Published on Tuesday, 21 August 2018
Abstract
Neuroblastoma (NB) is the most common neoplasm during infancy. Unfortunately, NB is still a lethal cancer.
Therefore, innovative curative therapies are immediately required.
In this study, we showed the pro-death activity of TPGS in human NB SK-N-SH cancer cells. NB cells were exposed to TPGS (10-80 μM).
We report for the first time that TPGS induces cell death by apoptosis in NB cells via a pro-oxidant-mediated signaling pathway.
Certainly, H2O2 directly oxidizes DJ-1 cysteine106-thiolate into DJ-1 cysteine106-sulfonate; indirectly activates the transcription factors NF-kappaB, P53 and c-JUN; induces up-regulation of mitochondria regulator proteins BAX/PUMA; provokes loss of mitochondrial membrane potential (ΔΨm) and activation of CASPASE-3/AIF, leading to nuclear disintegration, demonstrated by cellular and biochemical techniques such as fluorescence microscopy, flow cytometry and Western blot analysis.
Since TPGS is a U.S. Food and Drug Administration (FDA) -approved pharmaceutical excipient, this molecule might be used in clinical trials for NB treatment.
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