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Oxidant-induced autophagy and ferritin degradation contribute to epithelial-mesenchymal transition through lysosomal iron

Sioutas, Apostolos (author)
Linköpings universitet,Avdelningen för kardiovaskulär medicin,Medicinska fakulteten,Region Östergötland, Lungmedicinska kliniken US
Vainikka, Linda (author)
Linköpings universitet,Avdelningen för cellbiologi,Medicinska fakulteten
Kentson, Magnus (author)
Division of Medicine, Ryhov Hospital, Jönköping, Sweden
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Dam-Larsen, Sören (author)
Division of Medicine, Hospital of Eksjö, Eksjö, Sweden
Wennerström, Urban (author)
Division of Medicine, Hospital of Västervik, Västervik, Sweden
Jacobson, Petra (author)
Linköpings universitet,Institutionen för medicin och hälsa,Medicinska fakulteten,Region Östergötland, Lungmedicinska kliniken US
Persson, Hans Lennart, 1961- (author)
Linköpings universitet,Avdelningen för kardiovaskulär medicin,Medicinska fakulteten,Region Östergötland, Lungmedicinska kliniken US
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 (creator_code:org_t)
Dove Medical Press, 2017
2017
English.
In: Journal of Inflammation Research. - : Dove Medical Press. - 1178-7031. ; 10, s. 29-39
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Transforming growth factor (TGF)-ß1 triggers epithelial-mesenchymal transition (EMT) through autophagy, which is partly driven by reactive oxygen species (ROS). The aim of this study was to determine whether leaking lysosomes and enhanced degradation of H-ferritin could be involved in EMT and whether it could be possible to prevent EMT by iron chelation targeting of the lysosome.

Subject headings

NATURVETENSKAP  -- Biologi -- Immunologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Immunology (hsv//eng)

Keyword

A549 cells; COPD; pulmonary disease; pulmonary fibrosis; transforming growth factor; tumor necrosis factor

Publication and Content Type

ref (subject category)
art (subject category)

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