Volume 26, Issue 8 pp. 1649-1658
ORIGINAL ARTICLE

Benzo[a]pyrene promotes progression in tongue squamous cell carcinoma

Linxuan Huang

Linxuan Huang

MOE Key Laboratory of Gene Function and Regulation, State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-sen University, Guangzhou, China

Contribution: Data curation, Formal analysis, ​Investigation, Methodology, Writing - original draft, Writing - review & editing

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Xiaofen Xiao

Xiaofen Xiao

Department of Stomatology, Shenzhen People’s Hospital, 2nd Clinical Medical College of Jinan University, Shenzhen, China

Contribution: Funding acquisition, Resources, Writing - review & editing

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Yupeng Yao

Yupeng Yao

MOE Key Laboratory of Gene Function and Regulation, State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-sen University, Guangzhou, China

Contribution: Methodology, Validation

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Jianping Yu

Jianping Yu

MOE Key Laboratory of Gene Function and Regulation, State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-sen University, Guangzhou, China

Contribution: Data curation, Software

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Qingjian Chen

Qingjian Chen

MOE Key Laboratory of Gene Function and Regulation, State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-sen University, Guangzhou, China

Contribution: Data curation, Methodology

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Puping Liang

Corresponding Author

Puping Liang

MOE Key Laboratory of Gene Function and Regulation, State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-sen University, Guangzhou, China

Correspondence

Puping Liang and Yan Zhang, Guangzhou Higher Education Mega Center, Guangzhou 510006, P. R. China.

Emails: [email protected] (P. L.); [email protected] (Y. Z.)

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Yan Zhang

Corresponding Author

Yan Zhang

MOE Key Laboratory of Gene Function and Regulation, State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-sen University, Guangzhou, China

Correspondence

Puping Liang and Yan Zhang, Guangzhou Higher Education Mega Center, Guangzhou 510006, P. R. China.

Emails: [email protected] (P. L.); [email protected] (Y. Z.)

Contribution: Conceptualization, Data curation, Funding acquisition, Project administration, Resources, Supervision, Validation, Visualization, Writing - original draft, Writing - review & editing

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First published: 18 June 2020
Citations: 11

Linxuan Huang and Xiaofen Xiao contributed equally to this work.

Funding information

This work was supported by grants from Guangdong Provincial Key Scientific and Technological Projects (2017B020230002 and 2016B030231001) and National Natural Science Foundation of China (No. 31871413), and the Shenzhen Science and Technology Project (JCYJ20160422144656321).

Abstract

Objectives

Benzo[a]pyrene (B[a]P) is a member of the polycyclic aromatic hydrocarbon (PAH) family. Although the potent carcinogenicity of high-dose B[a]P has been extensively reported, the effects of long-term exposure to B[a]P on the progression of tongue squamous cell carcinoma (TSCC) are poorly understood.

Methods

In the present study, TSCC cells were treated with 5 or 50 nM of B[a]P for three months. The proliferation and chemoresistance of B[a]P-treated cells to 5-fluorouracil or cisplatin were detected by CCK8. The motility of the B[a]P-treated cells was evaluated with wound healing analysis, invasion assay, and three-dimensional culture in decellularized mouse tongue matrix. Xenograft assay was used to investigate the aggressiveness of B[a]P-treated cells. Immunofluorescence staining, terminal restriction fragment assay, and whole-genome sequence were used to determine the mutation spectrums.

Results

Long-term 50 nM B[a]P-treated cells exhibited increased aggressiveness and chemoresistance to 5-fluorouracil or cisplatin. In addition, data from whole-genome sequencing demonstrated that C:T to A:T transitions were the predominant nucleotide substitutions occurred in 50 nM B[a]P-treated CAL27 cells. Furthermore, 102 non-synonymous or stop-gain mutations were enriched in the extracellular-matrix-receptor interactive pathway.

Conclusions

B[a]P exposure may contribute to genomic instability, and therefore, B[a]P may promote the progression of TSCC.

CONFLICT OF INTEREST

The authors declare that they have no conflict of interest.

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