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Mechanism of YBX1/NOTCH1 Axis-Mediated Monocyte Apoptosis Under Benzene Exposure.

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Journal of biochemical and molecular toxicology 2026 Vol.40(4) p. e70827
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Chen QJ, Wu LM, Zeng WF, Yang ZQ, Kuang L, Liu ZH, Liu DB, Liu XH, Liao HX, Liu SY, Wu SG

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Long-term exposure to the chemical industry pollutant benzene induces hematopoietic damage; however, the mechanism of this injury is unclear.

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BibTeX ↓ RIS ↓
APA Chen QJ, Wu LM, et al. (2026). Mechanism of YBX1/NOTCH1 Axis-Mediated Monocyte Apoptosis Under Benzene Exposure.. Journal of biochemical and molecular toxicology, 40(4), e70827. https://doi.org/10.1002/jbt.70827
MLA Chen QJ, et al.. "Mechanism of YBX1/NOTCH1 Axis-Mediated Monocyte Apoptosis Under Benzene Exposure.." Journal of biochemical and molecular toxicology, vol. 40, no. 4, 2026, pp. e70827.
PMID 41987593
DOI 10.1002/jbt.70827

Abstract

Long-term exposure to the chemical industry pollutant benzene induces hematopoietic damage; however, the mechanism of this injury is unclear. Using an integrative RNA-seq analysis of benzene-exposed samples, we identified Y-box binding protein 1 (YBX1) and neurogenic locus notch homolog protein 1 (NOTCH1) as the most significantly dysregulated apoptosis-related molecules, prompting us to investigate their functional interplay. While neurogenic locus notch homolog protein 1 (NOTCH1) drives the progression of both benign and malignant disorders, the involvement of Y-box binding protein 1 (YBX1) despite being extensively characterized in tumorigenesis remains unexplored in the context of benzene-induced hematopoietic injury. This study examines the molecular mechanism of the YBX1/NOTCH1 axis in benzene-mediated monocyte apoptosis. Accordingly, we combined clinical data with RNA seqenceing (RNA-seq) analysis and examined the mechanistic basis of benzene-induced apoptosis in human monocytic leukemia cells using Cell Counting Kit-8 (CCK-8) cell viability assays, flow cytometry (FC), DNA pull-down coupled with liquid chromatography-tandem mass spectrometry (LC-MS), and western blotting (WB). Analysis of 1,4-BQ-treated THP-1 cells revealed that 1,4-Benzoquinone (1,4-BQ) upregulated NOTCH1/transcription coactivator BCL3 (BCL3) and downregulated YBX1/apoptosis regulator Bcl-2 (BCL2) in their gene profiles and protein levels. Furthermore, the differentially expressed genes were enriched in apoptotic pathways. Treatment with 1,4-BQ inhibited THP-1 cell proliferation, induced S-phase arrest, and triggered apoptosis in a concentration- and time-dependent manner. Knockdown of NOTCH1 or overexpression YBX1 significantly eliminated the inhibitory effects of 1,4-BQ on upregulated BCL3 and downregulated BCL2 expression. Furthermore, the inhibitory effects on apoptosis were considerably offset by YBX1 overexpression or NOTCH1 knockdown. YBX1 regulates BCL2/BCL3 by inhibiting NOTCH1, mediating benzene-induced monocyte apoptosis. Taken together, our results uncovered a critical role of YBX1/NOTCH1 in the benzene-induced monocyte apoptosis, which may have great potential as a biomarker and therapeutic target in benzene-induced hematotoxicity.

MeSH Terms

Humans; Receptor, Notch1; Benzene; Apoptosis; Y-Box-Binding Protein 1; Monocytes; Male; THP-1 Cells; Female; Signal Transduction