Phenotypic alterations of mucins and cytokeratins during gallbladder carcinogenesis

Pathology International - Tập 54 Số 8 - Trang 576-584 - 2004
Hee Jin Chang1, Sun‐Whe Kim2, Byung Lan Lee3,4, Eun Kyung Hong1, Woo Ho Kim4,5
1Department of Pathology, National Cancer Center and
2Department of Surgery
3Anatomy and
4BK21 Project for Medicine, Dentistry and Pharmacy, Seoul National University College of Medicine, Seoul, Korea
5*Cancer Research Institute and

Tóm tắt

In order to evaluate the significance of altered expression of mucin and cytokeratin during gallbladder carcinogenesis, we characteriazed the expressional profiles of MUC1, MUC2, MUC5AC, MUC6, CK7 and CK20 in 33 normal mucosa, 31 adenomas, 55 dysplasias and 131 carcinomas of the gallbladder. In normal gallbladder mucosa, the expressions of MUC5AC and MUC6 were diffuse and MUC1 expression was absent. However, in adenomas, dysplasias and carcinomas, the expressions of MUC5AC and MUC6 tended to decrease, whereas MUC1 expression was elevated. MUC2 and CK20 were infrequently expressed in all of the gallbladder epithelia, but adenomas expressing MUC2 and/or CK20 were more frequently associated with carcinomas and showed a higher grade of atypia than those without these antigens. In carcinomas, MUC1 expression was related to invasive growth, lymph node metastasis and a non‐papillotubular type, whereas MUC6 expression was related to non‐invasive growth. CK7 was diffusely expressed in almost all lesions, but carcinomas with a loss of CK7 expression showed poor survival. In conclusion, normal gallbladder mucosa has a gastric phenotype, but during carcinogenesis and tumor progression, the gastric phenotype is gradually lost and the aberrant expression of MUC1 occurs. The intestinal phenotype is not common in the gallbladder.

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Tài liệu tham khảo

10.1016/S0968-0004(01)02052-7

10.2741/Moniaux

10.1023/A:1008332602541

10.1002/(SICI)1096-9896(199905)188:1<30::AID-PATH291>3.0.CO;2-Q

10.1046/j.1440-1827.1999.00822.x

10.1016/S0046-8177(97)90134-9

10.1002/hep.510300609

10.1046/j.1440-1827.2002.01414.x

Albores‐Saavedra J, 2000, Tumors of the Gallbladder, Extrahepatic Bile Ducts and Ampulla of Vater., 21

Yamagiwa H, 1986, Intestinal metaplasia‐dysplasia‐carcinoma sequence of the gallbladder, Acta Pathol Jpn, 36, 989

Moll R, 1992, Cytokeratin 20 in human carcinomas. A new histodiagnostic marker detected by monoclonal antibodies, Am J Pathol, 140, 427

Ramaekers F, 1990, Use of monoclonal antibodies to keratin 7 in the differential diagnosis of adenocarcinomas, Am J Pathol, 136, 641

10.1097/01.MP.0000067683.84284.66

10.1007/978-3-642-84241-2

10.1007/978-1-4757-3656-4

Shirai Y, 1992, Early carcinoma of the gallbladder, Eur J Surg, 158, 545

10.1002/1097-0142(19861015)58:8<1702::AID-CNCR2820580821>3.0.CO;2-Z

Frierson HF, 1992, Histology for Pathologists, 639

10.1023/A:1005573213100

Kashiwagi H, 2001, MUC1 and MUC2 expression in human gallbladder carcinoma: a clinicopathological study and relationship with prognosis, Oncol Report, 8, 485

Kohlgraf KG, 2003, Contribution of the MUC1 tandem repeat and cytoplasmic tail to invasive and metastatic properties of a pancreatic cancer cell line, Cancer Res, 63, 5011

10.5858/2000-124-1196-EOCAIC

10.1002/mc.2940030608

10.1136/jcp.48.1.26

Smedts F, 1990, Changing patterns of keratin expression during progression of cervical intraepithelial neoplasia, Am J Pathol, 136, 657

10.1111/j.1349-7006.2003.tb01368.x

10.1016/S0002-9440(10)65002-X