Claudin7 and moesin in endometrial Adenocarcinoma; A retrospective study of 265 patients

Paulette Mhawech-Fauceglia, Dan Wang, Shashikant Lele, Peter J. Frederick, Tanja Pejovic, Song Liu

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

Background: Metastasis is the main cause of death in cancer and is a multistep process. Moesin (MSN), a member of the ezrin-rdixin-moesin family and Claudin7 (CLDN7), a tight junction protein, both play a role in tumor cell metastasis. Previously, we found an over-expression of MSN and under-expression of CLDN7 at the mRNA level in uterine serous carcinoma in comparison to uterine endometrioid adenocarcinoma. The purpose of this study is to determine the protein expression of MSN and CLDN7 in endometrial cancer (EC) and to evaluate their prognostic value. Two hundred sixty-five patients with EC were retrieved from the archives. MSN and CLDN7 immunostaining were performed on the tissue paraffin sections. The expression of each antibody was reported and then correlated with clinicopathological prognostic factors including age, tumor grade, tumor stage, lympho-vascular involvement, depth of myometrial invasion, overall survival (OS), disease free survival (DFS) and death of disease (DOD). Results: MSN and CLDN were expressed in 46% and 52% of overall cases. We observed an association between MSN + staining and tumor grade, and serous and clear cell carcinoma subtypes (p <0.001 each). There was an association between CLDN7 + staining and low tumor grade and endometrioid adenocarcinoma subtype (p <0.001 and 0.001 respectively). However, no association between MSN and CLDN7 expression and outcome including OS, DOD, and DFS was found. Conclusion: A significant prognostic value of MSN and CLDN7 in predicting disease outcomes in patients with EC was not demonstrated. Nevertheless, the high percentage of EC cases with MSN and CLDN7 immunoexpression, and their association with tumor grade and subtypes, suggests that these proteins might play a role in tumorigenesis of endometrial adenocarcinomas. Future studies are needed to shed light on their mechanistic properties in EC cells.

Original languageEnglish (US)
Article number65
JournalBMC Research Notes
Volume5
DOIs
StatePublished - 2012
Externally publishedYes

Fingerprint

Adenocarcinoma
Retrospective Studies
Endometrial Neoplasms
Tumors
Neoplasms
Endometrioid Carcinoma
Disease-Free Survival
Cells
moesin
Staining and Labeling
Neoplasm Metastasis
Tight Junction Proteins
Carcinoma
Survival
Paraffin
Blood Vessels
Cause of Death
Carcinogenesis
Proteins
Tissue

Keywords

  • Claudin7
  • Clinical outcome
  • Endometrial adenocarcinoma
  • Moesin

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)
  • Medicine(all)

Cite this

Claudin7 and moesin in endometrial Adenocarcinoma; A retrospective study of 265 patients. / Mhawech-Fauceglia, Paulette; Wang, Dan; Lele, Shashikant; Frederick, Peter J.; Pejovic, Tanja; Liu, Song.

In: BMC Research Notes, Vol. 5, 65, 2012.

Research output: Contribution to journalArticle

Mhawech-Fauceglia, Paulette ; Wang, Dan ; Lele, Shashikant ; Frederick, Peter J. ; Pejovic, Tanja ; Liu, Song. / Claudin7 and moesin in endometrial Adenocarcinoma; A retrospective study of 265 patients. In: BMC Research Notes. 2012 ; Vol. 5.
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abstract = "Background: Metastasis is the main cause of death in cancer and is a multistep process. Moesin (MSN), a member of the ezrin-rdixin-moesin family and Claudin7 (CLDN7), a tight junction protein, both play a role in tumor cell metastasis. Previously, we found an over-expression of MSN and under-expression of CLDN7 at the mRNA level in uterine serous carcinoma in comparison to uterine endometrioid adenocarcinoma. The purpose of this study is to determine the protein expression of MSN and CLDN7 in endometrial cancer (EC) and to evaluate their prognostic value. Two hundred sixty-five patients with EC were retrieved from the archives. MSN and CLDN7 immunostaining were performed on the tissue paraffin sections. The expression of each antibody was reported and then correlated with clinicopathological prognostic factors including age, tumor grade, tumor stage, lympho-vascular involvement, depth of myometrial invasion, overall survival (OS), disease free survival (DFS) and death of disease (DOD). Results: MSN and CLDN were expressed in 46{\%} and 52{\%} of overall cases. We observed an association between MSN + staining and tumor grade, and serous and clear cell carcinoma subtypes (p <0.001 each). There was an association between CLDN7 + staining and low tumor grade and endometrioid adenocarcinoma subtype (p <0.001 and 0.001 respectively). However, no association between MSN and CLDN7 expression and outcome including OS, DOD, and DFS was found. Conclusion: A significant prognostic value of MSN and CLDN7 in predicting disease outcomes in patients with EC was not demonstrated. Nevertheless, the high percentage of EC cases with MSN and CLDN7 immunoexpression, and their association with tumor grade and subtypes, suggests that these proteins might play a role in tumorigenesis of endometrial adenocarcinomas. Future studies are needed to shed light on their mechanistic properties in EC cells.",
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AU - Mhawech-Fauceglia, Paulette

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AU - Frederick, Peter J.

AU - Pejovic, Tanja

AU - Liu, Song

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N2 - Background: Metastasis is the main cause of death in cancer and is a multistep process. Moesin (MSN), a member of the ezrin-rdixin-moesin family and Claudin7 (CLDN7), a tight junction protein, both play a role in tumor cell metastasis. Previously, we found an over-expression of MSN and under-expression of CLDN7 at the mRNA level in uterine serous carcinoma in comparison to uterine endometrioid adenocarcinoma. The purpose of this study is to determine the protein expression of MSN and CLDN7 in endometrial cancer (EC) and to evaluate their prognostic value. Two hundred sixty-five patients with EC were retrieved from the archives. MSN and CLDN7 immunostaining were performed on the tissue paraffin sections. The expression of each antibody was reported and then correlated with clinicopathological prognostic factors including age, tumor grade, tumor stage, lympho-vascular involvement, depth of myometrial invasion, overall survival (OS), disease free survival (DFS) and death of disease (DOD). Results: MSN and CLDN were expressed in 46% and 52% of overall cases. We observed an association between MSN + staining and tumor grade, and serous and clear cell carcinoma subtypes (p <0.001 each). There was an association between CLDN7 + staining and low tumor grade and endometrioid adenocarcinoma subtype (p <0.001 and 0.001 respectively). However, no association between MSN and CLDN7 expression and outcome including OS, DOD, and DFS was found. Conclusion: A significant prognostic value of MSN and CLDN7 in predicting disease outcomes in patients with EC was not demonstrated. Nevertheless, the high percentage of EC cases with MSN and CLDN7 immunoexpression, and their association with tumor grade and subtypes, suggests that these proteins might play a role in tumorigenesis of endometrial adenocarcinomas. Future studies are needed to shed light on their mechanistic properties in EC cells.

AB - Background: Metastasis is the main cause of death in cancer and is a multistep process. Moesin (MSN), a member of the ezrin-rdixin-moesin family and Claudin7 (CLDN7), a tight junction protein, both play a role in tumor cell metastasis. Previously, we found an over-expression of MSN and under-expression of CLDN7 at the mRNA level in uterine serous carcinoma in comparison to uterine endometrioid adenocarcinoma. The purpose of this study is to determine the protein expression of MSN and CLDN7 in endometrial cancer (EC) and to evaluate their prognostic value. Two hundred sixty-five patients with EC were retrieved from the archives. MSN and CLDN7 immunostaining were performed on the tissue paraffin sections. The expression of each antibody was reported and then correlated with clinicopathological prognostic factors including age, tumor grade, tumor stage, lympho-vascular involvement, depth of myometrial invasion, overall survival (OS), disease free survival (DFS) and death of disease (DOD). Results: MSN and CLDN were expressed in 46% and 52% of overall cases. We observed an association between MSN + staining and tumor grade, and serous and clear cell carcinoma subtypes (p <0.001 each). There was an association between CLDN7 + staining and low tumor grade and endometrioid adenocarcinoma subtype (p <0.001 and 0.001 respectively). However, no association between MSN and CLDN7 expression and outcome including OS, DOD, and DFS was found. Conclusion: A significant prognostic value of MSN and CLDN7 in predicting disease outcomes in patients with EC was not demonstrated. Nevertheless, the high percentage of EC cases with MSN and CLDN7 immunoexpression, and their association with tumor grade and subtypes, suggests that these proteins might play a role in tumorigenesis of endometrial adenocarcinomas. Future studies are needed to shed light on their mechanistic properties in EC cells.

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KW - Clinical outcome

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KW - Moesin

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