Search Results - "Smith, Yvonne E"
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Functional and molecular characterisation of EO771.LMB tumours, a new C57BL/6-mouse-derived model of spontaneously metastatic mammary cancer
Published in Disease models & mechanisms (01-03-2015)“…The translation of basic research into improved therapies for breast cancer patients requires relevant preclinical models that incorporate spontaneous…”
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Cleavage of the extracellular domain of junctional adhesion molecule-A is associated with resistance to anti-HER2 therapies in breast cancer settings
Published in Breast cancer research : BCR (20-11-2018)“…Junctional adhesion molecule-A (JAM-A) is an adhesion molecule whose overexpression on breast tumor tissue has been associated with aggressive cancer…”
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Antibiotic Tetrocarcin-A Down-regulates JAM-A, IAPs and Induces Apoptosis in Triple-negative Breast Cancer Models
Published in Anticancer research (01-03-2019)“…Triple-negative breast cancers (TNBC) lack expression of three important receptors, and have limited treatment options. High expression of junctional adhesion…”
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Diterpenoid natural compound C4 (Crassin) exerts cytostatic effects on triple-negative breast cancer cells via a pathway involving reactive oxygen species
Published in Cellular oncology (Dordrecht) (01-02-2018)“…Purpose Triple-negative breast cancers (TNBC) lack expression of three common cell surface receptors, i.e., estrogen receptor (ER), progesterone receptor (PR)…”
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Functional Antagonism of Junctional Adhesion Molecule-A (JAM-A), Overexpressed in Breast Ductal Carcinoma In Situ (DCIS), Reduces HER2-Positive Tumor Progression
Published in Cancers (03-03-2022)“…Breast ductal carcinoma in situ (DCIS) is clinically challenging, featuring high diagnosis rates and few targeted therapies. Expression/signaling from…”
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Dynamic interplay between adhesion surfaces in carcinomas:Cell-cell and cell-matrix crosstalk
Published in World journal of biological chemistry (26-02-2016)“…Cell-cell and cell-matrix signaling and communication between adhesion sites involve mechanisms which are required for cellular functions during normal…”
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Abstract P3-06-01: Junctional adhesion molecule-A (JAM-A) as a novel future drug target in ductal carcinoma in situ (DCIS)
Published in Cancer research (Chicago, Ill.) (15-02-2020)“…Background/Aim: Increased expression of the cell-cell adhesion molecule Junctional Adhesion Molecule-A (JAM-A) has been associated with poor prognosis and HER2…”
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The Contribution of Ig-Superfamily and MARVEL D Tight Junction Proteins to Cancer Pathobiology
Published in Current pathobiology reports (01-06-2016)“…The epithelial linings of eukaryotic organs form dynamically-regulated selectively-permeable barriers that control the movement of substances into (and out of)…”
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