OncoTargets and Therapy (Oct 2020)

Metformin Combined with 4SC-202 Inhibited the Migration and Invasion of OSCC via STAT3/TWIST1

  • He Y,
  • Fan Z,
  • He L,
  • Zhang C,
  • Ping F,
  • Deng M,
  • Liu S,
  • Wang Y,
  • Cheng B,
  • Xia J

Journal volume & issue
Vol. Volume 13
pp. 11019 – 11029

Abstract

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Yuan He,1,2,* Zhaona Fan,1,2,* Lihong He,1,2 Chi Zhang,1,2 Fan Ping,1,2 Miao Deng,1,2 Suyang Liu,1,2 Yanting Wang,1,2 Bin Cheng,1,2 Juan Xia1,2 1Hospital of Stomatology, Sun Yat-Sen University, Guangzhou, People’s Republic of China; 2Guangdong Provincial Key Laboratory of Stomatology, Guanghua School of Stomatology, Sun Yat-Sen University, Guangzhou, People’s Republic of China*These authors contributed equally to this workCorrespondence: Bin Cheng; Juan XiaGuangdong Provincial Key Laboratory of Stomatology, Guanghua School of Stomatology, Sun Yat-Sen University, No. 55 Linyuan Xi Road, Guangzhou, Guangdong 510055, People’s Republic of ChinaTel +862083741891Fax +86 20 83822807Email [email protected]; [email protected]: Oral squamous cell carcinoma (OSCC), the most common epithelial malignant neoplasm in the head and neck, characterizes with local infiltration and metastasis of lymph nodes. The five-year survival rate of OSCC remains low despite the advances in clinical methods. Thus, it is necessary to develop a new effective therapeutic scheme for OSCC. Our previous results showed that metformin and 4SC-202 synergistically promoted the intrinsic apoptosis of OSCC in vitro and in vivo, but the effects on invasion and migration remained unclear.Methods: Human OSCC cell lines HSC6 and CAL33 were cultured with metformin (16 mM) or/and 4SC-202 (0.4 μM) for 72 h. STAT3 inhibitor S31-201 was applied at concentration of 60 μM for 48 h. Wound-healing assays and transwell assays were used to determine the invasion and migration ability of OSCC. qRT-PCR and Western blot were performed to detect mRNA levels and protein levels.Results: Metformin or/and 4SC-202 suppressed the migration and invasion of OSCC cells. Importantly, the expression of TWIST1 was suppressed by metformin and 4SC-202, while the invasion and migration inhibitory effects of metformin and 4SC-202 were countered by the overexpression of TWIST1. In addition, the phosphorylation level of STAT3 decreased after the administration of metformin or/and 4SC-202. Furthermore, inhibition of STAT3 by S31-201 suppressed the expression of TWIST1 and led to a decline in migration and invasion of OSCC, while overexpression of TWIST1 attenuated these effects.Conclusion: Metformin and 4SC-202 suppressed the invasion and migration of OSCC through inhibition of STAT3/TWIST1, and this scheme can serve as a novel therapeutic strategy for OSCC.Keywords: oral squamous cell carcinoma, metformin, 4SC-202, invasion, migration

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