Literature DB >> 26931459

How Research on Human Progeroid and Antigeroid Syndromes Can Contribute to the Longevity Dividend Initiative.

Fuki M Hisama1, Junko Oshima2, George M Martin3.   

Abstract

Although translational applications derived from research on basic mechanisms of aging are likely to enhance health spans and life spans for most of us (the longevity dividend), there will remain subsets of individuals with special vulnerabilities. Medical genetics is a discipline that describes such "private" patterns of aging and can reveal underlying mechanisms, many of which support genomic instability as a major mechanism of aging. We review examples of three classes of informative disorders: "segmental progeroid syndromes" (those that appear to accelerate multiple features of aging), "unimodal progeroid syndromes" (those that impact on a single disorder of aging), and "unimodal antigeroid syndromes," variants that provide enhanced protection against specific disorders of aging; we urge our colleagues to expand our meager research efforts on the latter, including ancillary somatic cell genetic approaches.
Copyright © 2016 Cold Spring Harbor Laboratory Press; all rights reserved.

Entities:  

Mesh:

Year:  2016        PMID: 26931459      PMCID: PMC4817739          DOI: 10.1101/cshperspect.a025882

Source DB:  PubMed          Journal:  Cold Spring Harb Perspect Med        ISSN: 2157-1422            Impact factor:   6.915


  163 in total

1.  Spartan/C1orf124, a reader of PCNA ubiquitylation and a regulator of UV-induced DNA damage response.

Authors:  Richard C Centore; Stephanie A Yazinski; Alice Tse; Lee Zou
Journal:  Mol Cell       Date:  2012-06-08       Impact factor: 17.970

Review 2.  Genome-wide significant loci: how important are they? Systems genetics to understand heritability of coronary artery disease and other common complex disorders.

Authors:  Johan L M Björkegren; Jason C Kovacic; Joel T Dudley; Eric E Schadt
Journal:  J Am Coll Cardiol       Date:  2015-03-03       Impact factor: 24.094

Review 3.  Genetics of Alzheimer's disease.

Authors:  Vincent Chouraki; Sudha Seshadri
Journal:  Adv Genet       Date:  2014       Impact factor: 1.944

4.  DNA damage responses in progeroid syndromes arise from defective maturation of prelamin A.

Authors:  Yiyong Liu; Antonio Rusinol; Michael Sinensky; Youjie Wang; Yue Zou
Journal:  J Cell Sci       Date:  2006-10-24       Impact factor: 5.285

Review 5.  A polygenic model of inherited predisposition to cancer.

Authors:  T A Dragani; F Canzian; M A Pierotti
Journal:  FASEB J       Date:  1996-06       Impact factor: 5.191

6.  Men born in 1913 followed to age 100 years.

Authors:  Lars Wilhelmsen; Mikael Dellborg; Lennart Welin; Kurt Svärdsudd
Journal:  Scand Cardiovasc J       Date:  2015-02-11       Impact factor: 1.589

Review 7.  Dissecting the Mechanisms Underlying Unusually Successful Human Health Span and Life Span.

Authors:  Sofiya Milman; Nir Barzilai
Journal:  Cold Spring Harb Perspect Med       Date:  2015-12-04       Impact factor: 6.915

Review 8.  The multifaceted nature of amyloid precursor protein and its proteolytic fragments: friends and foes.

Authors:  Hoang S Nhan; Karen Chiang; Edward H Koo
Journal:  Acta Neuropathol       Date:  2014-10-07       Impact factor: 17.088

9.  Mutations in SPRTN cause early onset hepatocellular carcinoma, genomic instability and progeroid features.

Authors:  Davor Lessel; Bruno Vaz; Swagata Halder; Paul J Lockhart; Ivana Marinovic-Terzic; Jaime Lopez-Mosqueda; Melanie Philipp; Joe C H Sim; Katherine R Smith; Judith Oehler; Elisa Cabrera; Raimundo Freire; Kate Pope; Amsha Nahid; Fiona Norris; Richard J Leventer; Martin B Delatycki; Gotthold Barbi; Simon von Ameln; Josef Högel; Marina Degoricija; Regina Fertig; Martin D Burkhalter; Kay Hofmann; Holger Thiele; Janine Altmüller; Gudrun Nürnberg; Peter Nürnberg; Melanie Bahlo; George M Martin; Cora M Aalfs; Junko Oshima; Janos Terzic; David J Amor; Ivan Dikic; Kristijan Ramadan; Christian Kubisch
Journal:  Nat Genet       Date:  2014-09-28       Impact factor: 38.330

10.  Diagnosis of fanconi anemia: chromosomal breakage analysis.

Authors:  Anneke B Oostra; Aggie W M Nieuwint; Hans Joenje; Johan P de Winter
Journal:  Anemia       Date:  2012-05-24
View more
  12 in total

1.  Lack of resemblance between Myhre syndrome and other "segmental progeroid" syndromes warrants restraint in applying this classification.

Authors:  Angela E Lin; Nicola Brunetti-Pierri; Bert Callewaert; Valérie Cormier-Daire; Sofia Douzgou; T Bernard Kinane; Mark E Lindsay; Lois J Starr
Journal:  Geroscience       Date:  2021-02-25       Impact factor: 7.713

Review 2.  Review of How Genetic Research on Segmental Progeroid Syndromes Has Documented Genomic Instability as a Hallmark of Aging But Let Us Now Pursue Antigeroid Syndromes!

Authors:  George M Martin; Fuki M Hisama; Junko Oshima
Journal:  J Gerontol A Biol Sci Med Sci       Date:  2021-01-18       Impact factor: 6.053

Review 3.  Peptide Hormone Regulation of DNA Damage Responses.

Authors:  Vera Chesnokova; Shlomo Melmed
Journal:  Endocr Rev       Date:  2020-07-01       Impact factor: 19.871

Review 4.  Geroscience: Addressing the mismatch between its exciting research opportunities, its economic imperative and its current funding crisis.

Authors:  George M Martin
Journal:  Exp Gerontol       Date:  2016-11-19       Impact factor: 4.032

5.  SMAD4 mutations and cross-talk between TGF-β/IFNγ signaling accelerate rates of DNA damage and cellular senescence, resulting in a segmental progeroid syndrome-the Myhre syndrome.

Authors:  Renuka Kandhaya-Pillai; Deyin Hou; Jiaming Zhang; Xiaomeng Yang; Goli Compoginis; Takayasu Mori; Tamara Tchkonia; George M Martin; Fuki M Hisama; James L Kirkland; Junko Oshima
Journal:  Geroscience       Date:  2021-01-05       Impact factor: 7.713

6.  Ageing: Dietary protection for genes.

Authors:  Junko Oshima; George M Martin
Journal:  Nature       Date:  2016-08-24       Impact factor: 49.962

Review 7.  WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects.

Authors:  Koutaro Yokote; Sirisak Chanprasert; Lin Lee; Katharina Eirich; Minoru Takemoto; Aki Watanabe; Naoko Koizumi; Davor Lessel; Takayasu Mori; Fuki M Hisama; Paula D Ladd; Brad Angle; Hagit Baris; Kivanc Cefle; Sukru Palanduz; Sukru Ozturk; Antoinette Chateau; Kentaro Deguchi; T K M Easwar; Antonio Federico; Amy Fox; Theresa A Grebe; Beverly Hay; Sheela Nampoothiri; Karen Seiter; Elizabeth Streeten; Raul E Piña-Aguilar; Gemma Poke; Martin Poot; Renata Posmyk; George M Martin; Christian Kubisch; Detlev Schindler; Junko Oshima
Journal:  Hum Mutat       Date:  2016-10-07       Impact factor: 4.878

8.  Biallelic WRN Mutations in Newly Identified Japanese Werner Syndrome Patients.

Authors:  Yoshiro Maezawa; Hisaya Kato; Minoru Takemoto; Aki Watanabe; Masaya Koshizaka; Takahiro Ishikawa; Forough Sargolzaeiaval; Masafumi Kuzuya; Hiroshi Wakabayashi; Takashi Kusaka; Koutaro Yokote; Junko Oshima
Journal:  Mol Syndromol       Date:  2018-05-15

Review 9.  Mutations Involved in Premature-Ageing Syndromes.

Authors:  Fabio Coppedè
Journal:  Appl Clin Genet       Date:  2021-06-02

10.  Accelerated epigenetic aging in Werner syndrome.

Authors:  Anna Maierhofer; Julia Flunkert; Junko Oshima; George M Martin; Thomas Haaf; Steve Horvath
Journal:  Aging (Albany NY)       Date:  2017-04       Impact factor: 5.682

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.