Cited by 3Angiogenesis and VEGF in CancerMyasthenia Gravis and ThymomaVascular Tumors and Angiosarcomas

Neoplastic transformation and angiogenesis in the thymus of transgenic mice expressing SV40 T and t antigen under an l‐pyruvate kinase promoter (SV12 mice)

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Nabarra, Bernadette, Pontoux, Christiane, Godard, Cecile, Osborne‐Pellegrin, Mary, Ezine, Sophie·2005·International Journal of Experimental Pathology

Abstract

Summary: Using several techniques, we have assessed morphological characteristics of a malignant thymic tumour in SV12 transgenic (Tg) mice expressing SV40 T and t antigens under control of an L‐PK promoter. We describe the development of a carcinoma originating from thymic hyperplasia and followed by the formation of a benign tumour composed chiefly of medullary epithelial cells expressing the transgene and of lymphocytes, a pathology very rarely reported in mice. Our study of the SV12 Tg mice represents the first description of a model of a pure malignant thymic tumour associated with extensive angiogenesis maintained in numerous descendants. The formation of a large tumoral neovascular network, observed here, has never been described in human and/or experimental thymic tumours. Tumoral transformation and angiogenesis are demonstrated by immunolabelling with antibodies against various cytokeratins (CKs) of different molecular weights, vascular endothelial cell markers and VEGF/receptor‐2 (Flk‐1) present on the neovascular endothelial cells. Different points raised by the originality of this model are discussed. These include the medullary nature of the cells expressing the SV40 transgene and their relationship with the tumoral development. The subset of different molecular weight CK components and their modifications are also considered, as well as the presence of type IV epithelial cells, progenitors of medullary epithelial cells. Finally, the cell signals involved in angiogenesis and the possible action of an angiogenic factor, probably secreted by the tumoral cells themselves, are discussed.

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Crossref · 10.1111/j.0959-9673.2005.00451.x

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  • The bladder cancer cell line T24 was established in 1972 and has contributed to several cell line cross-contamination.

    “The bladder cancer cell line T24 was established in 1972 and has contributed to several cell line cross-contamination [20, 21].”

    From Investigation of Cross-Contamination and Misidentification of 278 Widely Used Tumor Cell Lines (2017) · cites this paper as [21]

    The Abstract and Materials and methods describe SV12 transgenic mice and thymic tumours, not the T24 bladder cancer cell line. Searches for T24, its establishment in 1972, and cell-line cross-contamination found no passage addressing either part of the claim. (LLM, conf=0.75)

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Authors
Nabarra, B., Pontoux, C., Godard, C., Osborne‐Pellegrin, M., & Ezine, S.
Affiliations
Inserm (FR)
Corresponding author
Nabarra, Bernadette
Venue
International Journal of Experimental Pathology
Publisher
Wiley
Published
2005-11-24
Volume
86
Issue
6
Pages
397-413
ISSN
  • 0959-9673 (ISSN-L)
  • 1365-2613
OpenAlex
W1823981504
Cited by
3
References
0
Citations by year
2017: 1 · 2014: 1
FWCI
0.00
Type
journal article
Language
en
Open access
Locations
  • International Journal of Experimental Pathology (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Angiogenesis and VEGF in Cancer
  • Health Sciences › Medicine › Neurology › Myasthenia Gravis and Thymoma
  • Health Sciences › Medicine › Oncology › Vascular Tumors and Angiosarcomas
Keywords
thymic carcinoma, SV40 T antigen, transgenic mice, tumor angiogenesis, thymic hyperplasia, cytokeratin, tumor models
MeSH terms
Animals, Antigens, Polyomavirus Transforming, Antigens, Viral, Tumor, Cell Transformation, Neoplastic, Female, Immunohistochemistry, Male, Mice, Inbred CBA, Mice, Transgenic, Neovascularization, Pathologic, Promoter Regions, Genetic, Pyruvate Kinase, Thymus Gland, Thymus Neoplasms, Biomarkers, Tumor, Microscopy, Immunoelectron, Mice

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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

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