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Abstract A23: Insulin-like growth factor 2 mRNA binding protein 1 (IGF2BP1) drives growth, metastasis and chemoresistance in human and canine osteosarcoma

Authors :
Brian T. Kalet
Deanna D. Dailey
Liza E. Pfaff
Dawn L. Duval
Source :
Molecular Cancer Research. 12:A23-A23
Publication Year :
2014
Publisher :
American Association for Cancer Research (AACR), 2014.

Abstract

Osteosarcoma (OSA) is the most common bone tumor in children. Dose intensive therapies have resulted in survival rates of 75%, however for patients with metastasis at diagnosis, the survival rate is only 20%, indicating the need for improved therapeutic strategies for metastatic osteosarcoma. Unfortunately, the availability of human OSA samples for study is extremely limited; however, over 10,000 canine patients spontaneously develop OSA annually and canine tumors share common histological features, genetic mutations and gene expression profiles with human OSA. To identify factors that contribute to metastasis and chemotherapeutic resistance of OSA, we assessed the gene expression signatures of normal bone and groups of primary canine OSA tumors surgically resected from dogs with short (300 day) disease free intervals (DFI) following standard treatment. Insulin-like growth factor 2 mRNA binding protein 1 (IGF2BP1) was identified as a negative prognostic indicator in this canine OSA study. IGF2BP1 is an oncofetal protein that binds multiple RNA targets to regulate their nuclear transport, stability, translation and subcellular localization. We have further investigated the role of IGF2BP1 in the development and metastatic progression of both human and canine osteosarcoma. IGF2BP1 transcripts were virtually undetectable on microarray analysis of normal bone and up-regulated greater-than 65-fold in both canine tumor groups relative to normal bone. RT-qPCR analysis validated these findings demonstrating a stair-step pattern of expression in which normal bone had virtually no IGF2BP1 expression, and IGF2BP1 expression was elevated 132-fold and 915-fold compared to normal bone in the long and short DFI tumor groups, respectively. Array CGH analysis revealed no genomic amplification of the IGF2BP1 locus, but 3′ UTR truncation may contribute to increased IGF2BP1 mRNA half-life. Similarly, human osteosarcoma cell lines, on average, expressed 14-fold higher levels of IGF2BP1 transcripts compared to human osteoblasts. Further, in the MG63.2 cell line, a metastatic variant of the MG63 human OSA cell line, we measured elevated mRNA transcripts (five-fold, p=0.0368) and protein levels (seven-fold), implicating IGF2BP1 in metastasis of osteosarcoma. IGF2BP1 knockdown in shRNA-expressing MG63.2 clones resulted in a three-fold (p Citation Format: Liza E. Pfaff, Brian T. Kalet, Deanna D. Dailey, Dawn L. Duval. Insulin-like growth factor 2 mRNA binding protein 1 (IGF2BP1) drives growth, metastasis and chemoresistance in human and canine osteosarcoma. [abstract]. In: Proceedings of the AACR Special Conference: The Translational Impact of Model Organisms in Cancer; Nov 5-8, 2013; San Diego, CA. Philadelphia (PA): AACR; Mol Cancer Res 2014;12(11 Suppl):Abstract nr A23.

Details

ISSN :
15573125 and 15417786
Volume :
12
Database :
OpenAIRE
Journal :
Molecular Cancer Research
Accession number :
edsair.doi...........aada8bfb0594a39a7f8e5f787eec3654