Expression of pin1 and ki67 in cervical cancer and their significance

Li Hongyu , Shen Hongling , Xu Qian , Deng Dongrui , Wang Shixuan , Lu Yunping , Ma Ding

Current Medical Science ›› 2006, Vol. 26 ›› Issue (34) : 120 -122.

PDF
Current Medical Science ›› 2006, Vol. 26 ›› Issue (34) : 120 -122. DOI: 10.1007/BF02828056
Article

Expression of pin1 and ki67 in cervical cancer and their significance

Author information +
History +
PDF

Abstract

In order to investigate the expression levels of Pin1 mRNA and protein in cervical cancer and its association with Ki67 and their clinical significance, amplification of Pin1 gene was examined by RT-PCR, and the expression of both Pin1 and Ki67 protein was detected by immunohistochemistry in cervical cancer tissues. It was shown that the expression levels of Pin1 were higher in cervical cancer than in normal cervical tissues (P<0.05). The expression of Pin1 protein was increased progressively along with the disease process from normal cervix to CIN and to cervical cancer (P<0.05). No significant difference in the Pin1 expression was found between disease stages (FIGO), pathological grades or pelvic lymph node metastasis status (P>0.05). The expression of Pin1 was significantly higher in adenocarcinoma than in squamous carcinoma of the uterine cervix (P<0.05). In cervical cancer, the overexpression of Pin1 was positively correlated with that of Ki67 (P<0.05). These results suggested that the overexpression of Pin1 was closely related with cancer cell proliferation or progression of cervical cancer and contributed to oncogenesis. Pin1 may serve as a potential marker for cervical cancer diagnosis.

Keywords

peptidyl-prolyl cis/trans Isomerase PPIase Pin1 / cervical cancer / Ki67

Cite this article

Download citation ▾
Li Hongyu, Shen Hongling, Xu Qian, Deng Dongrui, Wang Shixuan, Lu Yunping, Ma Ding. Expression of pin1 and ki67 in cervical cancer and their significance. Current Medical Science, 2006, 26(34): 120-122 DOI:10.1007/BF02828056

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

RyoA, LiouY C, LuK P, et al.. Prolyl isomerase Pin1: a catalyst for oncogenesis and a potential therapeutic target in cancer. J Cell Sci, 2003, 116(5): 773-83

[2]

AyalaG, WangD, WulfG, et al.. The prolyl isomerase Pin1 is a novel prognostic marker in human prostate cancer. Cancer Res, 2003, 63: 6244-6251

[3]

BaoL, KimzeyA, SauterG, et al.. Prevalent overexpression of prolyl isomerase Pin1 in human cancers. Am J Pathol, 2004, 164(5): 1727-1737

[4]

MiyashitaH, MoriS, MotegiK, et al.. Pin1 is overexpressed in oral squamous cell carcinoma and its levels correlate with cyclin D1 overexpression. Oncol Rep, 2003, 10(2): 455-461

[5]

LuK P. Pinning down cell signaling, cancer and Alzheimer's disease. Trends Biochem Sci, 2004, 29(4): 200-209

[6]

WulfG, FinnG, SuizuF, et al.. Phosphorylation-specific prolyl isomerization: is there an underlying theme?. Nat Cell Biol, 2005, 7(5): 435-441

[7]

WulfG M, RyoA, WulfG G, et al.. Pin1 is overexpressed in breast cancer and potentiates the transcriptional activity of phosphorylated c-Jun towards the cyclin D1 gene. EMBO J, 2001, 20(13): 3459-3472

[8]

LuP J, ZhouX Z, LiouY C, et al.. Critical role of WW domain phosphorylation in regulating its phosphoserine-binding activity and the Pin1 function. J Biol Chem, 2002, 277(4): 2381-2384

[9]

LiH, ByeonI J, JuY, et al.. Structure of human Ki67 FHA domain and its binding to a phosphoprotein fragment from hNIFK reveal unique recognition sites and new views to the structural basis of FHA domain functions. J Mol Biol, 2004, 335(1): 371-381

AI Summary AI Mindmap
PDF

74

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/