TABLE OF CONTENTS |
March 13 2014, Volume 7 / Issue 10 |
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 | Analysis Cover Story Translational Notes Targets and Mechanisms Tools
The Distillery: Therapeutics Cancer Endocrine/metabolic disease Hematology Infectious disease Musculoskeletal disease Neurology Other Pulmonary disease Renal disease
The Distillery: Techniques Assays and screens Disease models Drug delivery Drug platforms Markers
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Analysis |
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Cover Story | Top |
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Killer targets in metastasis Amy Donner doi:10.1038/scibx.2014.274
An international team has found a new pathway in NK cells that leads to the rejection of metastatic tumors. It remains unclear which components of the pathway will make the best targets.
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Translational Notes | Top |
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Repairing reproducibility C. Simone Fishburn doi:10.1038/scibx.2014.275
Although the NIH is taking steps to improve the reproducibility of preclinical data, many researchers are not waiting for guidelines and instead are angling to elevate standards at their own institutions.
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Targets and Mechanisms | Top |
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Zinc-ing about diabetes Kai-Jye Lou doi:10.1038/scibx.2014.276
ZNT8 burst onto the scene in 2007 as a promising diabetes target, and follow-up studies suggested that stimulating the zinc transporter protein could have therapeutic benefit. A new study suggests that the preferred approach might be to inhibit the target.
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Tools | Top |
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Hitchhiker's guide to the lymph node Benjamin Boettner doi:10.1038/scibx.2014.277
An MIT team has provided a recipe for delivering cancer vaccines to lymph nodes by tethering them to albumin. In proof-of-concept studies in mice, lymph node–targeted tumor antigens and adjuvants elicited strong immune responses and reduced tumor growth.
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Distillery: Therapeutics |
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Cancer | Top |
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DNA (cytosine-5-)-methyltransferase 3α (DNMT3A) doi:10.1038/scibx.2014.278
In vitro and mouse studies suggest eliminating DNMT3A-mutant preleukemia cells could help prevent AML.
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Myeloid-lymphoid or mixed-lineage leukemia (MLL; HRX); multiple endocrine neoplasia I (MEN1; menin) doi:10.1038/scibx.2014.279
SAR studies suggest compounds that disrupt the interaction between MLL and menin could be useful for treating some forms of AML and ALL.
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V-rel reticuloendotheliosis viral oncogene homolog A (RELA; p65); chromosome 11 open reading frame 95 (C11orf95) doi:10.1038/scibx.2014.280
Patient sample and cell culture studies suggest targeting a C11orf95-RELA fusion protein could help treat supratentorial ependymomas.
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Casitas B cell lymphoma-b (CBL-B); TYRO3 protein tyrosine kinase (TYRO3; SKY); AXL receptor tyrosine kinase (AXL; UFO); c-Mer proto-oncogene tyrosine kinase (MERTK) doi:10.1038/scibx.2014.281
In vitro and mouse studies suggest TYRO3, AXL and MERTK receptor (TAM receptor) inhibitors could help prevent metastasis by activating NK cells.
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IL-17A doi:10.1038/scibx.2014.282
Mouse studies suggest IL-17A inhibitors could help treat hepatocellular carcinoma (HCC).
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CREB binding protein (CREBBP; CBP); enhancer of zeste homolog 2 (EZH2); histone deacetylase (HDAC) doi:10.1038/scibx.2014.283
In vitro and mouse studies suggest HDAC or EZH2 inhibitors could help treat PTEN (MMAC1; TEP1)-deficient prostate cancers lacking CBP.
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E1A binding protein p300 (EP300; p300); PTEN (MMAC1; TEP1) doi:10.1038/scibx.2014.284
In vitro and mouse studies suggest inhibiting p300 could help treat PTEN-deficient prostate cancers.
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Endocrine/metabolic disease | Top |
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Solute carrier family 30 zinc transporter member 8 (SLC30A8; ZNT8) doi:10.1038/scibx.2014.285
Human genetic studies suggest inhibiting SLC30A8 could help prevent or treat type 2 diabetes.
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Hematology | Top |
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Activin receptor–like kinase 3 (ALK3) doi:10.1038/scibx.2014.286
Mouse studies suggest inhibiting the bone morphogenetic protein type I receptor ALK3 could help treat anemia.
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Infectious disease | Top |
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Quinolone resistance protein (NorA) doi:10.1038/scibx.2014.287
In vitro studies suggest boronic acid derivatives that inhibit the NorA bacterial efflux pump could help prevent antibiotic resistance.
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Musculoskeletal disease | Top |
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Sialic acid binding Ig-like lectin 15 (SIGLEC15) doi:10.1038/scibx.2014.288
Cell-based and mouse studies suggest inhibition of SIGLEC15 could help prevent osteoclast-mediated bone destruction in osteoporosis and other bone-loss disorders.
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Neurology | Top |
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Neurotensin (NTS) doi:10.1038/scibx.2014.289
In vitro and rodent studies suggest a conjugate of NTS and the brain-penetrating peptide Angiopep could help treat pain.
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Other | Top |
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Toll-like receptor 9 (TLR9) doi:10.1038/scibx.2014.290
In vitro, mouse and primate studies suggest a CpG DNA nanoparticle wrapped in the polysaccharide schizophyllan could be used as a vaccine adjuvant that activates B cells and plasmacytoid dendritic cells (pDCs).
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Pulmonary disease | Top |
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Thrombospondin-1 (TSP-1; THBS1) doi:10.1038/scibx.2014.291
In vitro and mouse studies suggest TSP-1 could help stimulate alveolar lung repair after injury.
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Renal disease | Top |
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Adenosine A3 receptor (ADORA3) doi:10.1038/scibx.2014.292
In vitro and cell-based studies identified an ADORA3 partial agonist that could help treat kidney disease caused by renal fibrosis.
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Distillery: Techniques |
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Assays and screens | Top |
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Measurement of β-amyloid (Aβ) oligomers in cerebrospinal fluid (CSF) to diagnose and monitor the progression of Alzheimer's disease (AD) doi:10.1038/scibx.2014.293
An assay that measures Aβ oligomers levels in CSF could help diagnose AD and monitor disease progression in patients.
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Protein M, an IgG-binding protein with a new mode of antibody interaction doi:10.1038/scibx.2014.294
In vitro studies suggest Protein M, a broadly reactive, antibody-binding protein, could complement Proteins A and G as a reagent for large-scale antibody purification.
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Disease models | Top |
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Long-term, Plasmodium cynomolgi–infected primary hepatocyte culture to screen for malaria therapeutics doi:10.1038/scibx.2014.295
Long-term, P. cynomolgi–infected primary hepatocyte cultures could be used to identify therapeutics that prevent malaria relapse.
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Transcription activator–like effector nuclease (TALEN)-mediated genome editing to generate genetically modified monkeys doi:10.1038/scibx.2014.296
Primate studies suggest TALENs could be used to generate genetically modified monkeys to model disease.
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Transgenic mouse models of Netherton syndrome expressing human kallikrein-related peptidase 5 (KLK5) doi:10.1038/scibx.2014.297
Transgenic mice expressing human KLK5 in the epidermis could be used to study the biology of Netherton syndrome and screen for drugs to treat the indication.
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Drug delivery | Top |
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Drug-loaded, neutrophil-targeting nanoparticles to prevent inflammation-induced tissue damage doi:10.1038/scibx.2014.298
Neutrophil-targeting nanoparticles could help prevent tissue damage involving vascular inflammation.
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Drug platforms | Top |
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Gene catalog for differentiating human pluripotent stem cells (hPSCs) into mature, insulin-producing pancreatic β cells doi:10.1038/scibx.2014.299
In vitro and computational studies identified genes that could help develop strategies for β cell production from hPSCs.
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Lymph node–targeting cancer vaccines doi:10.1038/scibx.2014.300
Mouse studies suggest albumin-binding DNA and peptide vaccines could help stimulate antitumor immunity in lymph nodes to help treat cancer.
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Markers | Top |
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Injectable, synthetic markers for paper-based detection of disease in urine samples doi:10.1038/scibx.2014.301
Mouse studies suggest nanoparticles coated with protease-sensitive peptides that release biomarkers into urine can be used with paper-based assays to diagnose colorectal cancer and thrombosis.
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