Urine supernatant reveals a signature that predicts survival in clear-cell renal cell carcinoma

被引:4
作者
Daza, Jorge [1 ,2 ,3 ,4 ,10 ]
Salome, Berengere [2 ,3 ,4 ]
Okhawere, Kennedy [1 ]
Bane, Octavia [5 ,6 ]
Meilika, Kirolos N. [1 ]
Korn, Talia G. [1 ]
Qi, Jingjing [3 ]
Xe, Hui [3 ]
Patel, Manishkumar [3 ]
Brody, Rachel [7 ]
Kim-Schultz, Seunghee [3 ]
Sfakianos, John P. [1 ]
Lewis, Sara [5 ,6 ]
Rich, Jordan M. [1 ]
Zuluaga, Laura [1 ]
Badani, Ketan K. [1 ,9 ]
Horowitz, Amir [2 ,3 ,4 ,8 ]
机构
[1] Icahn Sch Med Mt Sinai, Dept Urol, New York, NY USA
[2] Icahn Sch Med Mt Sinai, Dept Oncol Sci, New York, NY USA
[3] Icahn Sch Med Mt Sinai, Precis Immunol Inst, New York, NY USA
[4] Icahn Sch Med Mt Sinai, Tisch Canc Inst, New York, NY USA
[5] Icahn Sch Med Mt Sinai, Dept Diagnost Mol & Intervent Radiol, New York, NY USA
[6] Icahn Sch Med Mt Sinai, Biomed Engn & Imaging Inst, New York, NY USA
[7] Icahn Sch Med Mt Sinai, Dept Pathol, New York, NY USA
[8] Icahn Sch Med, Precis Immunol Inst, Tischcancer Inst, Dept Oncol Sci, 1425 Madison Ave, 12 Fl, New York, NY 10029 USA
[9] Icahn Sch Med, Dept Urol, 5 East 98th St, 6 Fl, New York, NY 10029 USA
[10] Icahn Sch Med, Dept Urol, 5 East 98th St, 6 Fl, New York, NY 10029 USA
关键词
kidney cancer; molecular biomarkers; risk group; outcomes; inflammation; tumour microenvironment; #kcsm; #KidneyCancer; #uroonc; PROSTATE-CANCER; RECURRENCE; TRIALS; SCORE;
D O I
10.1111/bju.15989
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
ObjectiveTo profile the cell-free urine supernatant and plasma of a small cohort of clear-cell renal cell carcinoma (ccRCC) patients by measuring the relative concentrations of 92 proteins related to inflammation. Using The Cancer Genome Atlas (TCGA), we then performed a targeted mRNA analysis of genes encoding the above proteins and defined their effects on overall survival (OS). Subjects/patients and MethodsSamples were collected prospectively from ccRCC patients. A multiplex proximity extension assay was used to measure the concentrations of 92 inflammation-related proteins in cell-free urine supernatants and plasma. Transcriptomic and clinical information from ccRCC patients was obtained from TCGA. Unsupervised clustering and differential protein expression analyses were performed on protein concentration data. Targeted mRNA analysis on genes encoding significant differentially expressed proteins was performed using TCGA. Backward stepwise regression analyses were used to build a nomogram. The performance of the nomogram and clinical benefit was assessed by discrimination and calibration, and a decision curve analysis, respectively. ResultsUnsupervised clustering analysis revealed inflammatory signatures in the cell-free urine supernatant of ccRCC patients. Backward stepwise regressions using TCGA data identified transcriptomic risk factors and risk groups associated with OS. A nomogram to predict 2-year and 5-year OS was developed using these risk factors. The decision curve analysis showed that our model was associated with a net benefit improvement compared to the treat-all/none strategies. ConclusionWe defined four novel biomarkers using proteomic and transcriptomic data that distinguish severity of prognosis in ccRCC. We showed that these biomarkers can be used in a model to predict 2-year and 5-year OS in ccRCC across different tumour stages. This type of analysis, if validated in the future, provides non-invasive prognostic information that could inform either management or surveillance strategies for patients.
引用
收藏
页码:75 / 83
页数:9
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