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Anti-cancer effects of plant-derived Micromonospora sp. M2 against A549 and MCF-7 cell lines.
Jeong, Gyeong Han; Bak, Dong-Ho; Lee, Hanui; Cho, Ja Young; Kang, Seong Hee; Chung, Byung Yeoup; Park, Sanghwa; Bai, Hyoung-Woo.
Afiliação
  • Jeong GH; Research division for Biotechnology, Advanced Radiation Technology Institute (ARTI), Korea Atomic Energy Research Institute (KAERI), Jeongeup, Republic of Korea.
  • Bak DH; Research division for Biotechnology, Advanced Radiation Technology Institute (ARTI), Korea Atomic Energy Research Institute (KAERI), Jeongeup, Republic of Korea.
  • Lee H; Research division for Biotechnology, Advanced Radiation Technology Institute (ARTI), Korea Atomic Energy Research Institute (KAERI), Jeongeup, Republic of Korea.
  • Cho JY; Department of Biological Sciences and Research Center of Ecomimetics, College of Natural Science, Chonnam National University, Gwangju, Republic of Korea.
  • Kang SH; Bacteria Research Team, Nakdonggang National Institute of Biological Resources (NNIBR), Sangju, Republic of Korea.
  • Chung BY; Research division for Biotechnology, Advanced Radiation Technology Institute (ARTI), Korea Atomic Energy Research Institute (KAERI), Jeongeup, Republic of Korea.
  • Park S; Research division for Biotechnology, Advanced Radiation Technology Institute (ARTI), Korea Atomic Energy Research Institute (KAERI), Jeongeup, Republic of Korea.
  • Bai HW; Bacteria Research Team, Nakdonggang National Institute of Biological Resources (NNIBR), Sangju, Republic of Korea.
Biosci Biotechnol Biochem ; 88(6): 608-619, 2024 May 22.
Article em En | MEDLINE | ID: mdl-38573835
ABSTRACT
The huge diversity of secondary bioactive metabolites, such as antibiotic and anticancer compounds produced by Micromonospora sp., makes it an attractive target for study. Here, we explored the anti-proliferative activities of Micromonospora sp. M2 extract (MBE) in relation to its pro-oxidative activities in A549 and MCF7 cell lines. Anti-proliferative effects were assessed by treating cells with MBE. We found that treatment with MBE decreased cell proliferation and increased intracellular reactive oxygen species, and that these observations were facilitated by the suppression of the PI3K-AKT pathway, alterations to the Bcl/Bad ratio, and increased caspase activity. These observations also demonstrated that MBE induced apoptotic cell death in cell lines. In addition, the phosphorylation of P38 and c-Jun N-terminal kinase (JNK) were upregulated following MBE treatment in both cell lines. Collectively, these results indicate that MBE acts as an anticancer agent via oxidative stress and JNK/mitogen-activated protein kinase pathway activation, enhancing apoptotic cell death in cell lines.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Espécies Reativas de Oxigênio / Apoptose / Proliferação de Células / Micromonospora Limite: Humans Idioma: En Revista: Biosci Biotechnol Biochem Assunto da revista: BIOQUIMICA / BIOTECNOLOGIA Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Espécies Reativas de Oxigênio / Apoptose / Proliferação de Células / Micromonospora Limite: Humans Idioma: En Revista: Biosci Biotechnol Biochem Assunto da revista: BIOQUIMICA / BIOTECNOLOGIA Ano de publicação: 2024 Tipo de documento: Article