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Kallikrein-related peptidase 7 overexpression in melanoma cells modulates cell adhesion leading to a malignant phenotype

Haddada, Meriem (author)
Draoui, Hend (author)
Deschamps, Lydia (author)
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Walker, Francine (author)
Delaunay, Tiphaine (author)
Brattsand, Maria (author)
Umeå universitet,Patologi
Magdolen, Viktor (author)
Darmoul, Dalila (author)
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 (creator_code:org_t)
2018-03-02
2018
English.
In: Biological chemistry (Print). - : Walter de Gruyter. - 1431-6730 .- 1437-4315. ; 399:9, s. 1099-1105
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • We recently reported that human melanoma cells, but not benign melanocytes, aberrantly express kallikrein-related peptidase 7 (KLK7). Here, we show a KLK7 overexpression-mediated decrease of cell adhesion to extracellular matrix binding proteins, associated with downregulation of alpha 5/beta 1/alpha v/beta 3 integrin expression. We also report an up-regulation of MCAM/CD146 and an increase in spheroid formation of these cells. Our results demonstrate that aberrant KLK7 expression leads to a switch to a more malignant phenotype suggesting a potential role of KLK7 in melanoma invasion. Thus, KLK7 may represent a biomarker for melanoma progression and may be a potential therapeutic target for melanoma.

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)

Keyword

E-cadherin
integrins
kallikrein-related peptidase 7
MCAM/CD146
melanoma
spheroid

Publication and Content Type

ref (subject category)
art (subject category)

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