Search Results - "Cooke, Vesselina G"
-
1
Origin and function of myofibroblasts in kidney fibrosis
Published in Nature medicine (01-08-2013)“…Myofibroblasts are associated with organ fibrosis, but their origin and functional role remain unknown. Using multiple genetically engineered mice, the authors…”
Get full text
Journal Article -
2
Pericyte Depletion Results in Hypoxia-Associated Epithelial-to-Mesenchymal Transition and Metastasis Mediated by Met Signaling Pathway
Published in Cancer cell (17-01-2012)“…The functional role of pericytes in cancer progression remains unknown. Clinical studies suggest that low numbers of vessel-associated pericytes correlated…”
Get full text
Journal Article -
3
Targeting Vascular Pericytes in Hypoxic Tumors Increases Lung Metastasis via Angiopoietin-2
Published in Cell reports (Cambridge) (24-02-2015)“…Strategies to target angiogenesis include inhibition of the vessel-stabilizing properties of vascular pericytes. Pericyte depletion in early-stage non-hypoxic…”
Get full text
Journal Article -
4
Studying clonal dynamics in response to cancer therapy using high-complexity barcoding
Published in Nature medicine (01-05-2015)“…The authors have developed a barcoded library that enables the high-throughput tracking of tumor cell dynamics and clonal evolution in response to therapy…”
Get full text
Journal Article -
5
An F876L mutation in androgen receptor confers genetic and phenotypic resistance to MDV3100 (enzalutamide)
Published in Cancer discovery (01-09-2013)“…Castration-resistant prostate cancer (CRPC) is the most aggressive, incurable form of prostate cancer. MDV3100 (enzalutamide), an antagonist of the androgen…”
Get more information
Journal Article -
6
VEGF-A and Tenascin-C produced by S100A4+ stromal cells are important for metastatic colonization
Published in Proceedings of the National Academy of Sciences - PNAS (20-09-2011)“…Increased numbers of S100A4+ cells are associated with poor prognosis in patients who have cancer. Although the metastatic capabilities of S100A4+ cancer cells…”
Get full text
Journal Article -
7
Global chromatin profiling reveals NSD2 mutations in pediatric acute lymphoblastic leukemia
Published in Nature genetics (01-11-2013)“…Frank Stegmeier, Levi Garraway and colleagues apply a targeted mass spectrometry approach that measures level of histone modifications and identify a recurrent…”
Get full text
Journal Article -
8
Antitumor Properties of RAF709, a Highly Selective and Potent Inhibitor of RAF Kinase Dimers, in Tumors Driven by Mutant RAS or BRAF
Published in Cancer research (Chicago, Ill.) (15-03-2018)“…Resistance to the RAF inhibitor vemurafenib arises commonly in melanomas driven by the activated BRAF oncogene. Here, we report antitumor properties of RAF709,…”
Get full text
Journal Article -
9
Inhibition of Wild-Type p53-Expressing AML by the Novel Small Molecule HDM2 Inhibitor CGM097
Published in Molecular cancer therapeutics (01-10-2015)“…The tumor suppressor p53 is a key regulator of apoptosis and functions upstream in the apoptotic cascade by both indirectly and directly regulating Bcl-2…”
Get full text
Journal Article -
10
Design and Discovery of N‑(2-Methyl-5′-morpholino-6′-((tetrahydro‑2H‑pyran-4-yl)oxy)-[3,3′-bipyridin]-5-yl)-3-(trifluoromethyl)benzamide (RAF709): A Potent, Selective, and Efficacious RAF Inhibitor Targeting RAS Mutant Cancers
Published in Journal of medicinal chemistry (22-06-2017)“…RAS oncogenes have been implicated in >30% of human cancers, all representing high unmet medical need. The exquisite dependency on CRAF kinase in KRAS mutant…”
Get full text
Journal Article -
11
Fibroblast Growth Factor-2 Failed to Induce Angiogenesis in Junctional Adhesion Molecule-A–Deficient Mice
Published in Arteriosclerosis, thrombosis, and vascular biology (01-09-2006)“…OBJECTIVE—We have previously shown that JAM-A regulates fibroblast growth factor-2 (FGF-2)–induced endothelial cell morphology, proliferation, and migration…”
Get full text
Journal Article -
12
Identification of amino acids essential for the antiangiogenic activity of tumstatin and its use in combination antitumor activity
Published in Proceedings of the National Academy of Sciences - PNAS (30-09-2008)“…Tumstatin is an angiogenesis inhibitor that binds to αvβ3 integrin and suppresses tumor growth. Previous deletion mutagenesis studies identified a 25-aa…”
Get full text
Journal Article -
13
Pharmacological and genomic profiling identifies NF-κB–targeted treatment strategies for mantle cell lymphoma
Published in Nature medicine (01-01-2014)“…A screen for compounds that may inhibit the growth of hematological malignancies reveals the specific dependence of some mantle cell lymphoma (MCL) cell lines…”
Get full text
Journal Article -
14
LXH254, a Potent and Selective ARAF-Sparing Inhibitor of BRAF and CRAF for the Treatment of MAPK-Driven Tumors
Published in Clinical cancer research (01-04-2021)“…Targeting RAF for antitumor therapy in RAS-mutant tumors holds promise. Herein, we describe in detail novel properties of the type II RAF inhibitor, LXH254…”
Get full text
Journal Article -
15
Discovery of Darovasertib (NVP-LXS196), a Pan-PKC Inhibitor for the Treatment of Metastatic Uveal Melanoma
Published in Journal of medicinal chemistry (25-01-2024)“…Uveal melanoma (UM) is the most common primary intraocular malignancy in the adult eye. Despite the aggressive local management of primary UM, the development…”
Get full text
Journal Article -
16
Deletion of JAM-A causes morphological defects in the corneal epithelium
Published in The international journal of biochemistry & cell biology (2007)“…Junctional adhesion molecule-A (JAM-A, JAM-1, F11R) is an Ig domain containing transmembrane protein that has been proposed to function in diverse processes…”
Get full text
Journal Article -
17
Design and Discovery of N‑(3-(2-(2-Hydroxyethoxy)-6-morpholinopyridin-4-yl)-4-methylphenyl)-2-(trifluoromethyl)isonicotinamide, a Selective, Efficacious, and Well-Tolerated RAF Inhibitor Targeting RAS Mutant Cancers: The Path to the Clinic
Published in Journal of medicinal chemistry (12-03-2020)“…Direct pharmacological inhibition of RAS has remained elusive, and efforts to target CRAF have been challenging due to the complex nature of RAF signaling,…”
Get full text
Journal Article -
18
The Public Repository of Xenografts Enables Discovery and Randomized Phase II-like Trials in Mice
Published in Cancer cell (11-07-2016)Get full text
Journal Article -
19
Inhibiting Tankyrases Sensitizes KRAS-Mutant Cancer Cells to MEK Inhibitors via FGFR2 Feedback Signaling
Published in Cancer research (Chicago, Ill.) (15-06-2014)“…Tankyrases (TNKS) play roles in Wnt signaling, telomere homeostasis, and mitosis, offering attractive targets for anticancer treatment. Using unbiased…”
Get full text
Journal Article -
20
JAM-A is present in mammalian spermatozoa where it is essential for normal motility
Published in Developmental biology (01-01-2008)“…Junctional adhesion molecules (JAMs) that are expressed in endothelial and epithelial cells and function in tight junction assembly, also perform important…”
Get full text
Journal Article