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      Cancer Stem Cells: Emergent Nature of Tumor Emergency

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          Abstract

          A functional analysis of 167 genes overexpressed in Krebs-2 tumor initiating cells was performed. In the first part of the study, the genes were analyzed for their belonging to one or more of the three groups, which represent the three major phenotypic manifestation of malignancy of cancer cells, namely (1) proliferative self-sufficiency, (2) invasive growth and metastasis, and (3) multiple drug resistance. 96 genes out of 167 were identified as possible contributors to at least one of these fundamental properties. It was also found that substantial part of these genes are also known as genes responsible for formation and/or maintenance of the stemness of normal pluri-/multipotent stem cells. These results suggest that the malignancy is simply the ability to maintain the stem cell specific genes expression profile, and, as a consequence, the stemness itself regardless of the controlling effect of stem niches. In the second part of the study, three stress factors combined into the single concept of “generalized cellular stress,” which are assumed to activate the expression of these genes, were defined. In addition, possible mechanisms for such activation were identified. The data obtained suggest the existence of a mechanism for the de novo formation of a pluripotent/stem phenotype in the subpopulation of “committed” tumor cells.

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          Most cited references408

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          Revisiting the hallmarks of cancer.

          The hallmarks of cancer described by Hanahan and Weinberg have proved seminal in our understanding of cancer's common traits and in rational drug design. Not free of critique and with understanding of different aspects of tumorigenesis coming into clearer focus in the recent years, we attempt to draw a more organized and updated picture of the cancer hallmarks. We define seven hallmarks of cancer: selective growth and proliferative advantage, altered stress response favoring overall survival, vascularization, invasion and metastasis, metabolic rewiring, an abetting microenvironment, and immune modulation, while highlighting some considerations for the future of the field.
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            Anoikis: an emerging hallmark in health and diseases.

            Anoikis is a programmed cell death occurring upon cell detachment from the correct extracellular matrix, thus disrupting integrin ligation. It is a critical mechanism in preventing dysplastic cell growth or attachment to an inappropriate matrix. Anoikis prevents detached epithelial cells from colonizing elsewhere and is thus essential for tissue homeostasis and development. As anchorage-independent growth and epithelial-mesenchymal transition, two features associated with anoikis resistance, are crucial steps during tumour progression and metastatic spreading of cancer cells, anoikis deregulation has now evoked particular attention from the scientific community. The aim of this review is to analyse the molecular mechanisms governing both anoikis and anoikis resistance, focusing on their regulation in physiological processes, as well as in several diseases, including metastatic cancers, cardiovascular diseases and diabetes. Copyright © 2011 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
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              Control of neuronal precursor proliferation in the cerebellum by Sonic Hedgehog.

              Cerebellar granule cells are the most abundant type of neuron in the brain, but the molecular mechanisms that control their generation are incompletely understood. We show that Sonic hedgehog (Shh), which is made by Purkinje cells, regulates the division of granule cell precursors (GCPs). Treatment of GCPs with Shh prevents differentiation and induces a potent, long-lasting proliferative response. This response can be inhibited by basic fibroblast growth factor or by activation of protein kinase A. Blocking Shh function in vivo dramatically reduces GCP proliferation. These findings provide insight into the mechanisms of normal growth and tumorigenesis in the cerebellum.
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                Author and article information

                Contributors
                Journal
                Front Genet
                Front Genet
                Front. Genet.
                Frontiers in Genetics
                Frontiers Media S.A.
                1664-8021
                16 November 2018
                2018
                : 9
                : 544
                Affiliations
                [1] 1Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences , Novosibirsk, Russia
                [2] 2Department of Natural Sciences, Novosibirsk State University , Novosibirsk, Russia
                [3] 3The State Research Center of Virology and Biotechnology Vector , Koltsovo, Russia
                [4] 4Research Institute of Fundamental and Clinical Immunology , Novosibirsk, Russia
                Author notes

                Edited by: Darius Widera, University of Reading, United Kingdom

                Reviewed by: Pierfrancesco Pagella, University of Zurich, Switzerland; Cristiana Tanase, Victor Babes National Institute of Pathology, Romania

                *Correspondence: Sergey S. Bogachev labmolbiol@ 123456mail.ru

                This article was submitted to Stem Cell Research, a section of the journal Frontiers in Genetics

                Article
                10.3389/fgene.2018.00544
                6250818
                0fdcc4d7-09bf-4827-8fdf-d15c9717a49d
                Copyright © 2018 Efremov, Proskurina, Potter, Dolgova, Efremova, Taranov, Ostanin, Chernykh, Kolchanov and Bogachev.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 09 July 2018
                : 26 October 2018
                Page count
                Figures: 2, Tables: 6, Equations: 0, References: 460, Pages: 29, Words: 27450
                Categories
                Genetics
                Hypothesis and Theory

                Genetics
                cancer stem cell,tamra+ cells,induction of pluripotency,hypoxia,oxidative stress,xenobiotics,carcinogenesis,genes-markers of stemness

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