Zobrazeno 1 - 10
of 15
pro vyhledávání: '"G C, Tucker"'
Autor:
Stéphane Léonce, V. Perez, Nicolas Guilbaud, Alain Pierré, A A Cordi, A D Morris, G C Tucker, Ghanem Atassi, M. Jan
Publikováno v:
Anti-Cancer Drugs. 8:746-755
The polyanionic species suramin is a potential anti-cancer agent of narrow therapeutic index. Among other pharmacological characteristics, suramin is an inhibitor of angiogenesis. We have targeted its angiostatic properties as part of a program to di
Publikováno v:
Medicinal chemistry (Shariqah (United Arab Emirates)). 5(3)
Among the newer and promising weapons against cancer are Farnesyl Transferase Inhibitors (FTI). Indeed it is known that the enzyme Farnesyl Transferase (FT), catalyses the prenylation of cysteine residues of several proteins associated with cancer pr
Publikováno v:
Angiogenesis. 3(3)
The microenvironment of the majority of solid tumours in which new vessels must grow and survive is acidic. Whilst recent reports suggest a role of the low tumour pH in the invasive and metastatic potential of tumour cells, little is known as to its
Publikováno v:
Angiogenesis. 5(3)
Matrix metalloproteinases (MMPs) constitute a large family of extracellular matrix degrading proteases implicated in a number of physiological and pathological processes, including angiogenesis. However, the relative importance of the individual MMPs
Autor:
G C, Tucker
Publikováno v:
Therapie. 56(5)
The multiplicity of experimental models of angiogenesis in vitro and in vivo complicates the choice of a straightforward strategy to accurately identify the anti-angiogenic potential of a natural or synthetic compound with antitumoral activity. In th
Autor:
J M, Henlin, J A, Boutin, N, Kucharczyk, C, Desmet-Beaufort, A, Loynel, M, Bertrand, A, Genton, G C, Tucker, G, Atassi, J L, Fauchére
Publikováno v:
The journal of peptide research : official journal of the American Peptide Society. 57(2)
A complete 331,776-member library of tetrapeptides made of 24 amino acid building blocks was synthesized robotically on solid phase and subjected to a deconvolution based on the inhibitory potency of the sublibraries in a HPLC assay of the S-farnesyl
Autor:
David Ricol, Jean Paul Thiery, El Marjou A, G C Tucker, Ferry G, Yoshida T, François Radvanyi, Marie-France Poupon, Dominique K. Chopin, Girault Jm, Gil-Diez-de-Medina S, David Cappellen
Publikováno v:
Oncogene. 18(51)
FGFRs (fibroblast growth factor receptors) are encoded by four genes (FGFR1 – 4). Alternative splicing results in various receptor isoforms. The FGFR2-IIIb variant is present in a wide variety of epithelia, including the bladder epithelium. Recentl
Publikováno v:
International journal of cancer. 68(5)
In situ changes in the repertoire of integrins and proteolytic enzymes have been demonstrated during melanoma metastasis. To investigate whether established human melanoma cell lines, injected into nude mice, could undergo phenotypic changes similar
Publikováno v:
Symposia of the Society for Experimental Biology. 47
Since one crucial step in tumor progression consists of the acquisition of invasive and metastatic properties, it is important to analyze the mechanisms used by cancer cells to disperse. Among the possible mechanisms of cell dispersion, cell motility
Publikováno v:
Cancer cells (Cold Spring Harbor, N.Y. : 1989). 3(12)
Tumor metastasis is associated with an increase in the plasticity of malignant cells, a phenomenon that is characterized by changes in cell morphology and a decrease in intercellular cohesiveness. The plasticity of cells is correlated with their moti