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High Level of Ezrin Expression in Colorectal Cancer Tissues is Closely Related to Tumor Malignancy

Overview
Specialty Gastroenterology
Date 2009 Apr 29
PMID 19399936
Citations 20
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Abstract

Aim: To investigate the ezrin expression in normal colorectal mucosa and colorectal cancer tissues, and study the correlation between ezrin expression in colorectal cancer tissues and tumor invasion and metastasis.

Methods: Eighty paraffin-embedded cancer tissue samples were selected from primary colorectal adenocarcinoma. Twenty-eight patients had well-differentiated, 22 had moderately differentiated and 30 had poorly differentiated adenocarcinoma. Forty-five patients and 35 patients had lymph node metastasis. Forty-five patients were of Dukes A to B stage, and 35 were of C to D stage. Another 22 paraffin-embedded tissue blocks of normal colorectal epithelium (> 5 cm away from the edge of the tumor) were selected as the control group. All patients with colorectal cancer were treated surgically and diagnosed histologically, without preoperative chemotherapy or radiotherapy. The immunohistochemistry was used to detect the ezrin expression in paraffin-embedded normal colorectal mucosa tissues and colorectal cancer tissue samples.

Results: Ezrin expression in colorectal cancer was significantly higher than in normal colorectal mucosa (75.00% vs 9.09%, P < 0.01), and there was a close relationship between ezrin expression and the degree of tumor differentiation, lymph node metastasis and Dukes stage (88.46% vs 50.00%, P < 0.01; 94.28% vs 51.11%, P < 0.01; 94.28% vs 51.11%, P < 0.01).

Conclusion: Ezrin expression is obviously higher in colorectal cancer tissues than in normal colorectal mucosa tissues, and the high level of ezrin expression is closely related to the colorectal cancer invasion and metastasis process.

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References
1.
Ferrari S, Zanella L, Alberghini M, Palmerini E, Staals E, Bacchini P . Prognostic significance of immunohistochemical expression of ezrin in non-metastatic high-grade osteosarcoma. Pediatr Blood Cancer. 2007; 50(4):752-6. DOI: 10.1002/pbc.21360. View

2.
Oishi K, Sato N, Sagara J, Kawai A, Tsukita S . ERM family members as molecular linkers between the cell surface glycoprotein CD44 and actin-based cytoskeletons. J Cell Biol. 1994; 126(2):391-401. PMC: 2200023. DOI: 10.1083/jcb.126.2.391. View

3.
Yu Y, Khan J, Khanna C, Helman L, Meltzer P, Merlino G . Expression profiling identifies the cytoskeletal organizer ezrin and the developmental homeoprotein Six-1 as key metastatic regulators. Nat Med. 2004; 10(2):175-81. DOI: 10.1038/nm966. View

4.
Dransfield D, Bradford A, Smith J, Martin M, Roy C, Mangeat P . Ezrin is a cyclic AMP-dependent protein kinase anchoring protein. EMBO J. 1997; 16(1):35-43. PMC: 1169611. DOI: 10.1093/emboj/16.1.35. View

5.
Koon N, Schneider-Stock R, Sarlomo-Rikala M, Lasota J, Smolkin M, Petroni G . Molecular targets for tumour progression in gastrointestinal stromal tumours. Gut. 2004; 53(2):235-40. PMC: 1774925. DOI: 10.1136/gut.2003.021238. View