Seed Oil of Brucea javanica Induces Apoptotic Death of Acute Myeloid Leukemia Cells via Both the Death Receptors and the Mitochondrial-Related Pathways.

Evid Based Complement Alternat Med

Department of Pharmacology, Key Laboratory of New Drug Screening of Liaoning Province, Shenyang Pharmaceutical University, Shenyang 110016, China.

Published: November 2011

Seed oil of Brucea javanica (BJO) is extracted from the seeds of herb medicine Brucea javanica (L.), and its emulsion formulation (BJOE) has been used clinically to treat carcinomas for many years in China. The antileukemia potential of BJO was investigated in human acute myeloid leukemia cell lines (AML) U937 and HL-60 in vitro and in a mouse U937 xenograft tumor model. BJO induced AML cell apoptosis through activation of caspase-8 and modulation of apoptosis-related proteins. Meanwhile, the inhibition of survivin and XIAP increased the cytotoxicity of BJO. Consistent with these findings, BJO also increased subG(1) phase cells and cause PARP cleavage in AML patients' leukemia cells. In contrast, only weak cytotoxicity of BJO was found in peripheral blood lymphocytes (PBLs) of healthy volunteers. Moreover, oleic acid and linoleic acid were found to be the active components of BJO. Our study provided strong evidence for the first time that BJO induced apoptosis of both cultured and primary AML cells. Furthermore, intravenous injection of BJO significantly inhibited U937 tumor growth in the xenograft mouse model. These results suggest that BJO may have a therapeutic role in the treatment of human leukemia.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3132896PMC
http://dx.doi.org/10.1155/2011/965016DOI Listing

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Article Synopsis
  • Lung cancer has a poor prognosis, but recent studies suggest that inducing ferroptosis, a form of cell death, could be a promising treatment approach.
  • This study specifically investigates oleic acid (OA), the main component of Brucea javanica oil (BJO), and its effects on lung cancer cell lines A549 and H1299.
  • Findings indicate that OA inhibits cancer cell growth and migration, suppresses SDC4 expression, and promotes ferroptosis by altering the levels of several key proteins involved in this process, highlighting its potential for lung cancer therapy.
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