2000
DOI: 10.1002/1097-0045(20000901)44:4<265::aid-pros1>3.3.co;2-9
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Distinction between intraductal carcinoma of the prostate (IDC‐P), high‐grade dysplasia (PIN), and invasive prostatic adenocarcinoma, using molecular markers of cancer progression

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Cited by 23 publications
(39 citation statements)
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“…[6][7][8][9][10][11][12] The concept of ductal adenocarcinoma as a specific entity has been challenged, most recently by Bock and Bostwick. 13 In a study utilizing LOH analysis of 12 polymorphic microsatellite markers, frequently lost in prostate cancer, Dawkins et al 14 reported LOH in none of the Gleason grade 3 tumors studied, 9% of high-grade prostatic intraepithelial neoplasia (HGPIN) lesions, 29% of Gleason grade 4 cancers and 60% of ductal adenocarcinomas, suggesting that these are in fact a different lesion.…”
Section: Prostatic Ductal Adenocarcinomamentioning
confidence: 99%
“…[6][7][8][9][10][11][12] The concept of ductal adenocarcinoma as a specific entity has been challenged, most recently by Bock and Bostwick. 13 In a study utilizing LOH analysis of 12 polymorphic microsatellite markers, frequently lost in prostate cancer, Dawkins et al 14 reported LOH in none of the Gleason grade 3 tumors studied, 9% of high-grade prostatic intraepithelial neoplasia (HGPIN) lesions, 29% of Gleason grade 4 cancers and 60% of ductal adenocarcinomas, suggesting that these are in fact a different lesion.…”
Section: Prostatic Ductal Adenocarcinomamentioning
confidence: 99%
“…Prostate cancer arises from multiple genetic and epigenetic aberrations (7). Common aberrations in human prostate cancer are reduced expression of pRb (8) and frequent inactivation of phosphatase and tensin homologue (PTEN; ref.…”
Section: Introductionmentioning
confidence: 99%
“…A number of clinic tests, including the measurement of the serum level of prostate specific antigen (PSA), MRI, and gene expression profiling, are increasingly used in the clinic, whereas none of those could predict which of the PIN lesions will progress [24][25][26][27][28][29]. The only established approach to monitor PIN progression is repeat biopsy [25][26][27][28][29], which is costly and painful.…”
Section: Focal Basal Cell Alterations and Disruptions In Tumor Capsulesmentioning
confidence: 99%
“…The only established approach to monitor PIN progression is repeat biopsy [25][26][27][28][29], which is costly and painful. Since over 90% of prostate cancer related mortality result from invasion-related illnesses, and the incidence of PIN could be up to 16.5%-25% in routine or ultrasound guided prostate biopsies [25][26][27][28][29], there is an urgent need to uncover the intrinsic mechanism of tumor invasion, and to develop novel approaches to identify the specific precursor of invasive prostate lesions.…”
Section: Focal Basal Cell Alterations and Disruptions In Tumor Capsulesmentioning
confidence: 99%