Particulate matter facilitates amphiregulin-dependent lung cancer proliferation through glutamine metabolism

Although many cohort studies have reported that long-term exposure to particulate matter (PM) causes lung cancer, the molecular mechanisms underlying the PM-induced increases in lung cancer progression remain unclear. We applied the lung cancer cell line A549 (Parental; A549.Par) to PM for an extend...

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Veröffentlicht in:International journal of biological sciences 2024-01, Vol.20 (8), p.3126-3139
Hauptverfasser: Jiang, Ya-Jing, Ho, Trung-Loc, Chao, Chia-Chia, He, Xiu-Yuan, Chen, Po-Chun, Cheng, Fang-Ju, Huang, Wei-Chien, Huang, Chang-Lun, Liu, Po-I, Tang, Chih-Hsin
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Sprache:eng
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Zusammenfassung:Although many cohort studies have reported that long-term exposure to particulate matter (PM) causes lung cancer, the molecular mechanisms underlying the PM-induced increases in lung cancer progression remain unclear. We applied the lung cancer cell line A549 (Parental; A549.Par) to PM for an extended period to establish a mimic PM-exposed lung cancer cell line, A549.PM. Our results indicate that A549.PM exhibits higher cell growth and proliferation abilities compared to A549.Par cells and . The RNA sequencing analysis found amphiregulin (AREG) plays a critical role in PM-induced cell proliferation. We observed that PM increases AREG-dependent lung cancer proliferation through glutamine metabolism. In addition, the EGFR/PI3K/AKT/mTOR signaling pathway is involved in PM-induced solute carrier family A1 member 5 (SLC1A5) expression and glutamine metabolism. Our findings offer important insights into how lung cancer proliferation develops upon exposure to PM.
ISSN:1449-2288
1449-2288
DOI:10.7150/ijbs.96210