TY - JOUR
T1 - Cdx2 protein expression in normal and malignant human tissues
T2 - An immunohistochemical survey using tissue microarrays
AU - Moskaluk, Christopher A.
AU - Zhang, Hong
AU - Powell, Steven M.
AU - Cerilli, Lisa A.
AU - Hampton, Garret M.
AU - Frierson, Henry F.
N1 - Funding Information:
Copyright © 2003 by The United States and Canadian Academy of Pathology, Inc. VOL. 16, NO. 9, P. 913, 2003 Printed in the U.S.A. Date of acceptance: May 29, 2003. Hong Zhang is an ITREID fellow in the Center for Global Health at The University of Virginia and is supported by NIH Fogerty Grant D43TW00909-05. Address reprint requests to: Christopher A. Moskaluk, M.D., Ph.D., Department of Pathology, University of Virginia Health System, Rm. 3890 Old Medical School Bldg., Jefferson Park Ave., Charlottesville, VA 22908; fax: 434-243-6757; e-mail: [email protected].
PY - 2003/9/1
Y1 - 2003/9/1
N2 - Cdx2 has been identified as a marker of colon cancer in RNA-profiling experiments. We show here that the detection of Cdx2 protein by immunohistochemistry correlates well with RNA transcript levels as detected by oligonucleotide microarrays. Using tissue microarrays containing most normal tissue types and an antibody to the Cdx2 protein, strong diffuse Cdx2 staining was only seen in the nuclei of small and large intestinal epithelium and portions of the pancreatic duct system. In tissue microarrays containing 745 cancers from many anatomic sites, colonic adenocarcinomas showed strong extensive staining in 90% of cases, with adenocarcinomas of the stomach, esophagus, and ovary (endometrioid and mucinous types) showing extensive staining in only 20-30% of cases. Other types of carcinomas showed extensive staining in only ≤1% of cases. Of 30 neuroendocrine tumors examined, carcinoids of the midgut and hindgut had the most cases with extensive staining (73% and 44%, respectively), thus paralleling the distribution of Cdx2 expression in adenocarcinomas. Cdx2 shows a limited range of expression in the spectrum of human tissues and neoplasia and thus may have utility in determining the site of origin of tumors in certain clinical situations.
AB - Cdx2 has been identified as a marker of colon cancer in RNA-profiling experiments. We show here that the detection of Cdx2 protein by immunohistochemistry correlates well with RNA transcript levels as detected by oligonucleotide microarrays. Using tissue microarrays containing most normal tissue types and an antibody to the Cdx2 protein, strong diffuse Cdx2 staining was only seen in the nuclei of small and large intestinal epithelium and portions of the pancreatic duct system. In tissue microarrays containing 745 cancers from many anatomic sites, colonic adenocarcinomas showed strong extensive staining in 90% of cases, with adenocarcinomas of the stomach, esophagus, and ovary (endometrioid and mucinous types) showing extensive staining in only 20-30% of cases. Other types of carcinomas showed extensive staining in only ≤1% of cases. Of 30 neuroendocrine tumors examined, carcinoids of the midgut and hindgut had the most cases with extensive staining (73% and 44%, respectively), thus paralleling the distribution of Cdx2 expression in adenocarcinomas. Cdx2 shows a limited range of expression in the spectrum of human tissues and neoplasia and thus may have utility in determining the site of origin of tumors in certain clinical situations.
KW - Cdx2
KW - Immunohistochemistry
KW - RNA profiling
KW - Tissue microarray
UR - http://www.scopus.com/inward/record.url?scp=0141742109&partnerID=8YFLogxK
U2 - 10.1097/01.MP.0000086073.92773.55
DO - 10.1097/01.MP.0000086073.92773.55
M3 - Article
C2 - 13679455
AN - SCOPUS:0141742109
SN - 0893-3952
VL - 16
SP - 913
EP - 919
JO - Modern Pathology
JF - Modern Pathology
IS - 9
ER -