Increased expression of SKP2 and phospho-MAPK/ERK1/2 and decreased expression of p27 during tumor progression of cervical neoplasms

被引:42
作者
Chen, Tzu-Ping
Chen, Chien-Ming
Chang, Hsueh-Wen
Wang, Jyh-seng
Chang, Wei-Chi
Hsu, Su-In
Cho, Chung-Lung [1 ]
机构
[1] Natl Sun Yat Sen Univ, Dept Biol Sci, 70 Lien Hai Rd, Kaohsiung 804, Taiwan
[2] E Da Hosp, Dept Pathol, Kaohsiung, Taiwan
[3] Vet Gen Hosp, Dept Pathol, Kaohsiung, Taiwan
[4] Gao Bo Pathol Lab, Kaohsiung, Taiwan
关键词
SKP2; p27; phospho-MAPK/ERK1/2; cervical neoplasm; progression;
D O I
10.1016/j.ygyno.2006.09.015
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective. The objective of this study was to investigate whether the expression of SKP2, p27 and phospho-MAPK/ERK1/2 is associated with the progression of human cervical neoplasia. Methods. We performed immunohistochemical detection to stain formalin-fixed paraffin-embedded cervical tissues with anti-SKP2 and anti-p27 monoclonal antibodies and anti-phospho-p42/44 MAPK antibody. The study sample included 23 normal cervical epithelium, 25 low-grade squamous intraepithelial lesion (LSIL), 19 high-grade squamous intraepithelial lesion (HSIL), and 31 squamous cell carcinomas (SCC). In addition, 14 frozen cervical biopsies, including 1 normal, 6 HSIL, 2 adenocarcinoma and 5 SCC, and a human cervical cancer cell line (HeLa), were analyzed the expression levels of mRNA and protein of SKP2 and p27 by RT-PCR and Western blot analysis, respectively. Results. The expression of SKP2, p27 and phospho-MAPK/ERK1/2 were strongly associated with cervical neoplastic progression (P < 0.0001, P=0.006, P=0.003, respectively; Fisher's Exact Test). In addition, SKP2 expression was positively correlated with phospho-MAPK/ERK1/2 expression (Spearman correlation coefficient= 0.480, P=0.0002). The association between SKP2 and phospho-MAPK/ERK1/2 was significant after controlling for the four histologic grades (P=0.038, Mantel-Haenszel test). Conclusions. These results suggest that expression levels of SKP2, p27 and phospho-MAPK/ERK1/2 may serve as markers for progression in human cervical carcinoma and may also play roles in cervical carcinoma progression and cervical carcinogenesis. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:516 / 523
页数:8
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