Research Topics
Genomes and Genes | Ishtiaq RehmanSummaryAffiliation: University of Sheffield Country: UK Publications
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Publications
iTRAQ identification of candidate serum biomarkers associated with metastatic progression of human prostate cancerIshtiaq Rehman
Department of Human Metabolism, The Medical School, The Mellanby Centre for Bone Research, University of Sheffield, Sheffield, United Kingdom
PLoS ONE 7:e30885. 2012..Our proteomic approach has identified leads for potentially useful serum biomarkers associated with the metastatic progression of prostate cancer. The panels identified, including eEF1A1 warrant further investigation and validation...
Promoter hyper-methylation of calcium binding proteins S100A6 and S100A2 in human prostate cancerIshtiaq Rehman
Academic Urology Unit, Division of Clinical Sciences South, University of Sheffield, United Kingdom, and Service d Urologie, Groupe Hospitalier Pitie Salpetriere, Paris, France
Prostate 65:322-30. 2005..S100A6 and S100A2 are members of the S100 family of calcium binding proteins, which are down regulated in prostate cancer, however the molecular mechanism(s) underlying their loss of expression is unknown...
DNA methylation and immunohistochemical analysis of the S100A4 calcium binding protein in human prostate cancerIshtiaq Rehman
Academic Urology Unit, Division of Clinical Sciences South, University of Sheffield, Sheffield, UK
Prostate 67:341-7. 2007..The role of DNA methylation in the transcriptional regulation of S100A4 is unknown in human prostate cancer...
S100A6 (Calcyclin) is a prostate basal cell marker absent in prostate cancer and its precursorsI Rehman
Academic Urology Unit, Division of Clinical Sciences South, University of Sheffield, Floor K, Royal Hallamshire Hospital, Glossop Road, Sheffield S10 2JF, UK
Br J Cancer 91:739-44. 2004..The finding of intense S100A6 expression in the basal cells of benign glands but loss of expression in cancer could be useful as a novel diagnostic marker for prostate cancer...
Eight-plex iTRAQ analysis of variant metastatic human prostate cancer cells identifies candidate biomarkers of progression: An exploratory studyAdam Glen
Department of Human Metabolism, The Mellanby Centre for Bone Research, University of Sheffield Medical School, Sheffield, UK
Prostate 70:1313-32. 2010..Due to the heterogeneity in the biological behavior of prostate cancer, biomarkers that can reliably distinguish indolent from aggressive disease are urgently needed to inform treatment choices...
Promoter hypermethylation is associated with tumor location, stage, and subsequent progression in transitional cell carcinomaJames W F Catto
Academic Urology Unit, K Floor, Royal Hallamshire Hospital, Glossop Rd, Sheffield, S10 2JF United Kingdom
J Clin Oncol 23:2903-10. 2005..Here we investigate the extent of promoter hypermethylation in TCC throughout the urinary tract...
Human prostate cancer cells express neuroendocrine cell markers PGP 9.5 and chromogranin AAaron Leiblich
Section of Oncology, Academic Urology Unit, University of Sheffield, Royal Hallamshire Hospital, Sheffield, UK
Prostate 67:1761-9. 2007..To identify novel candidates associated with metastatic progression, we compared the proteomic profiles of LNCaP (lymph-node metastatic, androgen-dependant) and PC-3 (bone metastatic, androgen-independent), human prostate cancer cells...
Promoter hypermethylation in circulating blood cells identifies prostate cancer progressionMorgan Roupret
Institute for Cancer Studies, University of Sheffield, Royal Hallamshire Hospital, Sheffield, United Kingdom
Int J Cancer 122:952-6. 2008..The extent of this hypermethylation increases during disease progression and can be used to identify the extent and duration of treatment response in prostate cancer...
iTRAQ-facilitated proteomic analysis of human prostate cancer cells identifies proteins associated with progressionAdam Glen
Academic Urology Unit, Section of Oncology, University of Sheffield, Floor K, Royal Hallamshire Hospital, Glossop Road, Sheffield, S10 2JF, UK
J Proteome Res 7:897-907. 2008..0005, Mann-Whitney U). Our study is the first to report the application of iTRAQ technology and its potential for the global proteomic profiling of prostate cancer cells, including the identification of absent protein expression...
Promoter hypermethylation identifies progression risk in bladder cancerDavid R Yates
Institute of Cancer Studies, Academic Urology Unit, Academic Pathology Unit, and Department of Automatic Control and Systems Engineering, The University of Sheffield, Sheffield, United Kingdom
Clin Cancer Res 13:2046-53. 2007..Here, we investigate a panel of methylated loci in a prospectively collected cohort of bladder tumors to determine whether hypermethylation has a useful role in the management of patients with bladder cancer...
Clinically localised prostate cancer is microsatellite stableAbdel Rahmene Azzouzi
Service d Urologie, CHU d Angers, Centre de Recherche pour les Pathologies Protatiques, Universite Paris VII, Paris, France, and Department of Pathology, Royal Hallamshire Hospital, Sheffield, UK
BJU Int 99:1031-5. 2007..To determine the frequency of microsatellite instability (MSI) change with mono-, di- and tetranucleotide markers in clinically localized prostate cancer, and to correlate those markers with clinical and pathological variables...
Dysregulated expression of S100A11 (calgizzarin) in prostate cancer and precursor lesionsIshtiaq Rehman
Academic Urology Unit, Division of Clinical Sciences South, University of Sheffield, UK
Hum Pathol 35:1385-91. 2004..Our finding of frequent dysregulated expression of S100A11 in cancer and precursor lesions, together with an association with high histological stage, suggests that S100A11 may be involved in prostate cancer development and progression...
Distinct microRNA alterations characterize high- and low-grade bladder cancerJames W F Catto
Academic Urology Unit, University of Sheffield, Sheffield, United Kingdom
Cancer Res 69:8472-81. 2009..In conclusion, distinct microRNA alterations characterize UCC and target genes in a pathway-specific manner. These data reveal new insights into the disease biology and have implications regarding tumor diagnosis, prognosis and therapy...
Evaluation of the frequency of putative prostate cancer stem cells in primary and metastatic prostate cancerColby L Eaton
School of Medicine, University of Sheffield, Sheffield, UK
Prostate 70:875-82. 2010..In this study we have, for the first time, assessed matched primary and bone marrow biopsies from prostate cancer patients for the distribution of cells carrying these and a number of other putative stem cell markers...
The application of artificial intelligence to microarray data: identification of a novel gene signature to identify bladder cancer progressionJames W F Catto
Academic Urology Unit, University of Sheffield, Sheffield, United Kingdom
Eur Urol 57:398-406. 2010..Gene expression microarrays can reveal insights into disease biology and identify novel biomarkers. However, these experiments produce large datasets that are difficult to interpret...
Molecular detection of localized prostate cancer using quantitative methylation-specific PCR on urinary cells obtained following prostate massageMorgan Roupret
Institute for Cancer Studies and Academic Urology Unit, University of Sheffield, Royal Hallamshire Hospital, Sheffield, UK
Clin Cancer Res 13:1720-5. 2007..Many patients require repeat prostate biopsies to diagnose the disease. We investigated whether aberrant promoter hypermethylation in prostatic fluid could reliably detect prostate cancer...
The antibody MAB8051 directed against osteoprotegerin detects carbonic anhydrase II: implications for association studies with human cancersElizabeth A Waterman
Academic Unit of Urology, School of Medicine and Biomedical Sciences, University of Sheffield, Beech Hill Road, Sheffield, S10 2RX, United Kingdom
Int J Cancer 121:1958-66. 2007..We conclude that care should be exercised using this antibody for immunohistochemistry studies, without additional in situ hybridisation, or parallel use of other OPG-specific antibodies...
Multifocal urothelial cancers with the mutator phenotype are of monoclonal origin and require panurothelial treatment for tumor clearanceJames W F Catto
Academic Urology Unit, University of Sheffield, Sheffield, United Kingdom
J Urol 175:2323-30. 2006..Tumors with high MSI have numerous DNA mutations, of which many provide no selection benefit. While these tumors represent an ideal model for studying UC clonality, their low frequency has prevented their previous investigation...
Distinct patterns of microsatellite instability are seen in tumours of the urinary tractJames W F Catto
The Institute for Cancer Studies, University of Sheffield, UK
Oncogene 22:8699-706. 2003..In addition, we have confirmed that MSI and EMAST are discrete forms of MSI, and that the presence of EMAST does not affect tumour phenotype...
Behavior of urothelial carcinoma with respect to anatomical locationJ W F Catto
Academic Urology Unit, University of Sheffield, Sheffield, United Kingdom
J Urol 177:1715-20. 2007..Observational studies conflict as to the significance of anatomical location on the behavior of urothelial carcinoma. We compared the biological outcome in a large series of urothelial carcinoma with respect to anatomical location...
Expression of S100 proteins in normal human tissues and common cancers using tissue microarrays: S100A6, S100A8, S100A9 and S100A11 are all overexpressed in common cancersS S Cross
Academic Unit of Pathology, Division of Genomic Medicine, School of Medicine and Biomedical Sciences, University of Sheffield, Sheffield, UK
Histopathology 46:256-69. 2005..S100A6, S100A8, S100A9 and S100A11 have all been suggested to have potential roles in carcinogenesis and tumour progression but their expression has not been described in a wide range of human tissues and tumours...
Lactate dehydrogenase-B is silenced by promoter hypermethylation in human prostate cancerA Leiblich
Academic Urology Unit, Division of Clinical Sciences South, University of Sheffield, UK
Oncogene 25:2953-60. 2006..001). Absent LDHB expression was also seen in 7/7 (100%) cases of metastatic cancer in bone. Our data are the first to show loss of LDHB expression in prostate cancer, the mechanism of which appears to involve promoter hypermethylation...
Evidence for the early onset of aberrant promoter methylation in urothelial carcinomaD Dhawan
Academic Urology Unit, University of Sheffield, and Department of Urology, Royal Hallamshire Hospital, UK
J Pathol 209:336-43. 2006..03). Promoter methylation occurs early in the urothelial carcinogenic pathway and appears to be a good biomarker of the invasive urothelial carcinoma phenotype...
iTRAQ underestimation in simple and complex mixtures: "the good, the bad and the ugly"Saw Yen Ow
ChELSI Institute, Chemical and Process Engineering, University of Sheffield, Mappin Street, S1 3JD Sheffield, United Kingdom
J Proteome Res 8:5347-55. 2009..In light of our results, we propose a list of advice for iTRAQ data analysis that could routinely ameliorate quantitative interpretation of proteomic data sets...
Proteomic analysis of voided urine after prostatic massage from patients with prostate cancer: a pilot studyI Rehman
Academic Urology Unit, Division of Clinical Sciences (South, University of Sheffield, Sheffield, United Kingdom
Urology 64:1238-43. 2004..CONCLUSIONS: The role of urinary calgranulin B/MRP-14 as a potential novel marker for prostate cancer needs additional investigation...
Methylational urinalysis: a prospective study of bladder cancer patients and age stratified benign controlsD R Yates
Institute for Cancer Studies, University of Sheffield, Royal Hallamshire Hospital, Sheffield, UK
Oncogene 25:1984-8. 2006..The frequency and extent of methylation appears to increase with age and malignancy. The lack of tumour specificity suggests that further investigation is required before this test is introduced into clinical practice...
Methylation of the O6-methylguanine-DNA methyltransferase promoter suppresses expression in mouse skin tumors and varies with the tumor induction protocolRana Abdel-Fattah
Laboratory of Cellular Carcinogenesis and Tumor Promotion, National Cancer Institute, NIH, Bethesda, MD 20892, USA
Int J Cancer 118:527-31. 2006....
