Literature DB >> 35523998

Components of IGF-axis in growth disorders: a systematic review and patent landscape report.

Amit Singh1, Ketan Pajni2, Inusha Panigrahi3, Navdeep Dhoat4, Sabyasachi Senapati2, Preeti Khetarpal5.   

Abstract

PURPOSE: In this review, epi/genetic mutations of IGF-axis components associated with growth disorders have been summarized alongwith assessment of relevant diagnostic and therapeutic technology through patent literature.
METHODOLOGY: PROSPERO protocol registration CRD42021279468. For scientific literature search Literature databases (PubMed, EMBASE, ScienceDirect, and Google Scholar) were queried using the appropriate syntax. Various filters were applied based on inclusion and exclusion criteria. Search results were further refined by two authors for finalizing studies to be included in this synthesis. For patent documents search Patent databases (Patentscope and Espacenet) were queried using keywords: IGF or IGFBP. Filters were applied according to International Patent Classification (IPC) and Cooperative Patent Classification (CPC). Search results were reviewed by two authors for inclusion in the patent landscape report.
RESULTS: For scientific literature analysis, out of 545 search results, 196 were selected for review based on the inclusion criteria. For Patent literature search, out of 485 results, 37 were selected for this synthesis.
CONCLUSION: Dysregulation of IGF-axis components leads to various abnormalities and their key role in growth and development suggests epi/mutations or structural defects among IGF-axis genes can be associated with growth disorders and may explain some of the idiopathic short stature cases. Trend of patent filings indicate advent of recombinant technology for therapeutics.
© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Diagnosis; Growth disorders; Insulin-like growth factors; Patent; Therapeutics

Mesh:

Substances:

Year:  2022        PMID: 35523998     DOI: 10.1007/s12020-022-03063-2

Source DB:  PubMed          Journal:  Endocrine        ISSN: 1355-008X            Impact factor:   3.925


  69 in total

1.  A heterozygous mutation of the insulin-like growth factor-I receptor causes retention of the nascent protein in the endoplasmic reticulum and results in intrauterine and postnatal growth retardation.

Authors:  Tillmann Wallborn; Stefan Wüller; Jürgen Klammt; Tassilo Kruis; Jürgen Kratzsch; Gabriele Schmidt; Marina Schlicke; Eva Müller; Hildegard Schmitz van de Leur; Wieland Kiess; Roland Pfäffle
Journal:  J Clin Endocrinol Metab       Date:  2010-03-31       Impact factor: 5.958

2.  Fanconi Anemia and Laron Syndrome.

Authors:  Inma Castilla-Cortazar; Julieta Rodriguez de Ita; Gabriel Amador Aguirre; Fabiola Castorena-Torres; Jesús Ortiz-Urbina; Mariano García-Magariño; Rocío García de la Garza; Carlos Diaz Olachea; Martha Irma Elizondo Leal
Journal:  Am J Med Sci       Date:  2017-02-04       Impact factor: 2.378

3.  Uniparental disomy and pretreatment IGF-1 may predict elevated IGF-1 levels in Prader-Willi patients on GH treatment.

Authors:  Viviana Valeria Palmieri; Antonella Lonero; Sarah Bocchini; Gilda Cassano; Alessio Convertino; Domenico Corica; Antonio Crinò; Valentina Fattorusso; Silvio Ferraris; Danilo Fintini; Adriana Franzese; Graziano Grugni; Lorenzo Iughetti; Rosanna Lia; Francesca Macchi; Simona Filomena Madeo; Patrizia Matarazzo; Luana Nosetti; Sara Osimani; Roberta Pajno; Giuseppa Patti; Maria Chiara Pellegrin; Annamaria Perri; Letizia Ragusa; Irene Rutigliano; Michele Sacco; Alessandro Salvatoni; Emanuela Scarano; Stefano Stagi; Gianluca Tornese; Giuliana Trifirò; Malgorzata Wasniewska; Rita Fischetto; Paola Giordano; Maria Rosaria Licenziati; Maurizio Delvecchio
Journal:  Growth Horm IGF Res       Date:  2019-08-28       Impact factor: 2.372

4.  Adult height and epigenotype in children with Silver-Russell syndrome treated with GH.

Authors:  G Binder; M Liebl; J Woelfle; T Eggermann; G Blumenstock; R Schweizer
Journal:  Horm Res Paediatr       Date:  2013-09-18       Impact factor: 2.852

Review 5.  Insulin-like growth factor (IGF) axis in cancerogenesis.

Authors:  Aldona Kasprzak; Wojciech Kwasniewski; Agnieszka Adamek; Anna Gozdzicka-Jozefiak
Journal:  Mutat Res Rev Mutat Res       Date:  2016-09-04       Impact factor: 5.657

6.  A New Homozygous IGF1R Variant Defines a Clinically Recognizable Incomplete Dominant form of SHORT Syndrome.

Authors:  Paolo Prontera; Lucia Micale; Alberto Verrotti; Valerio Napolioni; Gabriela Stangoni; Giuseppe Merla
Journal:  Hum Mutat       Date:  2015-08-24       Impact factor: 4.878

Review 7.  The GH/IGF-1 axis in ageing and longevity.

Authors:  Riia K Junnila; John J Kopchick; Edward O List; Darlene E Berryman; John W Murrey
Journal:  Nat Rev Endocrinol       Date:  2013-04-16       Impact factor: 43.330

8.  Identification of a novel heterozygous IGF1 splicing mutation in a large kindred with familial short stature.

Authors:  John S Fuqua; Michael Derr; Ron G Rosenfeld; Vivian Hwa
Journal:  Horm Res Paediatr       Date:  2012-07-20       Impact factor: 2.852

9.  Mosaic uniparental disomy in Beckwith-Wiedemann syndrome.

Authors:  R E Slatter; M Elliott; K Welham; M Carrera; P N Schofield; D E Barton; E R Maher
Journal:  J Med Genet       Date:  1994-10       Impact factor: 6.318

10.  Hemizygosity at the insulin-like growth factor I receptor (IGF1R) locus and growth failure in the ring chromosome 15 syndrome.

Authors:  R Peoples; A Milatovich; U Francke
Journal:  Cytogenet Cell Genet       Date:  1995
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