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  1. Article ; Online: Nephronectin promotes breast cancer brain metastatic colonization via its integrin-binding domains.

    Magnussen, Synnøve Norvoll / Toraskar, Jimita / Wilhelm, Imola / Hasko, Janos / Figenschau, Stine Linn / Molnar, Judit / Seppola, Marit / Steigen, Sonja E / Steigedal, Tonje S / Hadler-Olsen, Elin / Krizbai, Istvan A / Svineng, Gunbjørg

    Scientific reports

    2020  Volume 10, Issue 1, Page(s) 12237

    Abstract: This study demonstrates a role for the extracellular matrix protein nephronectin (NPNT) in promoting experimental breast cancer brain metastasis, possibly through enhanced binding to- and migration through brain endothelial cells. With the introduction ... ...

    Abstract This study demonstrates a role for the extracellular matrix protein nephronectin (NPNT) in promoting experimental breast cancer brain metastasis, possibly through enhanced binding to- and migration through brain endothelial cells. With the introduction of more targeted breast cancer treatments, a prolonged survival has resulted during the last decade. Consequently, an increased number of patients develop metastasis in the brain, a challenging organ to treat. We recently reported that NPNT was highly expressed in primary breast cancer and associated with unfavourable prognosis. The current study addresses our hypothesis that NPNT promotes brain metastases through its integrin-binding motifs. SAGE-sequencing revealed that NPNT was significantly up-regulated in human breast cancer tissue compared to pair-matched normal breast tissue. Human brain metastatic breast cancers expressed both NPNT and its receptor, integrin α8β1. Using an open access repository; BreastMark, we found a correlation between high NPNT mRNA levels and poor prognosis for patients with the luminal B subtype. The 66cl4 mouse cell line was used for expression of wild-type and mutant NPNT, which is unable to bind α8β1. Using an in vivo model of brain metastatic colonization, 66cl4-NPNT cells showed an increased ability to form metastatic lesions compared to cells with mutant NPNT, possibly through reduced endothelial adhesion and transmigration.
    MeSH term(s) Animals ; Brain/metabolism ; Brain/pathology ; Brain Neoplasms/metabolism ; Brain Neoplasms/pathology ; Breast/metabolism ; Breast/pathology ; Breast Neoplasms/metabolism ; Breast Neoplasms/pathology ; Cell Differentiation/physiology ; Endothelial Cells/metabolism ; Endothelial Cells/pathology ; Extracellular Matrix Proteins/metabolism ; Female ; Humans ; Integrins/metabolism ; Mice ; Mice, Inbred BALB C ; Prognosis ; RNA, Messenger/metabolism
    Chemical Substances Extracellular Matrix Proteins ; Integrins ; RNA, Messenger ; integrin alpha8beta1 ; nephronectin
    Language English
    Publishing date 2020-07-22
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-020-69242-1
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Kidney Tertiary Lymphoid Structures in Lupus Nephritis Develop into Large Interconnected Networks and Resemble Lymph Nodes in Gene Signature.

    Dorraji, Seyed Esmaeil / Kanapathippillai, Premasany / Hovd, Aud-Malin Karlsson / Stenersrød, Mikael Ryan / Horvei, Kjersti Daae / Ursvik, Anita / Figenschau, Stine Linn / Thiyagarajan, Dhivya / Fenton, Christopher Graham / Pedersen, Hege Lynum / Fenton, Kristin Andreassen

    The American journal of pathology

    2020  Volume 190, Issue 11, Page(s) 2203–2225

    Abstract: Immune aggregates organized as tertiary lymphoid structures (TLS) are observed within the kidneys of patients with systemic lupus erythematosus and lupus nephritis (LN). Renal TLS was characterized in lupus-prone New Zealand black × New Zealand white F1 ... ...

    Abstract Immune aggregates organized as tertiary lymphoid structures (TLS) are observed within the kidneys of patients with systemic lupus erythematosus and lupus nephritis (LN). Renal TLS was characterized in lupus-prone New Zealand black × New Zealand white F1 mice analyzing cell composition and vessel formation. RNA sequencing was performed on transcriptomes isolated from lymph nodes, macrodissected TLS from kidneys, and total kidneys of mice at different disease stages by using a personal genome machine and RNA sequencing. Formation of TLS was found in anti-double-stranded DNA antibody-positive mice, and the structures were organized as interconnected large networks with distinct T/B cell zones with adjacent dendritic cells, macrophages, plasma cells, high endothelial venules, supporting follicular dendritic cells network, and functional germinal centers. Comparison of gene profiles of whole kidney, renal TLS, and lymph nodes revealed a similar gene signature of TLS and lymph nodes. The up-regulated genes within the kidneys of lupus-prone mice during LN development reflected TLS formation, whereas the down-regulated genes were involved in metabolic processes of the kidney cells. A comparison with human LN gene expression revealed similar up-regulated genes as observed during the development of murine LN and TLS. In conclusion, kidney TLS have a similar cell composition, structure, and gene signature as lymph nodes and therefore may function as a kidney-specific type of lymph node.
    MeSH term(s) Animals ; Dendritic Cells/metabolism ; Dendritic Cells/pathology ; Gene Expression Profiling ; Gene Expression Regulation ; Kidney/metabolism ; Kidney/pathology ; Lupus Nephritis/metabolism ; Lupus Nephritis/pathology ; Lymph Nodes/metabolism ; Lymph Nodes/pathology ; Mice
    Language English
    Publishing date 2020-08-17
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2943-9
    ISSN 1525-2191 ; 0002-9440
    ISSN (online) 1525-2191
    ISSN 0002-9440
    DOI 10.1016/j.ajpath.2020.07.015
    Database MEDical Literature Analysis and Retrieval System OnLINE

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