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2,6-DMBQ suppresses cell proliferation and migration via inhibiting mTOR/AKT and p38 MAPK signaling pathways in NSCLC cells.
Xie, Xiaomeng; Zu, Xueyin; Laster, Kyle; Dong, Zigang; Kim, Dong Joon.
Affiliation
  • Xie X; Department of Pathophysiology, School of Basic Medical Sciences, Academy of Medical Science, College of Medicine, Zhengzhou University, Zhengzhou, Henan, 450008, China; China-US (Henan) Hormel Cancer Institute, Zhengzhou, Henan, 450008, China.
  • Zu X; Department of Pathophysiology, School of Basic Medical Sciences, Academy of Medical Science, College of Medicine, Zhengzhou University, Zhengzhou, Henan, 450008, China; China-US (Henan) Hormel Cancer Institute, Zhengzhou, Henan, 450008, China.
  • Laster K; China-US (Henan) Hormel Cancer Institute, Zhengzhou, Henan, 450008, China.
  • Dong Z; Department of Pathophysiology, School of Basic Medical Sciences, Academy of Medical Science, College of Medicine, Zhengzhou University, Zhengzhou, Henan, 450008, China; China-US (Henan) Hormel Cancer Institute, Zhengzhou, Henan, 450008, China; The Collaborative Innovation Center of Henan Province fo
  • Kim DJ; Department of Pathophysiology, School of Basic Medical Sciences, Academy of Medical Science, College of Medicine, Zhengzhou University, Zhengzhou, Henan, 450008, China; China-US (Henan) Hormel Cancer Institute, Zhengzhou, Henan, 450008, China; The Collaborative Innovation Center of Henan Province fo
J Pharmacol Sci ; 145(3): 279-288, 2021 Mar.
Article in En | MEDLINE | ID: mdl-33602509
2,6-Dimethoxy-1,4-benzoquinone (2,6-DMBQ) is the major bioactive compound found in fermented wheat germ extract. Although fermented wheat germ extract has been reported to show anti-proliferative and anti-metabolic effects in various cancers, the anticancer potential and molecular mechanisms exerted by 2,6-DMBQ have not been investigated in non-small cell lung cancer (NSCLC) cells. Here, we report that 2,6-DMBQ suppresses NSCLC cell growth and migration through inhibiting activation of AKT and p38 MAPK. 2,6-DMBQ significantly suppressed anchorage-dependent and independent cell growth. Additionally, 2,6-DMBQ induced G2 phase cell cycle arrest through inhibiting the expression and phosphorylation of cyclin B1 and CDC2, respectively. Furthermore, 2,6-DMBQ strongly suppressed NSCLC cell migration through induction of E-cadherin expression. To determine the molecular mechanism(s) exerted by 2,6-DMBQ upon NSCLC cell lines, various signaling kinases were screened; the results indicate that 2,6-DMBQ strongly inhibits the phosphorylation of AKT and p38 MAPK. Additionally, the growth kinetics of cells treated with an AKT or p38 MAPK inhibitor in combination with 2,6-DMBQ indicate that 2,6-DMBQ suppresses NSCLC cell growth and migration through inhibition of AKT and p38 MAPK. Taken together, our results suggest that 2,6-DMBQ is a potential anticancer reagent against NSCLC cells and could be useful for treating lung cancer patients.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Signal Transduction / Cell Movement / Benzoquinones / Carcinoma, Non-Small-Cell Lung / MAP Kinase Signaling System / Cell Proliferation / Proto-Oncogene Proteins c-akt / TOR Serine-Threonine Kinases / Lung Neoplasms / Antineoplastic Agents Limits: Humans Language: En Journal: J Pharmacol Sci Journal subject: FARMACOLOGIA Year: 2021 Document type: Article Affiliation country: China Country of publication: Japón

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Signal Transduction / Cell Movement / Benzoquinones / Carcinoma, Non-Small-Cell Lung / MAP Kinase Signaling System / Cell Proliferation / Proto-Oncogene Proteins c-akt / TOR Serine-Threonine Kinases / Lung Neoplasms / Antineoplastic Agents Limits: Humans Language: En Journal: J Pharmacol Sci Journal subject: FARMACOLOGIA Year: 2021 Document type: Article Affiliation country: China Country of publication: Japón