2021
DOI: 10.1016/j.biopha.2021.111628
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Pinus kesiya Royle ex Gordon induces apoptotic cell death in hepatocellular carcinoma HepG2 cell via intrinsic pathway by PARP and Topoisomerase I suppression

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Cited by 7 publications
(3 citation statements)
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“…This observation suggested that pure isolated abietic acid could have more specific effects on cell cycles and may induce cell population shifts in different phases due to its standardization, thereby avoiding endo-interactions with other bioactive ingredients. Hence, the purity potentiates its apoptotic effects, as opposed to the complex nature of the pine extract [ 55 , 56 , 57 , 58 , 59 , 60 , 61 ]. Our data concurred with previously reported results showing that abietic acid showed antitumor activity through apoptosis induction and alteration of apoptosis-related proteins (Bax, caspase 3 and 9) in nasopharyngeal carcinoma (NPC) and triggered cell cycle arrest at G 2 /M phase [ 50 ].…”
Section: Discussionmentioning
confidence: 99%
“…This observation suggested that pure isolated abietic acid could have more specific effects on cell cycles and may induce cell population shifts in different phases due to its standardization, thereby avoiding endo-interactions with other bioactive ingredients. Hence, the purity potentiates its apoptotic effects, as opposed to the complex nature of the pine extract [ 55 , 56 , 57 , 58 , 59 , 60 , 61 ]. Our data concurred with previously reported results showing that abietic acid showed antitumor activity through apoptosis induction and alteration of apoptosis-related proteins (Bax, caspase 3 and 9) in nasopharyngeal carcinoma (NPC) and triggered cell cycle arrest at G 2 /M phase [ 50 ].…”
Section: Discussionmentioning
confidence: 99%
“…Moreover, these plants as well as G. daltonii, P. kesiya, C. filiformis, C. formosum spp. pruniflorum are reported to possess different degrees of cytotoxicity in the hepatocellular carcinoma HepG2 cells [44][45][46][47][48][49][50][51].…”
Section: Discussionmentioning
confidence: 99%
“…After that, the cells were resuspended in the binding buffer and analyzed using the BD FACSCantoII Flow cytometer (BD Biosciences, San Jose, CA, USA). The sample data were analyzed using BD FACSDiva software Version 6.1.3 (BD Biosciences, San Jose, CA, USA) [ 45 ]. The untreated cells were the control.…”
Section: Methodsmentioning
confidence: 99%