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      Bmi-1: At the crossroads of physiological and pathological biology

      review-article
      , , , ,
      Genes & Diseases
      Chongqing Medical University
      Aging, Bmi-1, Cancer, Post translational modification, Stem cell, ASC, adult stem cell, ATM, Ataxia telangiectasia mutated, BASC, bronchioalveolar stem cell, Bmi-1, B-cell specific Moloney murine virus integration site 1, CIC, cancer initiating cell, CSC, cancer stem cell, EMT, epithelial–mesenchymal transition, ESC, embryonic stem cell, HCC, hepatocellular carcinoma, HDACi, histone deacetylase inhibitor, HSC, hematopoietic stem cell, hTERT, human telomerase reverse transcriptase, HTH, helix-turn-helix, ISC, intestinal stem cell, MEC, mammary epithelial cell, NSC, neural stem cell, PcG, polycomb group, PEST, domain rich in proline, glutamic acid, serine, and threonine, PRC, polycomb repressive complex, PTM, post-translational modification, RING, really interesting new gene, Rb, retinoblastoma, TSC, trophectodermal stem cell, UTR, untranslated region, XEN, extraembryonic stem cell

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          Abstract

          Bmi-1 is a member of the Polycomb repressor complex 1 that mediates gene silencing by regulating chromatin structure and is indispensable for self-renewal of both normal and cancer stem cells. Despite three decades of research that have elucidated the transcriptional regulation, post-translational modifications and functions of Bmi-1 in regulating the DNA damage response, cellular bioenergetics, and pathologies, the entire potential of a protein with such varied functions remains to be realized. This review attempts to synthesize the current knowledge on Bmi-1 with an emphasis on its role in both normal physiology and cancer. Additionally, since cancer stem cells are emerging as a new paradigm for therapy resistance, the role of Bmi-1 in this perspective is also highlighted. The wide spectrum of malignancies that implicate Bmi-1 as a signature for stemness and oncogenesis also make it a suitable candidate for therapy. Nonetheless, new approaches are vitally needed to further characterize physiological roles of Bmi-1 with the long-term goal of using Bmi-1 as a prognostic marker and a therapeutic target.

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          Most cited references125

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          A reserve stem cell population in small intestine renders Lgr5-positive cells dispensable.

          The small intestine epithelium renews every 2 to 5 days, making it one of the most regenerative mammalian tissues. Genetic inducible fate mapping studies have identified two principal epithelial stem cell pools in this tissue. One pool consists of columnar Lgr5-expressing cells that cycle rapidly and are present predominantly at the crypt base. The other pool consists of Bmi1-expressing cells that largely reside above the crypt base. However, the relative functions of these two pools and their interrelationship are not understood. Here we specifically ablated Lgr5-expressing cells in mice using a human diphtheria toxin receptor (DTR) gene knocked into the Lgr5 locus. We found that complete loss of the Lgr5-expressing cells did not perturb homeostasis of the epithelium, indicating that other cell types can compensate for the elimination of this population. After ablation of Lgr5-expressing cells, progeny production by Bmi1-expressing cells increased, indicating that Bmi1-expressing stem cells compensate for the loss of Lgr5-expressing cells. Indeed, lineage tracing showed that Bmi1-expressing cells gave rise to Lgr5-expressing cells, pointing to a hierarchy of stem cells in the intestinal epithelium. Our results demonstrate that Lgr5-expressing cells are dispensable for normal intestinal homeostasis, and that in the absence of these cells, Bmi1-expressing cells can serve as an alternative stem cell pool. These data provide the first experimental evidence for the interrelationship between these populations. The Bmi1-expressing stem cells may represent both a reserve stem cell pool in case of injury to the small intestine epithelium and a source for replenishment of the Lgr5-expressing cells under non-pathological conditions.
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            Bmi-1 is required for maintenance of adult self-renewing haematopoietic stem cells.

            A central issue in stem cell biology is to understand the mechanisms that regulate the self-renewal of haematopoietic stem cells (HSCs), which are required for haematopoiesis to persist for the lifetime of the animal. We found that adult and fetal mouse and adult human HSCs express the proto-oncogene Bmi-1. The number of HSCs in the fetal liver of Bmi-1-/- mice was normal. In postnatal Bmi-1-/- mice, the number of HSCs was markedly reduced. Transplanted fetal liver and bone marrow cells obtained from Bmi-1-/- mice were able to contribute only transiently to haematopoiesis. There was no detectable self-renewal of adult HSCs, indicating a cell autonomous defect in Bmi-1-/- mice. A gene expression analysis revealed that the expression of stem cell associated genes, cell survival genes, transcription factors, and genes modulating proliferation including p16Ink4a and p19Arf was altered in bone marrow cells of the Bmi-1-/- mice. Expression of p16Ink4a and p19Arf in normal HSCs resulted in proliferative arrest and p53-dependent cell death, respectively. Our results indicate that Bmi-1 is essential for the generation of self-renewing adult HSCs.
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              Creation of human tumour cells with defined genetic elements.

              During malignant transformation, cancer cells acquire genetic mutations that override the normal mechanisms controlling cellular proliferation. Primary rodent cells are efficiently converted into tumorigenic cells by the coexpression of cooperating oncogenes. However, similar experiments with human cells have consistently failed to yield tumorigenic transformants, indicating a fundamental difference in the biology of human and rodent cells. The few reported successes in the creation of human tumour cells have depended on the use of chemical or physical agents to achieve immortalization, the selection of rare, spontaneously arising immortalized cells, or the use of an entire viral genome. We show here that the ectopic expression of the telomerase catalytic subunit (hTERT) in combination with two oncogenes (the simian virus 40 large-T oncoprotein and an oncogenic allele of H-ras) results in direct tumorigenic conversion of normal human epithelial and fibroblast cells. These results demonstrate that disruption of the intracellular pathways regulated by large-T, oncogenic ras and telomerase suffices to create a human tumor cell.
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                Author and article information

                Contributors
                Journal
                Genes Dis
                Genes Dis
                Genes & Diseases
                Chongqing Medical University
                2352-4820
                2352-3042
                05 May 2015
                September 2015
                05 May 2015
                : 2
                : 3
                : 225-239
                Affiliations
                [1]Department of Obstetrics and Gynecology, Stephenson Cancer Center, University of Oklahoma Health Science Center, Oklahoma City, OK 73104, United States of America
                Author notes
                []Corresponding Author. Peggy and Charles Stephenson Cancer Center, OUHSC, 975 NE 10th Street, BRC-1409B, Oklahoma City, OK 73104, United States of America. Tel.: +1 405 271 7184; fax: +1 405 271 2141. Resham-Bhattacharya@ 123456ouhsc.edu
                Article
                S2352-3042(15)00027-6
                10.1016/j.gendis.2015.04.001
                4593320
                26448339
                ab63cfe9-d4ac-4cbf-92fd-cef19105b1f4

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 16 March 2015
                : 15 April 2015
                Categories
                Article

                aging,bmi-1,cancer,post translational modification,stem cell,asc, adult stem cell,atm, ataxia telangiectasia mutated,basc, bronchioalveolar stem cell,bmi-1, b-cell specific moloney murine virus integration site 1,cic, cancer initiating cell,csc, cancer stem cell,emt, epithelial–mesenchymal transition,esc, embryonic stem cell,hcc, hepatocellular carcinoma,hdaci, histone deacetylase inhibitor,hsc, hematopoietic stem cell,htert, human telomerase reverse transcriptase,hth, helix-turn-helix,isc, intestinal stem cell,mec, mammary epithelial cell,nsc, neural stem cell,pcg, polycomb group,pest, domain rich in proline, glutamic acid, serine, and threonine,prc, polycomb repressive complex,ptm, post-translational modification,ring, really interesting new gene,rb, retinoblastoma,tsc, trophectodermal stem cell,utr, untranslated region,xen, extraembryonic stem cell

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