Biomedicines (Aug 2021)

Low Blood-As Levels and Selected Genotypes Appears to Be Promising Biomarkers for Occurrence of Colorectal Cancer in Women

  • Piotr Baszuk,
  • Paulina Stadnik,
  • Wojciech Marciniak,
  • Róża Derkacz,
  • Anna Jakubowska,
  • Cezary Cybulski,
  • Tomasz Huzarski,
  • Jacek Gronwald,
  • Tadeusz Dębniak,
  • Katarzyna Białkowska,
  • Sandra Pietrzak,
  • Józef Kładny,
  • Rodney J. Scott,
  • Jan Lubiński,
  • Marcin R. Lener

DOI
https://doi.org/10.3390/biomedicines9091105
Journal volume & issue
Vol. 9, no. 9
p. 1105

Abstract

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In following study we examined whether blood arsenic (As) levels combined with specific polymorphisms in MT1B, GSTP1, ABCB1, NQO1, CRTC3, GPX1, SOD2, CAT, XRCC1, ERCC2 can be used as a marker for the detection of colorectal cancer (CRC) among Polish women. A retrospective case-control study of CRC included 83 CRC cases and 78 healthy controls. From each study participant pre-treatment peripheral blood was collected for As level measurement by inductively coupled–plasma mass spectrometry (ICP-MS). We estimated the odds ratio (OR) of the association between blood-As levels and CRC using multivariable unconditional logistic regression models. A low blood-As level (0.27–0.67 µg/L) was associated with an increased frequency of CRC (OR: 3.69; p = 0.005). This correlation was significantly greater when participants carried particular gene variants: CAT, rs1001179-nonCC (OR: 19.4; p = 0.001); ABCB1 rs2032582–CC (OR: 14.8; p = 0.024); GPX1 rs1050450-CC (OR: 11.6; p = 0.002) and CRTC3 rs12915189-nonGG (OR: 10.3; p = 0.003). Our study provides strong evidence that low blood-As levels are significantly associated with increased CRC occurrence and that particular gene variants significantly enhanced this correlation however, due to the novelty of these findings, we suggest further validation before a definitive statement that the combined effect of low blood-As levels with specific gene polymorphisms is a suitable CRC biomarker.

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