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Low-level internalization of cystatin E/M affects legumain activity and migration of melanoma cells

Wallin, Hanna (author)
Lund University,Lunds universitet,Proteasinhibitorforskning,Forskargrupper vid Lunds universitet,Protease Inhibitor Research,Lund University Research Groups
Apelqvist, Jenny (author)
Lund University,Lunds universitet,Proteasinhibitorforskning,Forskargrupper vid Lunds universitet,Protease Inhibitor Research,Lund University Research Groups
Andersson, Freddi (author)
Lund University,Lunds universitet,Proteasinhibitorforskning,Forskargrupper vid Lunds universitet,Protease Inhibitor Research,Lund University Research Groups
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Ekström, Ulf (author)
Lund University,Lunds universitet,Proteasinhibitorforskning,Forskargrupper vid Lunds universitet,Protease Inhibitor Research,Lund University Research Groups
Abrahamson, Magnus (author)
Lund University,Lunds universitet,Proteasinhibitorforskning,Forskargrupper vid Lunds universitet,Protease Inhibitor Research,Lund University Research Groups
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 (creator_code:org_t)
2017
2017
English 12 s.
In: Journal of Biological Chemistry. - 0021-9258. ; 292:35, s. 14413-14424
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The ratio between proteases and their inhibitors is unbalanced in cancer. The cysteine protease inhibitor cystatin C is internalized by some cancer cells, which affects cellular properties. Here we aimed to investigate if uptake of cystatin C and the related inhibitor cystatin E/M occur in melanoma cell lines and to evaluate to what extent the uptake affects the legumain activity that is typically increased in melanoma. First we studied the basic expression, secretion, and intracellular content of all type 2 cystatins as well as expression and activity of their possible target enzymes legumain and cathepsin B in MDA-MB-435S, A375, and C8161 melanoma cells. Legumain activity was mea-sureable in all cell lines, and of the potential legumain inhibitors, cystatin C, E/M, and F, cystatin C was the one mainly produced. All cells internalized cystatin C added to culture media, leading to increased intracellular cystatin C levels by 120 –200%. Cystatin E/M was internalized as well but at a modest rate. The effects on intracellular legumain activity were nevertheless pronounced, probably because the cells lacked this inhibitor, and its affinity for legumain is 100-fold higher than that of cystatin C. Likewise, the low-degree uptake resulted in reduced migration and invasion of A375 cells in Matrigel to an extent comparable with the W106F variant of cystatin C with optimal uptake properties and resulting in much higher intracellular levels. Thus, cystatin E/M appears to be a good candidate to efficiently down-regulate the increased legumain activity, possibly important for the malignant phenotype of melanoma cells.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

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Wallin, Hanna
Apelqvist, Jenny
Andersson, Fredd ...
Ekström, Ulf
Abrahamson, Magn ...
About the subject
MEDICAL AND HEALTH SCIENCES
MEDICAL AND HEAL ...
and Basic Medicine
and Cell and Molecul ...
MEDICAL AND HEALTH SCIENCES
MEDICAL AND HEAL ...
and Clinical Medicin ...
and Cancer and Oncol ...
Articles in the publication
Journal of Biolo ...
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Lund University

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