Antitumor Effects of Astaxanthin on Esophageal Squamous Cell Carcinoma by up-Regulation of PPARγ.

Esophageal squamous cell carcinoma is a malignant tumor that is difficult to find and has a poor prognosis. The aim of this study is to explore the chemoprevention effect of Astaxanthin (AST) and reveal the possible mechanism of AST on the development of esophageal cancer based on PPARγ. We found th...

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Publicado en:Nutrition & Cancer Vol. 74; no. 4; pp. 1399 - 1411
Autores principales: Cui, Lingling, Li, Zhonglei, Xu, Fan, Tian, Yalan, Chen, Tingting, Li, Jiaxin, Guo, Yingying, Lyu, Quanjun
Formato: research tables/charts Journal Article
Publicado: Taylor & Francis Ltd 2022
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 2022
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      pub: Taylor & Francis Ltd
      place: Philadelphia, Pennsylvania
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        10.1080/01635581.2021.1952449
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        atl: Antitumor Effects of Astaxanthin on Esophageal Squamous Cell Carcinoma by up-Regulation of PPARγ.
      aug:
        au:
          Cui, Lingling
          Li, Zhonglei
          Xu, Fan
          Tian, Yalan
          Chen, Tingting
          Li, Jiaxin
          Guo, Yingying
          Lyu, Quanjun
        affil: College of Public Health, Zhengzhou University, Zhengzhou, Henan, China
      sug:
        subj:
          Esophageal Squamous Cell Carcinoma Drug Therapy
          Carotenoids Therapeutic Use
          Antineoplastic Agents Pharmacodynamics
          Peroxisome Proliferator-Activated Receptors Drug Effects
          Chemoprevention
          Cell Line, Tumor Drug Effects
          Data Analysis Software
          Incidence
          Cell Viability
          Superoxide Dismutase
          Antioxidants
          Caspases
          Apoptosis
          Human
          Descriptive Statistics
          Rats
          Animal Studies
      ab: Esophageal squamous cell carcinoma is a malignant tumor that is difficult to find and has a poor prognosis. The aim of this study is to explore the chemoprevention effect of Astaxanthin (AST) and reveal the possible mechanism of AST on the development of esophageal cancer based on PPARγ. We found that a stable and strong binding between PPARγ molecules and AST molecules using Autodock 4.0 software. AST significantly inhibited the viability of EC109 cells in a dose and time dependent manners (all P < 0.05), and up-regulated the protein expression level of PPARγ from the concentration of 6.25 µM (P < 0.05). Animal experiment showed that AST significantly decreased the incidences of NMBzA-induced esophageal carcinogenesis at 50 mg/kg AST in F344 rats (P < 0.05). AST inhibited the oxidative stress by improving the levels of superoxide dismutase (SOD), total antioxidant capacity (TAOC) and suppressing malondialdehyde (MDA) in serum, and increasing the protein of PPARγ, Bax/Bcl-2, Caspase-3 in esophagus tissue, especially in the 50 mg/kg of AST intervention group (all P < 0.05). In conclusion, our data suggested that protective effect of AST on esophageal cancer by inhibiting oxidative stress, up-regulating PPARγ, and activating the apoptotic pathway, which could provide a basis for clinical application of AST.
      pubtype: Academic Journal
      doctype:
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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