4.3 Article

Effects of Sinapic Acid Combined with Cisplatin on the Apoptosis and Autophagy of the Hepatoma Cells HepG2 and SMMC-7721

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Publisher

HINDAWI LTD
DOI: 10.1155/2021/6095963

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Funding

  1. National Natural Science Foundation of China [81560530, 81760589, 81960590]
  2. Funding Scheme for High-level Overseas Chinese Students, Return of the Ministry of Human Resources and Social Security [RSTH[2019]160]
  3. Natural Science Foundation of Guangxi Zhuang Autonomous Region of China [2016GXNSFCA380026, 2020GCNSFAA159160]
  4. Open Project of Key Laboratory of Early Prevention and Treatment of Regional High Incidence Tumor, the Ministry of Education, China [GKE2018KF03]
  5. Scientific Research Foundation for Returned Scholars of Guilin Medical University [04010150001]
  6. Foundation for University Key Teacher by the Education Department of Guangxi Zhuang Autonomous Region [GRJ[2018]18]

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The combination of sinapic acid and cisplatin showed promising antitumor effects on liver cancer cells by inhibiting cell proliferation and migration, inducing apoptosis, and activating autophagy. This suggests that phenolic acid compounds could be a potential adjuvant therapy strategy for hepatocellular carcinoma.
Sinapic acid (Sa) is a small-molecule phenolic acid compound predominant in fruits, vegetables, and grains. This study investigated the antitumor effects of cisplatin (DDP) combined with Sa (Sa/DDP) on the hepatic cancer cells (HCC), HepG2 and SMMC-7721. The HepG2 and SMMC-7721 cells were treated with Sa or Sa/DDP, and the cell proliferation and cell cycle were detected using the MTT assay. The cell migration was detected using the transwell and scratch assays, while apoptosis and autophagy were detected using Hoechst, MDC, and Annexin V-FITC/PI staining. The protein expression was quantitated using the western blot. Sa/DDP was found to not only inhibit cancer cell proliferation and migration but also induce cell apoptosis. Simultaneously, the Sa/DDP combination was found to activate autophagy, and the HCQ autophagy inhibitor enhanced the apoptosis in the Sa/DDP-induced liver cancer cells. The combined use of Sa and DDP makes it an attractive adjuvant therapy strategy for tumors, establishing the prospect of phenolic acid compounds for the adjuvant treatment of hepatocellular carcinoma.

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