Comparison of MUC4 expression in primary pancreatic cancer and paired lymph node metastases

被引:18
作者
Ansari, Daniel
Urey, Carlos
Gundewar, Chinmay
Bauden, Monika Posaric
Andersson, Roland [1 ,2 ]
机构
[1] Lund Univ, Clin Sci Lund, Dept Surg, SE-22185 Lund, Sweden
[2] Skane Univ Hosp, SE-22185 Lund, Sweden
关键词
Immunohistochemistry; matched; metastasis; MUC4; pancreatic ductal adenocarcinoma; primary; DUCTAL ADENOCARCINOMA; PRIMARY TUMORS; PROGRESSION; SURVIVAL; INVASION; CELLS;
D O I
10.3109/00365521.2013.832368
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objective. Mucin 4 (MUC4) is a transmembrane glycoprotein that is expressed in pancreatic ductal adenocarcinoma (PDAC), but not in normal pancreatic tissue. MUC4 has a proposed role in pancreatic tumor progression and metastasis. The purpose of this pilot study was to investigate MUC4 expression during PDAC metastasis by comparing the expression in the primary tumor and paired lymph node metastases from the same patient. Material and methods. Surgical specimens from 17 cases of primary PDAC and paired lymph node metastases were immunohistochemically analyzed for MUC4 expression. The modified histochemical score (H-score) was used for staining assessment. Results. Positive staining for MUC4 was detected in most primary and metastatic PDAC tumors (15/17 vs. 14/17). The concordance for MUC4 expression in primary tumors and corresponding lymph node metastases was 82%. In two cases, the primary tumor was MUC4-positive and the lymph node metastases were negative, while in one patient with a MUC4-negative primary tumor, the lymph node metastasis was positive. The distribution of H-score for expression of MUC4 significantly correlated (r = 0.615; p = 0.009) between primary tumors and paired metastatic lesions. Conclusions: MUC4 was observed in both primary and matched metastatic tumors with a high level of concordance, suggesting that MUC4 expression is retained following PDAC metastasis.
引用
收藏
页码:1183 / 1187
页数:5
相关论文
共 27 条
[1]   Mucins and CD56 as markers of tumour invasion and prognosis in periampullary cancer [J].
Aloysius, M. M. ;
Zaitoun, A. M. ;
Awad, S. ;
Ilyas, M. ;
Rowlands, B. J. ;
Lobo, D. N. .
BRITISH JOURNAL OF SURGERY, 2010, 97 (08) :1269-1278
[2]   Pancreatic cancer cells resistance to gemcitabine: the role of MUC4 mucin [J].
Bafna, S. ;
Kaur, S. ;
Momi, N. ;
Batra, S. K. .
BRITISH JOURNAL OF CANCER, 2009, 101 (07) :1155-1161
[3]  
Chakraborty Subhankar, 2008, Expert Opin Med Diagn, V2, P891, DOI 10.1517/17530059.2.8.891
[4]   Structure, evolution, anal biology of the MUC4 mucin [J].
Chaturvedi, Pallavi ;
Singh, Ajay P. ;
Batra, Surinder K. .
FASEB JOURNAL, 2008, 22 (04) :966-981
[5]   MUC4 mucin interacts with and stabilizes the HER2 oncoprotein in human pancreatic cancer cells [J].
Chaturvedi, Pallavi ;
Singh, Ajay P. ;
Chakraborty, Subhankar ;
Chauhan, Subhash C. ;
Bafna, Sangeeta ;
Meza, Jane L. ;
Singh, Pankaj K. ;
Hollingsworth, Michael A. ;
Mehta, Parmender P. ;
Batra, Surinder K. .
CANCER RESEARCH, 2008, 68 (07) :2065-2070
[6]   MUC4 mucin potentiates pancreatic tumor cell proliferation, survival, and invasive properties and interferes with its interaction to extracellular matrix proteins [J].
Chaturvedi, Pallavi ;
Singh, Ajay P. ;
Moniaux, Nicolas ;
Senapati, Shantibhushan ;
Chakraborty, Subhankar ;
Meza, Jane L. ;
Batra, Surinder K. .
MOLECULAR CANCER RESEARCH, 2007, 5 (04) :309-320
[7]   MUC4 mucin expression in human pancreatic tumours is affected by organ environment:: the possible role of TGFβ2 [J].
Choudhury, A ;
Moniaux, N ;
Ulrich, AB ;
Schmied, BM ;
Standop, J ;
Pour, PM ;
Gendler, SJ ;
Hollingsworth, MA ;
Aubert, JP ;
Batra, SK .
BRITISH JOURNAL OF CANCER, 2004, 90 (03) :657-664
[8]   The Mucin MUC4 and Its Membrane Partner ErbB2 Regulate Biological Properties of Human CAPAN-2 Pancreatic Cancer Cells via Different Signalling Pathways [J].
Jonckheere, Nicolas ;
Skrypek, Nicolas ;
Merlin, Johann ;
Dessein, Anne Frederique ;
Dumont, Patrick ;
Leteurtre, Emmanuelle ;
Harris, Ann ;
Desseyn, Jean-Luc ;
Susini, Christiane ;
Frenois, Frederic ;
Van Seuningen, Isabelle .
PLOS ONE, 2012, 7 (02)
[9]  
Jonckheere Nicolas, 2010, Cancers (Basel), V2, P1794, DOI 10.3390/cancers2041794
[10]   Parallel progression of primary tumours and metastases [J].
Klein, Christoph A. .
NATURE REVIEWS CANCER, 2009, 9 (04) :302-312