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PMID: 15623633 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

MAP2K4/MKK4 expression in pancreatic cancer: genetic validation of immunohistochemistry and relationship to disease course.

Xin W, Yun KJ, Ricci F, Zahurak M, Qiu W, Su GH, Yeo CJ, Hruban RH, Kern SE, Iacobuzio-Donahue CA

Abstract

MKK4 (MAP2K4/SEK1) is a member of the mitogen-activated protein kinase family, originally identified as a kinase involved in the stress-activated protein kinase pathway by directly phosphorylating c-Jun NH2-terminal kinase. MKK4 genetic inactivation has been observed in a subset of pancreatic carcinomas, implicating deregulation of the stress-activated protein kinase pathway in pancreatic carcinogenesis. We evaluated Mkk4 protein expression patterns by immunohistochemical labeling in a series of 60 resected primary infiltrating pancreatic adenocarcinomas (24 cases with known MKK4 genetic status), and 14 different tissue arrays representing the primary carcinoma and all of the gross metastases from 26 patients that died of metastatic pancreatic cancer. Among the surgically resected carcinomas, focal or diffuse-positive immunolabeling for Mkk4 protein was found in 52 of 60 cases (86.7%). Among the eight carcinomas with negative Mkk4 immunolabeling, three harbored a homozygous deletion or intragenic mutation of the MKK4 gene, in contrast to none of the 52 cases with positive Mkk4 immunolabeling (P < 0.01). Loss of Mkk4 immunolabeling showed a trend toward shorter survival, with Mkk4-positive carcinomas having half the risk of death than Mkk4-negative carcinomas (P = 0.09). Mkk4 immunolabeling patterns were also evaluated among unresectable primary and metastatic cancer tissues from autopsy specimens, indicating intact Mkk4 immunolabeling in 88.8% of the unresectable primary carcinomas as compared with 63.3% of distant metastases (P < 0.001). Our data indicate that the loss of Mkk4 protein expression in pancreatic carcinomas may be more frequent than suggested by the rates of genetic inactivation alone and that MKK4 loss may contribute to disease progression. The correlation of MKK4 genetic status with immunolabeling patterns validate this approach for the evaluation of MKK4 status in routine histologic sections and may provide useful information regarding patient prognosis.

MeSH Terms
Adenocarcinoma/enzymology,pathology Adult Aged Aged, 80 and over Disease Progression Female Gene Expression Regulation, Enzymologic/physiology Humans Immunoenzyme Techniques MAP Kinase Kinase 4/genetics,metabolism Male Middle Aged Pancreatic Neoplasms/enzymology,pathology
Chemicals
MAP Kinase Kinase 4 MAP2K4 protein, human
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Xin Wei
Department of Pathology, The University of Michigan Medical Center, Ann Arbor, Michigan, USA.
Yun Ki J
Ricci Francesca
Zahurak Marianna
Qiu Wanglong
Su Gloria H
Yeo Charles J
Hruban Ralph H
Kern Scott E
Iacobuzio-Donahue Christine A
Article Info
Journal
Clinical cancer research : an official journal of the American Association for Cancer Research
Abbr.
Clin Cancer Res
ISSN
1078-0432
Published
2004-12-15
Pages
8516-20
Language
English
Region
United States
NLM ID
9502500
Subset
IM
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