AI Article Synopsis

  • * Results showed that low blood arsenic levels (0.27-0.67 µg/L) were linked to a higher frequency of CRC, with odds ratios (OR) indicating a significant association (e.g., OR: 3.69).
  • * Furthermore, certain gene variants enhanced this correlation, with very high odds ratios for specific polymorphisms, suggesting a potential biomarker role, but the authors recommend further research for validation due to the new insights.

Article Abstract

In following study we examined whether blood arsenic (As) levels combined with specific polymorphisms in , , , , , , , , , 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; = 0.005). This correlation was significantly greater when participants carried particular gene variants: , rs1001179-nonCC (OR: 19.4; = 0.001); rs2032582-CC (OR: 14.8; = 0.024); rs1050450-CC (OR: 11.6; = 0.002) and rs12915189-nonGG (OR: 10.3; = 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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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8469608PMC
http://dx.doi.org/10.3390/biomedicines9091105DOI Listing

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