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Liriodenine, an aporphine alkaloid from Enicosanthellum pulchrum, inhibits proliferation of human ovarian cancer cells through induction of apoptosis via the mitochondrial signaling pathway and blocking cell cycle progression.

Nordin N, Majid NA, Hashim NM, Rahman MA, Hassan Z, Ali HM - Drug Des Devel Ther (2015)

Bottom Line: The result showed that liriodenine inhibits proliferation of CAOV-3 cells at 37.3 μM after 24 hours of exposure.Involvement of the intrinsic pathway in the mitochondria could be seen, with a significant increase in mitochondrial permeability and cytochrome c release, whereas the mitochondrial membrane potential was decreased.These findings indicate that liriodenine could be considered as a promising anticancer agent.

View Article: PubMed Central - PubMed

Affiliation: Department of Pharmacy, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.

ABSTRACT
Enicosanthellum pulchrum is a tropical plant from Malaysia and belongs to the Annonaceae family. This plant is rich in isoquinoline alkaloids. In the present study, liriodenine, an isoquinoline alkaloid, was examined as a potential anticancer agent, particularly in ovarian cancer. Liriodenine was isolated by preparative high-performance liquid chromatography. Cell viability was performed to determine the cytotoxicity, whilst the detection of morphological changes was carried out by acridine orange/propidium iodide assay. Initial and late apoptosis was examined by Annexin V-fluorescein isothiocyanate and DNA laddering assays, respectively. The involvement of pathways was detected via caspase-3, caspase-8, and caspase-9 analyses. Confirmation of pathways was further performed in mitochondria using a cytotoxicity 3 assay. Apoptosis was confirmed at the protein level, including Bax, Bcl-2, and survivin, while interruption of the cell cycle was used for final validation of apoptosis. The result showed that liriodenine inhibits proliferation of CAOV-3 cells at 37.3 μM after 24 hours of exposure. Changes in cell morphology were detected by the presence of cell membrane blebbing, chromatin condensation, and formation of apoptotic bodies. Early apoptosis was observed by Annexin V-fluorescein isothiocyanate bound to the cell membrane as early as 24 hours. Liriodenine activated the intrinsic pathway by induction of caspase-3 and caspase-9. Involvement of the intrinsic pathway in the mitochondria could be seen, with a significant increase in mitochondrial permeability and cytochrome c release, whereas the mitochondrial membrane potential was decreased. DNA fragmentation occurred at 72 hours upon exposure to liriodenine. The presence of DNA fragmentation indicates the CAOV-3 cells undergo late apoptosis or final stage of apoptosis. Confirmation of apoptosis at the protein level showed overexpression of Bax and suppression of Bcl-2 and survivin. Liriodenine inhibits progression of the CAOV-3 cell cycle in S phase. These findings indicate that liriodenine could be considered as a promising anticancer agent.

No MeSH data available.


Related in: MedlinePlus

Electrophoretic separation of fragmented DNA for CAOV-3 cells treated or not treated with liriodenine.Notes: Lane A is the positive control, where HL-60 cells were treated with actinomycin D. Lanes B–C are cells treated with liriodenine for 72 and 48 hours, respectively. Lane D shows untreated cells. Lane E shows the DNA marker (50 bp).Abbreviation: bp, base pairs.
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f7-dddt-9-1437: Electrophoretic separation of fragmented DNA for CAOV-3 cells treated or not treated with liriodenine.Notes: Lane A is the positive control, where HL-60 cells were treated with actinomycin D. Lanes B–C are cells treated with liriodenine for 72 and 48 hours, respectively. Lane D shows untreated cells. Lane E shows the DNA marker (50 bp).Abbreviation: bp, base pairs.

Mentions: CAOV-3 cells treated with liriodenine at concentrations of 37 μM showed the presence of DNA laddering after 72 hours of treatment (Figure 7). The presence of laddering indicated DNA fragmentation in CAOV-3 cells. The positive control used in this study comprised HL-60 cells treated with actinomycin D, which showed formation of a clear ladder and had close similarities to the marker.


Liriodenine, an aporphine alkaloid from Enicosanthellum pulchrum, inhibits proliferation of human ovarian cancer cells through induction of apoptosis via the mitochondrial signaling pathway and blocking cell cycle progression.

Nordin N, Majid NA, Hashim NM, Rahman MA, Hassan Z, Ali HM - Drug Des Devel Ther (2015)

Electrophoretic separation of fragmented DNA for CAOV-3 cells treated or not treated with liriodenine.Notes: Lane A is the positive control, where HL-60 cells were treated with actinomycin D. Lanes B–C are cells treated with liriodenine for 72 and 48 hours, respectively. Lane D shows untreated cells. Lane E shows the DNA marker (50 bp).Abbreviation: bp, base pairs.
© Copyright Policy
Related In: Results  -  Collection

License
Show All Figures
getmorefigures.php?uid=PMC4362660&req=5

f7-dddt-9-1437: Electrophoretic separation of fragmented DNA for CAOV-3 cells treated or not treated with liriodenine.Notes: Lane A is the positive control, where HL-60 cells were treated with actinomycin D. Lanes B–C are cells treated with liriodenine for 72 and 48 hours, respectively. Lane D shows untreated cells. Lane E shows the DNA marker (50 bp).Abbreviation: bp, base pairs.
Mentions: CAOV-3 cells treated with liriodenine at concentrations of 37 μM showed the presence of DNA laddering after 72 hours of treatment (Figure 7). The presence of laddering indicated DNA fragmentation in CAOV-3 cells. The positive control used in this study comprised HL-60 cells treated with actinomycin D, which showed formation of a clear ladder and had close similarities to the marker.

Bottom Line: The result showed that liriodenine inhibits proliferation of CAOV-3 cells at 37.3 μM after 24 hours of exposure.Involvement of the intrinsic pathway in the mitochondria could be seen, with a significant increase in mitochondrial permeability and cytochrome c release, whereas the mitochondrial membrane potential was decreased.These findings indicate that liriodenine could be considered as a promising anticancer agent.

View Article: PubMed Central - PubMed

Affiliation: Department of Pharmacy, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.

ABSTRACT
Enicosanthellum pulchrum is a tropical plant from Malaysia and belongs to the Annonaceae family. This plant is rich in isoquinoline alkaloids. In the present study, liriodenine, an isoquinoline alkaloid, was examined as a potential anticancer agent, particularly in ovarian cancer. Liriodenine was isolated by preparative high-performance liquid chromatography. Cell viability was performed to determine the cytotoxicity, whilst the detection of morphological changes was carried out by acridine orange/propidium iodide assay. Initial and late apoptosis was examined by Annexin V-fluorescein isothiocyanate and DNA laddering assays, respectively. The involvement of pathways was detected via caspase-3, caspase-8, and caspase-9 analyses. Confirmation of pathways was further performed in mitochondria using a cytotoxicity 3 assay. Apoptosis was confirmed at the protein level, including Bax, Bcl-2, and survivin, while interruption of the cell cycle was used for final validation of apoptosis. The result showed that liriodenine inhibits proliferation of CAOV-3 cells at 37.3 μM after 24 hours of exposure. Changes in cell morphology were detected by the presence of cell membrane blebbing, chromatin condensation, and formation of apoptotic bodies. Early apoptosis was observed by Annexin V-fluorescein isothiocyanate bound to the cell membrane as early as 24 hours. Liriodenine activated the intrinsic pathway by induction of caspase-3 and caspase-9. Involvement of the intrinsic pathway in the mitochondria could be seen, with a significant increase in mitochondrial permeability and cytochrome c release, whereas the mitochondrial membrane potential was decreased. DNA fragmentation occurred at 72 hours upon exposure to liriodenine. The presence of DNA fragmentation indicates the CAOV-3 cells undergo late apoptosis or final stage of apoptosis. Confirmation of apoptosis at the protein level showed overexpression of Bax and suppression of Bcl-2 and survivin. Liriodenine inhibits progression of the CAOV-3 cell cycle in S phase. These findings indicate that liriodenine could be considered as a promising anticancer agent.

No MeSH data available.


Related in: MedlinePlus