Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (2/2 displayed)

  • 2016Doxorubicin loaded dual pH- and thermo-responsive magnetic nanocarrier for combined magnetic hyperthermia and targeted controlled drug delivery applicationscitations
  • 2005TIMP-I expression in anaplastic large cell lymphoma is usually restricted to macrophages and only seldom observed in tumour cells7citations

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Chart of shared publication
Maenosono, S.
1 / 3 shared
Dunn, A.
1 / 1 shared
Nguyen, Ttk
1 / 1 shared
Mott, D.
1 / 1 shared
Boyer, C.
1 / 2 shared
Hervault, A.
1 / 2 shared
Poppema, S.
1 / 1 shared
Van Den Berg, Anke
1 / 1 shared
Rust, R.
1 / 1 shared
Blokzijl, T.
1 / 1 shared
Harms, G.
1 / 1 shared
Visser, Lydia
1 / 1 shared
Kamps, Wa
1 / 1 shared
Chart of publication period
2016
2005

Co-Authors (by relevance)

  • Maenosono, S.
  • Dunn, A.
  • Nguyen, Ttk
  • Mott, D.
  • Boyer, C.
  • Hervault, A.
  • Poppema, S.
  • Van Den Berg, Anke
  • Rust, R.
  • Blokzijl, T.
  • Harms, G.
  • Visser, Lydia
  • Kamps, Wa
OrganizationsLocationPeople

article

TIMP-I expression in anaplastic large cell lymphoma is usually restricted to macrophages and only seldom observed in tumour cells

  • Poppema, S.
  • Van Den Berg, Anke
  • Lim, M.
  • Rust, R.
  • Blokzijl, T.
  • Harms, G.
  • Visser, Lydia
  • Kamps, Wa
Abstract

<p>Anaplastic large cell lymphomas (ALCLs) can be subdivided into two subgroups on the basis of their expression of the ALK protein. ALK protein expression leads to activation of signal transducer and activator of transcription (STAT) 3, which is more commonly expressed in ALK-positive than in ALK-negative tumours. Activated STAT3 leads to the induction of several genes such as Mcl-1, Bcl-2 and Bcl-X-L, and tissue inhibitor of metalloproteinase (TIMP)-1. In this study, we analysed TIMP-1 expression in five ALCL cell lines and 11 tumours by quantitative RT-PCR and immunohistochemistry. We identified high-level TIMP-1 expression by RT-PCR in three ALK-positive ALCL-derived cell lines and in all ALK-positive ALCLs, whereas ALK-negative ALCLs generally demonstrated a lower level of TIMP-1 expression. Concordant with these results, we observed TIMP-1 immunostaining in all ALK-positive ALCLs and in only two of six ALK-negative ALCLs. No relationship was observed between the levels of ALK and TIMP-1 expression in the ALK-positive tumours. STAT3 expression levels were similar in all ALCL samples. Double staining with either CD30 or CD68 demonstrated that TIMP-1 expression was restricted to macrophages in the majority of TIMP-1-positive tumours. Expression of the TIMP-1 substrate MMP-2 was more prominent in ALK-negative tumours, while MMP-9 levels were low in all cases. Expression levels of IL-6 and TGF-beta 1, which are cytokines known to induce TIMP-1 were higher in ALK-negative ALCLs and moderate in ALK-positive tumours. No clear relationship was observed between IL-10 expression and ALK positivity. Overall, no correlation was seen in ALCLs between the expression of TIMP-1 and that of cytokines that induce TIMP-1. Lack of TIMP-I expression in the tumour cells of ALK-positive ALCLs argues against a direct role for ALK-induced activation of STAT3 in the regulation of TIMP-1 expression in ALCL. Copyright (c) 2005 Pathological Society of Great Britain and Ireland. Published by John Wiley &amp; Sons, Ltd.</p>

Topics
  • impedance spectroscopy
  • activation