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      Synopsis: Special Issue on “Disruption of signaling homeostasis induced crosstalk in the carcinogenesis paradigm Epistemology of the origin of cancer

      review-article
      1 , 2 , 3 , * , , 1 , 2 , 4
      4open
      EDP Sciences
      Akt, Aneuploidy, AP-2, bcl-2, BRCA, Cancer, Carcinogenesis, CD44, Cell transition, CHK2, Chronic inflammation, Crosstalk, Disruption, DNA, ECM, EGFR, Eicosanoid, Epidemiology, Epigenetics, FADS2, Fibrosis, Genetics, Genomics, GLUT-4, HBV, HCC, HCV, HETE, Homeostasis, IKK, JNK, Lipid, LOX, LOXL2, LOXL3, LTA4, LTB4, LTD4, LTE4, Lysyl oxidase, LXA4, LXB4, MaR1, MaR2, Metabolism, MicroRNA, MMP, mRNA, Microbiome, Morbid obesity, Mutation, NPD1, p16, p53, p120, Pathogenesis, PAX, PCN, PGG2, PGH2, PI3K, PPAR, Precancerous niche, Proteomics, PUFA, Radiation, Reproducibility, RvD1, RvD2, RvD3, RvD4, RvD5, RvD6, Signaling, SMT, Somatic mutation theory, SOX-2, SPM, STAT3, Stem cell, Targeting therapy, Technology, TGF, Warburg

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          Abstract

          It is increasingly evident that carcinogenesis, in the vast majority of cancers, cannot be explained simply through an accumulation of somatic mutations, or epigenetics, the stem cell theory, or the Warburg effect. Here, decades of thinking based on incorrect assumptions has resulted in an incorrect hypothesis on the origin of cancer. Many papers studying DNA, genetics, RNA, miRNA, proteomics, and epigenetics have increased our understanding of biology. Our paradigm, though more complex, is more reliable and plausible. It states that cancer originates from a disruption of homeostasis. This essential biological phenomenon, homeostasis, maintains the interrelationships of various signaling pathways and induced crosstalk which modify cellular functions together with the interactions of surrounding cells and structures such that the equilibrium lies towards the optimal health of the organism. This Special Issue “ Disruption of signaling homeostasis induced crosstalk in the carcinogenesis paradigm Epistemology of the origin of cancer ” provides compelling evidence that carcinogenesis is explained by a six-step sequence of events for the vast majority of cancers. These six steps include, (1) a pathogenic stimulus followed by (2) chronic inflammation, from which develops (3) fibrosis with associated remodeling in the cellular microenvironment. From these changes a (4) pre-cancerous niche develops which triggers the deployment of (5) a chronic stress escape strategy, and when this fails to resolve, and (6) the transition of a normal cell to a cancer cell occurs. This paradigm provides opportunities to move away from a symptom-oriented understanding of cancer and is much closer to a cause-based understanding, which opens the door for early preventative strategies to mitigate cancer as a disease, and to interdict metastases. This is underpinned by the fact that an independent recently published proof of this paradigm showed how a stimulus trigger the proposed multi-sequence cascade of events as abrupt involution-induced chronic inflammation, followed by fibrosis with remodeling, which describes the pre-cancerous niche followed by hyperplasia, metaplasia, and cancer.

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          Most cited references338

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          Matrix elasticity directs stem cell lineage specification.

          Microenvironments appear important in stem cell lineage specification but can be difficult to adequately characterize or control with soft tissues. Naive mesenchymal stem cells (MSCs) are shown here to specify lineage and commit to phenotypes with extreme sensitivity to tissue-level elasticity. Soft matrices that mimic brain are neurogenic, stiffer matrices that mimic muscle are myogenic, and comparatively rigid matrices that mimic collagenous bone prove osteogenic. During the initial week in culture, reprogramming of these lineages is possible with addition of soluble induction factors, but after several weeks in culture, the cells commit to the lineage specified by matrix elasticity, consistent with the elasticity-insensitive commitment of differentiated cell types. Inhibition of nonmuscle myosin II blocks all elasticity-directed lineage specification-without strongly perturbing many other aspects of cell function and shape. The results have significant implications for understanding physical effects of the in vivo microenvironment and also for therapeutic uses of stem cells.
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            The epithelial-mesenchymal transition generates cells with properties of stem cells.

            The epithelial-mesenchymal transition (EMT) is a key developmental program that is often activated during cancer invasion and metastasis. We here report that the induction of an EMT in immortalized human mammary epithelial cells (HMLEs) results in the acquisition of mesenchymal traits and in the expression of stem-cell markers. Furthermore, we show that those cells have an increased ability to form mammospheres, a property associated with mammary epithelial stem cells. Independent of this, stem cell-like cells isolated from HMLE cultures form mammospheres and express markers similar to those of HMLEs that have undergone an EMT. Moreover, stem-like cells isolated either from mouse or human mammary glands or mammary carcinomas express EMT markers. Finally, transformed human mammary epithelial cells that have undergone an EMT form mammospheres, soft agar colonies, and tumors more efficiently. These findings illustrate a direct link between the EMT and the gain of epithelial stem cell properties.
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              Epigenetics in cancer.

              Epigenetic mechanisms are essential for normal development and maintenance of tissue-specific gene expression patterns in mammals. Disruption of epigenetic processes can lead to altered gene function and malignant cellular transformation. Global changes in the epigenetic landscape are a hallmark of cancer. The initiation and progression of cancer, traditionally seen as a genetic disease, is now realized to involve epigenetic abnormalities along with genetic alterations. Recent advancements in the rapidly evolving field of cancer epigenetics have shown extensive reprogramming of every component of the epigenetic machinery in cancer including DNA methylation, histone modifications, nucleosome positioning and non-coding RNAs, specifically microRNA expression. The reversible nature of epigenetic aberrations has led to the emergence of the promising field of epigenetic therapy, which is already making progress with the recent FDA approval of three epigenetic drugs for cancer treatment. In this review, we discuss the current understanding of alterations in the epigenetic landscape that occur in cancer compared with normal cells, the roles of these changes in cancer initiation and progression, including the cancer stem cell model, and the potential use of this knowledge in designing more effective treatment strategies.
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                Author and article information

                Journal
                fopen
                https://www.4open-sciences.org
                4open
                4open
                EDP Sciences
                2557-0250
                01 October 2019
                01 October 2019
                2019
                : 2
                : ( publisher-idID: fopen/2019/01 )
                : 28
                Affiliations
                [1 ] Theodor-Billroth-Akademie®, , Germany, USA,
                [2 ] INCORE, International Consortium of Research Excellence of the Theodor-Billroth-Academy®, , Germany, USA,
                [3 ] Department of Surgery, Carl-Thiem-Klinikum, , Cottbus, Germany,
                [4 ] Risk-Based Decisions Inc., , Sacramento, CA, USA,
                Author notes
                [* ]Corresponding author: b-bruecher@ 123456gmx.de
                Article
                fopen180008
                10.1051/fopen/2019023
                6c92bc93-8a91-49f8-953b-ed9d73c5ab6c
                © B.L.D.M. Brücher & I.S. Jamall, Published by EDP Sciences, 2019

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 27 March 2018
                : 10 September 2019
                Page count
                Figures: 5, Tables: 0, Equations: 0, References: 334, Pages: 30
                Categories
                Life Sciences - Medicine
                Review Article
                Disruption of homeostasis-induced signaling and crosstalk in the carcinogenesis paradigm “Epistemology of the origin of cancer”
                Custom metadata
                4open 2019, 2, 28
                2019
                2019
                2019

                Medicine,Chemistry,Physics,Mathematics,Materials science,Life sciences
                Warburg,MaR1,Genetics,RvD3,Genomics,Technology,GLUT-4,BRCA,RvD2,HBV,RvD1,HCC,HCV,Reproducibility,HETE,Radiation,Homeostasis,IKK,Cancer,PUFA,JNK,Proteomics,Lipid,LOX,Precancerous niche,LOXL2,Aneuploidy,Targeting therapy,PPAR,LOXL3,LTA4,Carcinogenesis,PI3K,LTB4,PGH2,LTD4,LTE4,PGG2,Lysyl oxidase,PCN,LXA4,Stem cell,LXB4,CD44,PAX,Pathogenesis,MaR2,Metabolism,p120,MicroRNA,p53,MMP,Akt,mRNA,Cell transition,p16,Microbiome,NPD1,Morbid obesity,Mutation,STAT3,CHK2,SPM,Chronic inflammation,Crosstalk,AP-2,SOX-2,Disruption,Somatic mutation theory,DNA,ECM,SMT,EGFR,TGF,Signaling,Eicosanoid,Epidemiology,bcl-2,RvD6,Epigenetics,RvD5,FADS2,Fibrosis,RvD4

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