Molecular biology reports · 2026
The potential anticancer effect of Jasonia montana against hepatocellular carcinoma.
СтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Abdellateif Mona S, Mounir Dalia M, Abdelsalam Hani M, Diab Abdelaziz Abbas, Ahmed Wafaa A
Аннотация
AIM: Hepatocellular Carcinoma (HCC) is a fundamental health problem with an overall poor prognosis. Jasonia montana (J. montana) was evaluated for its biological activities against HCC cells (in vitro study).
METHODS: The efficacy of J. montana was evaluated for its cytotoxic activity on HepG2 cells. Its impacts on cell cycle phases, apoptosis pathways, DNA damage, cellular oxidative stress, and inflammation were assessed. Additionally, the expression levels of PTEN and SOX2 were also evaluated.
RESULTS: The ethanol extract of J. montana produced a cytotoxic effect on HepG2 cells at (IC50) of 24 μg/mL. There was a significant increase in the cell number in the 2n, G0/G1, and G2/M phases (p < 0.001, p = 0.001, and p = 0.022; respectively), while a significant decrease in the cell number in the S phase (p < 0.001) and 4n phase (p = 0.011) compared to the untreated HepG2 cells. Caspase-8 [2.6 ± 0.56 ng/mL versus 0.9 ± 0.06 ng/mL, p < 0.001], Caspase-9 [11.9 ± 1.18 ng/mL versus 5.8 ± 0.85 ng/mL, p < 0.001], and Caspase-3 [19.9 ± 1.01 ng/mL versus 4.0 ± 0.88 ng/mL, p < 0.001] were significantly increased in HepG2 cells treated with J. montana compared to untreated control cells. There was a significant increase in the PTEN expression (FC = 3.04 ± 0.85, p = 0.030), and a significant decrease in SOX2 expression (FC = 0.54 ± 0.02, p = 0.039). There was a significant decrease in IL-6 and TNF-α levels (P < 0.001). Moreover, the total antioxidant (TA) and glutathione reductase (GSH) were significantly increased (P < 0.001).
CONCLUSION: J. montana could be a potentially useful chemotherapeutic agent against HCC cells.
METHODS: The efficacy of J. montana was evaluated for its cytotoxic activity on HepG2 cells. Its impacts on cell cycle phases, apoptosis pathways, DNA damage, cellular oxidative stress, and inflammation were assessed. Additionally, the expression levels of PTEN and SOX2 were also evaluated.
RESULTS: The ethanol extract of J. montana produced a cytotoxic effect on HepG2 cells at (IC50) of 24 μg/mL. There was a significant increase in the cell number in the 2n, G0/G1, and G2/M phases (p < 0.001, p = 0.001, and p = 0.022; respectively), while a significant decrease in the cell number in the S phase (p < 0.001) and 4n phase (p = 0.011) compared to the untreated HepG2 cells. Caspase-8 [2.6 ± 0.56 ng/mL versus 0.9 ± 0.06 ng/mL, p < 0.001], Caspase-9 [11.9 ± 1.18 ng/mL versus 5.8 ± 0.85 ng/mL, p < 0.001], and Caspase-3 [19.9 ± 1.01 ng/mL versus 4.0 ± 0.88 ng/mL, p < 0.001] were significantly increased in HepG2 cells treated with J. montana compared to untreated control cells. There was a significant increase in the PTEN expression (FC = 3.04 ± 0.85, p = 0.030), and a significant decrease in SOX2 expression (FC = 0.54 ± 0.02, p = 0.039). There was a significant decrease in IL-6 and TNF-α levels (P < 0.001). Moreover, the total antioxidant (TA) and glutathione reductase (GSH) were significantly increased (P < 0.001).
CONCLUSION: J. montana could be a potentially useful chemotherapeutic agent against HCC cells.