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Endocrine-disrupting compounds and metabolomic reprogramming in breast cancer

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WILEY
DOI: 10.1002/jbt.23506

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bisphenols; breast cancer; endocrine-disrupting compounds; metabolomics; phthalates; zeranol

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Endocrine-disrupting chemicals, due to their structural similarity to hormones like estrogen, can interfere with endocrine signaling and contribute to the development of breast cancer. They may dysregulate cell signaling pathways related to cellular metabolism, which play a role in cancer progression. Studying these altered pathways through metabolomic analysis can provide insights into the mechanisms by which these chemicals promote breast cancer development.
Endocrine-disrupting chemicals pose a growing threat to human health through their increasing presence in the environment and their potential interactions with the mammalian endocrine systems. Due to their structural similarity to hormones like estrogen, these chemicals can interfere with endocrine signaling, leading to many deleterious effects. Exposure to estrogenic endocrine-disrupting compounds (EDC) is a suggested risk factor for the development of breast cancer, one of the most frequently diagnosed cancers in women. However, the mechanisms through which EDCs contribute to breast cancer development remain elusive. To rapidly proliferate, cancer cells undertake distinct metabolic programs to utilize existing nutrients in the tumor microenvironment and synthesize macromolecules de novo. EDCs are known to dysregulate cell signaling pathways related to cellular metabolism, which may be an important mechanism through which they exert their cancer-promoting effects. These altered pathways can be studied via metabolomic analysis, a new advancement in -omics technologies that can interrogate molecular pathways that favor cancer development and progression. This review will summarize recent discoveries regarding EDCs and the metabolic reprogramming that they may induce to facilitate the development of breast cancer.

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