4.6 Article

Epidermal Growth Factor Receptor (EGFR) Gene Polymorphism May be a Modifier for Cadmium Kidney Toxicity

期刊

GENES
卷 12, 期 10, 页码 -

出版社

MDPI
DOI: 10.3390/genes12101573

关键词

cadmium; EGFR polymorphism; estimated glomerular filtration rate; kidney function

资金

  1. Ministry of Science and Technology [MOST108-2314-B-037-062]
  2. Kaohsiung Medical University Hospital [MOST108-2314-B-037-062]
  3. [KMU-TC109A01-1]
  4. [KMUH109-9T05]

向作者/读者索取更多资源

The study investigated the impact of cadmium exposure on human kidney health and found that EGFR gene polymorphisms could modify Cd kidney toxicity, with certain genotypes potentially having a protective effect, while interactions between cadmium and specific genes could affect kidney function.
The results of many studies indicate that cadmium (Cd) exposure is harmful to humans, with the proximal tubule of the kidney being the main target of Cd accumulation and toxicity. Studies have also shown that Cd has the effect of activating the pathway of epidermal growth factor receptor (EGFR) signaling and cell growth. The EGFR is a family of transmembrane receptors, which are widely expressed in the human kidney. The aim of this study was to investigate the kidney function estimated glomerular filtration rate (eGFR), and its relationship with plasma Cd level and EGFR gene polymorphism. Using data from Academia Sinica Taiwan biobank, 489 subjects aged 30-70 years were analyzed. The demographic characteristics was determined from questionnaires, and biological sampling of urine and blood was determined from physical examination. Kidney function was assessed by the eGFR with CKD-EPI formula. Plasma Cd (ug/L) was measured by inductively coupled plasma mass spectrometry. A total of 97 single-nucleotide polymorphisms (SNPs) were identified in the EGFR on the Taiwan biobank chip, however 4 SNPs did not pass the quality control. Multiple regression analyses were performed to achieve the study aim. The mean (& PLUSMN;SD) plasma Cd level of the study subjects was 0.02 (& PLUSMN;0.008) ug/L. After adjusting for confounding variables, rs13244925 AA, rs6948867 AA, rs35891645 TT and rs6593214 AA types had higher eGFR (4.89 mL/min/1.73 m(2) (p = 0.035), 5.54 mL/min/1.73 m(2) (p = 0.03), 4.96 mL/min/1.73 m(2) (p = 0.048) and 5.16 mL/min/1.73 m(2) (p = 0.048), respectively). Plasma cadmium and rs845555 had an interactive effect on eGFR. In conclusion, EGFR polymorphisms could be modifiers of Cd kidney toxicity, in which rs13244925 AA, rs6948867 AA, rs35891645 TT and rs6593214 AA may be protective, and Cd interacting with rs845555 may affect kidney function.

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