4.7 Article

Pyrrolizidine alkaloids from Liparis nervosa with antitumor activity by modulation of autophagy and apoptosis

Journal

PHYTOCHEMISTRY
Volume 153, Issue -, Pages 147-155

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.phytochem.2018.06.001

Keywords

Liparis nervosa; Orchidaceae; Pyrrolizidine alkaloids; Cytotoxicity; Human colorectal cancer cell line; Autophagy; Apoptosis

Funding

  1. National Natural Science Foundation of China [81402803]
  2. project of Science and Technology Bureau of Chengdu [2015-HM01-00041-SF]
  3. United States of America National Institutes of Health [R01 HL128647]

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Seven pyrrolizidine alkaloids, nervosine X-XV and nervosine VII N-oxide, together with a reaction product, namely chloride-(N-chloromethyl nervosine VII), were isolated from Liparis nervosa. Their structures were elucidated by extensive spectroscopic analyses. Most of these compounds were investigated for their cytotoxicity in vitro against HCT116 human cancer cell line, and the results showed that chloride-(N-chloromethyl nervosine VII) induced tumor cell death in a dose-dependent mariner. Furthermore, the mechanisms underlying its cytotoxicity were investigated, including apoptosis and autophagy. Apoptosis in HCT116 cells was associated with up-regulation of caspase-3 and -9 expressions by activation of the mitochondrial pathway. The autophagy inducing effect was associated with the regulation of autophagic markers, including LC3-II, p62, and Beclin 1. Mechanistic studies showed that JNK, ERK1/2, and p38 MAPKs signaling cascades play an important role in chloride-(N-chloromethyl nervosine VII) induced autophagy and apoptosis.

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