Properties of geopolymer binders prepared from milled pond ash

Alkali-activated materials were prepared from pond ash from the Darkhan city (Mongolia) thermal power station. This ash contains about 60 wt % X-ray amorphous material in addition to quartz, mullite, hematite and magnesioferrite, and presents significant storage problems since it is accumulating in large amounts and is a hazardous waste, containing 90-100 ppm of the heavy metals As, Pb and Cr, and about 800 ppm Sr. Alkali-activated materials synthesized from the as-received pond ash achieved compressive strengths of only 3.25 MPa. Reduction of the particle size by mechanical milling for up to 30 min progressively increases the compressive strength of the resulting alkali-activated geopolymer up to 15.4 MPa. Leaching tests indicate that the combination of milling and alkali treatment does not cause the release of the hazardous heavy metals from the product, making it suitable for construction applications. © 2017 CSIC

Tracing TET1 expression in prostate cancer: discovery of malignant cells with a distinct oncogenic signature

Background!#!Ten-eleven translocation methylcytosine dioxygenase 1 (TET1) is involved in DNA demethylation and transcriptional regulation, plays a key role in the maintenance of stem cell pluripotency, and is dysregulated in malignant cells. The identification of cancer stem cells (CSCs) driving tumor growth and metastasis is the primary objective of biomarker discovery in aggressive prostate cancer (PCa). In this context, we analyzed TET1 expression in PCa.!##!Methods!#!A large-scale immunohistochemical analysis of TET1 was performed in normal prostate (NOR) and PCa using conventional slides (50 PCa specimens) and tissue microarrays (669 NOR and 1371 PCa tissue cores from 371 PCa specimens). Western blotting, RT-qPCR, and 450 K methylation array analyses were performed on PCa cell lines. Genome-wide correlation, gene regulatory network, and functional genomics studies were performed using publicly available data sources and bioinformatics tools.!##!Results!#!In NOR, TET1 was exclusively expressed in normal cytokeratin 903 (CK903)-positive basal cells. In PCa, TET1 was frequently detected in alpha-methylacyl-CoA racemase (AMACR)-positive tumor cell clusters and was detectable at all tumor stages and Gleason scores. Pearson's correlation analyses of PCa revealed 626 TET1-coactivated genes (r > 0.5) primarily encoding chromatin remodeling and mitotic factors. Moreover, signaling pathways regulating antiviral processes (62 zinc finger, ZNF, antiviral proteins) and the pluripotency of stem cells were activated. A significant proportion of detected genes exhibited TET1-correlated promoter hypomethylation. There were 161 genes encoding transcription factors (TFs), of which 133 were ZNF-TFs with promoter binding sites in TET1 and in the vast majority of TET1-coactivated genes.!##!Conclusions!#!TET1-expressing cells are an integral part of PCa and may represent CSCs with oncogenic potential