Supplementary Table 3: Non-proteomic studies to discover biomarkers of renal cell carcinoma (RCC) Biomarker(s) ‡: Samples† VEGF/bFGF n = 10 donors (stable disease), n = 19 donors (progressive disease). Soluble-CAIX n = 5 non-RCC donors, n = 22 RCC donors. NMP22 n = 23 RCC (n = 21 with radical nephrectomy, n = 2 with partial nephrectomy), n = 20 control donors. N=30 confirmed RCC cases, n=2 patients with oncocytomas, n=33 patients with abdominal trauma/pain or with kidney stones/renal cysts. n = 42 patients with renal tumours, n=30 control patients, and n=10 prostate cancer patients. n = 34 RCC donors sampled before and after nephrectomy. Human Kidney-Injury Molecule-1 (hKIM-1). Urinary glycosaminoglycans Aquaporin-1 and adipophilin-1. n = 42 RCC patients, n = 19 healthy volunteers, n = 15 patients undergoing non-renal surgery. Study design and diagnostic/prognostic utility‡. Reference(s) ELISA-Based study: Urinary concentrations increase during progressive disease but not within patients with stable disease. WB-based study: Soluble CAIX levels decrease within urine following nephrectomy. ELISA-Based study: NMP22 levels are higher in the group with RCC and drop post nephrectomy. ), (1) Immunological NMP22 Test: NMP22 levels higher within RCC-patients than controls. Statistically significant difference observed between the two groups (p<0.005). ELISA-Based study: hKIM-1 detectable within RCC urine and decreases post nephrectomy. hKIM-1 levels distinguished RCC from other conditions with p<0.005. Biochemical measurement. Higher glycosaminoglycans secretion in patients with larger tumours. Higher rate of glycosaminoglycan secretion with increasing tumour size (r = 0.8235, p < 0.001), no correlation of glycosaminoglycan excretion observed with tumour stage. In n = 3 donors with multiple tumour foci very high rates of glycosaminoglycan secretion. WB-based study. The level of AQP1 and ADFP was observed to be greater within the urine of patients with clear cell and papillary carcinoma urinary than within the urine of cancer patients with RCC tumours of non-proximal tubular origin. AQP1 and ADFP levels correlate with tumour size (r = 0.82 AQP1, and r = 0.76 ADFP, p<0.001 in both cases). (4) (2) (3) (5) (6) (7) †All samples are human and urine unless otherwise specified; n numbers refer to number with condition unless otherwise stated, ‡Abbreviations used for proteomic techniques are defined within the text and list of common abbreviations. 1. Braybrooke JP, O'Byrne KJ, Propper DJ, Blann A, Saunders M, Dobbs N, et al. A phase II study of razoxane, an antiangiogenic topoisomerase II inhibitor, in renal cell cancer with assessment of potential surrogate markers of angiogenesis. Clin Cancer Res. 2000 Dec;6(12):4697-704. 2. Zavada J, Zavadova Z, Zat'ovicova M, Hyrsl L, Kawaciuk I. Soluble form of carbonic anhydrase IX (CA IX) in the serum and urine of renal carcinoma patients. Br J Cancer. 2003 Sep 15;89(6):1067-71. 3. Ozer G, Altinel M, Kocak B, Yazicioglu A, Gonenc F. Value of urinary NMP-22 in patients with renal cell carcinoma. Urology. 2002 Oct;60(4):593-7. 4. Huang S, Rhee E, Patel H, Park E, Kaswick J. Urinary NMP22 and renal cell carcinoma. Urology. 2000 Feb;55(2):227-30. 5. Han WK, Alinani A, Wu CL, Michaelson D, Loda M, McGovern FJ, et al. Human kidney injury molecule1 is a tissue and urinary tumor marker of renal cell carcinoma. J Am Soc Nephrol. 2005 Apr;16(4):1126-34. 6. Sarica K, Turkolmez K, Soygur T, Ozer G, Yaman MO, Baltaci S, et al. Evaluation of urinary glycosaminoglycan excretion in patients with renal cell carcinoma. Eur Urol. 1997;31(1):54-7. 7. Morrissey JJ, London AN, Luo J, Kharasch ED. Urinary biomarkers for the early diagnosis of kidney cancer. Mayo Clin Proc. 2010 May;85(5):413-21.