Tumor size, stage and grade alterations of urinary peptidome in RCC

被引:31
作者
Chinello, Clizia [1 ]
Cazzaniga, Marta [1 ]
De Sio, Gabriele [1 ]
Smith, Andrew James [1 ]
Grasso, Angelica [2 ]
Rocco, Bernardo [2 ]
Signorini, Stefano [3 ]
Grasso, Marco [4 ]
Bosari, Silvano [5 ]
Zoppis, Italo [6 ]
Mauri, Giancarlo [6 ]
Magni, Fulvio [1 ]
机构
[1] Univ Milano Bicocca UNIMIB, Sch Med, Dept Hlth Sci, I-20900 Monza, Italy
[2] Osped Maggiore Policlin Fdn, Dept Specialist Surg Sci, Urol Unit, Milan, Italy
[3] Hosp Desio, Dept Lab Med, Desio, Italy
[4] Azienda Osped San Gerardo, Dept Surg Pathol Cytol Med Genet & Nephropathol, Monza, Italy
[5] Univ Milan, IRCCS Policlin Fdn Mangiagalli & Regina Elena, Dept Med Surg & Dent Sci, Pathol Unit, Milan, Italy
[6] Univ Milano Bicocca, Dept Informat Syst & Commun, Milan, Italy
关键词
Mass spectrometry; Proteomics; Urine; Renal cell carcinoma; Tumour size; Tumour progression; Stage; Grade; Cancer; Peptidomics; RENAL-CELL CARCINOMA; COLORECTAL-CANCER CELL; PROTEOMIC ANALYSIS; EXPRESSION; BIOMARKERS; INVASION; DREBRIN; PROTEIN; ADAMS;
D O I
10.1186/s12967-015-0693-8
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Several promising biomarkers have been found for RCC, but none of them has been used in clinical practice for predicting tumour progression. The most widely used features for predicting tumour aggressiveness still remain the cancer stage, size and grade. Therefore, the aim of our study is to investigate the urinary peptidome to search and identify peptides whose concentrations in urine are linked to tumour growth measure and clinical data. Methods: A proteomic approach applied to ccRCC urinary peptidome (n = 117) based on prefractionation with activated magnetic beads followed by MALDI-TOF profiling was used. A systematic correlation study was performed on urinary peptide profiles obtained from MS analysis. Peptide identity was obtained by LC-ESI-MS/MS. Results: Fifteen, twenty-six and five peptides showed a statistically significant alteration of their urinary concentration according to tumour size, pT and grade, respectively. Furthermore, 15 and 9 signals were observed to have urinary levels statistically modified in patients at different pT or grade values, even at very early stages. Among them, C1RL, A1AGx, ZAG2G, PGBM, MMP23, GP162, ADA19, G3P, RSPH3, DREB, NOTC2 SAFB2 and CC168 were identified. Conclusions: We identified several peptides whose urinary abundance varied according to tumour size, stage and grade. Among them, several play a possible role in tumorigenesis, progression and aggressiveness. These results could be a useful starting point for future studies aimed at verifying their possible use in the managements of RCC patients.
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页数:11
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