Literature DB >> 10918395

Decreased expression of the INK4 family of cyclin-dependent kinase inhibitors in Wilms tumor.

M Y Arcellana-Panlilio1, R M Egeler, E Ujack, A Pinto, D J Demetrick, S M Robbins, M J Coppes.   

Abstract

Cyclin-dependent kinase (CDK) inhibitors represented by the INK4 family (including p16(INK4a, CDKN2A), p15(INK4b, CDKN2B), p18(INK4c, CDKN2C), and p19(INK4d, CDKN2D)) are regulators of the cell cycle shown to be aberrant in many types of human cancer. We tested the hypothesis that these CDK inhibitors are a target for altered gene expression in Wilms tumor. Using RT-PCR, gene expression of the INK4 family was found to be decreased in 9 of 38 Wilms tumor samples obtained from the National Wilms Tumor Study Group (NWTSG) tissue bank. All the affected tumor samples were of favorable histology. Methylation-specific PCR revealed that methylation in the p16 promoter region may be responsible for altered expression. The incidence of loss of p16 expression may increase with increasing tumor stage, i.e., 1/10 (10%) with stage I/II FH Wilms tumor, 2/10 (20%) with stage III FH Wilms tumor, and 4/10 (40%) with stage IV FH Wilms tumor. Thus, determining the expression status of the INK4 family may have potential prognostic value in the management of Wilms tumor. Copyright 2000 Wiley-Liss, Inc.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 10918395     DOI: 10.1002/1098-2264(2000)9999:9999<::aid-gcc1006>3.0.co;2-l

Source DB:  PubMed          Journal:  Genes Chromosomes Cancer        ISSN: 1045-2257            Impact factor:   5.006


  5 in total

1.  Correlations between histological characterizations and methylation statuses of tumour suppressor genes in Wilms' tumours.

Authors:  Yen-Chein Lai; Meng-Yao Lu; Wen-Chung Wang; Tai-Cheng Hou; Chen-Yun Kuo
Journal:  Int J Exp Pathol       Date:  2022-04-18       Impact factor: 2.793

2.  The IGF signalling pathway in Wilms tumours--a report from the ENCCA Renal Tumours Biology-driven drug development workshop.

Authors:  Mariana Maschietto; Jocelyn Charlton; Daniela Perotti; Paolo Radice; James I Geller; Kathy Pritchard-Jones; Mark Weeks
Journal:  Oncotarget       Date:  2014-09-30

3.  SLIT2 promoter methylation analysis in neuroblastoma, Wilms' tumour and renal cell carcinoma.

Authors:  D Astuti; N F Da Silva; A Dallol; D Gentle; T Martinsson; P Kogner; R Grundy; T Kishida; M Yao; F Latif; E R Maher
Journal:  Br J Cancer       Date:  2004-01-26       Impact factor: 7.640

4.  Distinct clinicopathological features in metanephric adenoma harboring BRAF mutation.

Authors:  Anna Caliò; John N Eble; Ondrej Hes; Guido Martignoni; Saul E Harari; Sean R Williamson; Matteo Brunelli; Adeboye O Osunkoya; Lisha Wang; Eva Comperat; Antonio Lopez-Beltran; Mingsheng Wang; Shaobo Zhang; Kendra L Curless; Kristin M Post; Hsim-Yee Chang; Claudio Luchini; Lee Ann Baldrige; Gregory T MacLennan; Rodolfo Montironi; David J Grignon; Liang Cheng
Journal:  Oncotarget       Date:  2016-08-08

5.  Genetic and epigenetic analyses guided by high resolution whole-genome SNP array reveals a possible role of CHEK2 in Wilms tumour susceptibility.

Authors:  Sara Ciceri; Beatrice Gamba; Paola Corbetta; Patrizia Mondini; Monica Terenziani; Serena Catania; Marilina Nantron; Maurizio Bianchi; Paolo D'Angelo; Federica Torri; Fabio Macciardi; Paola Collini; Martina Di Martino; Fraia Melchionda; Andrea Di Cataldo; Filippo Spreafico; Paolo Radice; Daniela Perotti
Journal:  Oncotarget       Date:  2018-09-25
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.