cancer cell;
integrins;
splice variant;
Stromal cell;
tenascin-C;
EPITHELIAL-MESENCHYMAL TRANSITION;
MESSENGER-RNA EXPRESSION;
SQUAMOUS-CELL CARCINOMA;
HUMAN BREAST-CANCER;
GROWTH-FACTOR-BETA;
SPLICE VARIANTS;
ANNEXIN-II;
PROTEIN DISTRIBUTION;
ENDOTHELIAL-CELLS;
COLORECTAL-CANCER;
D O I:
10.1080/19336918.2015.1008332
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Tenascin-C (TNC) is highly expressed in cancer tissues. Its cellular sources are cancer and stromal cells, including fibroblasts/myofibroblasts, and also vascular cells. TNC expressed in cancer tissues dominantly contains large splice variants. Deposition of the stroma promotes the epithelial-mesenchymal transition, proliferation, and migration of cancer cells. It also facilitates the formation of cancer stroma including desmoplasia and angiogenesis. Integrin receptors that mediate the signals of TNC have also been discussed.
机构:
Polish Acad Sci, Mossakowski Med Res Ctr, Neuromuscular Unit, PL-02106 Warsaw, PolandPolish Acad Sci, Mossakowski Med Res Ctr, Neuromuscular Unit, PL-02106 Warsaw, Poland
机构:
Univ London Imperial Coll Sci Technol & Med, Fac Med, Div Rheumatol, Kennedy Inst, London W6 8LH, EnglandUniv London Imperial Coll Sci Technol & Med, Fac Med, Div Rheumatol, Kennedy Inst, London W6 8LH, England
Udalova, Irina A.
Ruhmann, Michaela
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Univ London Imperial Coll Sci Technol & Med, Fac Med, Div Rheumatol, Kennedy Inst, London W6 8LH, EnglandUniv London Imperial Coll Sci Technol & Med, Fac Med, Div Rheumatol, Kennedy Inst, London W6 8LH, England
Ruhmann, Michaela
Thomson, Scott J. P.
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Univ London Imperial Coll Sci Technol & Med, Fac Med, Div Rheumatol, Kennedy Inst, London W6 8LH, EnglandUniv London Imperial Coll Sci Technol & Med, Fac Med, Div Rheumatol, Kennedy Inst, London W6 8LH, England
Thomson, Scott J. P.
Midwood, Kim S.
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机构:
Univ London Imperial Coll Sci Technol & Med, Fac Med, Div Rheumatol, Kennedy Inst, London W6 8LH, EnglandUniv London Imperial Coll Sci Technol & Med, Fac Med, Div Rheumatol, Kennedy Inst, London W6 8LH, England
机构:
Department of Oral Medicine/Pathology, School of Dentistry, Aristotle University of ThessalonikiDepartment of Oral Medicine/Pathology, School of Dentistry, Aristotle University of Thessaloniki
Epivatianos A.
Iordanidis F.
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机构:
Department of Histopathology, General Hospital Papanikolaou, ThessalonikiDepartment of Oral Medicine/Pathology, School of Dentistry, Aristotle University of Thessaloniki
Iordanidis F.
Andreadis D.
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机构:
Department of Oral Medicine/Pathology, School of Dentistry, Aristotle University of ThessalonikiDepartment of Oral Medicine/Pathology, School of Dentistry, Aristotle University of Thessaloniki
Andreadis D.
Iordanidis S.
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机构:
Department of Oral and Maxillofacial Surgery, School of Dentistry, Aristotle University of Thessaloniki, ThessalonikiDepartment of Oral Medicine/Pathology, School of Dentistry, Aristotle University of Thessaloniki
Iordanidis S.
Poulopoulos A.
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Department of Oral Medicine/Pathology, School of Dentistry, Aristotle University of ThessalonikiDepartment of Oral Medicine/Pathology, School of Dentistry, Aristotle University of Thessaloniki
Poulopoulos A.
Markopoulos A.
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机构:
Department of Oral Medicine/Pathology, School of Dentistry, Aristotle University of ThessalonikiDepartment of Oral Medicine/Pathology, School of Dentistry, Aristotle University of Thessaloniki