Pristimerin effectively inhibits the malignant phenotypes of uveal melanoma cells by targeting NF‑κB pathway.
@article{Zhang2017PristimerinEI,
title={Pristimerin effectively inhibits the malignant phenotypes of uveal melanoma cells by targeting NF‑$\kappa$B pathway.},
author={Biao Zhang and Jing Zhang and Jingxuan Pan},
journal={International journal of oncology},
year={2017},
volume={51 3},
pages={
887-898
}
}Uveal melanoma (UM) is a highly aggressive intraocular malignancy that lacks any effective targeted-therapy. Neither survival nor prognosis has been improved for the past decades in patients with metastatic UM. NF‑κB pathway is reported to be abnormally activated in UM. However, the role of NF‑κB pathway as a potential therapeutical target in UM remains unclear. Here, the effect of pristimerin, a potent inhibitor of NF‑κB pathway, on UM cells in terms of growth, apoptosis, motility, invasion…
13 Citations
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Evidence is provided for the development of pristimerin to be a new therapeutic agent for ESCC by suppressing tumour necrosis factor α (TNFα)‐induced IκBα phosphorylation, p65 translocation, and NF‐κB‐dependent gene expression.
Pristimerin‐induced uveal melanoma cell death via inhibiting PI3K/Akt/FoxO3a signalling pathway
- Biology, ChemistryJournal of cellular and molecular medicine
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Findings indicate that Pristimerin may be considered as a potential chemotherapeutic agent for patients with UM and induced apoptotic cell death through inhibition of PI3K/Akt/FoxO3a pathway in UM‐1 cells.
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- Biology, ChemistryInternational journal of molecular medicine
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Western blotting revealed that Pris effectively synergized with Cis to induce cell apoptosis by inhibiting the microRNA-23a/Akt/glycogen synthase kinase 3β signaling pathway and suppressing autophagy, suggesting that this may be a potential therapeutic strategy to overcome lung cancer.
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- Biology, ChemistryFrontiers in Oncology
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Pristimerin reverses multidrug resistance of cancer cells and exerts synergizing effects with other chemotherapeutic drugs and multi-targeted biological and molecular regulations in cancers.
MicroRNA-29a Inhibits Growth, Migration and Invasion of Melanoma A375 Cells in Vitro by Directly Targeting BMI1
- BiologyCellular Physiology and Biochemistry
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Background/Aims: Melanoma is one of the most aggressive malignant tumors, with increasing incidence, poor prognosis, and lack of any effective targeted therapies. Abnormal expression of miR-29a has…
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- 2019
In vivo and in vitro studies that illustrate the relationship between aldehyde dehydrogenase and MICs are summarized, rendering ALDH a potential marker to evaluate the efficacy of anti-neoplastic therapies or an adjuvant anti-melanoma target.
Clinicopathological relevance of NFκB1/p50 nuclear immunoreactivity and its relationship with the inflammatory environment of uveal melanoma.
- Biology, MedicineExperimental and molecular pathology
- 2019
Triptolide ameliorates fine particulate matter-induced podocytes injury via regulating NF-κB signaling pathway
- Biology, MedicineBMC Molecular and Cell Biology
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Identification of differentially expressed genes and functional annotations associated with metastases of the uveal melanoma
- BiologyJournal of cellular biochemistry
- 2019
It is suggested that SCD5, SPTBN1, FABP5, SQLE, PTPLA, and CDC25B transcription levels were of high prognostic value, which might assist to understand the underlying carcinogenesis or advancement of UVM better.
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