TY - JOUR
T1 - In vitro evaluation of chemically analyzed Hypericum Triquetrifolium extract efficacy in apoptosis induction and cell cycle arrest of the HCT-116 colon cancer cell line
AU - Mahajna, Shahinaz
AU - Kadan, Sleman
AU - Tietel, Zipora
AU - Saad, Bashar
AU - Khasib, Said
AU - Tumeh, Aziz
AU - Ginsberg, Doron
AU - Zaid, Hilal
N1 - Publisher Copyright:
© 2019 by the authors.
PY - 2019/11/15
Y1 - 2019/11/15
N2 - Naturally derived drugs and plant-based products are attractive commodities that are being explored for cancer treatment. This in vitro study aimed to investigate the role of Hypericum triquetrifolium (50% ethanol: 50% water) extract (HTE) treatment on apoptosis, cell cycle modulation, and cell cycle arrest in human colon cancer cell line (HCT-116). HTE induced cell death via an apoptotic process, as assayed by an Annexin V-Cy3 assay. Exposing HCT-116 cells to 0.064, 0.125, 0.25, and 0.5mg/mL of HTE for 24 h led to 50 ± 9%, 71.6 ± 8%, 85 ± 5%, and 96 ± 1.5% apoptotic cells, respectively. HCT-116 cells treated with 0.25 and 0.5 mg/mL HTE for 3 h resulted in 38.9 ± 1.5% and 57.2 ± 3% cleavage of caspase-3-specific substrate, respectively. RT-PCR analysis revealed that theHTE extract had no effect onmRNA levels of Apaf-1 and NOXA. Moreover, the addition of 0.125mg/mL and 0.25mg/mL HTE for 24 h was clearly shown to attenuate the cell cycle progression machinery in HCT-116 cells. GC/MS analysis of the extract identified 21 phytochemicals that are known as apoptosis inducers and cell cycle arrest agents. All the compounds detected are novel in H. triquetrifolium. These results suggest that HTE-induced apoptosis of human colon cells ismediated primarily through the caspase-dependent pathway. Thus, HTE appears to be a potent therapeutic agent for colon cancer treatment.
AB - Naturally derived drugs and plant-based products are attractive commodities that are being explored for cancer treatment. This in vitro study aimed to investigate the role of Hypericum triquetrifolium (50% ethanol: 50% water) extract (HTE) treatment on apoptosis, cell cycle modulation, and cell cycle arrest in human colon cancer cell line (HCT-116). HTE induced cell death via an apoptotic process, as assayed by an Annexin V-Cy3 assay. Exposing HCT-116 cells to 0.064, 0.125, 0.25, and 0.5mg/mL of HTE for 24 h led to 50 ± 9%, 71.6 ± 8%, 85 ± 5%, and 96 ± 1.5% apoptotic cells, respectively. HCT-116 cells treated with 0.25 and 0.5 mg/mL HTE for 3 h resulted in 38.9 ± 1.5% and 57.2 ± 3% cleavage of caspase-3-specific substrate, respectively. RT-PCR analysis revealed that theHTE extract had no effect onmRNA levels of Apaf-1 and NOXA. Moreover, the addition of 0.125mg/mL and 0.25mg/mL HTE for 24 h was clearly shown to attenuate the cell cycle progression machinery in HCT-116 cells. GC/MS analysis of the extract identified 21 phytochemicals that are known as apoptosis inducers and cell cycle arrest agents. All the compounds detected are novel in H. triquetrifolium. These results suggest that HTE-induced apoptosis of human colon cells ismediated primarily through the caspase-dependent pathway. Thus, HTE appears to be a potent therapeutic agent for colon cancer treatment.
KW - Apoptosis
KW - Cell cycle
KW - Colon cancer
KW - Hypericum triquetrifolium
KW - Phytochemicals
UR - http://www.scopus.com/inward/record.url?scp=85075081458&partnerID=8YFLogxK
U2 - 10.3390/molecules24224139
DO - 10.3390/molecules24224139
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
C2 - 31731693
AN - SCOPUS:85075081458
SN - 1420-3049
VL - 24
JO - Molecules
JF - Molecules
IS - 22
M1 - 4139
ER -