44 research outputs found
MRP3: a molecular target for human glioblastoma multiforme immunotherapy.
<p>Abstract</p> <p>Background</p> <p>Glioblastoma multiforme (GBM) is refractory to conventional therapies. To overcome the problem of heterogeneity, more brain tumor markers are required for prognosis and targeted therapy. We have identified and validated a promising molecular therapeutic target that is expressed by GBM: human multidrug-resistance protein 3 (MRP3).</p> <p>Methods</p> <p>We investigated MRP3 by genetic and immunohistochemical (IHC) analysis of human gliomas to determine the incidence, distribution, and localization of MRP3 antigens in GBM and their potential correlation with survival. To determine MRP3 mRNA transcript and protein expression levels, we performed quantitative RT-PCR, raising MRP3-specific antibodies, and IHC analysis with biopsies of newly diagnosed GBM patients. We used univariate and multivariate analyses to assess the correlation of RNA expression and IHC of MRP3 with patient survival, with and without adjustment for age, extent of resection, and KPS.</p> <p>Results</p> <p>Real-time PCR results from 67 GBM biopsies indicated that 59/67 (88%) samples highly expressed <it>MRP3 </it>mRNA transcripts, in contrast with minimal expression in normal brain samples. Rabbit polyvalent and murine monoclonal antibodies generated against an extracellular span of MRP3 protein demonstrated reactivity with defined <it>MRP3</it>-expressing cell lines and GBM patient biopsies by Western blotting and FACS analyses, the latter establishing cell surface MRP3 protein expression. IHC evaluation of 46 GBM biopsy samples with anti-MRP3 IgG revealed MRP3 in a primarily membranous and cytoplasmic pattern in 42 (91%) of the 46 samples. Relative RNA expression was a strong predictor of survival for newly diagnosed GBM patients. Hazard of death for GBM patients with high levels of <it>MRP3 </it>RNA expression was 2.71 (95% CI: 1.54-4.80) times that of patients with low/moderate levels (p = 0.002).</p> <p>Conclusions</p> <p>Human GBMs overexpress MRP3 at both mRNA and protein levels, and elevated MRP3 mRNA levels in GBM biopsy samples correlated with a higher risk of death. These data suggest that the tumor-associated antigen MRP3 has potential use for prognosis and as a target for malignant glioma immunotherapy.</p
A GATA4-regulated tumor suppressor network represses formation of malignant human astrocytomas
GATA4 loss as a result of promoter hypermethylation or somatic mutation promotes growth and chemotherapy resistance of human astrocytomas
Metabolomics and Natural-Products Strategies to Study Chemical Ecology in Nematodes
Synopsis This review provides an overview of two complementary approaches to identify biologically active compounds for studies in chemical ecology. The first is activity-guided fractionation and the second is metabolomics, particularly focusing on a new liquid chromatography-mass spectrometry-based method called isotopic ratio outlier analysis. To illustrate examples using these approaches, we review recent experiments using Caenorhabditis elegans and related freeliving nematodes
An Overview of Methods using 13C for Improved Compound Identification in Metabolomics and Natural Products
Compound identification is a major bottleneck in metabolomics studies. In nuclear magnetic resonance (NMR) investigations, resonance overlap often hinders unambiguous database matching or de novo compound identification. In liquid chromatography-mass spectrometry (LC-MS), discriminating between biological signals and background artifacts and reliable determination of molecular formulae are not always straightforward. We have designed and implemented several NMR and LC-MS approaches that utilize 13C, either enriched or at natural abundance, in metabolomics applications. For LC-MS applications, we describe a technique called isotopic ratio outlier analysis (IROA), which utilizes samples that are isotopically labeled with 5% (test) and 95% (control) 13C. This labeling strategy leads to characteristic isotopic patterns that allow the differentiation of biological signals from artifacts and yield the exact number of carbons, significantly reducing possible molecular formulae. The relative abundance between the test and control samples for every IROA feature can be determined simply by integrating the peaks that arise from the 5% and 95% channels. For NMR applications, we describe two 13C-based approaches. For samples at natural abundance, we have developed a workflow to obtain 13C-13C and 13C-1H statistical correlations using 1D 13C and 1H NMR spectra. For samples that can be isotopically labeled, we describe another NMR approach to obtain direct 13C-13C spectroscopic correlations. These methods both provide extensive information about the carbon framework of compounds in the mixture for either database matching or de novo compound identification. We also discuss strategies in which 13C NMR can be used to identify unknown compounds from IROA experiments. By combining technologies with the same samples, we can identify important biomarkers and corresponding metabolites of interest
Triflic Acid Treatment Enables LC-MS/MS Analysis of Insoluble Bacterial Biomass
The
lysis and extraction of soluble bacterial proteins from cells is a
common practice for proteomics analyses, but insoluble bacterial biomasses
are often left behind. Here, we show that with triflic acid treatment,
the insoluble bacterial biomass of Gram<sup>–</sup> and Gram<sup>+</sup> bacteria can be rendered soluble. We use LC-MS/MS shotgun
proteomics to show that bacterial proteins in the soluble and insoluble
postlysis fractions differ significantly. Additionally, in the case
of Gram<sup>–</sup> Pseudomonas aeruginosa, triflic acid treatment enables the enrichment of cell-envelope-associated
proteins. Finally, we apply triflic acid to a human microbiome sample
to show that this treatment is robust and enables the identification
of a new, complementary subset of proteins from a complex microbial
mixture
Triflic Acid Treatment Enables LC-MS/MS Analysis of Insoluble Bacterial Biomass
The
lysis and extraction of soluble bacterial proteins from cells is a
common practice for proteomics analyses, but insoluble bacterial biomasses
are often left behind. Here, we show that with triflic acid treatment,
the insoluble bacterial biomass of Gram<sup>–</sup> and Gram<sup>+</sup> bacteria can be rendered soluble. We use LC-MS/MS shotgun
proteomics to show that bacterial proteins in the soluble and insoluble
postlysis fractions differ significantly. Additionally, in the case
of Gram<sup>–</sup> Pseudomonas aeruginosa, triflic acid treatment enables the enrichment of cell-envelope-associated
proteins. Finally, we apply triflic acid to a human microbiome sample
to show that this treatment is robust and enables the identification
of a new, complementary subset of proteins from a complex microbial
mixture