Mutational and expressional analyses of STAG2 gene in solid cancers

被引:29
作者
Kim, M. S. [1 ]
Kim, S. S. [2 ]
Je, E. M. [1 ]
Yoo, N. J. [1 ]
Lee, S. H. [1 ,3 ]
机构
[1] Catholic Univ Korea, Coll Med, Dept Pathol, Seoul 137701, South Korea
[2] Catholic Univ Korea, Coll Med, Dept Internal Med, Seoul 137701, South Korea
[3] Catholic Univ Korea, Coll Med, Res Ctr Genome Polymorphism, Seoul 137701, South Korea
关键词
STAG2; aneuploidy; expression; mutation; gastric cancer; colorectal cancer; prostate cancer; COPY NUMBER; ANEUPLOIDY; TUMORIGENESIS; INSTABILITY; LEUKEMIA; IDENTIFICATION; TRANSFORMATION; INHIBITOR; PCR;
D O I
10.4149/neo_2012_067
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aneuploidy is frequently observed in cancers and is considered a crucial mechanism in cancer development. STAG2 is a gene that encodes a component of cohesion complex required for normal chromosomal segregation. Recently, somatic mutation of STAG2 gene and loss of STAG2 protein have been reported in glioblastoma, Ewing's sarcoma and melanoma. The aim of this study was to see whether such alterations of STAG2 are also common in other cancers. In this study, we analyzed STAG2 somatic mutation in 45 colorectal carcinomas (CRC), 45 gastric carcinomas (GC), 45 breast carcinomas, 45 non-small cell lung cancers and 45 prostate carcinomas (PCA) by single-strand conformation polymorphism. We analyzed also STAG2 protein expression in 100 GC, 103 CRC and 107 PCA by immunohistochemistry. STAG2 protein was well expressed in normal stomach, colon and prostate epithelial cells, while it was lost in 27% of GC, 23% of CRC and 30% of PCA. The loss of STAG2 was observed irrespective of subtypes, stages and grades of the cancers. However, we could not find any STAG2 mutations in these cancers. The loss of expression of STAG2 in GC, CRC and PCA tissues compared to their corresponding normal cells indicates that STAG2 loss is common in carcinomas as well. The data suggest also that loss of expression of STAG2, but not somatic mutation, might be responsible to STAG2 inactivation and is common in studied types of carcinomas.
引用
收藏
页码:524 / 529
页数:6
相关论文
共 22 条
[1]   Are There Any More Ovarian Tumor Suppressor Genes? A New Perspective Using Ultra High-Resolution Copy Number and Loss of Heterozygosity Analysis [J].
Gorringe, Kylie L. ;
Ramakrishna, Manasa ;
Williams, Louise H. ;
Sridhar, Anita ;
Boyle, Samantha E. ;
Bearfoot, Jennifer L. ;
Li, Jason ;
Anglesio, Michael S. ;
Campbell, Ian G. .
GENES CHROMOSOMES & CANCER, 2009, 48 (10) :931-942
[2]   TRISOMY IN MAN [J].
HASSOLD, TJ ;
JACOBS, PA .
ANNUAL REVIEW OF GENETICS, 1984, 18 :69-97
[3]  
Hayashi K, 1991, PCR Methods Appl, V1, P34
[4]   Boveri revisited: chromosomal instability, aneuploidy and tumorigenesis [J].
Holland, Andrew J. ;
Cleveland, Don W. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2009, 10 (07) :478-487
[5]   Human T cell leukemia virus type 1 oncoprotein tax targets the human mitotic checkpoint protein MAD1 [J].
Jin, DY ;
Spencer, F ;
Jeang, KT .
CELL, 1998, 93 (01) :81-91
[6]   Decreased expression of Bax-interacting factor-1 (Bif-1) in invasive urinary bladder and gallbladder cancers [J].
Kim, Su Young ;
Oh, Young Lyun ;
Kim, Kyung Mee ;
Jeong, Eun Goo ;
Kim, Min Sung ;
Yoo, Nam Jin ;
Lee, Sug Hyung .
PATHOLOGY, 2008, 40 (06) :553-557
[7]   Association between structural and numerical chromosomal aberrations in acute myeloblastic leukemia:: a study by RT-PCR and FISH in 447 patients with de-novo AML [J].
Krauter, J ;
Ganser, A ;
Bergmann, L ;
Raghavachar, A ;
Hoelzer, D ;
Lübbert, M ;
Schlimok, G ;
Arnold, R ;
Kirchner, H ;
Port, M ;
Heil, G .
ANNALS OF HEMATOLOGY, 1999, 78 (06) :265-269
[8]   PIK3CA gene is frequently mutated in breast carcinomas and hepatocellular carcinomas [J].
Lee, JW ;
Soung, YH ;
Kim, SY ;
Lee, HW ;
Park, WS ;
Nam, SW ;
Kim, SH ;
Lee, JY ;
Yoo, NJ ;
Lee, SH .
ONCOGENE, 2005, 24 (08) :1477-1480
[9]   Alterations of Fas (Apo-1/CD95) gene in non-small cell lung cancer [J].
Lee, SH ;
Shin, MS ;
Park, WS ;
Kim, SY ;
Kim, HS ;
Han, JY ;
Park, GS ;
Dong, SM ;
Pi, JH ;
Kim, CS ;
Kim, SH ;
Lee, JY ;
Yoo, NJ .
ONCOGENE, 1999, 18 (25) :3754-3760
[10]   Genetic instability in colorectal cancers [J].
Lengauer, C ;
Kinzler, KW ;
Vogelstein, B .
NATURE, 1997, 386 (6625) :623-627