2013
DOI: 10.1016/j.eururo.2013.03.043
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Prospective Evaluation of a Molecular Marker Panel for Prediction of Recurrence and Cancer-specific Survival After Radical Cystectomy

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Cited by 70 publications
(39 citation statements)
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“…Since this marker panel was previously validated in bladder cancer (BC), we previously conducted a study to rule out significant differences in marker expression between BC and UTUC [15,16]. The results of our current study indicate that in this population, UTUC exhibits similar molecular expression of cell cycle and proliferative markers when stratified by stage, regardless of tumor location.…”
Section: Discussionmentioning
confidence: 55%
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“…Since this marker panel was previously validated in bladder cancer (BC), we previously conducted a study to rule out significant differences in marker expression between BC and UTUC [15,16]. The results of our current study indicate that in this population, UTUC exhibits similar molecular expression of cell cycle and proliferative markers when stratified by stage, regardless of tumor location.…”
Section: Discussionmentioning
confidence: 55%
“…Bright-field microscopy imaging coupled with advanced color detection software (Automated Cellular Imaging System, Clarinet, CA, USA) was used for automated scoring. Cutoff points to determine alteration of the specified markers were determined previously [15,20]. Briefly, p21 was considered altered if immunoreactivity of staining was <10 %, p27 and cyclin E were considered altered when nuclear staining was <30 %, p53 was considered altered if nuclear activity demonstrated ≥10 % staining, and Ki-67 was considered altered if samples showed >20 % staining [15,20].…”
Section: Methodsmentioning
confidence: 99%
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“…A semiquantitative H-score for each sample was calculated multiplying the staining intensities (0: negative, 1: weak staining, 2: moderate staining, 3: strong staining) by the distributions (0: areas that were negative, 1: <25%, 2: 26-50%, 3: 51-75% 4:76-100%), and ranged from 0 to 12 (Wang et al, 2013). To estimate a cut point for dichotomizing ST6Gal-I expression into high versus low expression, we used the training cohort and chose the cut point that maximized the concordance index (Lotan et al, 2013). As a result, tumors with ST6Gal-I expression ≤2 IHC score categorized as "low"; those >2 IHC score were categorized as "high" (Supplementary Figure 1).…”
Section: Immunohistochemistrymentioning
confidence: 99%