Expression of cell cycle proteins in T1a and T1b urothelial bladder carcinoma and their value in predicting tumor progression

BACKGROUND Cell cycle proteins are important markers in predicting tumor behavior in urothelial carcinoma of the bladder. The objectives of this study were 1) to determine the expression levels of some of those markers in a series of patients with bladder carcinoma, 2) to define their value in disti...

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Veröffentlicht in:Cancer 2004-06, Vol.100 (11), p.2367-2375
Hauptverfasser: Mhawech, Paulette, Greloz, Vincent, Oppikofer, Chantal, Szalay‐Quinodoz, Idliko, Herrmann, Francois
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container_end_page 2375
container_issue 11
container_start_page 2367
container_title Cancer
container_volume 100
creator Mhawech, Paulette
Greloz, Vincent
Oppikofer, Chantal
Szalay‐Quinodoz, Idliko
Herrmann, Francois
description BACKGROUND Cell cycle proteins are important markers in predicting tumor behavior in urothelial carcinoma of the bladder. The objectives of this study were 1) to determine the expression levels of some of those markers in a series of patients with bladder carcinoma, 2) to define their value in distinguishing T1a (minimally invasive) from T1b (invasive) tumors, and 3) to evaluate their use as predictive factors in the progression of T1a and T1b tumors. METHODS Tumor specimens from 101 patients were included (22 Ta specimens, 34 T1a specimens, 15 T1b specimens, and 30 T2 specimens). A tissue microarray from the 101 paraffin embedded tissue blocks was constructed. Immunohistochemistry for p16, p27, p21, p53, cyclin D1, and Ki‐67 were performed. To evaluate T1a and T1b tumor progression, clinical and follow‐up data were available for all 49 patients. RESULTS Cyclin D1 and p27 were the only markers that showed a significant association with tumor stage and tumor grade (cyclin D1: P = 0.002 and P > 0.00, respectively; p27: P = 0.024 and P = 0.031, respectively). The results indicated that a combination of p21 (odds ratio, 5.7; 95% confidence interval [95% CI], 1.3–24.8 [P = 0.022]) and p16 (odds ratio, 3.7; 95% CI, 0.8–16.5 [P = 0.081]) may have potential use in distinguishing T1b tumors from T1a tumors. Finally, none of the markers examined were found to have predictive value for T1a and T1b tumor progression. CONCLUSIONS The expression of cyclin D1 and p27 was associated with the most important prognostic factors (tumor stage and grade). The combination of p21 and p16 may have value in distinguishing T1b tumors from T1a tumors, although this finding must be evaluated in much larger series. Finally, none of the markers studied appeared to have predictive value for disease progression in patients with T1a and T1b urothelial bladder tumors. Cancer 2004. © 2004 American Cancer Society. Cyclin D1 and p27 expression levels were associated significantly with tumor grade and stage in patients with urothelial carcinoma of the bladder. Potentially, p21/p16 may be useful for distinguishing T1b (invasive) tumors from T1a (minimally invasive) tumors, although this finding must be investigated first in a much larger series. None of the markers evaluated appeared to have the ability to predict disease progression in patients with T1a or T1b tumors.
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The objectives of this study were 1) to determine the expression levels of some of those markers in a series of patients with bladder carcinoma, 2) to define their value in distinguishing T1a (minimally invasive) from T1b (invasive) tumors, and 3) to evaluate their use as predictive factors in the progression of T1a and T1b tumors. METHODS Tumor specimens from 101 patients were included (22 Ta specimens, 34 T1a specimens, 15 T1b specimens, and 30 T2 specimens). A tissue microarray from the 101 paraffin embedded tissue blocks was constructed. Immunohistochemistry for p16, p27, p21, p53, cyclin D1, and Ki‐67 were performed. To evaluate T1a and T1b tumor progression, clinical and follow‐up data were available for all 49 patients. RESULTS Cyclin D1 and p27 were the only markers that showed a significant association with tumor stage and tumor grade (cyclin D1: P = 0.002 and P &gt; 0.00, respectively; p27: P = 0.024 and P = 0.031, respectively). The results indicated that a combination of p21 (odds ratio, 5.7; 95% confidence interval [95% CI], 1.3–24.8 [P = 0.022]) and p16 (odds ratio, 3.7; 95% CI, 0.8–16.5 [P = 0.081]) may have potential use in distinguishing T1b tumors from T1a tumors. Finally, none of the markers examined were found to have predictive value for T1a and T1b tumor progression. CONCLUSIONS The expression of cyclin D1 and p27 was associated with the most important prognostic factors (tumor stage and grade). The combination of p21 and p16 may have value in distinguishing T1b tumors from T1a tumors, although this finding must be evaluated in much larger series. Finally, none of the markers studied appeared to have predictive value for disease progression in patients with T1a and T1b urothelial bladder tumors. Cancer 2004. © 2004 American Cancer Society. Cyclin D1 and p27 expression levels were associated significantly with tumor grade and stage in patients with urothelial carcinoma of the bladder. Potentially, p21/p16 may be useful for distinguishing T1b (invasive) tumors from T1a (minimally invasive) tumors, although this finding must be investigated first in a much larger series. None of the markers evaluated appeared to have the ability to predict disease progression in patients with T1a or T1b tumors.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/cncr.20306</identifier><identifier>PMID: 15160340</identifier><identifier>CODEN: CANCAR</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Aged ; Aged, 80 and over ; Biological and medical sciences ; Biomarkers, Tumor - analysis ; Carcinoma, Transitional Cell - chemistry ; Carcinoma, Transitional Cell - pathology ; cell cycle protein ; Cell Cycle Proteins - metabolism ; Cyclin D1 ; Cyclin-Dependent Kinase Inhibitor p16 - metabolism ; Cyclin-Dependent Kinase Inhibitor p21 ; Cyclin-Dependent Kinase Inhibitor p27 ; Cyclins - metabolism ; Disease Progression ; Female ; Humans ; Ki-67 Antigen - metabolism ; Ki‐67 ; Male ; Medical sciences ; Middle Aged ; Neoplasm Invasiveness - pathology ; prediction of progression ; Predictive Value of Tests ; Prognosis ; T1a ; T1b ; Tumor Suppressor Protein p53 - metabolism ; Tumor Suppressor Proteins - metabolism ; Tumors ; Urinary Bladder Neoplasms - chemistry ; Urinary Bladder Neoplasms - pathology ; Urothelium - chemistry</subject><ispartof>Cancer, 2004-06, Vol.100 (11), p.2367-2375</ispartof><rights>Copyright © 2004 American Cancer Society</rights><rights>2004 INIST-CNRS</rights><rights>Copyright 2004 American Cancer Society.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3546-99c36a25bb7a68449d80d9ebadaf0cf587dc8a4407efba95785ac6f8bdbf71533</citedby><cites>FETCH-LOGICAL-c3546-99c36a25bb7a68449d80d9ebadaf0cf587dc8a4407efba95785ac6f8bdbf71533</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fcncr.20306$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcncr.20306$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,1428,27905,27906,45555,45556,46390,46814</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=15748387$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15160340$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mhawech, Paulette</creatorcontrib><creatorcontrib>Greloz, Vincent</creatorcontrib><creatorcontrib>Oppikofer, Chantal</creatorcontrib><creatorcontrib>Szalay‐Quinodoz, Idliko</creatorcontrib><creatorcontrib>Herrmann, Francois</creatorcontrib><title>Expression of cell cycle proteins in T1a and T1b urothelial bladder carcinoma and their value in predicting tumor progression</title><title>Cancer</title><addtitle>Cancer</addtitle><description>BACKGROUND Cell cycle proteins are important markers in predicting tumor behavior in urothelial carcinoma of the bladder. The objectives of this study were 1) to determine the expression levels of some of those markers in a series of patients with bladder carcinoma, 2) to define their value in distinguishing T1a (minimally invasive) from T1b (invasive) tumors, and 3) to evaluate their use as predictive factors in the progression of T1a and T1b tumors. METHODS Tumor specimens from 101 patients were included (22 Ta specimens, 34 T1a specimens, 15 T1b specimens, and 30 T2 specimens). A tissue microarray from the 101 paraffin embedded tissue blocks was constructed. Immunohistochemistry for p16, p27, p21, p53, cyclin D1, and Ki‐67 were performed. To evaluate T1a and T1b tumor progression, clinical and follow‐up data were available for all 49 patients. RESULTS Cyclin D1 and p27 were the only markers that showed a significant association with tumor stage and tumor grade (cyclin D1: P = 0.002 and P &gt; 0.00, respectively; p27: P = 0.024 and P = 0.031, respectively). The results indicated that a combination of p21 (odds ratio, 5.7; 95% confidence interval [95% CI], 1.3–24.8 [P = 0.022]) and p16 (odds ratio, 3.7; 95% CI, 0.8–16.5 [P = 0.081]) may have potential use in distinguishing T1b tumors from T1a tumors. Finally, none of the markers examined were found to have predictive value for T1a and T1b tumor progression. CONCLUSIONS The expression of cyclin D1 and p27 was associated with the most important prognostic factors (tumor stage and grade). The combination of p21 and p16 may have value in distinguishing T1b tumors from T1a tumors, although this finding must be evaluated in much larger series. Finally, none of the markers studied appeared to have predictive value for disease progression in patients with T1a and T1b urothelial bladder tumors. Cancer 2004. © 2004 American Cancer Society. Cyclin D1 and p27 expression levels were associated significantly with tumor grade and stage in patients with urothelial carcinoma of the bladder. Potentially, p21/p16 may be useful for distinguishing T1b (invasive) tumors from T1a (minimally invasive) tumors, although this finding must be investigated first in a much larger series. None of the markers evaluated appeared to have the ability to predict disease progression in patients with T1a or T1b tumors.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biological and medical sciences</subject><subject>Biomarkers, Tumor - analysis</subject><subject>Carcinoma, Transitional Cell - chemistry</subject><subject>Carcinoma, Transitional Cell - pathology</subject><subject>cell cycle protein</subject><subject>Cell Cycle Proteins - metabolism</subject><subject>Cyclin D1</subject><subject>Cyclin-Dependent Kinase Inhibitor p16 - metabolism</subject><subject>Cyclin-Dependent Kinase Inhibitor p21</subject><subject>Cyclin-Dependent Kinase Inhibitor p27</subject><subject>Cyclins - metabolism</subject><subject>Disease Progression</subject><subject>Female</subject><subject>Humans</subject><subject>Ki-67 Antigen - metabolism</subject><subject>Ki‐67</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neoplasm Invasiveness - pathology</subject><subject>prediction of progression</subject><subject>Predictive Value of Tests</subject><subject>Prognosis</subject><subject>T1a</subject><subject>T1b</subject><subject>Tumor Suppressor Protein p53 - metabolism</subject><subject>Tumor Suppressor Proteins - metabolism</subject><subject>Tumors</subject><subject>Urinary Bladder Neoplasms - chemistry</subject><subject>Urinary Bladder Neoplasms - pathology</subject><subject>Urothelium - chemistry</subject><issn>0008-543X</issn><issn>1097-0142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUuLFDEUhYMoTtu68QdINroQakwqSSW1lGZ8wKAgI7grbl5jJJVqky61F_53U1aBrnR1SO6Xc7g5CD2m5JIS0r4wyeTLljDS3UE7SnrZEMrbu2hHCFGN4OzTBXpQypd6lK1g99EFFbQjjJMd-nn145hdKWFKePLYuBixOZvo8DFPJxdSwSHhGwoYkq2q8VzvP7sYIGIdwVqXsYFsQprGFarTkPE3iLNb3lZ7G8wppFt8mscpL8a3W-RDdM9DLO7Rpnv08dXVzeFNc_3-9dvDy-vGMMG7pu8N66AVWkvoFOe9VcT2ToMFT4wXSlqjgHMindfQC6kEmM4rbbWXVDC2R89W35r9dXblNIyhLLtCctNcBkl7Ljuq_gtSKSin9Uv36PkKmjyVkp0fjjmMkM8DJcPSyrC0MvxupcJPNtdZj87-QbcaKvB0A6AYiD5DMqH8xUmumJKVoyv3PUR3_kfkcHh3-LCG_wJN96Zv</recordid><startdate>20040601</startdate><enddate>20040601</enddate><creator>Mhawech, Paulette</creator><creator>Greloz, Vincent</creator><creator>Oppikofer, Chantal</creator><creator>Szalay‐Quinodoz, Idliko</creator><creator>Herrmann, Francois</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TO</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20040601</creationdate><title>Expression of cell cycle proteins in T1a and T1b urothelial bladder carcinoma and their value in predicting tumor progression</title><author>Mhawech, Paulette ; Greloz, Vincent ; Oppikofer, Chantal ; Szalay‐Quinodoz, Idliko ; Herrmann, Francois</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3546-99c36a25bb7a68449d80d9ebadaf0cf587dc8a4407efba95785ac6f8bdbf71533</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biological and medical sciences</topic><topic>Biomarkers, Tumor - analysis</topic><topic>Carcinoma, Transitional Cell - chemistry</topic><topic>Carcinoma, Transitional Cell - pathology</topic><topic>cell cycle protein</topic><topic>Cell Cycle Proteins - metabolism</topic><topic>Cyclin D1</topic><topic>Cyclin-Dependent Kinase Inhibitor p16 - metabolism</topic><topic>Cyclin-Dependent Kinase Inhibitor p21</topic><topic>Cyclin-Dependent Kinase Inhibitor p27</topic><topic>Cyclins - metabolism</topic><topic>Disease Progression</topic><topic>Female</topic><topic>Humans</topic><topic>Ki-67 Antigen - metabolism</topic><topic>Ki‐67</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neoplasm Invasiveness - pathology</topic><topic>prediction of progression</topic><topic>Predictive Value of Tests</topic><topic>Prognosis</topic><topic>T1a</topic><topic>T1b</topic><topic>Tumor Suppressor Protein p53 - metabolism</topic><topic>Tumor Suppressor Proteins - metabolism</topic><topic>Tumors</topic><topic>Urinary Bladder Neoplasms - chemistry</topic><topic>Urinary Bladder Neoplasms - pathology</topic><topic>Urothelium - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mhawech, Paulette</creatorcontrib><creatorcontrib>Greloz, Vincent</creatorcontrib><creatorcontrib>Oppikofer, Chantal</creatorcontrib><creatorcontrib>Szalay‐Quinodoz, Idliko</creatorcontrib><creatorcontrib>Herrmann, Francois</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mhawech, Paulette</au><au>Greloz, Vincent</au><au>Oppikofer, Chantal</au><au>Szalay‐Quinodoz, Idliko</au><au>Herrmann, Francois</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of cell cycle proteins in T1a and T1b urothelial bladder carcinoma and their value in predicting tumor progression</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>2004-06-01</date><risdate>2004</risdate><volume>100</volume><issue>11</issue><spage>2367</spage><epage>2375</epage><pages>2367-2375</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><coden>CANCAR</coden><abstract>BACKGROUND Cell cycle proteins are important markers in predicting tumor behavior in urothelial carcinoma of the bladder. The objectives of this study were 1) to determine the expression levels of some of those markers in a series of patients with bladder carcinoma, 2) to define their value in distinguishing T1a (minimally invasive) from T1b (invasive) tumors, and 3) to evaluate their use as predictive factors in the progression of T1a and T1b tumors. METHODS Tumor specimens from 101 patients were included (22 Ta specimens, 34 T1a specimens, 15 T1b specimens, and 30 T2 specimens). A tissue microarray from the 101 paraffin embedded tissue blocks was constructed. Immunohistochemistry for p16, p27, p21, p53, cyclin D1, and Ki‐67 were performed. To evaluate T1a and T1b tumor progression, clinical and follow‐up data were available for all 49 patients. RESULTS Cyclin D1 and p27 were the only markers that showed a significant association with tumor stage and tumor grade (cyclin D1: P = 0.002 and P &gt; 0.00, respectively; p27: P = 0.024 and P = 0.031, respectively). The results indicated that a combination of p21 (odds ratio, 5.7; 95% confidence interval [95% CI], 1.3–24.8 [P = 0.022]) and p16 (odds ratio, 3.7; 95% CI, 0.8–16.5 [P = 0.081]) may have potential use in distinguishing T1b tumors from T1a tumors. Finally, none of the markers examined were found to have predictive value for T1a and T1b tumor progression. CONCLUSIONS The expression of cyclin D1 and p27 was associated with the most important prognostic factors (tumor stage and grade). The combination of p21 and p16 may have value in distinguishing T1b tumors from T1a tumors, although this finding must be evaluated in much larger series. Finally, none of the markers studied appeared to have predictive value for disease progression in patients with T1a and T1b urothelial bladder tumors. Cancer 2004. © 2004 American Cancer Society. Cyclin D1 and p27 expression levels were associated significantly with tumor grade and stage in patients with urothelial carcinoma of the bladder. Potentially, p21/p16 may be useful for distinguishing T1b (invasive) tumors from T1a (minimally invasive) tumors, although this finding must be investigated first in a much larger series. None of the markers evaluated appeared to have the ability to predict disease progression in patients with T1a or T1b tumors.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>15160340</pmid><doi>10.1002/cncr.20306</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects Aged
Aged, 80 and over
Biological and medical sciences
Biomarkers, Tumor - analysis
Carcinoma, Transitional Cell - chemistry
Carcinoma, Transitional Cell - pathology
cell cycle protein
Cell Cycle Proteins - metabolism
Cyclin D1
Cyclin-Dependent Kinase Inhibitor p16 - metabolism
Cyclin-Dependent Kinase Inhibitor p21
Cyclin-Dependent Kinase Inhibitor p27
Cyclins - metabolism
Disease Progression
Female
Humans
Ki-67 Antigen - metabolism
Ki‐67
Male
Medical sciences
Middle Aged
Neoplasm Invasiveness - pathology
prediction of progression
Predictive Value of Tests
Prognosis
T1a
T1b
Tumor Suppressor Protein p53 - metabolism
Tumor Suppressor Proteins - metabolism
Tumors
Urinary Bladder Neoplasms - chemistry
Urinary Bladder Neoplasms - pathology
Urothelium - chemistry
title Expression of cell cycle proteins in T1a and T1b urothelial bladder carcinoma and their value in predicting tumor progression
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