Diagnostic and prognostic impact of osteopontin expression in endometrial cancer

Han Byoul Cho; Eun Suk Kang; Young Tae Kim; Jae Hoon Kim

doi:10.1080/07357900802375738

Diagnostic and prognostic impact of osteopontin expression in endometrial cancer

Han Byoul Cho, Eun Suk Kang, Young Tae Kim, Jae Hoon Kim

Department of Obstetrics and Gynecology

Research output: Contribution to journal › Article › peer-review

14 Citations (Scopus)

Abstract

The role of osteopontin as a biomarker in endometrial cancer has not been conclusively established. We evaluated the expression and potential of osteopontin as a biomarker for endometrial cancer. Real-time polymerase chain reaction and immunohistochemistry revealed osteopontin overexpression in endometrial cancer. The plasma osteopontin level in endometrial cancer was significantly higher than in healthy controls (P < 0.001). In FIGO stage I endometrial cancer, osteopontin correctly identified 18 of 29 cases (62.1%) that were not detected by CA125. By Cox multivariate analysis, osteopontin positivity was an independent prognostic factor for disease-free survival (hazard ratio = 3.18, P= 0.035).

Original language	English
Pages (from-to)	313-323
Number of pages	11
Journal	Cancer Investigation
Volume	27
Issue number	3
DOIs	https://doi.org/10.1080/07357900802375738
Publication status	Published - 2009 Mar

Bibliographical note

Funding Information:
This work was supported, in part, by the National R&D Program for Cancer Control, Ministry of Health and Welfare, Republic of Korea (7-2006-0153), a CMB-YUHAN research grant of Yonsei University College of Medicine for 2006 (6-2006-0030), and the Korea Research Foundation Grant funded by the Korean Government (MOEHRD, Basic Research Promotion Fund) (KRF-2006-311-e00339).

All Science Journal Classification (ASJC) codes

Oncology
Cancer Research

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1080/07357900802375738

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title = "Diagnostic and prognostic impact of osteopontin expression in endometrial cancer",

abstract = "The role of osteopontin as a biomarker in endometrial cancer has not been conclusively established. We evaluated the expression and potential of osteopontin as a biomarker for endometrial cancer. Real-time polymerase chain reaction and immunohistochemistry revealed osteopontin overexpression in endometrial cancer. The plasma osteopontin level in endometrial cancer was significantly higher than in healthy controls (P < 0.001). In FIGO stage I endometrial cancer, osteopontin correctly identified 18 of 29 cases (62.1%) that were not detected by CA125. By Cox multivariate analysis, osteopontin positivity was an independent prognostic factor for disease-free survival (hazard ratio = 3.18, P= 0.035).",

author = "Cho, {Han Byoul} and Kang, {Eun Suk} and Kim, {Young Tae} and Kim, {Jae Hoon}",

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AU - Cho, Han Byoul

AU - Kang, Eun Suk

AU - Kim, Young Tae

AU - Kim, Jae Hoon

N1 - Funding Information: This work was supported, in part, by the National R&D Program for Cancer Control, Ministry of Health and Welfare, Republic of Korea (7-2006-0153), a CMB-YUHAN research grant of Yonsei University College of Medicine for 2006 (6-2006-0030), and the Korea Research Foundation Grant funded by the Korean Government (MOEHRD, Basic Research Promotion Fund) (KRF-2006-311-e00339).

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N2 - The role of osteopontin as a biomarker in endometrial cancer has not been conclusively established. We evaluated the expression and potential of osteopontin as a biomarker for endometrial cancer. Real-time polymerase chain reaction and immunohistochemistry revealed osteopontin overexpression in endometrial cancer. The plasma osteopontin level in endometrial cancer was significantly higher than in healthy controls (P < 0.001). In FIGO stage I endometrial cancer, osteopontin correctly identified 18 of 29 cases (62.1%) that were not detected by CA125. By Cox multivariate analysis, osteopontin positivity was an independent prognostic factor for disease-free survival (hazard ratio = 3.18, P= 0.035).

AB - The role of osteopontin as a biomarker in endometrial cancer has not been conclusively established. We evaluated the expression and potential of osteopontin as a biomarker for endometrial cancer. Real-time polymerase chain reaction and immunohistochemistry revealed osteopontin overexpression in endometrial cancer. The plasma osteopontin level in endometrial cancer was significantly higher than in healthy controls (P < 0.001). In FIGO stage I endometrial cancer, osteopontin correctly identified 18 of 29 cases (62.1%) that were not detected by CA125. By Cox multivariate analysis, osteopontin positivity was an independent prognostic factor for disease-free survival (hazard ratio = 3.18, P= 0.035).

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Diagnostic and prognostic impact of osteopontin expression in endometrial cancer

Abstract

Bibliographical note

All Science Journal Classification (ASJC) codes

UN SDGs

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