Tissue-based proteomics reveals FXYD3, S100A11 and GSTM3 as novel markers for regional lymph node metastasis in colon cancer

被引:88
作者
Meding, Stephan [1 ]
Balluff, Benjamin [1 ]
Elsner, Mareike [1 ]
Schoene, Cedrik [1 ]
Rauser, Sandra [1 ]
Nitsche, Ulrich [2 ]
Maak, Matthias [2 ]
Schaefer, Alexander [3 ]
Hauck, Stefanie M. [3 ]
Ueffing, Marius [3 ,4 ]
Langer, Rupert [5 ]
Hoefler, Heinz [1 ,5 ]
Friess, Helmut [2 ]
Rosenberg, Robert [2 ,6 ]
Walch, Axel [1 ]
机构
[1] Helmholtz Zentrum Munchen, Inst Pathol, D-85764 Neuherberg, Germany
[2] Tech Univ Munich, Klinikum Rechts Isar, Dept Surg, D-80290 Munich, Germany
[3] Helmholtz Zentrum Munchen, Res Unit Prot Sci, D-85764 Neuherberg, Germany
[4] Univ Tubingen, Ctr Ophthalmol, Inst Ophthalm Res, Tubingen, Germany
[5] Tech Univ Munich, Inst Pathol, D-80290 Munich, Germany
[6] Kantonsspital Baden, Klin Allgemein Viszeral & Gefasschirurg, Baden, Switzerland
关键词
MALDI imaging; label-free quantitative proteomics; immunohistochemistry; regional lymph node metastasis; tissue proteomics; colorectal cancer; GLUTATHIONE-S-TRANSFERASE; BREAST-CANCER; LUNG-CANCER; PHOSPHOSERINE AMINOTRANSFERASE; HEPATOCELLULAR-CARCINOMA; GENE-EXPRESSION; IDENTIFICATION; PROTEINS; OVEREXPRESSION; PROGRESSION;
D O I
10.1002/path.4021
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Regional lymph node metastasis negatively affects prognosis in colon cancer patients. The molecular processes leading to regional lymph node metastasis are only partially understood and proteomic markers for metastasis are still scarce. Therefore, a tissue-based proteomic approach was undertaken for identifying proteins associated with regional lymph node metastasis. Two complementary tissue-based proteomic methods have been employed. MALDI imaging was used for identifying small proteins (<= 25 kDa) in situ and label-free quantitative proteomics was used for identifying larger proteins. A tissue cohort comprising primary colon tumours without metastasis (UICC II, pN0, n = 21) and with lymph node metastasis (UICC III, pN2, n = 33) was analysed. Subsequent validation of identified proteins was done by immunohistochemical staining on an independent tissue cohort consisting of primary colon tumour specimens (n = 168). MALDI imaging yielded ten discriminating m/z species, and label-free quantitative proteomics 28 proteins. Two MALDI imaging-derived candidate proteins (FXYD3 and S100A11) and one from the label-free quantitative proteomics (GSTM3) were validated on the independent tissue cohort. All three markers correlated significantly with regional lymph node metastasis: FXYD3 (p = 0.0110), S100A11 (p = 0.0071), and GSTM3 (p = 0.0173). FXYD3 and S100A11 were more highly expressed in UICC II patient tumour tissues. GSTM3 was more highly expressed in UICC III patient tumour tissues. By our tissue-based proteomic approach, we could identify a large panel of proteins which are associated with regional lymph node metastasis and which have not been described so far. Here we show that novel markers for regional lymph metastasis can be identified by MALDI imaging or label-free quantitative proteomics and subsequently validated on an independent tissue cohort. Copyright (C) 2012 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
引用
收藏
页码:459 / 470
页数:12
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