By a News Reporter-Staff News Editor at Cancer Gene Therapy Week -- Fresh data on Biotechnology are presented in a new report. According to news reporting originating in Cuernavaca, Mexico, by NewsRx journalists, research stated, "It has recently begun to be considered that cancer is a systemic disease and that it must be studied at every level of complexity using many of the currently available approaches, including high-throughput technologies and bioinformatics. To achieve such understanding in cervical cancer, we collected information on gene, protein and phosphoprotein expression of the HeLa cell line and performed a comprehensive analysis of the different signaling pathways, transcription networks and metabolic events in which they participate."
The news reporters obtained a quote from the research from National Autonomous University, "A total expression analysis by RNA-Seq of the HeLa cell line showed that 19,974 genes were transcribed. Of these, 3,360 were over-expressed, and 2,129 under-expressed when compared to the NHEK cell line. A protein-protein interaction network was derived from the over-expressed genes and used to identify central elements and, together with the analysis of over-represented transcription factor motifs, to predict active signaling and regulatory pathways. This was further validated by Metal-Oxide Affinity Chromatography (MOAC) and Tandem Mass Spectrometry (MS/MS) assays which retrieved phosphorylated proteins. The 14-3-3 family members emerge as important regulators in carcinogenesis and as possible clinical targets. We observed that the different over-and under-regulated pathways in cervical cancer could be interrelated through elements that participate in crosstalks, therefore belong to what we term 'meta-pathways'. Additionally, we highlighted the relations of each one of the differentially represented pathways to one or more of the ten hallmarks of cancer. These features could be maintained in many other types of cancer, regardless of mutations or genomic rearrangements, and favor their robustness, adaptations and the evasion of tissue control."
According to the news reporters, the research concluded: "Probably, this could explain why cancer cells are not eliminated by selective pressure and why therapy trials directed against molecular targets are not as effective as expected."
For more information on this research see: Analysis and prediction of pathways in HeLa cells by integrating biological levels of organization with systems-biology approaches. Plos One, 2013;8(6):e65433. (Public Library of Science - www.plos.org; Plos One - www.plosone.org)
Our news correspondents report that additional information may be obtained by contacting J.C. Higareda-Almaraz, Functional Genomics of Prokaryotes Research Program, Center for Genomic Sciences, National Autonomous University of Mexico, Cuernavaca, Morelos, Mexico. Additional authors for this research include I.A. Valtierra-Gutierrez, M. Hernandez-Ortiz, S. Contreras, E. Hernandez and S. Encarnacion (see also technology.html">Biotechnology).
Keywords for this news article include: Biotechnology, Mexico, Genetics, Oncology, Cuernavaca, Hela Cells, Epithelial Cells, Cancer Gene Therapy, North and Central America.
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