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RETRACTED ARTICLE: Frequency of TP53 Mutations and its Impact on Drug Sensitivity in Acute Myeloid Leukemia?

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Indian Journal of Clinical Biochemistry Aims and scope Submit manuscript

This article was retracted on 04 February 2014

Abstract

The purpose of this study is to find out the frequency of TP53 mutations in acute myeloid leukemia (AML) patients and correlate sensitivity of drug response with TP53 mutations. In AML more than 90 % of cases comprise of wild type TP53. 94.2 % of TP53 mutations are found within exon 5–8 of which 73 % are point mutations. TP53 mutations were analysed with high resolution melting curve analysis. We analysed 106 AML samples of which we found nine mutations which represents 8.5 % mutation rate and found one rare SNP. The effect of TP53 mutations were studied on the chemosensitivity of two new drugs AZD115 and RHPS4, an Aurora Kinase B inhibitor and Telomerase inhibitor respectively. Four mutations were found out of 17 for RHPS4 stating significant (p = 0.002) increase in sensitivity and no mutation found in AZD1152 database, but need more study to get definite conclusion.

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Acknowledgments

I thank my supervisor Dr Claire Seedhouse (Haematology department, city hospital) for support and help during the entire project and Martin Grundy for providing drug database. I am obliged to all my colleagues and my family who supported me to accomplish my project successfully.

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Correspondence to Ankur Shah.

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This article has been retracted at the request of the second author of the paper, Claire Seedhouse, whose name was included in the paper without her permission. Further, the data in the paper has been published without any approvals from the department or the institution, where the corresponding author, Ankur Shah, was working at the time of submitting this paper.

An erratum to this article is available at http://dx.doi.org/10.1007/s12291-014-0422-8.

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Shah, A., Seedhouse, C. RETRACTED ARTICLE: Frequency of TP53 Mutations and its Impact on Drug Sensitivity in Acute Myeloid Leukemia?. Ind J Clin Biochem 27, 121–126 (2012). https://doi.org/10.1007/s12291-012-0203-1

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  • DOI: https://doi.org/10.1007/s12291-012-0203-1

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