Literature DB >> 19148905

The insulin-like growth factor system and sarcomas.

Bart Rikhof1, Steven de Jong, Albert J H Suurmeijer, Coby Meijer, Winette T A van der Graaf.   

Abstract

Sarcomas are a diverse group of malignant mesenchymal tumours arising from bone and soft tissues. The identification of critical cellular signalling pathways in sarcomas is an important issue for the development of new targeted therapies. This review highlights the experimental and clinical evidence supporting the role of the insulin-like growth factor (IGF) signalling system in the cellular transformation and progression of several types of sarcoma, including rhabdomyosarcoma, synovial sarcoma, leiomyosarcoma, Ewing's sarcoma and osteosarcoma. Preclinical data suggest that the IGF system could be a promising target for therapy in these sarcomas. Currently, therapies interrupting IGF signalling have been or are being developed. In recent phase 1 clinical studies with humanized monoclonal antibodies directed against IGF receptor type 1 (IGF-1R), objective tumour responses were observed in several patients with Ewing's sarcoma, encouraging further clinical testing in Ewing's sarcoma and other sarcoma (sub)types. Moreover, the occasional occurrence of paraneoplastic hypoglycaemia as a result of the secretion of incompletely processed forms of pro-IGF-II by sarcomas is discussed.

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Year:  2009        PMID: 19148905     DOI: 10.1002/path.2499

Source DB:  PubMed          Journal:  J Pathol        ISSN: 0022-3417            Impact factor:   7.996


  63 in total

1.  Systematic therapy for unresectable or metastatic soft-tissue sarcomas: past, present, and future.

Authors:  Sherif S Morgan; Lee D Cranmer
Journal:  Curr Oncol Rep       Date:  2011-08       Impact factor: 5.075

Review 2.  Soft tissue sarcomas in children.

Authors:  Gauri Kapoor; Kunal Das
Journal:  Indian J Pediatr       Date:  2011-09-21       Impact factor: 1.967

Review 3.  Small is beautiful: insulin-like growth factors and their role in growth, development, and cancer.

Authors:  Robert G Maki
Journal:  J Clin Oncol       Date:  2010-10-25       Impact factor: 44.544

4.  A set of imprinted genes required for normal body growth also promotes growth of rhabdomyosarcoma cells.

Authors:  Geoffrey Rezvani; Julian C K Lui; Kevin M Barnes; Jeffrey Baron
Journal:  Pediatr Res       Date:  2012-01       Impact factor: 3.756

Review 5.  A review of treatment of uterine leiomyosarcomas.

Authors:  Nicholas Reed
Journal:  Curr Oncol Rep       Date:  2013-12       Impact factor: 5.075

6.  Prognostic and therapeutic relevance of the IGF pathway in Ewing's sarcoma patients.

Authors:  A C M van de Luijtgaarden; Y M H Versleijen-Jonkers; M H S Roeffen; H W B Schreuder; U E Flucke; W T A van der Graaf
Journal:  Target Oncol       Date:  2013-01-06       Impact factor: 4.493

7.  Specific glycogen synthase kinase-3 inhibition reduces neuroendocrine markers and suppresses neuroblastoma cell growth.

Authors:  Yvette M Carter; Selvi Kunnimalaiyaan; Herbert Chen; T Clark Gamblin; Muthusamy Kunnimalaiyaan
Journal:  Cancer Biol Ther       Date:  2014-02-12       Impact factor: 4.742

Review 8.  Osteoblast dysfunctions in bone diseases: from cellular and molecular mechanisms to therapeutic strategies.

Authors:  Pierre J Marie
Journal:  Cell Mol Life Sci       Date:  2014-12-09       Impact factor: 9.261

9.  High IGF2 and FGFR3 are associated with tumour progression in undifferentiated pleomorphic sarcomas, but EGFR and FGFR3 mutations are a rare event.

Authors:  Katinka Rüping; Annelore Altendorf-Hofmann; Yuan Chen; Eric Kampmann; Sebastian Gibis; Lars Lindner; Detlef Katenkamp; Iver Petersen; Thomas Knösel
Journal:  J Cancer Res Clin Oncol       Date:  2014-05-08       Impact factor: 4.553

10.  Epigenetic features of human mesenchymal stem cells determine their permissiveness for induction of relevant transcriptional changes by SYT-SSX1.

Authors:  Luisa Cironi; Paolo Provero; Nicola Riggi; Michalina Janiszewska; Domizio Suva; Mario-Luca Suva; Vincent Kindler; Ivan Stamenkovic
Journal:  PLoS One       Date:  2009-11-19       Impact factor: 3.240

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