| Literature DB >> 24600558 |
Houda Saadi1, Marion Seillier2, Maria José Sandi2, Sylvain Peuget2, Christine Kellenberger3, Gwenaëlle Gravis4, Nelson J Dusetti2, Juan L Iovanna2, Palma Rocchi2, Mohamed Amri5, Alice Carrier2.
Abstract
Tumor Protein 53-Induced Nuclear Protein 1 (TP53INP1) plays an important role during cell stress response in synergy with the potent "genome-keeper" p53. In human, the gene encoding TP53INP1 is expressed at very high level in some pathological situations, such as inflammation and prostate cancer (PC). TP53INP1 overexpression in PC seems to be a worse prognostic factor, particularly predictive of biological cancer relapse, making TP53INP1 a relevant specific target for molecular therapy of Castration Resistant (CR) PC. In that context, detection of TP53INP1 in patient biological fluids is a promising diagnostic avenue. We report here successful development of a new Enzyme-Linked Immunosorbent Assay (ELISA) detecting TP53INP1, taking advantage of molecular tools (monoclonal antibodies (mAbs) and recombinant proteins) generated in the laboratory during the course of basic functional investigations devoted to TP53INP1. The ELISA principle is based on a sandwich immunoenzymatic system, TP53INP1 protein being trapped by a first specific mAb coated on microplate then recognized by a second specific mAb. This new assay allows specific detection of TP53INP1 in serum of several PC patients. This breakthrough paves the way towards investigation of a large cohort of patients and assessment of clinical applications of TP53INP1 dosage.Entities:
Keywords: Biomarker; CR PC, castration resistant prostate cancer; ELISA; ELISA, enzyme-linked immunosorbent assay; HRP, horse radish peroxydase; Prostate cancer; SFM, serum free medium; TP53INP1; TP53INP1, tumor protein 53-induced nuclear protein 1; aa, amino acid; p53
Year: 2013 PMID: 24600558 PMCID: PMC3908328 DOI: 10.1016/j.rinim.2013.05.002
Source DB: PubMed Journal: Results Immunol ISSN: 2211-2839