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Philippe Clézardin

Researcher at University of Lyon

Publications -  227
Citations -  11739

Philippe Clézardin is an academic researcher from University of Lyon. The author has contributed to research in topics: Bone metastasis & Cancer. The author has an hindex of 61, co-authored 221 publications receiving 10852 citations. Previous affiliations of Philippe Clézardin include Harvard University & University of Bern.

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Journal Article

Bisphosphonates inhibit breast and prostate carcinoma cell invasion, an early event in the formation of bone metastases.

TL;DR: Evidence that BP pretreatment of breast and prostate carcinoma cells inhibited tumor cell invasion in a dose-dependent manner is provided and BPs may be useful agents for the prophylactic treatment of patients with cancers that are known to preferentially metastasize to bone is suggested.
Journal Article

Bisphosphonates inhibit angiogenesis in vitro and testosterone-stimulated vascular regrowth in the ventral prostate in castrated rats.

TL;DR: BPs have in vivo antiangiogenic properties, which could be of relevance to improve therapy and prevention of bone metastasis, and extend the potential clinical use of BPs to patients with early prostate cancer.
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Platelet-derived lysophosphatidic acid supports the progression of osteolytic bone metastases in breast cancer

TL;DR: The data suggest that, at the bone metastatic site, tumor cells stimulate the production of LPA from activated platelets, which enhances both tumor growth and cytokine-mediated bone destruction.
Journal Article

Bisphosphonates inhibit prostate and breast carcinoma cell adhesion to unmineralized and mineralized bone extracellular matrices

TL;DR: Evidence is provided for a direct cellular effect of BP in preventing tumor cell adhesion to bone, suggesting that BPs may be useful agents for the prophylactic treatment of patients with cancer that is known to preferentially metastasize to bone.
Journal Article

SiRNA-mediated Inhibition of Vascular Endothelial Growth Factor Severely Limits Tumor Resistance to Antiangiogenic Thrombospondin-1 and Slows Tumor Vascularization and Growth

TL;DR: Systemic in vivo administration of crude anti-VEGF siRNA reduced the growth of unaltered fibrosarcoma tumor cells, and was synergistic with the inhibitory effects derived from TSP1 secretion by the tumor cells themselves.