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      Resveratrol Induces Mitochondrial Apoptosis and Inhibits Epithelial-Mesenchymal Transition in Oral Squamous Cell Carcinoma Cells.

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          Abstract

          OSCC is the most common malignant cancer of the head and neck. EMT is an essential cellular process critical to the morphogenesis and homeostasis of solid tissues. It is also involved in the initial stage of cancer metastasis and invasion in which cells lose epithelial characteristics. While cancer therapy protocols such as surgery, radiation, and chemotherapy are effective and useful, the drug tolerance and toxicity of OSCC patients remain a problem. Resveratrol is mainly produced in red grape skin and exhibits anti-oxidative, anti-inflammatory, anti-proliferative, and anti-cancer properties. This study was undertaken to investigate the underlying mechanisms giving rise to the induction of apoptosis by resveratrol in the human tongue squamous cell carcinoma cell line. Resveratrol treatment resulted in a time- and dose-dependent decrease in cell viability and increased the apoptotic cell ratio in CAL-27, SCC15, and SCC25 cells. Resveratrol treatment of CAL-27 cells showed that several lines of apoptotic manifestation and decreased cell migration, invasion, and EMT-inducing transcription factor. Taken together, our findings demonstrate the inhibitory effect of resveratrol in human OSCC cells via the mitochondrial pathway and that resveratrol is able to inhibit cell invasion and migration by inhibiting the EMT-inducing transcription factors.

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          Author and article information

          Journal
          Nutr Cancer
          Nutrition and cancer
          Informa UK Limited
          1532-7914
          0163-5581
          Jan 2018
          : 70
          : 1
          Affiliations
          [1 ] a Department of Oral and Maxillofacial Surgery , Pusan National University Dental Hospital , Mulgeum-eup, Yangsan-si , Gyeongsangnam-do , South Korea.
          [2 ] b Department of Oral and Maxillofacial Surgery , Medical Center, Dong-A University , Busan , South Korea.
          [3 ] c Department of Oral Anatomy , School of Dentistry, Pusan National University, Busandaehak-ro , Yangsan-si , Gyeongsangnam-do , South Korea.
          [4 ] e BK21 PLUS Project, School of Dentistry, Pusan National University, Busandaehak-ro , Yangsan-si , Gyeongsangnam-do , South Korea.
          [5 ] d Department of Oral Pathology , School of Dentistry, Pusan National University, Busandaehak-ro , Yangsan-si , Gyeongsangnam-do , South Korea.
          Article
          10.1080/01635581.2018.1397708
          29148840
          a06e881f-79b7-476a-8930-8f86ac7aa672
          History

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