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ARHI/NOEY2失活在乳腺肿瘤发病机制中可能很重要。

ARHI/NOEY2 inactivation may be important in breast tumor pathogenesis.

作者信息

Hisatomi Hisashi, Nagao Kumi, Wakita Kazuyuki, Kohno Norio

机构信息

Center for Molecular Biology and Cytogenetics, SRL, Inc., Tokyo, Japan.

出版信息

Oncology. 2002;62(2):136-40. doi: 10.1159/000048259.

DOI:10.1159/000048259
PMID:11914599
Abstract

Allelic loss frequently occurs on the short arm of chromosome 1 in human breast carcinoma, suggesting that the ARHI/NOEY2 gene, an imprinted putative tumor suppressor gene, is involved in the pathogenesis of the tumor entity. To clarify the clinical importance of ARHI/NOEY2 mRNA in breast cancer, we studied whether ARHI/NOEY2 inactivation might contribute to tumors arising in the breast. An ARHI/NOEY2 message was detected by real-time PCR analysis in all noncancerous breast tissues, but was not detected in 2 of 26 breast cancer tissue samples. In 10 of 26 breast cancer tissue samples ARHI/NOEY2 mRNA was substantially reduced. ARHI/NOEY2 expression was lost or markedly reduced in 12 of 26 (46.15%) breast cancer tissue samples. In summary, we conclude that decreased ARHI/NOEY2 mRNA expression may play an important role in the pathogenesis of breast cancer.

摘要

等位基因缺失在人类乳腺癌中经常发生在1号染色体短臂上,这表明ARHI/NOEY2基因,一个印记的假定肿瘤抑制基因,参与了该肿瘤实体的发病机制。为了阐明ARHI/NOEY2 mRNA在乳腺癌中的临床重要性,我们研究了ARHI/NOEY2失活是否可能导致乳腺肿瘤的发生。通过实时PCR分析在所有非癌性乳腺组织中检测到ARHI/NOEY2信息,但在26个乳腺癌组织样本中的2个中未检测到。在26个乳腺癌组织样本中的10个中,ARHI/NOEY2 mRNA大幅减少。在26个(46.15%)乳腺癌组织样本中的12个中,ARHI/NOEY2表达缺失或显著降低。总之,我们得出结论,ARHI/NOEY2 mRNA表达降低可能在乳腺癌发病机制中起重要作用。

相似文献

1
ARHI/NOEY2 inactivation may be important in breast tumor pathogenesis.ARHI/NOEY2失活在乳腺肿瘤发病机制中可能很重要。
Oncology. 2002;62(2):136-40. doi: 10.1159/000048259.
2
NOEY2 (ARHI), an imprinted putative tumor suppressor gene in ovarian and breast carcinomas.NOEY2(ARHI),一种在卵巢癌和乳腺癌中印记的假定肿瘤抑制基因。
Proc Natl Acad Sci U S A. 1999 Jan 5;96(1):214-9. doi: 10.1073/pnas.96.1.214.
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Genomic structure and promoter characterization of an imprinted tumor suppressor gene ARHI.印记肿瘤抑制基因ARHI的基因组结构与启动子特征分析
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ARHI (DIRAS3)-mediated autophagy-associated cell death enhances chemosensitivity to cisplatin in ovarian cancer cell lines and xenografts.ARHI(DIRAS3)介导的自噬相关细胞死亡增强了卵巢癌细胞系和异种移植瘤对顺铂的化疗敏感性。
Cell Death Dis. 2015 Aug 6;6(8):e1836. doi: 10.1038/cddis.2015.208.
2
Somatic Mutation of ARHI Gene in Hepatocellular Carcinomas.肝细胞癌中ARHI基因的体细胞突变
Pathol Oncol Res. 2015 Sep;21(4):1277-9. doi: 10.1007/s12253-015-9924-9. Epub 2015 Jul 5.
3
JMJD2A contributes to breast cancer progression through transcriptional repression of the tumor suppressor ARHI.
JMJD2A通过对肿瘤抑制因子ARHI的转录抑制作用促进乳腺癌进展。
Breast Cancer Res. 2014 May 30;16(3):R56. doi: 10.1186/bcr3667.
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DIRAS3 regulates the autophagosome initiation complex in dormant ovarian cancer cells.DIRAS3调节休眠卵巢癌细胞中的自噬体起始复合物。
Autophagy. 2014 Jun;10(6):1071-92. doi: 10.4161/auto.28577.
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Over-expression of ARHI decreases tumor growth, migration, and invasion in human glioma.ARHI 的过表达可降低人神经胶质瘤中的肿瘤生长、迁移和侵袭。
Med Oncol. 2014 Mar;31(3):846. doi: 10.1007/s12032-014-0846-2. Epub 2014 Jan 24.
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Expression and epigenetic regulation of angiogenesis-related factors during dormancy and recurrent growth of ovarian carcinoma.血管生成相关因子在卵巢癌休眠和复发性生长过程中的表达及其表观遗传调控。
Epigenetics. 2013 Dec;8(12):1330-46. doi: 10.4161/epi.26675. Epub 2013 Oct 17.
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