Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/68440
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dc.contributor.authorChalermchai Pilapongen_US
dc.contributor.authorThipjutha Phatruengdeten_US
dc.contributor.authorSaowalak Krungchanuchaten_US
dc.date.accessioned2020-04-02T15:27:14Z-
dc.date.available2020-04-02T15:27:14Z-
dc.date.issued2020-03-21en_US
dc.identifier.issn20403372en_US
dc.identifier.issn20403364en_US
dc.identifier.other2-s2.0-85082093030en_US
dc.identifier.other10.1039/c9nr10131den_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85082093030&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/68440-
dc.description.abstract© 2020 The Royal Society of Chemistry. We herein report a new biological consequence from a unique interaction between nanoparticles of ferric-tannic complexes (Fe-TA NPs) and liver cancer cells (HepG2.2.15). The Fe-TA NPs were found to accumulate into the cells via specific cellular uptake mechanisms and thereafter disturbed cellular autophagy and cellular pH homeostasis, which led the cells to undergo autophagic stress and eventual death. According to biophysical analysis, the cells undergoing autophagic stress were found to lose their capability of attachment, migration, and movement. Similarly, KEGG analysis demonstrated the down-regulation of TGF-beta indicating that the autophagic stress is capable of reducing cancer cell invasion. Therefore, the Fe-TA NPs could be considered beneficial as a new pharmaceutical nanoplatform for liver cancer treatment via induction of autophagic stress.en_US
dc.subjectMaterials Scienceen_US
dc.titleAutophagic stress; A new cellular response to nanoparticles. Could it be a new strategy for inhibition of liver cancer cell invasion and metastasis?en_US
dc.typeJournalen_US
article.title.sourcetitleNanoscaleen_US
article.volume12en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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