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. 2004 May 15;10(10):1466-70.
doi: 10.3748/wjg.v10.i10.1466.

Overexpression of annexin 1 in pancreatic cancer and its clinical significance

Affiliations

Overexpression of annexin 1 in pancreatic cancer and its clinical significance

Xiao-Feng Bai et al. World J Gastroenterol. .

Abstract

Aim: To investigate the expression of annexin I in pancreatic cancer and its relationship with the clinicopathologic factors, and to evaluate its potential clinical significance.

Methods: Annexin I expression was analyzed by Western blot and immunohistochemical staining in pancreatic adenocarcinoma and multi-tissue microarrays (MTAs).

Results: Western blot analysis showed that annexin I was overexpressed in 84.6% (11/13) pancreatic ductal adenocarcinomas. Immunohistochemistry analysis of pancreatic cancer in MTAs showed that annexin I protein was 71.4%(30/42) positive which was markedly increased compared with that in the tumor matched normal pancreas tissues 18.4%(7/38) (P<0.01). In the meantime, the high expression of annexin 1 was correlated with the poor differentiation of pancreatic adenocarcinoma.

Conclusion: Annexin 1 overexpression is a frequent biological marker and correlates with the differentiation of pancreatic cancer during tumorigenesis.

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Figures

Figure 1
Figure 1
Western blot analysis of annexin I in pancreatic duc-tal adenocarcinoma. Ten micrograms of total protein extracts from pancreatic tissues and cell lines were run on 120 g/L SDS-PAGE, and annexin I protein expression was probed with mouse anti-annexin I monoclonal antibody and visualized by chemiluminescence (top panel). C: pancreatic ductal adenocar-cinoma tissues; N: normal pancreas tissues; BxPC-3: human pancreatic adenocarcinoma cell line. α-Tubulin was used as an internal control (bottom panel).
Figure 2
Figure 2
Immunohistochemical analysis of annexin I expression on pancreatic cancer MTAs. A and B: Overview of the H & E staining and immunohistochemical staining of annexin I on pancreatic cancer MTAs; C (× 200) and D (× 400): normal pancreas; E (× 200) and F (× 400): well differentiated ductal adenocarcinoma; G (× 200) and H (× 400): poorly differentiated ductal adenocarcinoma.

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