Abstract
The chloroform extract of the Japanese cypress Chamaecyparis obtusa was found to kill PANC-1 human pancreatic cancer cells preferentially in the nutrient-deprived medium without causing toxicity in the nutrient rich condition. Phytochemical investigation on this extract led to the isolation of a new sesquiterpene (1), together with the six sesquiterpenes (2-7) and a lignan (8). The isolated compounds were tested for their preferential cytotoxicity activity against five different human pancreatic cancer cell lines [PANC-1, MIA PaCa2, CAPAN-1, PSN-1, and KLM-1] by utilizing an antiausterity strategy. Among them, α-cadinol (2) was identified as the most active constituent. α-Cadinol (2) was found to inhibit the activation of Akt/mTOR pathway, and the hyperactivation of autophagy leading to preferential PANC-1 cell death during nutrient-starvation.
Keywords:
Antiausterity agents; Autophagy; Chamaecyparis obtusa; PANC-1; Pancreatic cancer.
Copyright © 2017 Elsevier Ltd. All rights reserved.
MeSH terms
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Antineoplastic Agents, Phytogenic / chemistry*
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Antineoplastic Agents, Phytogenic / isolation & purification
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Antineoplastic Agents, Phytogenic / toxicity
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Autophagy / drug effects
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Cell Line, Tumor
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Chamaecyparis / chemistry*
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Chamaecyparis / metabolism
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Cyclodecanes / chemistry*
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Cyclodecanes / isolation & purification
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Cyclodecanes / toxicity
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Drug Evaluation, Preclinical
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Drug Screening Assays, Antitumor
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Humans
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Magnetic Resonance Spectroscopy
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Microscopy, Fluorescence
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Molecular Conformation
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Proto-Oncogene Proteins c-akt / antagonists & inhibitors
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Proto-Oncogene Proteins c-akt / metabolism
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Sesquiterpenes / chemistry*
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Sesquiterpenes / isolation & purification
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Sesquiterpenes / toxicity
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TOR Serine-Threonine Kinases / antagonists & inhibitors
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TOR Serine-Threonine Kinases / metabolism
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Terpenes / chemistry*
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Terpenes / isolation & purification
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Terpenes / toxicity
Substances
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10-hydroxy-7-isopropyl-5,10-dimethylcyclodec-4-ene-3,6-dione
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Antineoplastic Agents, Phytogenic
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Cyclodecanes
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Sesquiterpenes
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Terpenes
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cadinol
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MTOR protein, human
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Proto-Oncogene Proteins c-akt
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TOR Serine-Threonine Kinases