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1.
Appl Radiat Isot ; 129: 67-75, 2017 Nov.
Article in English | MEDLINE | ID: mdl-28822270

ABSTRACT

Nanostructured materials attracted considerable attention because of its high surface area to volume ratio resulting from their nano-scale dimensions. This class of sorbents is expected to have a potential impact on enhancement the efficacy of radioisotope generators for diagnostic and therapeutic applications in nuclear medicine. This review provides a summary on the importance of nanostructured materials as effective sorbents for the development of clinical-scale radioisotope generators and outlining the assessment of recent developments, key challenges and promising access to the near future.

2.
Br J Cancer ; 85(7): 1037-46, 2001 Sep 28.
Article in English | MEDLINE | ID: mdl-11592777

ABSTRACT

Colorectal carcinoma is uncommon in Egypt, but a high proportion of cases occurs before age 40 years and in the rectum. We compared the molecular pathology of 59 representative Egyptian patients aged 10-72 to Western patients with sporadic, young-onset, or hereditary non-polyposis colorectal cancer syndrome (HNPCC)-associated carcinoma and found significant differences. Most Egyptian cancers were rectal (51%) and poorly differentiated (58%). High levels of microsatellite instability (MSI-H) were frequent (37%) and attributable in some cases (36%) to methylation of the promoter of the hMLH1 mismatch repair gene, but no MSI-H cancer had loss of hMSH2 mismatch repair gene product of the type seen with germline hMSH2 mutation in HNPCC. K-ras mutation was uncommon (11%). In subset analyses, high frequencies of MSI-H in rectal carcinomas (36%) and p53 gene product overexpression in MSI-H cancers (50%) were found. MSI-H and K-ras mutation in Egyptians under age 40 were unusual (17% and 0%, respectively), and schistosomiasis was associated with MSI and K-ras mutation. Cluster analysis identified 2 groups: predominantly young men with poorly differentiated mucinous and signet-ring cell colorectal carcinoma lacking K-ras mutation; older patients who had well- or moderately differentiated adenocarcinoma often with MSI-H, K-ras mutation and schistosomiasis. Our findings show that the molecular pathology of colorectal cancer in older as well as younger Egyptians has unique differences from Western patients, and schistosomiasis influences the molecular pathogenesis of some tumours.


Subject(s)
Colorectal Neoplasms, Hereditary Nonpolyposis/ethnology , Colorectal Neoplasms, Hereditary Nonpolyposis/genetics , Colorectal Neoplasms/ethnology , Colorectal Neoplasms/genetics , Microsatellite Repeats/genetics , Adolescent , Adult , Age of Onset , Aged , Cell Differentiation , Child , Colorectal Neoplasms/physiopathology , Colorectal Neoplasms, Hereditary Nonpolyposis/physiopathology , DNA Mutational Analysis , DNA Repair , Egypt , Female , Genes, ras/genetics , Humans , Male , Methylation , Middle Aged , Risk Factors , Schistosomiasis/complications
3.
J Biol Chem ; 273(46): 30419-26, 1998 Nov 13.
Article in English | MEDLINE | ID: mdl-9804808

ABSTRACT

Prior investigations document that proliferative signaling cascades, under some circumstances, initiate apoptosis, although mechanisms that dictate the final outcome are largely unknown. In COS-7 cells, ceramide signals Raf-1 activation through Ras (Zhang, Y., Yao, B., Delikat, S., Bayoumy, S., Lin, X. H., Basu, S., McGinley, M., Chan-Hui, P. Y., Lichenstein, H., and Kolesnick, R. (1997) Cell 89, 63-72), but not apoptosis. However, expression of small amounts of the pro-apoptotic Bcl-2 family member, BAD, conferred ceramide-induced apoptosis onto COS-7 cells. Ceramide signaled apoptosis in BAD-expressing cells by a pathway involving sequentially kinase suppressor of Ras (KSR)/ceramide-activated protein kinase, Ras, c-Raf-1, and MEK1. Downstream, this pathway linked to BAD dephosphorylation at serine 136 by prolonged inactivation of Akt/PKB. Further, mutation of BAD at serine 136 abrogated ceramide signaling of apoptosis. The present study indicates that when ceramide signals through the Ras/Raf cascade, the availability of a single target, BAD, may dictate an apoptotic outcome.


Subject(s)
Apoptosis , Carrier Proteins/physiology , Ceramides/physiology , Proto-Oncogene Proteins c-raf/physiology , Signal Transduction , ras Proteins/physiology , Animals , COS Cells , Phosphorylation , Protein Serine-Threonine Kinases/metabolism , Proto-Oncogene Proteins/metabolism , Proto-Oncogene Proteins c-akt , Serine/metabolism , bcl-Associated Death Protein
4.
Cell ; 89(1): 63-72, 1997 Apr 04.
Article in English | MEDLINE | ID: mdl-9094715

ABSTRACT

A proline-directed serine/threonine ceramide-activated protein (CAP) kinase mediates transmembrane signaling through the sphingomyelin pathway. CAP kinase reportedly initiates proinflammatory TNF alpha action by phosphorylating and activating Raf-1. The present studies delineate kinase suppressor of Ras (KSR), identified genetically in Caenorhabditis elegans and Drosophila, as CAP kinase. Mouse KSR, like CAP kinase, renatures and autophosphorylates as a 100-kDa membrane-bound polypeptide. KSR overexpression constitutively activates Raf-1. TNF alpha or ceramide analogs markedly enhance KSR autophosphorylation and its ability to complex with, phosphorylate, and activate Raf-1. In vitro, low nanomolar concentrations of natural ceramide stimulate KSR to autophosphorylate, and transactivate Raf-1. Other lipid second messengers were ineffective. Moreover, Thr269 the Raf-1 site phosphorylated by CAP kinase, is also recognized by KSR. Thus, by previously established criteria, KSR appears to be CAP kinase.


Subject(s)
Protein Kinases/metabolism , Protein Serine-Threonine Kinases/pharmacology , Signal Transduction/physiology , ras Proteins/antagonists & inhibitors , Amino Acid Sequence , Animals , COS Cells/enzymology , Caenorhabditis elegans , Ceramides/pharmacology , Drosophila , Gene Expression Regulation, Enzymologic/physiology , Humans , Mice , Molecular Sequence Data , Mutagenesis/physiology , Phosphorylation , Protein Kinases/drug effects , Protein Serine-Threonine Kinases/genetics , Proto-Oncogene Proteins c-raf , Threonine/genetics , Tumor Necrosis Factor-alpha/pharmacology
5.
J Exp Med ; 186(11): 1831-41, 1997 Dec 01.
Article in English | MEDLINE | ID: mdl-9382882

ABSTRACT

The endotoxic shock syndrome is characterized by systemic inflammation, multiple organ damage, circulatory collapse and death. Systemic release of tumor necrosis factor (TNF)-alpha and other cytokines purportedly mediates this process. However, the primary tissue target remains unidentified. The present studies provide evidence that endotoxic shock results from disseminated endothelial apoptosis. Injection of lipopolysaccharide (LPS), and its putative effector TNF-alpha, into C57BL/6 mice induced apoptosis in endothelium of intestine, lung, fat and thymus after 6 h, preceding nonendothelial tissue damage. LPS or TNF-alpha injection was followed within 1 h by tissue generation of the pro-apoptotic lipid ceramide. TNF-binding protein, which protects against LPS-induced death, blocked LPS-induced ceramide generation and endothelial apoptosis, suggesting systemic TNF is required for both responses. Acid sphingomyelinase knockout mice displayed a normal increase in serum TNF-alpha in response to LPS, yet were protected against endothelial apoptosis and animal death, defining a role for ceramide in mediating the endotoxic response. Furthermore, intravenous injection of basic fibroblast growth factor, which acts as an intravascular survival factor for endothelial cells, blocked LPS-induced ceramide elevation, endothelial apoptosis and animal death, but did not affect LPS-induced elevation of serum TNF-alpha. These investigations demonstrate that LPS induces a disseminated form of endothelial apoptosis, mediated sequentially by TNF and ceramide generation, and suggest that this cascade is mandatory for evolution of the endotoxic syndrome.


Subject(s)
Apoptosis/drug effects , Ceramides/biosynthesis , Endothelium, Vascular/drug effects , Lipopolysaccharides/pharmacology , Receptors, Tumor Necrosis Factor , Shock, Septic/pathology , Tumor Necrosis Factor-alpha/pharmacology , Adipose Tissue/blood supply , Animals , Capillaries/drug effects , Capillaries/pathology , Carrier Proteins/pharmacology , Endothelium, Vascular/pathology , Fibroblast Growth Factor 2/pharmacology , Intestinal Mucosa/blood supply , Lipopolysaccharides/antagonists & inhibitors , Lipopolysaccharides/toxicity , Lung/blood supply , Mice , Mice, Inbred C57BL , Receptors, Tumor Necrosis Factor, Type I , Shock, Septic/chemically induced , Signal Transduction , Specific Pathogen-Free Organisms , Sphingomyelin Phosphodiesterase/pharmacology , Sphingomyelins/metabolism , Thymus Gland/blood supply , Tumor Necrosis Factor Decoy Receptors
6.
Antonie Van Leeuwenhoek ; 67(4): 357-62, 1995.
Article in English | MEDLINE | ID: mdl-7574552

ABSTRACT

Some properties of an extracellular lipase produced by Lactobacillus delbrueckii subsp. bulgaricus were studied. Maximum enzyme activity was found against olive and butter oil as enzyme substrates. Addition of 9% acacia gum, 0.1% Na-deoxycholate and 0.01 M CaCl2 to the enzyme reaction mixture increased-lipase activity from 5.3 to 14.5 (FFA/mg protein/minute) at pH 6.0 and at 40 degrees C. Maximum lipase production was reached in the presence of glucose as a sole source of carbon, wheat bran as nitrogen source, olive oil as a sole lipid source and butyric acid as fatty acid supporting the growth medium. An initial pH value of the culture medium of 6.0 and a temperature of 35 degrees C gave the highest lipolytic activity.


Subject(s)
Lactobacillus/enzymology , Lipase/metabolism , Butyrates , Butyric Acid , Calcium Chloride/pharmacology , Deoxycholic Acid/pharmacology , Dietary Fiber , Glucose , Gum Arabic/pharmacology , Hydrogen-Ion Concentration , Lactobacillus/drug effects , Lipase/biosynthesis , Olive Oil , Plant Oils , Substrate Specificity , Temperature
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