better overall survival rate (HR 0.63; 95% CI 0.0.44-0.91). Regarding the CNV of GSTT1, no copies were associated with the chances of OSCC relapses, the overall survival, or the progression-free survival. Conclusions. The CNV of GSTM1 may be applied to predict OSCC relapses and aid the treatment management, which might improve the survival rates of patients.
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Referências
  1. Aires FT, 2017, ORL J OTO-RHINO-LARY, V79, P347, DOI 10.1159/000485627
  2. Almal SH, 2012, J HUM GENET, V57, P6, DOI 10.1038/jhg.2011.108
  3. Ambrosone CB, 2001, CANCER RES, V61, P7130
  4. Anantharaman D, 2007, CARCINOGENESIS, V28, P1455, DOI 10.1093/carcin/bgm038
  5. Brasch-Andersen C, 2004, HUM MUTAT, V24, P208, DOI 10.1002/humu.20074
  6. Bray F, 2018, CA-CANCER J CLIN, V68, P394, DOI 10.3322/caac.21492
  7. Carta A, 2018, INT J ENV RES PUB HE, V15, DOI 10.3390/ijerph15081563
  8. Choudhari SK, 2014, ORAL ONCOL, V50, P10, DOI 10.1016/j.oraloncology.2013.09.011
  9. Costa A, 2014, SEMIN CANCER BIOL, V25, P23, DOI 10.1016/j.semcancer.2013.12.007
  10. Curioni OA, 2013, J CANC THER, V4, P978
  11. Drummond SN, 2004, ORAL ONCOL, V40, P52, DOI 10.1016/S1368-8375(03)00132-5
  12. Drummond SN, 2005, ORAL ONCOL, V41, P515, DOI 10.1016/j.oraloncology.2004.12.014
  13. Ferlay J, 2021, INT J CANCER, V149, P778, DOI 10.1002/ijc.33588
  14. Gkouveris I, 2017, TUMOR BIOL, V39, P1, DOI 10.1177/1010428317711659
  15. Gleber-Netto FO, 2015, ORAL ONCOL, V51, P738, DOI 10.1016/j.oraloncology.2015.04.016
  16. Hayes JD, 2005, ANNU REV PHARMACOL, V45, P51, DOI 10.1146/annurev.pharmtox.45.120403.095857
  17. He QF, 2018, J CLIN LAB ANAL, V32, DOI 10.1002/jcla.22403
  18. Hosni A, 2019, RADIOTHER ONCOL, V134, P10, DOI 10.1016/j.radonc.2019.01.014
  19. Hung RJ, 2004, INT J CANCER, V110, P598, DOI 10.1002/ijc.20157
  20. Katakwar P, 2016, J CANCER RES THER, V12, P438, DOI 10.4103/0973-1482.151935
  21. Kim D, 2019, CURR TREAT OPTION ON, V20, DOI 10.1007/s11864-019-0631-8
  22. Leemans CR, 2011, NAT REV CANCER, V11, P9, DOI 10.1038/nrc2982
  23. Li SL, 2019, CANCER CELL INT, V19, DOI 10.1186/s12935-019-0792-3
  24. MILLER SA, 1988, NUCLEIC ACIDS RES, V16, P1215, DOI 10.1093/nar/16.3.1215
  25. Muddathir ARM, 2019, BOSNIAN J BASIC MED, V19, P350, DOI 10.17305/bjbms.2019.4176
  26. Nguyen T, 2003, ANNU REV PHARMACOL, V43, P233, DOI 10.1146/annurev.pharmtox.43.100901.140229
  27. Rhodus Nelson L, 2014, Dent Clin North Am, V58, P315, DOI 10.1016/j.cden.2013.12.004
  28. Olivieri EHR, 2009, ORAL ONCOL, V45, pE73, DOI 10.1016/j.oraloncology.2009.03.004
  29. Rivera C, 2015, INT J CLIN EXP PATHO, V8, P11884
  30. Rockville U.S. Department of Health and Human Services, 2010, CHEM TOX CIG SMOK BI
  31. Rushmore TH, 2002, CURR DRUG METAB, V3, P481, DOI 10.2174/1389200023337171
  32. Safi AF, 2017, J CRANIO MAXILL SURG, V45, P1749, DOI 10.1016/j.jcms.2017.07.012
  33. Sardaro N, 2019, IN VIVO, V33, P289, DOI 10.21873/invivo.11474
  34. Sato M, 2000, ORAL ONCOL, V36, P267, DOI 10.1016/S1368-8375(99)00090-1
  35. Sekikawa S, 2020, J ORAL MAXIL SURG, V78, P469, DOI 10.1016/j.joms.2019.10.018
  36. Singh S, 2015, CANCER CHEMOTH PHARM, V75, P1, DOI 10.1007/s00280-014-2566-x
  37. Speleman F, 2008, CYTOGENET GENOME RES, V123, P176, DOI 10.1159/000184706
  38. Stransky N, 2011, SCIENCE, V333, P1157, DOI 10.1126/science.1208130
  39. Sudmant PH, 2015, SCIENCE, V349, DOI 10.1126/science.aab3761
  40. Taningher M, 1999, MUTAT RES-REV MUTAT, V436, P227, DOI 10.1016/S1383-5742(99)00005-8
  41. Troeltzsch M, 2018, J ORAL MAXIL SURG, V76, P2650, DOI 10.1016/j.joms.2018.07.005
  42. Trueba GP, 2004, FRONT BIOSCI-LANDMRK, V9, P2029, DOI 10.2741/1335
  43. Weckx A, 2019, ORAL ONCOL, V94, P8, DOI 10.1016/j.oraloncology.2019.05.002
  44. Xu CJ, 2005, ARCH PHARM RES, V28, P249, DOI 10.1007/BF02977789
  45. Yanamoto S, 2012, INT J ORAL MAX SURG, V41, P1195, DOI 10.1016/j.ijom.2012.07.011
  46. Zarrei M, 2015, NAT REV GENET, V16, P172, DOI 10.1038/nrg3871
  47. Zhang XM, 2013, PHARMACOGEN PERS MED, V6, P9, DOI 10.2147/PGPM.S35949