Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/20739
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dc.contributor.authorRoukos, D. H.en
dc.date.accessioned2015-11-24T19:09:43Z-
dc.date.available2015-11-24T19:09:43Z-
dc.identifier.issn1744-8352-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/20739-
dc.rightsDefault Licence-
dc.subjectAlgorithmsen
dc.subject*Genome, Humanen
dc.subjectHelicobacter pylori/pathogenicityen
dc.subjectHumansen
dc.subjectMutationen
dc.subjectNeoplastic Stem Cellsen
dc.subjectStomach Neoplasms/genetics/*therapyen
dc.titleInnovative genomic-based model for personalized treatment of gastric cancer: integrating current standards and new technologiesen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primary10.1586/14737159.8.1.29-
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/18088228-
heal.identifier.secondaryhttp://www.expert-reviews.com/doi/abs/10.1586/14737159.8.1.29-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.publicationDate2008-
heal.abstractIn the era of network biology, understanding the complexity of the signaling pathways network in cancer origin, progression and metastasis will dramatically alter and improve treatment strategies. Prognosis of gastric cancer remains poor. Clinical decisions on treatment are based on tumor-node-metastasis (TNM) staging, but are suboptimal. This perspective review, integrating several concepts, including cancer stem cells, provides a novel treatment model for tailoring the best treatment in individual patients with gastric cancer. Biologic metastatic steps (invasion, angiogenesis, intra/extravasation, colonization and microenvironment at distant organs) are orchestrated by mutated genes. Identifying and profiling these key genes and their interactions with environmental factors such as Helicobacter pylori, driver mutations and interacting signaling pathways using high-throughput technologies (including omics, resequencing, genome-wide associations studies and RNAi) in unbiased studies can lead to the development of both novel biomarkers and targeted agents. A comprehensive bench-to-bedside treatment-guided algorithm is provided for optimum preoperative or postoperative combination of cytotoxic and targeted agents. The protocol can be applied with adequate modification for most solid tumors.en
heal.journalNameExpert Rev Mol Diagnen
heal.journalTypepeer-reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ

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