Jul 2026· Ecotoxicology and Environmental Safety· Vol 321, pp.
120411
· 0 citations· 35 references
Medicine
TL;DR
Findings from both the epidemiological cohort and murine models suggest a significant link between Cd exposure and colorectal neoplasms and reveal the critical roles of inflammation and gut microbiota alterations in Cd-promoted colorectal tumorigenesis.
Abstract
Cadmium (Cd) is a well-established carcinogenic heavy metal linked to the development of various cancers. However, its role in colorectal neoplasms remains unclear. Using a cross-sectional design involving 2332 Chinese participants, we examined the association between Cd exposure and colorectal neoplasms and further explored underlying mechanisms using murine models exposed to environmentally relevant Cd concentrations in drinking water. Epidemiological analysis showed that elevated whole-blood Cd levels were associated with an increased risk of both non-advanced (prevalence ratio [PR] per log2-transformed increment = 1.12, 95% confidence interval [CI]: 1.05-1.20) and advanced colorectal neoplasms (PR per log2-transformed increment = 1.18, 95% CI: 1.01-1.37). In mice, although Cd exposure did not adversely affect overall health status or intestinal structure, it significantly promoted tumorigenesis and malignant progression in the azoxymethane/dextran sulfate sodium (AOM/DSS) model. Notably, Cd exposure did not affect tumor development in the AOM-only model, suggesting that its tumor-promoting effect is dependent on concurrent intestinal inflammation. Indeed, Cd exposure exacerbated DSS-induced colitis in mice. Additionally, Cd exposure induced distinct gut microbiota alterations, characterized by depletion of Lactobacillus intestinalis, as well as members of Turicibacter and Gordonibacter, and enrichment of members of Enterorhabdus, Allobaculum, and Atopobiaceae. Collectively, findings from both the epidemiological cohort and murine models suggest a significant link between Cd exposure and colorectal neoplasms. Moreover, these data reveal the critical roles of inflammation and gut microbiota alterations in Cd-promoted colorectal tumorigenesis.
Findings demonstrate that subchronic Cd exposure promotes RCC cell proliferation in vitro and highlight Cd as a relevant environmental modifier of RCC progression and underscore the need for further investigation into its clinical implications for metastasis and disease management via in vivo mouse models currently in development.
Lifestyle assessment including smoking status may help identify people with metabolic and alcohol-associated liver disease who are at greater cancer risk, although the pattern was not consistent across every category.
Increasing PM2.5, NO2, NOx, and CO exposures were suggestively associated with increased CRC incidence, particularly among female and Latino participants and for left colon and rectal cancers.
U. Ihenacho, Chiu‐Cheng Tseng, Jun Wu et al.· Environmental Research· 0 citations
Current evidence supports that an association exists between select chemical exposures and TC development, but study limitations prevent any direct link to causation.
Rachael Caretti, H. Arain, Herbert Chen· The Oncologist· 0 citations
There was little evidence of an overall association between alcohol intake and stomach cancer risk, although modest positive associations were observed among never smokers and in Asian cohorts.
H. Jayasekara, Molin Wang, Yang Peng et al.· JNCI Cancer Spectrum· 0 citations
Exposure to toxic metals contributes to the growing burden of noncommunicable diseases (NCDs), yet evidence from sub‐Saharan Africa remains limited. This hospital‐based cross‐sectional study assessed heavy metal (arsenic [As], cadmium [Cd], lead [Pb]) exposure levels and their association with health risks in adult diabetic and hypertensive patients in Cameroon. It involved 178 participants (39 diabetics, 78 hypertensives, 61 comorbid), and the urinary metals were quantified using atomic absorption spectrophotometry and normalized to creatinine. Serum oxidative stress biomarkers including glutathione (GSH), thiobarbituric acid reactive substances (TBARS) and paraoxonase 1 (PON1) were measured. Health risk indices including estimated daily intake (EDI), chronic daily intake (CDI), hazard quotient (HQ), hazard index (HI) and cancer risk (CR), were computed. Proportion contribution trend (PCT), receiver operating characteristic (ROC) and ordinary least squares (OLS) regression were applied for risk and predictive analyses. Diabetic patients exhibited significantly higher (p < 0.05) urinary Cd (5.21 ± 0.83 μg/g creatinine) and Pb (0.66 ± 0.12 μg/g creatinine) levels compared with hypertensive and comorbid patients. GSH levels were markedly lower (p < 0.05) in diabetics than in hypertensives. Although HQs and HIs were < 1, diabetics recorded the highest HI (2.73 × 10−1 ± 2.27 × 10−2; p < 0.05), indicating increased chronic exposure risk. CR values for As and Cd exceeded USEPA thresholds (10−6), with diabetics showing the greatest risk. PCT identified Cd as the dominant contributor to HI across groups. ROC analysis showed that As CDI moderately predicted CR in diabetics (AUC = 0.604; p = 0.047). OLS regression revealed water source and residence as significant determinants of As and Pb exposure. Summarily, diabetic individuals demonstrated disproportionately higher heavy metal exposure and associated carcinogenic risk, largely driven by Cd. Integrating environmental biomonitoring into NCD management is essential to mitigate heavy metal–related health burdens in Cameroon.
Fombat Zenabou Mbebwoh, Muankang Junior Tegha Kum, C. Aphrodite et al.· Journal of Toxicology· 0 citations