2020
DOI: 10.1016/j.acthis.2020.151538
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β-elemene suppresses the malignant behavior of esophageal cancer cells by regulating the phosphorylation of AKT

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Cited by 16 publications
(9 citation statements)
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“…Liang et al found that β-elemene suppressed PD-L1 expression and cancer cell proliferation in esophageal cancer cells. In both in vitro and in vivo experiments, β-elemene consistently inhibited Akt activation as well as expression of its downstream molecule, PD-L1 [199]. Although the general mechanism by which β-elemene suppresses tumors remains unclear, several studies have drawn attention to Akt as a target [222][223][224][225].…”
Section: β-Elemenementioning
confidence: 99%
“…Liang et al found that β-elemene suppressed PD-L1 expression and cancer cell proliferation in esophageal cancer cells. In both in vitro and in vivo experiments, β-elemene consistently inhibited Akt activation as well as expression of its downstream molecule, PD-L1 [199]. Although the general mechanism by which β-elemene suppresses tumors remains unclear, several studies have drawn attention to Akt as a target [222][223][224][225].…”
Section: β-Elemenementioning
confidence: 99%
“…β-Elemene (1-methyl-1-vinyl-2,4-diisopropenyl-cyclohexane), extracted from the root of Curcuma wenyujin , presents a broad-spectrum, moderate, antitumor effect and is widely used as an adjunctive drug to enhance the efficacy, reduce the toxicity of chemoradiotherapy, and reverse drug resistance in cancer treatment. 43 Previous studies have indicated that β‐elemene could inhibit cell proliferation and induce apoptosis in various types of cancers, including melanoma, 44 hepatocellular, 23 lymphoma, 26 glioma, 29 esophageal, 31 gastric, 45 glioblastoma multiforme, 32 nonsmall-cell lung, 33 pancreatic, 39 and nasopharyngeal. 34 Recent studies have reported that β‐elemene significantly inhibited the migration and invasive capacity of BGC823, SGC7901 and multidrug resistant (MDR) SGC7901/ADR gastric cancer cells, TE-1 and KYSE-150 esophageal cancer cells in vitro and inhibited the capacity of BGC823 cells to diffuse peritoneally and metastasize in vivo.…”
Section: Pharmacologymentioning
confidence: 99%
“…34 Recent studies have reported that β‐elemene significantly inhibited the migration and invasive capacity of BGC823, SGC7901 and multidrug resistant (MDR) SGC7901/ADR gastric cancer cells, TE-1 and KYSE-150 esophageal cancer cells in vitro and inhibited the capacity of BGC823 cells to diffuse peritoneally and metastasize in vivo. 24,25,31 Moreover, the radio sensitivity of cancers, such as glioblastoma multiforme U87-MG, T98G, and U251 cells, 32 melanoma A375 cells, 44 and A549 lung adenocarcinoma xenograft 27,28 were also reported to be significantly enhanced by β-elemene.…”
Section: Pharmacologymentioning
confidence: 99%
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