Previous studies have revealed the antitumor potential of
Poria cocos Wolf against a broad spectrum of cancers. However, the biological activity of
P. cocos against lung cancer, which is known as the leading cause of cancer mortality worldwide, and its underlying chemical and
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Previous studies have revealed the antitumor potential of
Poria cocos Wolf against a broad spectrum of cancers. However, the biological activity of
P. cocos against lung cancer, which is known as the leading cause of cancer mortality worldwide, and its underlying chemical and molecular basis, remain to be investigated. We aimed to evaluate the in vitro cytotoxicity of
P. cocos toward human lung adenocarcinoma cells with different
p53 statuses, to identify the bioactive constituents of
P. cocos, and explicate the molecular mechanisms underlying the cytotoxicity of these constituents in human lung adenocarcinoma cells. An EtOH extract of the sclerotia of
P. cocos exhibited cytotoxicity toward four human lung cancer cell lines: A549, H1264, H1299, and Calu-6, regardless of their
p53 status. Chemical investigation of the extract resulted in the isolation of two triterpenoids, dehydroeburicoic acid monoacetate (
1) and acetyl eburicoic acid (
4); a sterol, 9,11-dehydroergosterol peroxide (
2); and a diterpenoid, dehydroabietic acid (
3). All of the isolated compounds were cytotoxic to the lung adenocarcinoma cell lines, exhibiting IC
50 values ranging from 63.6 μM to 171.0 μM at 48 h of treatment. The cytotoxicity of the extract and the isolated compounds were found to be mediated by apoptosis, and accompanied by elevated Bax expression and/or Bcl-2 phosphorylation along with caspase-3 activation. Our data demonstrate that the sclerotium of
P. cocos and its four bioactive constituents (
1–
4) exert cytotoxicity against human lung adenocarcinoma cells, regardless of their
p53 status, by inducing apoptosis associated with mitochondrial perturbation, and proposing the potential to employ
P. cocos in the treatment of lung cancer.
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