Evidence map›Paper›PMID 42665396›Full record

ArticleIn vivo (Athens, Greece)

Anti-gicerin Antibody Suppresses Early Pulmonary Metastatic Colonization of B16F10 Melanoma Cells.

Naoki Kirimura, Saaya Ueno, Ryusuke Yamazaki, Yasuhiro Tsukamoto

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Article in In vivo (Athens, Greece). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Naoki KirimuraLaboratory of Animal Hygiene, Department of Agricultural and Life Science, Faculty of Life and Environmental Sciences, Kyoto Prefectural University, Kyoto, Japan.
Saaya UenoLaboratory of Animal Hygiene, Department of Agricultural and Life Science, Faculty of Life and Environmental Sciences, Kyoto Prefectural University, Kyoto, Japan.
Ryusuke YamazakiLaboratory of Animal Hygiene, Department of Agricultural and Life Science, Faculty of Life and Environmental Sciences, Kyoto Prefectural University, Kyoto, Japan.
Yasuhiro TsukamotoLaboratory of Animal Hygiene, Department of Agricultural and Life Science, Faculty of Life and Environmental Sciences, Kyoto Prefectural University, Kyoto, Japan ytsuka@kpu.ac.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimAdhesion of circulating melanoma cells to the pulmonary vascular bed is a critical early step in hematogenous metastasis. Gicerin is an immunoglobulin superfamily cell adhesion molecule that can mediate homophilic cell-cell adhesion. We examined whether gicerin is expressed in B16F10 melanoma cells and pulmonary tissue and whether systemic anti-gicerin antibody suppresses experimental pulmonary colonization. MATERIALS AND

methodsGicerin expression was examined by immunofluorescence staining in cultured B16F10 cells, subcutaneous B16F10 tumors, pulmonary metastatic foci, and normal lung tissue, with matched rabbit pre-immune IgG controls processed in parallel. Histopathological features of subcutaneous and pulmonary lesions were evaluated by hematoxylin and eosin staining. Nude mice received a tail-vein injection of B16F10 cells followed immediately by intravenous administration of matched rabbit pre-immune IgG or rabbit polyclonal anti-gicerin IgG. Cell proliferation, adhesion to human umbilical vein endothelial cells (HUVECs), and wound-healing migration were assessed

resultsGicerin immunoreactivity was detected in cultured B16F10 cells, subcutaneous tumors, pulmonary metastatic foci, and normal pulmonary structures, whereas matched rabbit pre-immune IgG controls showed no specific fluorescence, supporting staining specificity under the assay conditions. Tail-vein injection produced early pulmonary metastatic foci, and anti-gicerin IgG at 10 μg/mouse significantly reduced metastatic colonization compared with pre-immune IgG, whereas the 1 μg/mouse dose did not. Anti-gicerin IgG significantly inhibited B16F10 adhesion to HUVEC monolayers and significantly reduced cell migration without significantly affecting cell proliferation.

conclusionGicerin contributes to early pulmonary colonization of B16F10 melanoma cells by supporting tumor-endothelial adhesion and tumor-cell migration. Gicerin blockade may represent a potential strategy for preventing hematogenous dissemination of melanoma.

Indexed as

AntibodiesLung NeoplasmsMelanoma, ExperimentalAnimalsCell AdhesionCell Line, TumorCell MovementCell ProliferationFemaleHumansHuman Umbilical Vein Endothelial CellsMiceRabbitsAntibodiesantibody therapyB16F10cell adhesiongicerinMelanomapulmonary metastasis

Identifiers

PMID42665396
PMCPMC13531101

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