Cell cycle progression score predicts metastatic progression of clear cell renal cell carcinoma after resection

BACKGROUND: The outcome of surgically resected, apparently localized, clear cell renal carcinoma (ccRCC) is uncertain. OBJECTIVE: To evaluate if cell cycle progression (CCP) gene expression can predict future metastasis. METHODS: Pathologic T2a-T3b tumors at University of Iowa were reviewed. Patient...

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Veröffentlicht in:Cancer biomarkers : section A of Disease markers 2015-01, Vol.15 (6), p.861-867
Hauptverfasser: Askeland, Eric J., Chehval, Vincent A., Askeland, Ryan W., Fosso, Placede G., Sangale, Zaina, Xu, Nafei, Rajamani, Saradha, Stone, Steven, Brown, James A.
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container_issue 6
container_start_page 861
container_title Cancer biomarkers : section A of Disease markers
container_volume 15
creator Askeland, Eric J.
Chehval, Vincent A.
Askeland, Ryan W.
Fosso, Placede G.
Sangale, Zaina
Xu, Nafei
Rajamani, Saradha
Stone, Steven
Brown, James A.
description BACKGROUND: The outcome of surgically resected, apparently localized, clear cell renal carcinoma (ccRCC) is uncertain. OBJECTIVE: To evaluate if cell cycle progression (CCP) gene expression can predict future metastasis. METHODS: Pathologic T2a-T3b tumors at University of Iowa were reviewed. Patients with known or suspected metastasis, lymph node involvement or who received neoadjuvant or adjuvant radiation, chemotherapy or immunotherapy were excluded. Case and control cohorts were defined as those who did or did not develop metastatic disease within 5 years. Measured levels of 31 cell cycle genes and 15 control genes from the tumor were calculated as a CCP score. Additionally, gene expression data for a separate ccRCC cohort was downloaded from The Cancer Genome Atlas (TCGA). RESULTS: Univariate analysis of 26 cases and 38 controls revealed that the CCP score predicted progression to metastasis (OR 2.65, p = 0.0091). In multivariate logistic regression modeling, CCP expression remained a significant independent predictor for progression (p = 0.026). The CCP score was also significantly associated with distant metastasis in the TCGA renal cancer cohort in both univariate (p = 1.0 × 10-9) and multivariate (p = 5.6 × 10-3) analysis. CONCLUSION: The CCP score has prognostic value in predicting metastatic progression after resection of organ-confined ccRCC.
doi_str_mv 10.3233/CBM-150530
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OBJECTIVE: To evaluate if cell cycle progression (CCP) gene expression can predict future metastasis. METHODS: Pathologic T2a-T3b tumors at University of Iowa were reviewed. Patients with known or suspected metastasis, lymph node involvement or who received neoadjuvant or adjuvant radiation, chemotherapy or immunotherapy were excluded. Case and control cohorts were defined as those who did or did not develop metastatic disease within 5 years. Measured levels of 31 cell cycle genes and 15 control genes from the tumor were calculated as a CCP score. Additionally, gene expression data for a separate ccRCC cohort was downloaded from The Cancer Genome Atlas (TCGA). RESULTS: Univariate analysis of 26 cases and 38 controls revealed that the CCP score predicted progression to metastasis (OR 2.65, p = 0.0091). In multivariate logistic regression modeling, CCP expression remained a significant independent predictor for progression (p = 0.026). The CCP score was also significantly associated with distant metastasis in the TCGA renal cancer cohort in both univariate (p = 1.0 × 10-9) and multivariate (p = 5.6 × 10-3) analysis. CONCLUSION: The CCP score has prognostic value in predicting metastatic progression after resection of organ-confined ccRCC.</description><identifier>ISSN: 1574-0153</identifier><identifier>EISSN: 1875-8592</identifier><identifier>DOI: 10.3233/CBM-150530</identifier><identifier>PMID: 26406412</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Biomarkers, Tumor - genetics ; Carcinoma, Renal Cell - genetics ; Carcinoma, Renal Cell - secondary ; Carcinoma, Renal Cell - surgery ; Case-Control Studies ; Cell Cycle - genetics ; Cell Cycle Proteins - genetics ; Female ; Follow-Up Studies ; Humans ; Kidney Neoplasms - genetics ; Kidney Neoplasms - pathology ; Kidney Neoplasms - surgery ; Lymphatic Metastasis ; Male ; Middle Aged ; Neoplasm Invasiveness ; Neoplasm Staging ; Prognosis ; Real-Time Polymerase Chain Reaction ; Retrospective Studies</subject><ispartof>Cancer biomarkers : section A of Disease markers, 2015-01, Vol.15 (6), p.861-867</ispartof><rights>IOS Press and the authors. 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OBJECTIVE: To evaluate if cell cycle progression (CCP) gene expression can predict future metastasis. METHODS: Pathologic T2a-T3b tumors at University of Iowa were reviewed. Patients with known or suspected metastasis, lymph node involvement or who received neoadjuvant or adjuvant radiation, chemotherapy or immunotherapy were excluded. Case and control cohorts were defined as those who did or did not develop metastatic disease within 5 years. Measured levels of 31 cell cycle genes and 15 control genes from the tumor were calculated as a CCP score. Additionally, gene expression data for a separate ccRCC cohort was downloaded from The Cancer Genome Atlas (TCGA). RESULTS: Univariate analysis of 26 cases and 38 controls revealed that the CCP score predicted progression to metastasis (OR 2.65, p = 0.0091). In multivariate logistic regression modeling, CCP expression remained a significant independent predictor for progression (p = 0.026). The CCP score was also significantly associated with distant metastasis in the TCGA renal cancer cohort in both univariate (p = 1.0 × 10-9) and multivariate (p = 5.6 × 10-3) analysis. CONCLUSION: The CCP score has prognostic value in predicting metastatic progression after resection of organ-confined ccRCC.</description><subject>Biomarkers, Tumor - genetics</subject><subject>Carcinoma, Renal Cell - genetics</subject><subject>Carcinoma, Renal Cell - secondary</subject><subject>Carcinoma, Renal Cell - surgery</subject><subject>Case-Control Studies</subject><subject>Cell Cycle - genetics</subject><subject>Cell Cycle Proteins - genetics</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Kidney Neoplasms - genetics</subject><subject>Kidney Neoplasms - pathology</subject><subject>Kidney Neoplasms - surgery</subject><subject>Lymphatic Metastasis</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neoplasm Invasiveness</subject><subject>Neoplasm Staging</subject><subject>Prognosis</subject><subject>Real-Time Polymerase Chain Reaction</subject><subject>Retrospective Studies</subject><issn>1574-0153</issn><issn>1875-8592</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>AFRWT</sourceid><sourceid>EIF</sourceid><recordid>eNptkE1LxDAQhoMo7rp68QdIb4pQTZqmbY5a_IIVL3oOaT6WLm2zZtLD_ntTqoIghGSYPPMyPAidE3xDM0pv6_vXlDDMKD5AS1KVLK0Yzw5jzco8xYTRBToB2GKcU5LxY7TIihwXOcmWyNWm6xK1V51Jdt5tvAFo3ZCAcn7qGN2qAElvgoQgQ6v-UM4mcVD6RE0p3gyym0slvWoH18tE2mB8_AKjQhw5RUdWdmDOvt8V-nh8eK-f0_Xb00t9t04V5UVISUUaixurTakry3kxnYYXusKS8wqXmhZUU8qaUnLLGt1keZ5JyjCmWHFGV-hqzo3rfo4GguhbmFaTg3EjCFLmRVXGO4_o9Ywq7wC8sWLn2176vSBYTIJFFCxmwRG--M4dm97oX_THaAQuZwDkxoitG32UAv9FfQFTUoLi</recordid><startdate>20150101</startdate><enddate>20150101</enddate><creator>Askeland, Eric J.</creator><creator>Chehval, Vincent A.</creator><creator>Askeland, Ryan W.</creator><creator>Fosso, Placede G.</creator><creator>Sangale, Zaina</creator><creator>Xu, Nafei</creator><creator>Rajamani, Saradha</creator><creator>Stone, Steven</creator><creator>Brown, James A.</creator><general>SAGE Publications</general><scope>AFRWT</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>7X8</scope></search><sort><creationdate>20150101</creationdate><title>Cell cycle progression score predicts metastatic progression of clear cell renal cell carcinoma after resection</title><author>Askeland, Eric J. ; 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OBJECTIVE: To evaluate if cell cycle progression (CCP) gene expression can predict future metastasis. METHODS: Pathologic T2a-T3b tumors at University of Iowa were reviewed. Patients with known or suspected metastasis, lymph node involvement or who received neoadjuvant or adjuvant radiation, chemotherapy or immunotherapy were excluded. Case and control cohorts were defined as those who did or did not develop metastatic disease within 5 years. Measured levels of 31 cell cycle genes and 15 control genes from the tumor were calculated as a CCP score. Additionally, gene expression data for a separate ccRCC cohort was downloaded from The Cancer Genome Atlas (TCGA). RESULTS: Univariate analysis of 26 cases and 38 controls revealed that the CCP score predicted progression to metastasis (OR 2.65, p = 0.0091). In multivariate logistic regression modeling, CCP expression remained a significant independent predictor for progression (p = 0.026). The CCP score was also significantly associated with distant metastasis in the TCGA renal cancer cohort in both univariate (p = 1.0 × 10-9) and multivariate (p = 5.6 × 10-3) analysis. CONCLUSION: The CCP score has prognostic value in predicting metastatic progression after resection of organ-confined ccRCC.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>26406412</pmid><doi>10.3233/CBM-150530</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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subjects Biomarkers, Tumor - genetics
Carcinoma, Renal Cell - genetics
Carcinoma, Renal Cell - secondary
Carcinoma, Renal Cell - surgery
Case-Control Studies
Cell Cycle - genetics
Cell Cycle Proteins - genetics
Female
Follow-Up Studies
Humans
Kidney Neoplasms - genetics
Kidney Neoplasms - pathology
Kidney Neoplasms - surgery
Lymphatic Metastasis
Male
Middle Aged
Neoplasm Invasiveness
Neoplasm Staging
Prognosis
Real-Time Polymerase Chain Reaction
Retrospective Studies
title Cell cycle progression score predicts metastatic progression of clear cell renal cell carcinoma after resection
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