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The link between microplastics and colorectal cancer
Anisha Lynch-Godrei1,2,3, Christopher Leung4,5,6
1Department of Medicine, The University of Melbourne, Parkville, VIC, 3010, Australia.
Abstract:
Microplastics and nanoplastics (MNPLs) are known to enter the human body and accumulate within different tissues. As MNPLs have been shown to exert toxic effects in vivo, we aimed to evaluate the link between MNPLs and colorectal cancer tumorigenesis. A literature review was conducted, using Ovid MEDLINE and PubMed databases. MeSH terms "colorectal carcinoma" and "microplastic" were the foundations for the search strategy. Forty-one studies were initially identified, of which fourteen were ultimately selected for analysis. MNPLs are found within human colorectal tumors and are present at higher levels in the feces of colorectal cancer patients. The tissue sample studies however are limited by small sample sizes (n = 10 or 25), and are representative of mainly Chinese populations (five of the six human studies conducted in China). The mouse studies observed increased tumor loads and dysbiosis in mice exposed to MNPLs, and the in vitro studies observed increased reactive oxygen species (ROS) when cells were exposed to MNPLs in culture. Although the direct link between MNPLs and de novo development of colorectal cancer remains to be elucidated, these findings suggest that MNPLs can induce the molecular changes involved in tumorigenesis, and tumorigenesis itself when combined with a compromised gastrointestinal barrier. Given that barrier disruption occurs with inflammatory bowel disease, smoking, alcohol, stress, and infections, these populations may be most vulnerable to the effects of MNPLs.
Insights
Microplastics and nanoplastics (MNPLs) accumulate in the body and are found in colorectal tumors. Exposure to MNPLs may promote colorectal cancer development, especially with a compromised gut barrier.
Area of Science:
- Environmental Health
- Oncology
- Toxicology
Background:
- Microplastics and nanoplastics (MNPLs) are pervasive environmental contaminants.
- Accumulation of MNPLs in human tissues is documented, with potential toxic effects.
- The link between MNPLs and colorectal cancer (CRC) tumorigenesis requires further investigation.
Purpose of the Study:
- To evaluate the association between MNPLs and colorectal cancer development.
- To synthesize current evidence on MNPLs in CRC tissues and patient samples.
- To explore the mechanistic pathways by which MNPLs might influence CRC.
Main Methods:
- A comprehensive literature review was performed using Ovid MEDLINE and PubMed.
- Search strategy focused on MeSH terms "colorectal carcinoma" and "microplastic".
- Fourteen relevant studies were selected from an initial pool of forty-one.
Main Results:
- MNPLs detected in human colorectal tumors and at higher concentrations in CRC patient feces.
- Animal studies showed increased tumor burden and gut dysbiosis following MNPL exposure.
- In vitro studies indicated MNPLs induce reactive oxygen species (ROS) production in cells.
Conclusions:
- While direct causation of CRC by MNPLs is unproven, evidence suggests MNPLs can drive tumorigenic molecular changes.
- Compromised gastrointestinal barrier function, common in conditions like IBD, may increase vulnerability to MNPLs.
- Populations with existing gut barrier disruptions may be at higher risk for MNPL-associated CRC development.
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