TY - JOUR
T1 - Tumor classification of six common cancer types based on proteomic profiling by MALDI imaging
AU - Meding, Stephan
AU - Nitsche, Ulrich
AU - Balluff, Benjamin
AU - Elsner, Mareike
AU - Rauser, Sandra
AU - Schöne, Cédrik
AU - Nipp, Martin
AU - Maak, Matthias
AU - Feith, Marcus
AU - Ebert, Matthias P.
AU - Friess, Helmut
AU - Langer, Rupert
AU - Höfler, Heinz
AU - Zitzelsberger, Horst
AU - Rosenberg, Robert
AU - Walch, Axel
PY - 2012/3/2
Y1 - 2012/3/2
N2 - In clinical diagnostics, it is of outmost importance to correctly identify the source of a metastatic tumor, especially if no apparent primary tumor is present. Tissue-based proteomics might allow correct tumor classification. As a result, we performed MALDI imaging to generate proteomic signatures for different tumors. These signatures were used to classify common cancer types. At first, a cohort comprised of tissue samples from six adenocarcinoma entities located at different organ sites (esophagus, breast, colon, liver, stomach, thyroid gland, n = 171) was classified using two algorithms for a training and test set. For the test set, Support Vector Machine and Random Forest yielded overall accuracies of 82.74 and 81.18%, respectively. Then, colon cancer liver metastasis samples (n = 19) were introduced into the classification. The liver metastasis samples could be discriminated with high accuracy from primary tumors of colon cancer and hepatocellular carcinoma. Additionally, colon cancer liver metastasis samples could be successfully classified by using colon cancer primary tumor samples for the training of the classifier. These findings demonstrate that MALDI imaging-derived proteomic classifiers can discriminate between different tumor types at different organ sites and in the same site.
AB - In clinical diagnostics, it is of outmost importance to correctly identify the source of a metastatic tumor, especially if no apparent primary tumor is present. Tissue-based proteomics might allow correct tumor classification. As a result, we performed MALDI imaging to generate proteomic signatures for different tumors. These signatures were used to classify common cancer types. At first, a cohort comprised of tissue samples from six adenocarcinoma entities located at different organ sites (esophagus, breast, colon, liver, stomach, thyroid gland, n = 171) was classified using two algorithms for a training and test set. For the test set, Support Vector Machine and Random Forest yielded overall accuracies of 82.74 and 81.18%, respectively. Then, colon cancer liver metastasis samples (n = 19) were introduced into the classification. The liver metastasis samples could be discriminated with high accuracy from primary tumors of colon cancer and hepatocellular carcinoma. Additionally, colon cancer liver metastasis samples could be successfully classified by using colon cancer primary tumor samples for the training of the classifier. These findings demonstrate that MALDI imaging-derived proteomic classifiers can discriminate between different tumor types at different organ sites and in the same site.
KW - CUP classification
KW - MALDI imaging
KW - MALDI-IMS
KW - MALDI-MSI
KW - imaging MS
KW - proteomic classification
KW - proteomic classifier
KW - tumor classification
KW - tumor diagnosis
UR - http://www.scopus.com/inward/record.url?scp=84857824513&partnerID=8YFLogxK
U2 - 10.1021/pr200784p
DO - 10.1021/pr200784p
M3 - Article
C2 - 22224404
AN - SCOPUS:84857824513
SN - 1535-3893
VL - 11
SP - 1996
EP - 2003
JO - Journal of Proteome Research
JF - Journal of Proteome Research
IS - 3
ER -