| Literature DB >> 31558023 |
Jin-Xuan Fan1, Rong-Hui Deng2, He Wang1, Xin-Hua Liu1, Xia-Nan Wang1, Ran Qin1, Xin Jin3, Tian-Run Lei2, Diwei Zheng1, Pang-Hu Zhou2, Yunxia Sun1, Xian-Zheng Zhang1.
Abstract
Pyroptosis is a lytic and inflammatory form of programmed cell death and could be induced by chemotherapy drugs via caspase-3 mediation. However, the key protein gasdermin E (GSDME, translated by the DFNA5 gene) during the caspase-3-mediated pyroptosis process is absent in most tumor cells because of the hypermethylation of DFNA5 (deafness autosomal dominant 5) gene. Here, we develop a strategy of combining decitabine (DAC) with chemotherapy nanodrugs to trigger pyroptosis of tumor cells by epigenetics, further enhancing the immunological effect of chemotherapy. DAC is pre-performed with specific tumor-bearing mice for demethylation of the DFNA5 gene in tumor cells. Subsequently, a commonly used tumor-targeting nanoliposome loaded with cisplatin (LipoDDP) is used to administrate drugs for activating the caspase-3 pathway in tumor cells and trigger pyroptosis. Experiments demonstrate that the reversal of GSDME silencing in tumor cells is achieved and facilitates the occurrence of pyroptosis. According to the anti-tumor activities, anti-metastasis results, and inhibition of recurrence, this pyroptosis-based chemotherapy strategy enhances immunological effects of chemotherapy and also provides an important insight into tumor immunotherapy.Entities:
Keywords: Tumor therapy; chemotherapy; demethylation; liposome; pyroptosis
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Year: 2019 PMID: 31558023 DOI: 10.1021/acs.nanolett.9b03245
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189