Journal of Microbiology and Biotechnology

  • 제34권2호
  • /
  • Pages.240-248
  • /
  • 2024
  • /
  • 1017-7825(pISSN)
  • /
  • 1738-8872(eISSN)
한국미생물·생명공학회 (The Korean Society for Microbiology and Biotechnology)
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(E)-2-Methoxy-4-(3-(4-Methoxyphenyl) Prop-1-en-1-yl) Phenol Suppresses Breast Cancer Progression by Dual-Regulating VEGFR2 and PPARγ

  • Na-Yeon Kim (Department of Bioscience and Biotechnology, Konkuk University) ;
  • Hyo-Min Park (Department of Bioscience and Biotechnology, Konkuk University) ;
  • Hee Pom Lee (College of Pharmacy & Medical Research Center, Chungbuk National University) ;
  • Jin Tae Hong (College of Pharmacy & Medical Research Center, Chungbuk National University) ;
  • Do-Young Yoon (Department of Bioscience and Biotechnology, Konkuk University)
  • 투고 : 2023.09.14
  • 심사 : 2023.10.26
  • 발행 : 2024.02.28
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초록

In cancer treatment, multi-target approach has paid attention to a reasonable strategy for the potential agents. We investigated whether (E)-2-methoxy-4-(3-(4-methoxyphenyl) prop-1-en-1-yl) phenol (MMPP) could exert an anticancer effect by dual-regulating VEGFR2 and PPARγ. MMPP showed modulating effects in TNBC type (MDA-MB-231 and MDA-MB-468) and luminal A type (MCF7) breast cancer cell lines. MMPP enhanced PPARγ transcriptional activity and inhibited VEGFR2 phosphorylation. MMPP-induced signaling by VEGFR2 and PPARγ ultimately triggered the downregulation of AKT activity. MMPP exhibited anticancer effects, as evidenced by growth inhibition, inducement of apoptosis, and suppression of migration and invasion. At the molecular level, MMPP activated pro-apoptotic proteins (caspase3, caspase8, caspase9, and bax), while inhibiting the anti-apoptotic proteins (bcl2). Additionally, MMPP inhibited the mRNA expressions of EMT-promoting transcription factors. Therefore, our findings showed molecular mechanisms of MMPP by regulating VEGFR2 and PPARγ, and suggested that MMPP has potential to treat breast cancer.

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참고문헌

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