4.6 Article

Magnolol induces apoptosis via caspase-independent pathways in non-small cell lung cancer cells

期刊

ARCHIVES OF PHARMACAL RESEARCH
卷 37, 期 4, 页码 548-557

出版社

PHARMACEUTICAL SOC KOREA
DOI: 10.1007/s12272-013-0232-1

关键词

Magnolol; Apoptosis; Caspase; Non-small cell lung cancer

资金

  1. Kaohsiung Medical University [KMUH9-9M63, KMUH9-9M64]
  2. National Science Council [NSC 100-2320-B-037-009, NSC 99-2221-E-037-006-MY3, NSC 102-2320-B-039-025]
  3. Taiwan Department of Health Clinical Trial and Research Center of Excellence [DOH102-TD-B-111-004]

向作者/读者索取更多资源

Magnolol, a hydroxylated biphenyl agent isolated from herbal planet Magnolia officinalis, is a component of traditional Asian herbal teas. It has been reported to have anti-microbial, anti-inflammatory, and anti-cancer activity. Non-small cell lung cancer (NSCLC) cell lines (A549, H441 and H520) and normal human bronchial epithelial cells (HBECs) were used to evaluate the cytotoxic effect of magnolol. We show that magnolol inhibited cellular proliferation, increased DNA fragmentation, and decreased mitochondrial membrane potential in all NSCLC cells, but had no cytotoxic effect on HBECs. Magnolol triggered the release of pro-apoptotic proteins: Bid, Bax and cytochrome c from mitochondria, but did not activate the caspase-3, -8, and -9, suggesting that magnolol induces apoptosis of NSCLC cell lines via a caspase-independent pathway. The caspase-independent pathway is mediated through the activation of nuclear translocation of apoptosis-inducing factor, endonuclease G and cleaved poly(ADP-ribose) polymerase, which played important roles in mediating cell death. Furthermore, magnolol inhibited PI3K/AKT and ERK1/2 activity, but up-regulated p38 and JNK activity in A549 cell lines. The results of this study provided a basis for understanding and developing magnolol as a novel treatment of NSCLC.

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