Enhanced ASGR2 by microplastic exposure leads to resistance to therapy in gastric cancer
Hyeongi Kim1,2, Javeria Zaheer1,3, Eui-Ju Choi2
1Division of RI Application, Korea Institute Radiological and Medical Sciences, Seoul 01812, Republic of Korea.
Abstract:
Background: Microplastics (MPs) are a new global environmental threat. Previously, we showed the biodistribution of MPs using [64Cu] polystyrene (PS) and PET in mice. Here, we aimed to identify whether PS exposure has malignant effects on the stomach and induces resistance to therapy. Methods: BALB/c nude mice were fed 1.72 × 104 particles/mL of MP. We investigated PS accumulation in the stomach using radioisotope-labeled and fluorescent-conjugated PS. Further, we evaluated whether PS exposure induced cancer stemness and multidrug resistance, and whether it affected tumor development, tumor growth, and survival rate in vivo using a 4-week PS-exposed NCI-N87 mouse model. Using RNA-Seq analysis, we analyzed whether PS exposure induced gene expression changes in gastric tissues of mice. Results: PET imaging results showed that a single dose of [64Cu]-PS remained for 24 h in the mice stomach. The 4-week daily repetitive dose of fluorescent conjugated PS was deposited in the gastric tissues of mice. When PS was exposed, a 2.9-fold increase in migration rate was observed for NCI-N87 cells. Immunocytochemistry results showed decreased E-cadherin and increased N-cadherin expression, and flow cytometry, qPCR, and western blot analysis indicated a 1.9-fold increase in N-cadherin expression after PS exposure. Further, PS-induced multidrug resistance to bortezomib, paclitaxel, gefitinib, lapatinib, and trastuzumab was observed in the NCI-N87 mouse model due to upregulated CD44 expression. RNA-seq results identified increased asialoglycoprotein receptor 2 (ASGR2) expression after PS exposure, and ASGR2 knockdown decreased cell proliferation, migration, invasion, and drug resistance. Conclusion: We demonstrated that ASGR2 enhanced cancer hallmarks on PS exposure and induced resistance to chemo- and monoclonal antibody-therapy. Our preclinical findings may provide an incentive for further epidemiological studies on the role of MP exposure and its association with gastric cancer.
Insights
Microplastic (MP) exposure in mice increased gastric cancer stemness and drug resistance, linked to ASGR2. This suggests MPs may promote gastric cancer development and treatment resistance.
Area of Science:
- Environmental Science
- Toxicology
- Oncology
Background:
- Microplastics (MPs) pose a growing environmental threat.
- Previous studies tracked MP biodistribution; this study investigates MP effects on gastric cancer.
Purpose of the Study:
- To determine if polystyrene (PS) microplastic exposure induces malignant effects in the stomach.
- To assess if PS exposure leads to cancer stemness and therapy resistance in a gastric cancer model.
Main Methods:
- Mice were exposed to polystyrene microplastics (MPs) via diet.
- PS accumulation, cancer stemness markers, multidrug resistance, and gene expression (RNA-Seq) were analyzed.
- A 4-week PS-exposed NCI-N87 gastric cancer mouse model was used for in vivo assessments.
Main Results:
- PS accumulated in gastric tissues and increased cancer cell migration and N-cadherin expression.
- PS exposure induced multidrug resistance to various therapies, linked to CD44 upregulation.
- RNA-Seq identified increased ASGR2 expression, which promoted cancer hallmarks and therapy resistance.
Conclusions:
- ASGR2 plays a key role in enhancing cancer hallmarks and therapy resistance following microplastic exposure.
- These findings highlight a potential link between MP exposure and gastric cancer, warranting further epidemiological research.
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