SATB2 in Combination With Cytokeratin 20 Identifies Over 95% of all Colorectal Carcinomas

Kristina Magnusson(Uppsala University), Meike de Wit(Amsterdam UMC Location VUmc), Donal J. Brennan(University College Dublin), Louis Banka Johnson(Skåne University Hospital), Sharon F. McGee(University College Dublin), Emma Lundberg(KTH Royal Institute of Technology), Kirsha Naicker(University College Dublin), Rut Klinger(University College Dublin), Caroline Kampf, Anna Asplund, Kenneth Wester, Marcus Gry(AlbaNova), Anders Bjartell(Skåne University Hospital), William M. Gallagher(University College Dublin), Elton Rexhepaj(University College Dublin), Sami Kilpinen(Finland University), Olli Kallioniemi(University of Helsinki), Eric J.T. Belt(Amsterdam UMC Location VUmc), Jeroen Goos(Amsterdam UMC Location VUmc), Gerrit A. Meijer(Amsterdam UMC Location VUmc), Helgi Birgisson(Amsterdam UMC Location VUmc), Bengt Glimelius(University College Dublin), Carl Borrebaeck(KTH Royal Institute of Technology), Sanjay Navani(Lund University), Mathias Uhlén(KTH Royal Institute of Technology), Darran P. O’Connor(University College Dublin), Karin Jirström(University of Helsinki), Fredrik Pontén
The American Journal of Surgical Pathology
June 15, 2011
Cited by 254

Abstract

The special AT-rich sequence-binding protein 2 (SATB2), a nuclear matrix-associated transcription factor and epigenetic regulator, was identified as a tissue type-specific protein when screening protein expression patterns in human normal and cancer tissues using an antibody-based proteomics approach. In this respect, the SATB2 protein shows a selective pattern of expression and, within cells of epithelial lineages, SATB2 expression is restricted to glandular cells lining the lower gastrointestinal tract. The expression of SATB2 protein is primarily preserved in cancer cells of colorectal origin, indicating that SATB2 could function as a clinically useful diagnostic marker to distinguish colorectal cancer (CRC) from other types of cancer. The aim of this study was to further explore and validate the specific expression pattern of SATB2 as a clinical biomarker and to compare SATB2 with the well-known cytokeratin 20 (CK20). Immunohistochemistry was used to analyze the extent of SATB2 expression in tissue microarrays with tumors from 9 independent cohorts of patients with primary and metastatic CRCs (n=1882). Our results show that SATB2 is a sensitive and highly specific marker for CRC with distinct positivity in 85% of all CRCs, and that SATB2 and/or CK20 was positive in 97% of CRCs. In conclusion, the specific expression of SATB2 in a large majority of CRCs suggests that SATB2 can be used as an important complementary tool for the differential diagnosis of carcinoma of unknown primary origin.


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