2021
DOI: 10.1016/j.jep.2020.113645
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Methoxyeugenol regulates the p53/p21 pathway and suppresses human endometrial cancer cell proliferation

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Cited by 13 publications
(9 citation statements)
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“…It was found that the protein expression level of p-Cdc42 was markedly decreased following the addition of Que; however, its expression after 4 h of Que treatment was slightly increased compared with that after 2 h. This may be caused by the negative feedback regulation mechanism, which requires further investigation. p21 was first discovered as a downstream gene of p53, and subsequently, scientists have conducted numerous studies examining p21 and have shown that it is an important cell cycle government target (52,53). p21 is involved in the process of cell proliferation, differentiation, senescence and death (54).…”
Section: Discussionmentioning
confidence: 99%
“…It was found that the protein expression level of p-Cdc42 was markedly decreased following the addition of Que; however, its expression after 4 h of Que treatment was slightly increased compared with that after 2 h. This may be caused by the negative feedback regulation mechanism, which requires further investigation. p21 was first discovered as a downstream gene of p53, and subsequently, scientists have conducted numerous studies examining p21 and have shown that it is an important cell cycle government target (52,53). p21 is involved in the process of cell proliferation, differentiation, senescence and death (54).…”
Section: Discussionmentioning
confidence: 99%
“…In a previous work by our research group, methoxyeugenol showed an effect in decreasing cell proliferation in human endometrial cancer (Costa et al, 2021). HSCs are responsible for extracellular matrix deposition and synthesis, and their activation and proliferation rate are closely linked to the development of fibrosis.…”
Section: Introductionmentioning
confidence: 79%
“…Many natural phytochemical products can suppress cancerous cell proliferation by halting cell cycle phases [21,23]. In the G0/G1 phase, cells are stopped at the G1 to S checkpoint transition by suppressing the function of the complex formed by combining cyclin E and cyclin dependent kinase-2, which are the main cell cycle regulators, to promote cell transition from the G1 phase to the S control point [24].…”
Section: Discussionmentioning
confidence: 99%