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

被引:5
作者
Jiang, Ya-Jing [1 ]
Ho, Trung-Loc [1 ]
Chao, Chia-Chia [2 ]
He, Xiu-Yuan [1 ]
Chen, Po-Chun [3 ]
Cheng, Fang-Ju [1 ,4 ]
Huang, Wei-Chien [1 ,4 ,5 ,6 ]
Huang, Chang-Lun [7 ]
Liu, Po-, I [8 ,9 ,12 ]
Tang, Chih-Hsin [1 ,5 ,6 ,10 ,11 ]
机构
[1] China Med Univ, Grad Inst Biomed Sci, Taichung, Taiwan
[2] Fu Jen Catholic Univ, Dept Resp Therapy, New Taipei City, Taiwan
[3] Natl Taiwan Normal Univ, Dept Life Sci, Taipei, Taiwan
[4] China Med Univ Hosp, Ctr Mol Med, Taichung, Taiwan
[5] China Med Univ, Hsinchu Hosp, Dept Med Res, Hsinchu, Taiwan
[6] Asia Univ, Dept Med Lab Sci & Biotechnol, Taichung, Taiwan
[7] Changhua Christian Hosp, Dept Surg, Div Gen Thorac Surg, Changhua, Taiwan
[8] Asia Univ, Dept Phys Therapy, Taichung, Taiwan
[9] Asia Univ Hosp, Dept Gen Thorac Surg, Taichung, Taiwan
[10] China Med Univ, Sch Med, Dept Pharmacol, 91,Hsueh Shih Rd, Taichung, Taiwan
[11] China Med Univ, Chinese Med Res Ctr, Taichung, Taiwan
[12] Asia Univ Hosp, Dept Thorac Surg, 222,Fuxin Rd, Taichung 41354, Taiwan
关键词
Lung cancer; Particulate matter; Glutamine metabolism; Amphiregulin; GROWTH-FACTOR; AIR-POLLUTION; CELLS; PROGRESSION; EXPRESSION; MORTALITY; AUTOPHAGY; EXPOSURE; CYCLE; RISK;
D O I
10.7150/ijbs.96210
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 in vitro and in vivo. 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.
引用
收藏
页码:3126 / 3139
页数:14
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