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The protooncogene CHOP/GADD153, involved in growth arrest and DNA damage response, is amplified in a subset of human sarcomas.

作者信息

Forus A, Flørenes V A, Maelandsmo G M, Fodstad O, Myklebost O

机构信息

Department of Tumor Biology, Norwegian Radium Hospital, Montebello, Oslo.

出版信息

Cancer Genet Cytogenet. 1994 Dec;78(2):165-71. doi: 10.1016/0165-4608(94)90085-x.

DOI:10.1016/0165-4608(94)90085-x
PMID:7828148
Abstract

The C/EBP-homologous transcription factor CHOP (GADD153) is inducible by growth inhibition or DNA damage, and has been shown to be oncogenically activated by the specific (12;16) translocation in human myxoid liposarcoma. We have now found CHOP amplification in two sarcoma cell lines with previously reported amplification of the nearby GLI gene. Among 98 other human sarcomas of various types, CHOP was amplified in a hemangiopericytoma, a liposarcoma, and two osteosarcoma. High constitutive expression levels of CHOP were observed in tumors with gene amplification, but also in some other samples. The nearby MDM2 gene, which codes for a protein that may inactivate wild-type p53, has previously been reported to be frequently amplified in sarcoma. In our sarcoma panel, MDM2 was amplified in 9 cases. MDM2 and CHOP were co-amplified in two of these, whereas the two osteosarcomas had amplified CHOP but not MDM2. CHOP was amplified in both cell lines with GLI amplification, and MDM2 only in one. No mutations in the TP53 gene have been found in samples with amplification of MDM2. In contrast, the cell line in which CHOP but not MDM2 was amplified had mutated TP53, suggesting that selection of this amplicon was not mediated through p53 inactivation.

摘要

相似文献

1
The protooncogene CHOP/GADD153, involved in growth arrest and DNA damage response, is amplified in a subset of human sarcomas.
Cancer Genet Cytogenet. 1994 Dec;78(2):165-71. doi: 10.1016/0165-4608(94)90085-x.
2
Mapping of amplification units in the q13-14 region of chromosome 12 in human sarcomas: some amplica do not include MDM2.人类肉瘤中12号染色体q13-14区域扩增单元的定位:一些扩增不包括MDM2。
Cell Growth Differ. 1993 Dec;4(12):1065-70.
3
MDM2 gene amplification and transcript levels in human sarcomas: relationship to TP53 gene status.人肉瘤中MDM2基因扩增及转录水平:与TP53基因状态的关系
J Natl Cancer Inst. 1994 Sep 7;86(17):1297-302. doi: 10.1093/jnci/86.17.1297.
4
Separate amplified regions encompassing CDK4 and MDM2 in human sarcomas.在人类肉瘤中包含CDK4和MDM2的独立扩增区域。
Genes Chromosomes Cancer. 1996 Dec;17(4):254-9. doi: 10.1002/(SICI)1098-2264(199612)17:4<254::AID-GCC7>3.0.CO;2-2.
5
The 12q13-q15 translocation breakpoints in pleomorphic adenoma and clear-cell sarcoma of tendons and aponeuroses are different from that in myxoid liposarcoma.
Genes Chromosomes Cancer. 1993 Jul;7(3):178-80. doi: 10.1002/gcc.2870070312.
6
Fusion of CHOP to a novel RNA-binding protein in human myxoid liposarcoma.在人类黏液样脂肪肉瘤中CHOP与一种新型RNA结合蛋白的融合。
Nature. 1993 Jun 17;363(6430):640-4. doi: 10.1038/363640a0.
7
HMGA2 is the partner of MDM2 in well-differentiated and dedifferentiated liposarcomas whereas CDK4 belongs to a distinct inconsistent amplicon.在高分化和去分化脂肪肉瘤中,HMGA2是MDM2的伙伴,而CDK4属于一个不同的不一致扩增子。
Int J Cancer. 2008 May 15;122(10):2233-41. doi: 10.1002/ijc.23380.
8
CHOP (GADD153) and its oncogenic variant, TLS-CHOP, have opposing effects on the induction of G1/S arrest.CHOP(GADD153)及其致癌变体TLS-CHOP对G1/S期阻滞的诱导具有相反的作用。
Genes Dev. 1994 Feb 15;8(4):453-64. doi: 10.1101/gad.8.4.453.
9
Amplification of the CDK4 gene in sarcomas: tumor specificity and relationship with the RB gene mutation.肉瘤中CDK4基因的扩增:肿瘤特异性及其与RB基因突变的关系。
Anticancer Res. 1998 Jul-Aug;18(4A):2317-21.
10
Loss of heterozygosity at 12q14-15 often occurs in stage I soft tissue sarcomas and is associated with MDM2 amplification in tumors at various stages.12q14 - 15位点的杂合性缺失在I期软组织肉瘤中经常出现,并且与各个阶段肿瘤中的MDM2扩增相关。
Mod Pathol. 2003 Nov;16(11):1109-16. doi: 10.1097/01.MP.0000096045.51700.66.

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