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Article ? AI-assigned paper type based on the abstract. Classification may not be perfect — flag errors using the feedback button. Tier 2 ? Original research — experimental, observational, or case-control study. Direct primary evidence. Environmental Sources Human Health Effects Remediation Sign in to save

Environmental Pollution and Breast Cancer: The Microplastic Component BPA Regulates the Intratumoral Immune Microenvironment and Increases Lung Metastasis

Preprints.org 2021 3 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 35 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Mariana Segovia‐Mendoza, Margarita Isabel Palacios‐Arreola, Mariana Segovia‐Mendoza, Karen Elizabeth Nava‐Castro, Margarita Isabel Palacios‐Arreola, Karen Elizabeth Nava‐Castro, Norma Angélica Mendoza-Moreno, Margarita Isabel Palacios‐Arreola, Norma Angélica Mendoza-Moreno, Jorge Morales‐Montor Mariana Segovia‐Mendoza, Jorge Morales‐Montor Karen Elizabeth Nava‐Castro, Armando Pérez‐Torres, Jorge Morales‐Montor Jorge Morales‐Montor

Summary

Bisphenol A (BPA), a chemical found in many plastics, was shown to alter the immune environment within breast tumors and increase lung metastasis in mice. The findings suggest that BPA exposure may worsen cancer outcomes by promoting spread of the disease.

Background: Metastasis is a complex process that involves the spread of the tumor to distant parts of the body from its original site. Metastatic dissemination represents the main physiopathology of cancer. Soluble factors such as cytokines have been closely related to breast cancer (BC) metastasis. Bisphenol A (BPA) is an endocrine disrupting chemical compound with estrogenic properties, which exposure in the early stages of neonatal life leads to an increase in the size and weight of breast tumors and cellular changes in the tumoral immune microenvironment. Methods: Thus, we used female BALB/c mice that were exposed neonatally to a single dose of BPA. Once sexual maturity was reached, a mammary tumor was induced injecting 4T1 cells in situ. After 25 days of injection, we evaluated endocrine alterations, cytokine expression, tissue alterations denoted by macro and micro metastases in the lung, and metastasis-induced cell infiltration. Results: BPA neonatal treatment did not show significant endocrine alterations. Nevertheless, BPA induced a great rate of metastasis to the lung associated with higher intratumoral expression of IL-1b, IL-6, IFN-g, TNF-a and VEGF. Conclusions Our data suggest that cytokines are key players in BC metastasis induction, and that BPA is a risk factor to be considered. This knowledge must be considered with the aim of recognizing environmental pollution in the clinical history of patients to possibly counter BC metastases.

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