Oncogenic Role of Skp2 and p27^(Kip1) in Intraductal Proliferative Lesions of the Breast  被引量:4

Oncogenic Role of Skp2 and p27^(Kip1) in Intraductal Proliferative Lesions of the Breast

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作  者:Yan Lv Yun Niu Xiu-min Ding Xu-qi Xiao 

机构地区:[1]Department of Acupuncture and Moxibustion,Tianjin University of Traditional Chinese Medicine,Tianjin 300193,China [2]Breast Cancer Research and Pathology Laboratory,Cancer Institute&Hospital of Tianjin Medical University,Tianjin 300060,China

出  处:《Chinese Medical Sciences Journal》2012年第3期161-166,共6页中国医学科学杂志(英文版)

基  金:Supported by the National Natural Science Foundation of China(30471967);research funding of Tianjin Cancer Institute&Hospitalof Tianjin Medical University

摘  要:Objective To investigate whether the connection of p27 Kip1 to S-phase kinase-associated protein 2 (Skp2) plays an oncogenic role in intraductal proliferative lesions of the breast. Methods Here we investigated the mechanism involved in association of Skp2's degradation of p27 Kip1 with the breast carcinogenesis by immunohistochemical method through detection of Skp2 and p27 Kip1 protein levels in 120 paraffin-embedded tissues of intraductal proliferative lesions including usual ductal hyperplasia (UDH, n=30), atypical ductal hyperplasia (n=30), flat epithelial atypia (FEA, n=30), and ductal carcinoma in situ (DCIS, n=30). Moreover, the expression status of Skp2 and p27 Kip1 in 30 cases of the normal breast paraffin-embedded tissues were explored. Results The DCIS group was with the highest Skp2 level and the lowest p27 Kip1 level, and the UDH group was with the lowest Skp2 level and the highest p27 Kip1 level. Both Skp2 and p27 Kip1 levels in the DCIS group were significantly different from those in the UDH group (all P<0.01). The levels of Skp2 and p27 Kip1 in the FEA group were significantly different from both the DCIS and UDH groups (all P<0.05). p27 Kip1 was negatively correlated with Skp2 in both the UDH group (r=-0.629, P=0.026) and DCIS group (r=-0.893, P=0.000). Conclusion Overexpression of Skp2 might be the mechanism underlying p27 Kip1 over degradation.

关 键 词:breast cancer intraductal proliferative lesions p27 ^Kip1 S-phase kinase-associated protein 2 

分 类 号:Q591.2[生物学—生物化学] X503.1[环境科学与工程—环境工程]

 

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