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      Hedgehog Signal and Genetic Disorders

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          Abstract

          The hedgehog (Hh) family comprises sonic hedgehog (Shh), Indian hedgehog (Ihh), and desert hedgehog (Dhh), which are versatile signaling molecules involved in a wide spectrum of biological events including cell differentiation, proliferation, and survival; establishment of the vertebrate body plan; and aging. These molecules play critical roles from embryogenesis to adult stages; therefore, alterations such as abnormal expression or mutations of the genes involved and their downstream factors cause a variety of genetic disorders at different stages. The Hh family involves many signaling mediators and functions through complex mechanisms, and achieving a comprehensive understanding of the entire signaling system is challenging. This review discusses the signaling mediators of the Hh pathway and their functions at the cellular and organismal levels. We first focus on the roles of Hh signaling mediators in signal transduction at the cellular level and the networks formed by these factors. Then, we analyze the spatiotemporal pattern of expression of Hh pathway molecules in tissues and organs, and describe the phenotypes of mutant mice. Finally, we discuss the genetic disorders caused by malfunction of Hh signaling-related molecules in humans.

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          Most cited references207

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          Patched1 regulates hedgehog signaling at the primary cilium.

          Primary cilia are essential for transduction of the Hedgehog (Hh) signal in mammals. We investigated the role of primary cilia in regulation of Patched1 (Ptc1), the receptor for Sonic Hedgehog (Shh). Ptc1 localized to cilia and inhibited Smoothened (Smo) by preventing its accumulation within cilia. When Shh bound to Ptc1, Ptc1 left the cilia, leading to accumulation of Smo and activation of signaling. Thus, primary cilia sense Shh and transduce signals that play critical roles in development, carcinogenesis, and stem cell function.
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            Centrioles, centrosomes, and cilia in health and disease.

            Centrioles are barrel-shaped structures that are essential for the formation of centrosomes, cilia, and flagella. Here we review recent advances in our understanding of the function and biogenesis of these organelles, and we emphasize their connection to human disease. Deregulation of centrosome numbers has long been proposed to contribute to genome instability and tumor formation, whereas mutations in centrosomal proteins have recently been genetically linked to microcephaly and dwarfism. Finally, structural or functional centriole aberrations contribute to ciliopathies, a variety of complex diseases that stem from the absence or dysfunction of cilia.
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              HEDGEHOG-GLI1 signaling regulates human glioma growth, cancer stem cell self-renewal, and tumorigenicity.

              Cancer stem cells are rare tumor cells characterized by their ability to self-renew and to induce tumorigenesis. They are present in gliomas and may be responsible for the lethality of these incurable brain tumors. In the most aggressive and invasive type, glioblastoma multiforme (GBM), an average of about one year spans the period between detection and death [1]. The resistence of gliomas to current therapies may be related to the existence of cancer stem cells [2-6]. We find that human gliomas display a stemness signature and demonstrate that HEDGEHOG (HH)-GLI signaling regulates the expression of stemness genes in and the self-renewal of CD133(+) glioma cancer stem cells. HH-GLI signaling is also required for sustained glioma growth and survival. It displays additive and synergistic effects with temozolomide (TMZ), the current chemotherapeutic agent of choice. TMZ, however, does not block glioma stem cell self-renewal. Finally, interference of HH-GLI signaling with cyclopamine or through lentiviral-mediated silencing demonstrates that the tumorigenicity of human gliomas in mice requires an active pathway. Our results reveal the essential role of HH-GLI signaling in controlling the behavior of human glioma cancer stem cells and offer new therapeutic possibilities.
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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
                08 November 2019
                2019
                : 10
                : 1103
                Affiliations
                [1] 1Developmental Biomedical Science, Division of Biological Sciences, Nara Institute of Science and Technology , Ikoma, Japan
                [2] 2Systems Neurobiology and Medicine, Division of Biological Sciences, Nara Institute of Science and Technology , Ikoma, Japan
                [3] 3Department of Biomedical Chemistry, School of Science and Technology, Kwansei Gakuin University , Sanda, Japan
                [4] 4Division of Stem Cell Biology, Institute for Genetic Medicine, Hokkaido University , Sapporo, Japan
                Author notes

                Edited by: William Cho, Queen Elizabeth Hospital (QEH), Hong Kong

                Reviewed by: Alain-Pierre Gadeau, Institut National de la Santé et de la Recherche Médicale (INSERM), France; Kulbhushan Sharma, Institute of Nuclear Medicine & Allied Sciences (DRDO), India

                *Correspondence: Noriaki Sasai, noriakisasai@ 123456bs.naist.jp ; Michinori Toriyama, toriyama@ 123456kwansei.ac.jp ; Toru Kondo, tkondo@ 123456igm.hokudai.ac.jp

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

                Article
                10.3389/fgene.2019.01103
                6856222
                13627cdb-204e-4e12-bf56-004d49b27687
                Copyright © 2019 Sasai, Toriyama and Kondo

                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
                : 15 April 2019
                : 11 October 2019
                Page count
                Figures: 1, Tables: 2, Equations: 0, References: 308, Pages: 23, Words: 11395
                Categories
                Genetics
                Review

                Genetics
                sonic hedgehog (shh),development,genetic disease,mouse model,ciliopathies,cancer
                Genetics
                sonic hedgehog (shh), development, genetic disease, mouse model, ciliopathies, cancer

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