标题:Detection of CHK1 and CCND1 gene copy number changes in breast cancer with dual-colour fluorescence in-situ hybridization.
作者:Mu K;Li L;Yang Q;Zhang T;Gao P;Meng B;Liu Z;Wang Y;Zhou G
作者机构:[Mu, K] Department of Pathology, Shandong University School of Medicine, Jinan, China;[ Li, L] Department of Pathology, Shandong University School of 更多
通讯作者:Zhou, GY
通讯作者地址:[Zhou, GY]Shandong Univ, Sch Med, Dept Pathol, 44 Wenhua Xi Rd, Jinan 250012, Shandong, Peoples R China.
来源:Histopathology: Official Journal of the British Division of the International Academy of Pathology
出版年:2011
卷:58
期:4
页码:601-607
DOI:10.1111/j.1365-2559.2011.03780.x
关键词:CCND1; CHK1; Breast Cancer; Fluorescence in-situ Hybridization
摘要:AIMS: To investigate the correlation between CCND1 amplification and CHK1 deletion in breast cancer, and to explore their role in tumorigenesis and progression, a comparative study of the gene copy number changes of CCND1 and CHK1 was performed with dual-colour fluorescence in-situ hybridization (FISH). METHODS AND RESULTS: Sixty-one infiltrating ductal breast carcinomas with foci of ductal carcinoma in situ (DCIS) components were selected for dual-colour FISH. A strong correlation was found between CCND1 amplification and CHK1 deletion (P<0.0001). Fourteen cases were detected that demonstrated both CCND1 amplification and CHK1 deletion. Interestingly, when comparing the infiltrating and non-invasive areas for the same tumour, we found three cases with CCND1 amplification in the infiltrating areas but not in the DCIS areas. We did not find a CHK1 gene profile difference between infiltrating and DCIS areas in the same lesions. CONCLUSIONS: Our findings suggest that CCND1 amplification and CHK1 deletion are common events in breast cancer, and that the two genetic alterations often coexist. Our data also suggest that CHK1 deletion is an early genetic event in the development of breast cancer and can be detected at the DCIS stage, whereas CCND1 amplification is more likely to be associated with tumour progression.
收录类别:SCOPUS;SCIE
WOS核心被引频次:10
Scopus被引频次:10
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-79952718383&doi=10.1111%2fj.1365-2559.2011.03780.x&partnerID=40&md5=dd7603c5586b1874a7b6140274ac2a90
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