Volume 111, Issue 6 pp. 595-598

Mutational analysis of salvador gene in human carcinomas

NAM JIN YOO

NAM JIN YOO

Department of Pathology, College of Medicine, The Catholic University of Korea, Seoul, Korea; and

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YOUNG HWA SOUNG

YOUNG HWA SOUNG

Department of Pathology, College of Medicine, The Catholic University of Korea, Seoul, Korea; and

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JONG WOO LEE

JONG WOO LEE

Department of Pathology, College of Medicine, The Catholic University of Korea, Seoul, Korea; and

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WON SANG PARK

WON SANG PARK

Department of Pathology, College of Medicine, The Catholic University of Korea, Seoul, Korea; and

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SU YOUNG KIM

SU YOUNG KIM

Department of Pathology, College of Medicine, The Catholic University of Korea, Seoul, Korea; and

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SUK WOO NAM

SUK WOO NAM

Department of Pathology, College of Medicine, The Catholic University of Korea, Seoul, Korea; and

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JUNG HO HAN

JUNG HO HAN

Department of Diagnostic Pathology, Samsung Medical Center, Sungkyunkwan University, Seoul, Korea

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SANG HO KIM

SANG HO KIM

Department of Pathology, College of Medicine, The Catholic University of Korea, Seoul, Korea; and

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JUNG YOUNG LEE

JUNG YOUNG LEE

Department of Pathology, College of Medicine, The Catholic University of Korea, Seoul, Korea; and

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SUG HYUNG LEE

SUG HYUNG LEE

Department of Pathology, College of Medicine, The Catholic University of Korea, Seoul, Korea; and

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First published: 12 September 2003
Citations: 5
Sug Hyung Lee, Department of Pathology, College of Medicine, The Catholic University of Korea, 505 Banpo-dong, Socho-gu, Seoul 137-701, Korea. e-mail: [email protected]

Abstract

It is believed that clonal expansion and cancer growth is the result of the deregulation of proliferation and cell death. Recently, salvador, a molecule that can regulate both cell proliferation and cell death, was identified. It was also reported that human salvador (hWW45) is mutated in some cancer cell lines. However, there have been no data regarding salvador gene mutations in human cancer tissues. To explore the hypothesis that the salvador gene might be similarly mutated in human cancer tissues, we analyzed the entire coding region of the salvador gene for the detection of somatic mutations in a series of human cancer tissues, including carcinomas from stomach, colon, liver and lung. However, using SSCP analysis, no mutation in the coding and splicing regions could be detected in the cancers. The data presented here suggest that salvador is not frequently mutated in human carcinoma tissues and that the mutation might be tumor-type specific.

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