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Computer-Aided Molecular Design Meets Network Toxicology and Molecular Docking: A Joint Strategy to Explore Common Molecular Mechanisms of Phthalates on Human Breast Cancer and Structure–Activity Relationship
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This study used network toxicology and molecular docking to identify shared mechanisms by which three common phthalates (DBP, BBP, DEHP) promote breast cancer, finding that all three interact with five key transcription factor-associated genes including TP53 and ESR1. Computer-aided molecular design revealed that alkyl chain length and phenyl groups are critical structural determinants of phthalate binding affinity to these cancer-relevant targets.
Distinct PAEs are implicated in breast cancer progression through multiple molecular pathways. This study aims to elucidate the potential mechanisms in common by which PAEs promote breast cancer progression. Dibutyl phthalate (DBP), benzyl butyl phthalate (BBP), and diethylhexyl phthalate (DEHP) were selected as representative PAE compounds. Network toxicology guided the construction of a regulatory network centered on five key transcription factor-associated genes: TP53, CTNNB1, PPARA, ESR1, and CDKN2A. Differential expression and survival analyses confirmed the significant impact of these hub genes on breast cancer (p < 0.05). Molecular docking results revealed direct interactions between the three PAEs and hub targets, while BBP had the strongest PAE-hub gene interaction and DEHP had the weakest one. Computer-aided molecular design (CAMD), combined with molecular docking, found the importance of alkyl chains and phenyl in PAE-hub gene interaction. A group addition/subtraction controlled experiment revealed that the binding affinities of modified BBP variants to hub genes are all weaker than the unmodified parent. The drop was significant whether the C17 alkyl chain was lengthened to match DEHP (p = 0.026) or the phenyl group was removed (p = 0.022). The findings provide novel insights into the mechanism in common of PAE-promoting breast cancer and offer a foundation for the unified intervention strategies and the design of safer plasticizer alternatives.
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This analysis investigates the molecular pathways through which phthalate exposure may contribute to depression, including effects on hormone signaling, neuroinflammation, and oxidative stress. Phthalates are ubiquitous plasticizers found in food packaging, personal care products, and medical devices, leading to near-universal human exposure. The findings suggest a biologically plausible link between phthalate burden and mental health outcomes, warranting further epidemiological study.
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