Gamma synuclein is a novel nicotine responsive protein in oral cancer malignancy.

Gamma synuclein Nicotine acetylcholine receptor Oral cancer Signal transduction

Journal

Cancer cell international
ISSN: 1475-2867
Titre abrégé: Cancer Cell Int
Pays: England
ID NLM: 101139795

Informations de publication

Date de publication:
2020
Historique:
received: 11 12 2019
accepted: 06 07 2020
entrez: 17 7 2020
pubmed: 17 7 2020
medline: 17 7 2020
Statut: epublish

Résumé

The mechanisms of neuronal protein γ-synuclein (SNCG) in the malignancy of oral squamous cell carcinoma (OSCC) are not clear. This study tested the hypothesis that SNCG is involved in nicotine-induced malignant behaviors of OSCC. The effect of nicotine on SNCG expression and epithelial-to-mesenchymal transition (EMT) markers were examined. Short hairpin RNA (shRNA) and an antagonist specific for α7-nicotine acetylcholine receptors (α7-nAChRs) were used to examine the role of α7-nAChRs in mediating the effects of nicotine. Knockdown of SNCG in nicotine-treated cells was performed to investigate the role of SNCG in cancer malignancy. The in vivo effect of nicotine was examined using a nude mouse xenotransplantation model. Nicotine increased SNCG expression in a time- and dose-dependent manner. Nicotine treatment also increased E-cadherin and ZO-1 and decreased fibronectin and vimentin expression. After specific knockdown of α7-nAChRs and inhibition of the PI3/AKT signal, the effect of nicotine on SNCG expression was attenuated. Silencing of SNCG abolished nicotine-induced invasion and migration of OSCC cells. The xenotransplantation model revealed that nicotine augmented tumor growth and SNCG expression. Nicotine upregulated SNCG expression by activating the α7-nAChRs/PI3/AKT signaling that are participated in nicotine-induced oral cancer malignancy.

Sections du résumé

BACKGROUND BACKGROUND
The mechanisms of neuronal protein γ-synuclein (SNCG) in the malignancy of oral squamous cell carcinoma (OSCC) are not clear. This study tested the hypothesis that SNCG is involved in nicotine-induced malignant behaviors of OSCC. The effect of nicotine on SNCG expression and epithelial-to-mesenchymal transition (EMT) markers were examined.
METHODS METHODS
Short hairpin RNA (shRNA) and an antagonist specific for α7-nicotine acetylcholine receptors (α7-nAChRs) were used to examine the role of α7-nAChRs in mediating the effects of nicotine. Knockdown of SNCG in nicotine-treated cells was performed to investigate the role of SNCG in cancer malignancy. The in vivo effect of nicotine was examined using a nude mouse xenotransplantation model.
RESULTS RESULTS
Nicotine increased SNCG expression in a time- and dose-dependent manner. Nicotine treatment also increased E-cadherin and ZO-1 and decreased fibronectin and vimentin expression. After specific knockdown of α7-nAChRs and inhibition of the PI3/AKT signal, the effect of nicotine on SNCG expression was attenuated. Silencing of SNCG abolished nicotine-induced invasion and migration of OSCC cells. The xenotransplantation model revealed that nicotine augmented tumor growth and SNCG expression.
CONCLUSION CONCLUSIONS
Nicotine upregulated SNCG expression by activating the α7-nAChRs/PI3/AKT signaling that are participated in nicotine-induced oral cancer malignancy.

Identifiants

pubmed: 32669976
doi: 10.1186/s12935-020-01401-w
pii: 1401
pmc: PMC7350738
doi:

Types de publication

Journal Article

Langues

eng

Pagination

300

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© The Author(s) 2020.

Déclaration de conflit d'intérêts

Competing interestsThe authors declare that they have no competing interests.

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Auteurs

Chia-Chen Hsu (CC)

Graduate Institute of Medical Sciences, National Defense Medical Center, Taipei, 114 Taiwan.

Yu-Fu Su (YF)

Graduate Institute of Medical Sciences, National Defense Medical Center, Taipei, 114 Taiwan.
Department of Radiation Oncology, Tri-Service General Hospital, National Defense Medical Center, Taipei, 114 Taiwan.

Kuo-Yang Tsai (KY)

Department of Oral and Maxillofacial Surgery, Changhua Christian Hospital, Changhua, 500 Taiwan.
College of Nursing and Health Science, Da-Yeh University, Changhua, 515 Taiwan.

Feng-Chih Kuo (FC)

Division of Endocrinology and Metabolism, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, 114 Taiwan.

Chi-Fu Chiang (CF)

Department of Dentistry, Tri-Service General Hospital, National Defense Medical Center, No.161, Sec.6, Min-Chuan East Rd., Nei-Hu, Taipei, 114 Taiwan.

Chu-Yen Chien (CY)

Graduate Institute of Medical Sciences, National Defense Medical Center, Taipei, 114 Taiwan.

Ying-Chen Chen (YC)

Molecular and Cell Biology, Taiwan International Graduate Program, Academia Sinica and Graduate Institute of Life Science, National Defense Medical Center, Taipei, 114 Taiwan.

Chien-Hsing Lee (CH)

Division of Endocrinology and Metabolism, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, 114 Taiwan.

Yu-Chiao Wu (YC)

Department of Dentistry, Tri-Service General Hospital, National Defense Medical Center, No.161, Sec.6, Min-Chuan East Rd., Nei-Hu, Taipei, 114 Taiwan.

Kun Wang (K)

Department of Internal Medicine, Cardinal Tien Hospital and School of Medicine, College of Medicine, Fu Jen Catholic University, New Taipei City, Taiwan.

Shyun-Yeu Liu (SY)

Department of Oral and Maxillofacial Surgery, Chi Mei Medical Center, Tainan, 710 Taiwan.

Yi-Shing Shieh (YS)

Department of Dentistry, Tri-Service General Hospital, National Defense Medical Center, No.161, Sec.6, Min-Chuan East Rd., Nei-Hu, Taipei, 114 Taiwan.
Department and Graduate Institute of Biochemistry, National Defense Medical Center, Taipei, 114 Taiwan.

Classifications MeSH