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Integrin α10, a novel therapeutic target in glioblastoma, regulates cell migration, proliferation, and survival

Thorén, Matilda Munksgaard (author)
Xintela AB, SE-22381 Lund, Sweden
Masoumi, Katarzyna Chmielarska (author)
Xintela AB, SE-22381 Lund, Sweden
Krona, Cecilia, 1976- (author)
Uppsala universitet,Uppsala University,Neuroonkologi,Science for Life Laboratory, SciLifeLab
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Huang, Xiaoli (author)
Xintela AB, SE-22381 Lund, Sweden
Kundu, Soumi (author)
Uppsala universitet,Uppsala University,Science for Life Laboratory, SciLifeLab,Neuroonkologi
Schmidt, Linnéa (author)
Xintela AB, SE-22381 Lund, Sweden
Forsberg Nilsson, Karin, 1963- (author)
Uppsala universitet,Uppsala University,Science for Life Laboratory, SciLifeLab,Neuroonkologi
Keep, Marcus Floyd (author)
University of North Dakota,Sanford Brain & Spine Inst, Dept Neurosurg, Fargo, ND 58102 USA;Univ North Dakota, Sch Med, Dept Surg, Fargo, ND 58102 USA
Englund, Elisabet (author)
Lund University,Lunds universitet,Tumörmikromiljö,Sektion I,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Tumor microenvironment,Section I,Department of Clinical Sciences, Lund,Faculty of Medicine,Lund Univ, Dept Clin Sci, Div Oncol & Pathol, Neuropathol Lab, SE-22184 Lund, Sweden
Nelander, Sven (author)
Uppsala universitet,Uppsala University,Science for Life Laboratory, SciLifeLab,Neuroonkologi
Holmqvist, Bo (author)
ImaGene iT AB, SE-22381 Lund, Sweden
Lundgren-Åkerlund, Evy (author)
Xintela AB, SE-22381 Lund, Sweden
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 (creator_code:org_t)
2019-04-25
2019
English.
In: Cancers. - : MDPI AG. - 2072-6694. ; 11:4
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • New, effective treatment strategies for glioblastomas (GBMs), the most malignant and invasive brain tumors in adults, are highly needed. In this study, we investigated the potential of integrin α10Β1 as a therapeutic target in GBMs. Expression levels and the role of integrin α10Β1 were studied in patient-derived GBM tissues and cell lines. The effect of an antibody-drug conjugate (ADC), an integrin a10 antibody conjugated to saporin, on GBM cells and in a xenograft mouse model was studied. We found that integrin α10Β1 was strongly expressed in both GBM tissues and cells, whereas morphologically unaffected brain tissues showed only minor expression. Partial or no overlap was seen with integrins α3, α6, and α7, known to be expressed in GBM. Further analysis of a subpopulation of GBM cells selected for high integrin α10 expression demonstrated increased proliferation and sphere formation. Additionally, siRNA-mediated knockdown of integrin α10 in GBM cells led to decreased migration and increased cell death. Furthermore, the ADC reduced viability and sphere formation of GBM cells and induced cell death both in vitro and in vivo. Our results demonstrate that integrin α10Β1 has a functional role in GBM cells and is a novel, potential therapeutic target for the treatment of GBM.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)
NATURVETENSKAP  -- Biologi -- Cellbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Cell Biology (hsv//eng)

Keyword

Antibody-drug conjugate (ADC)
Glioblastoma (GBM)
Glioma
Integrin α10
Saporin
glioblastoma (GBM)

Publication and Content Type

art (subject category)
ref (subject category)

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