Category Health/Medical

Gene Signature could lead to a new way of diagnosing Lyme Disease

Longitudinal differential gene expression and pathway analysis of Lyme disease. (A) Bar chart of the numbers of genes found to be upregulated or downregulated at Lyme disease diagnosis (V1), 3 weeks post-treatment (V2, after a standard course of antibiotics), and 6 months post-treatment (V5). (B) Venn diagram representing the number of DEGs between Lyme disease patients and controls at three time points. (C) Principal component analysis (PCA) of Lyme disease patients and controls at three time points on the basis of 1,759 unique DEGs identified at V1, V2, and V5. The asterisk represents a subject in the control group who looks like an outlier in the PCA plot but is not shown to be an outlier by PCA analysis of the control samples (see Fig. S2 in the supplemental material). Note that the PC3 axis in the PCA plot accounts for only 8% of the variance in the data set. (D to F) Top 10 disease and functional categories (D), top 10 canonical pathways (E), and top 10 upstream regulators (excluding drug categories) (F) predicted to be involved in Lyme disease at (V1, V2, and V5) with categories, pathways, and genes ranked by the negative log of the P value of the enrichment score. The color scheme is based on Z scores, with activation in orange, inhibition in blue, and undetermined directionality in gray. The red line represents the designated significance threshold (P < 0.05).

Longitudinal differential gene expression and pathway analysis of Lyme disease. (A) Bar chart of the numbers of genes found to be upregulated or downregulated at Lyme disease diagnosis (V1), 3 weeks post-treatment (V2, after a standard course of antibiotics), and 6 months post-treatment (V5). (B) Venn diagram representing the number of DEGs between Lyme disease patients and controls at three time points. (C) Principal component analysis (PCA) of Lyme disease patients and controls at three time points on the basis of 1,759 unique DEGs identified at V1, V2, and V5. The asterisk represents a subject in the control group who looks like an outlier in the PCA plot but is not shown to be an outlier by PCA analysis of the control samples (see Fig. S2 in the supplemental material)...

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Study finds mechanism by which Obesity Promotes Pancreatic and Breast Cancer

breast cancer

Micrograph showing a lymph node invaded by ductal breast carcinoma, with extension of the tumour beyond the lymph node. Credit: Nephron/Wikipedia

MGH team describes finding an association between obesity and an overabundance of a factor called PlGF (placental growth factor) and that PlGF’s binding to its receptor VEGFR-1, which is expressed on immune cells within tumors, promotes tumor progression. Their findings in cellular and animal models, as well as in patient tumor samples, indicate that targeting the PlGF/ VEGFR-1 pathway may be particularly effective in obese patients.

“We found that obesity increased infiltration of tumor-promoting immune cells and the growth and metastasis of pancreatic cancers,” says Dai Fukumura, MD, PhD...

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The Sleeping Giant NGC 4889 harbors a Dark Secret

This image shows the elliptical galaxy NGC 4889 in front of hundreds of background galaxies, and deeply embedded within the Coma galaxy cluster. Well-hidden from human eyes, there is a gigantic supermassive black hole at the center of the galaxy. Credit: NASA & ESA

This image shows the elliptical galaxy NGC 4889 in front of hundreds of background galaxies, and deeply embedded within the Coma galaxy cluster. Well-hidden from human eyes, there is a gigantic supermassive black hole at the center of the galaxy. Credit: NASA & ESA

The placid appearance of NGC 4889 can fool the unsuspecting observer. But the elliptical galaxy harbours one of the most supermassive black holes ever discovered. Located ~300 million light-years away in the Coma Cluster, the giant elliptical galaxy NGC 4889, the brightest and largest galaxy in this image has a black hole that is 21 billion times the mass of the Sun. The event horizon has a diameter of ~130 billion kilometres. This is about 15X the diameter of Neptune’s orbit from the Sun...

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New Nanoparticle Formulation of a Cancer Drug is both Effective and Nontoxic – qualities hard to achieve with the free drug

The polymeric nanoparticle Accurin encapsulates the clinical candidate AZD2811, an Aurora B kinase inhibitor. This material relates to a paper that appeared in the Feb. 10, 2016 issue of Science Translational Medicine, published by AAAS. The paper, by S. Ashton at institution in location, and colleagues was titled, "Aurora kinase inhibitor nanoparticles target tumors with favorable therapeutic index in vivo." Credit: Ashton et al., Science Translational Medicine (2016)

The polymeric nanoparticle Accurin encapsulates the clinical candidate AZD2811, an Aurora B kinase inhibitor. This material relates to a paper that appeared in the Feb. 10, 2016 issue of Science Translational Medicine, published by AAAS. The paper, by S. Ashton at institution in location, and colleagues was titled, “Aurora kinase inhibitor nanoparticles target tumors with favorable therapeutic index in vivo.” Credit: Ashton et al., Science Translational Medicine (2016)

Their nanoparticle creation releases the potent but toxic targeted cancer drug directly to tumors, while sparing healthy tissue. The findings in rodents with human tumors have helped launch clinical trials of the nanoparticle-encapsulated version of the drug, which are currently underway...

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