Literature DB >> 12171773

Mutations in the p53 gene in acute myeloid leukemia patients correlate with poor prognosis.

Mônica B Melo1, Nilofer N Ahmad, Carmen S P Lima, Katia B B Pagnano, Silvana Bordin, Irene Lorand-Metze, Sara T O SaAd, Fernando F Costa.   

Abstract

Inactivation of tumor suppressor genes, whose products exert an inhibitory influence on cell cycle progression, can lead to neoplastic transformation. In acute myeloid leukemia (AML), the frequency of p53 gene mutations ranges from 4 to 15% in populations from USA and Europe. In an attempt to investigate the frequency of point mutations in the p53 gene in AML Brazilian patients, DNA samples of 35 patients were studied using PCR-SSCP techniques, screening exons 4-10. Mutations were identified in bone marrow DNA in 5 of the 35 AML patients (14.3%), a frequency similar to those reported for Northern American and European populations. The overall survival of patients with mutations in the p53 gene was significantly shorter than for patients without mutations.

Entities:  

Mesh:

Year:  2002        PMID: 12171773     DOI: 10.1080/10245330290020090

Source DB:  PubMed          Journal:  Hematology        ISSN: 1024-5332            Impact factor:   2.269


  4 in total

1.  NFκB regulates p21 expression and controls DNA damage-induced leukemic differentiation.

Authors:  Claudia M Nicolae; Michael J O'Connor; Daniel Constantin; George-Lucian Moldovan
Journal:  Oncogene       Date:  2018-04-06       Impact factor: 9.867

2.  Bridge-Induced Translocation between NUP145 and TOP2 Yeast Genes Models the Genetic Fusion between the Human Orthologs Associated With Acute Myeloid Leukemia.

Authors:  Valentina Tosato; Nicole West; Jan Zrimec; Dmitri V Nikitin; Giannino Del Sal; Roberto Marano; Michael Breitenbach; Carlo V Bruschi
Journal:  Front Oncol       Date:  2017-09-29       Impact factor: 6.244

Review 3.  Rational Combinations of Targeted Agents in AML.

Authors:  Prithviraj Bose; Steven Grant
Journal:  J Clin Med       Date:  2015-04-10       Impact factor: 4.964

4.  Selective activation of TNFR1 and NF-κB inhibition by a novel biyouyanagin analogue promotes apoptosis in acute leukemia cells.

Authors:  Christiana G Savva; Sotirios Totokotsopoulos; Kyriakos C Nicolaou; Christiana M Neophytou; Andreas I Constantinou
Journal:  BMC Cancer       Date:  2016-04-20       Impact factor: 4.430

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.