Activation of apoptotic protein in U937 cells by a component of turmeric oil
1Department of Food and Biotechnology, Dongseo University, Busan 617-716, Korea. lyk@dongseo.ac.kr
Abstract:
Aromatic (ar)-turmerone from turmeric oil displays anti-tumorigenesis activity that includes inhibited cell proliferation. This study investigated ar-turmerone-mediated apoptotic protein activation in human lymphoma U937 cells. Ar-turmerone treatment inhibited U937 cell viability in a concentration-dependent fashion, with inhibition exceeding 84%. Moreover, the treatment produced nucleosomal DNA fragmentation and the percentage of sub-diploid cells increased in a concentration-dependent manner; both are hallmarks of apoptosis. The apoptotic effect of ar-turmerone was associated with the induction of Bax and p53 proteins, rather than Bcl-2 and p21. Activation of mitochondrial cytochrome c and caspase-3 demonstrated that the activation of caspases accompanied the apoptotic effect of ar-turmerone, which mediated cell death. These results suggest that the apoptotic effect of ar-turmerone on U937 cells may involve caspase-3 activation through the induction of Bax and p53, rather than Bcl-2 and p21.
Insights
Aromatic turmerone from turmeric oil induces apoptosis in human lymphoma cells by activating caspase-3. This natural compound effectively inhibits cancer cell proliferation and triggers programmed cell death via specific protein pathways.
Area of Science:
- Biochemistry
- Molecular Biology
- Pharmacology
Background:
- Aromatic (ar)-turmerone, a compound found in turmeric oil, exhibits anti-tumorigenesis properties, including the inhibition of cancer cell proliferation.
- Understanding the molecular mechanisms behind its anti-cancer effects is crucial for therapeutic development.
Purpose of the Study:
- To investigate the role of ar-turmerone in activating apoptotic proteins in human lymphoma U937 cells.
- To elucidate the specific molecular pathways involved in ar-turmerone-induced apoptosis.
Main Methods:
- Treatment of human lymphoma U937 cells with varying concentrations of ar-turmerone.
- Assessment of cell viability using assays.
- Analysis of DNA fragmentation and sub-diploid cell populations.
- Western blot analysis to detect the expression of apoptosis-related proteins (Bax, p53, Bcl-2, p21).
- Measurement of mitochondrial cytochrome c release and caspase-3 activation.
Main Results:
- Ar-turmerone significantly inhibited U937 cell viability in a dose-dependent manner (over 84% inhibition).
- The treatment induced characteristic hallmarks of apoptosis, including nucleosomal DNA fragmentation and an increase in sub-diploid cells.
- Apoptosis was associated with increased expression of Bax and p53, but not Bcl-2 or p21.
- Mitochondrial cytochrome c release and caspase-3 activation were observed, indicating caspase-dependent cell death.
Conclusions:
- Ar-turmerone induces apoptosis in human lymphoma U937 cells through a mechanism involving caspase-3 activation.
- The apoptotic effect appears to be mediated by the induction of Bax and p53 proteins.
- These findings highlight the potential of ar-turmerone as a therapeutic agent against lymphoma.
Related Concept Videos
The Extrinsic Apoptotic Pathway
The Intrinsic Apoptotic Pathway
Apoptosis
Phagocytosis of Apoptotic Cells
Normal cells contain receptors that prevent them from being recognized by phagocytes.
Caspases

