Biomarkers for Wilms Tumor: A Systematic Review

scientific article

Biomarkers for Wilms Tumor: A Systematic Review is …
instance of (P31):
scholarly articleQ13442814
editorialQ871232
review articleQ7318358

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P356DOI10.1016/J.JURO.2016.05.100
P932PMC publication ID5069120
P698PubMed publication ID27259655

P50authorMegan Van NoordQ57054862
Eugene ConeQ60058166
P2093author name stringJonathan C Routh
Henry E Rice
Elizabeth T Tracy
Stewart S Dalton
P2860cites workProgress in childhood cancer: 50 years of research collaboration, a report from the Children's Oncology GroupQ24657000
Advances in Wilms Tumor Treatment and Biology: Progress Through International CollaborationQ28083988
Tumor-associated B7-H1 promotes T-cell apoptosis: a potential mechanism of immune evasionQ28131654
End stage renal disease in patients with Wilms tumor: results from the National Wilms Tumor Study Group and the United States Renal Data SystemQ31010441
Expression of the neurotrophin receptor TrkB is associated with unfavorable outcome in Wilms' tumorQ31826551
Congestive heart failure after treatment for Wilms' tumor: a report from the National Wilms' Tumor Study groupQ33181845
Treatment with nephrectomy only for small, stage I/favorable histology Wilms' tumor: a report from the National Wilms' Tumor Study GroupQ33182388
Treatment of Wilms tumor relapsing after initial treatment with vincristine, actinomycin D, and doxorubicin. A report from the National Wilms Tumor Study GroupQ33375430
TP53 mutational status is a potential marker for risk stratification in Wilms tumour with diffuse anaplasiaQ34338441
Loss of heterozygosity for chromosomes 1p and 16q is an adverse prognostic factor in favorable-histology Wilms tumor: a report from the National Wilms Tumor Study GroupQ34446746
WT1 mutation and 11P15 loss of heterozygosity predict relapse in very low-risk wilms tumors treated with surgery alone: a children's oncology group studyQ34667826
Controversies and advances in the management of Wilms' tumourQ34794743
Allele loss at 16q defines poorer prognosis Wilms tumour irrespective of treatment approach in the UKW1-3 clinical trials: a Children's Cancer and Leukaemia Group (CCLG) StudyQ34949192
Gain of 1q is associated with inferior event-free and overall survival in patients with favorable histology Wilms tumor: a report from the Children's Oncology GroupQ35185392
Expression and prognostic relevance of vascular endothelial growth factor (VEGF) and its receptor (FLT-1) in nephroblastoma.Q35586613
Immunohistochemical detection of p53 in Wilms' tumors correlates with unfavorable outcome.Q35773597
Prognostic markers in nephroblastoma (Wilms' tumor).Q36142728
B7-H1 glycoprotein blockade: a novel strategy to enhance immunotherapy in patients with renal cell carcinoma.Q36272357
Tumor B7-H1 is associated with poor prognosis in renal cell carcinoma patients with long-term follow-up.Q36439488
The prognostic significance of apoptosis-associated proteins BCL-2, BAX and BCL-X in clinical nephroblastomaQ36623109
Subsets of very low risk Wilms tumor show distinctive gene expression, histologic, and clinical featuresQ37435558
B7-H1 expression in Wilms tumor: correlation with tumor biology and disease recurrenceQ37461823
Development and evaluation of BioScore: a biomarker panel to enhance prognostic algorithms for clear cell renal cell carcinomaQ37461830
Telomerase reverse transcriptase catalytic subunit expression and proliferation index in Wilms tumorQ38410435
Expression of the lipogenic enzyme fatty acid synthase (FAS) as a predictor of poor outcome in nephroblastoma: an interinstitutional studyQ38452956
Wilms tumors: relationship of nuclear deoxyribonucleic acid ploidy to patient survival.Q38491968
Second malignant neoplasms following treatment for Wilm's tumor: a report from the National Wilms' Tumor Study GroupQ38508700
Gain of 1q is a marker of poor prognosis in Wilms' tumorsQ39349862
B7-h1 as a biomarker for therapy failure in patients with favorable histology Wilms tumor.Q43784781
Differential expression of the heat shock protein 70 in the histological compartments of nephroblastomasQ43802065
Expression and prognostic value of platelet-derived growth factor-AA and its receptor α in nephroblastomaQ44007807
HER2/neu expression: a predictor for differentiation and survival in children with Wilms tumorQ44425783
Characteristics and outcomes of children with the Wilms tumor-Aniridia syndrome: a report from the National Wilms Tumor Study GroupQ44573108
Bilateral Wilms' tumor: long-term survival and some epidemiological featuresQ44614766
Loss of heterozygosity analysis at different chromosome regions in Wilms tumor confirms 1p allelic loss as a marker of worse prognosis: a study from the Italian Association of Pediatric Hematology and OncologyQ45760446
p53 Immunohistochemistry expression in Wilms tumor: a prognostic tool in the detection of tumor aggressivenessQ46629881
Microsatellite analysis of the DCC gene in nephroblastomas: pathologic correlations and prognostic implicationsQ46781654
Bilateral Wilms tumorQ47593815
Clinical relevance of mutations in the Wilms tumor suppressor 1 gene WT1 and the cadherin-associated protein beta1 gene CTNNB1 for patients with Wilms tumors: results of long-term surveillance of 71 patients from International Society of Pediatric OQ47670734
High telomerase RNA expression level is an adverse prognostic factor for favorable-histology Wilms' tumor.Q50754124
The expression of IL-6 and STAT3 might predict progression and unfavorable prognosis in Wilms' tumor.Q51001524
Increased tissue factor expression and poor nephroblastoma prognosis.Q51815120
Revised International Society of Paediatric Oncology (SIOP) working classification of renal tumors of childhood.Q53318349
Anaplasia in unilateral Wilms' tumor: a report from the National Wilms' Tumor Study Pathology Center.Q53520274
The expression of HSP70 and HSP90alpha in children with Wilms tumor.Q54597224
Decreased E-cadherin expression correlates with higher stage of Wilms' tumors.Q54676905
Astrocyte elevated gene-1 overexpression in histologically favorable Wilms tumor is related to poor prognosis.Q54771946
High telomerase reverse transcriptase (hTERT) messenger RNA level correlates with tumor recurrence in patients with favorable histology Wilms' tumorQ59282688
Loss of Imprinting of Insulin-Like Growth Factor-II (IGF2) Gene in Distinguishing Specific Biologic Subtypes of Wilms TumorQ63433243
MIB-1 (KI-67) Proliferation Index and Cyclin-Dependent Kinase Inhibitor p27Kip1 Protein Expression in NephroblastomaQ63966372
Prognostic value of proliferating cell nuclear antigen in Wilms' tumour in children.Q64981211
A third Wilms' tumor locus on chromosome 16qQ67848748
Molecular genetics of Wilms tumorQ70978673
Genotype/phenotype correlations in Wilms' tumorQ71580257
Loss of heterozygosity for chromosomes 16q and 1p in Wilms' tumors predicts an adverse outcomeQ72373963
Denys-Drash syndrome: relating a clinical disorder to genetic alterations in the tumor suppressor gene WT1Q72577728
Expression and prognostic value of Wilms' tumor 1 and early growth response 1 proteins in nephroblastomaQ73269404
16q heterozygosity loss in Wilms' tumour in children and its clinical importanceQ73550945
Expression and prognostic value Of CD44 isoforms in nephroblastoma (Wilms tumor)Q74493276
Immunohistochemical detection of p53 protein expression as a prognostic indicator in Wilms tumorQ77358795
Expression and prognostic value of epidermal growth factor receptor, transforming growth factor-alpha, and c-erb B-2 in nephroblastomaQ77380414
Immunohistochemical detection of p53 protein expression as a prognostic factor in Wilms tumorQ83985886
Assessment of promoter methylation and expression of SIX2 as a diagnostic and prognostic biomarker in Wilms' tumorQ87206471
P433issue5
P407language of work or nameEnglishQ1860
P921main subjectbiomarkerQ864574
systematic reviewQ1504425
P304page(s)1530-1535
P577publication date2016-05-31
P1433published inJournal of UrologyQ15709979
P1476titleBiomarkers for Wilms Tumor: A Systematic Review
P478volume196

Reverse relations

cites work (P2860)
Q91972546Aberrant expression and mechanism of miR-130b-3p/phosphatase and tensin homolog in nephroblastoma in children
Q47104294Association between long interspersed nuclear element-1 methylation levels and relapse in Wilms tumors
Q92016796Competitive endogenous RNA (ceRNA) regulation network of lncRNAs, miRNAs, and mRNAs in Wilms tumour
Q92703125Genes Controlled by DNA Methylation Are Involved in Wilms Tumor Progression
Q95643669HOXB2 and FOXC1 synergistically drive the progression of Wilms tumor
Q91817106Insights into the Chemical Biology of Childhood Embryonal Solid Tumors by NMR-Based Metabolomics
Q90041553Loss of Heterozygosity at Chromosome 16q Is a Negative Prognostic Factor in Korean Pediatric Patients with Favorable Histology Wilms Tumor: A Report of the Korean Pediatric Hematology Oncology Group (K-PHOG)
Q88912690MicroRNA‑92a‑3p inhibits the cell proliferation, migration and invasion of Wilms tumor by targeting NOTCH1
Q92134502Multi-Omics Integration Reveals a Competitive Endogenous RNAs Network for the Identification of Progression Biomarkers and the Stratification of Patients Diagnosed With Nephroblastoma
Q33772198Recent advances in the management of Wilms' tumor.
Q99630135Two rare cases of acute myeloid leukemia with t(8;16)(p11.2;p13.3) and 1q duplication: case presentation and literature review

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