Low cyclin F expression in hepatocellular carcinoma associates with poor differentiation and unfavorable prognosis. Issue 4 (17th February 2013)
- Record Type:
- Journal Article
- Title:
- Low cyclin F expression in hepatocellular carcinoma associates with poor differentiation and unfavorable prognosis. Issue 4 (17th February 2013)
- Main Title:
- Low cyclin F expression in hepatocellular carcinoma associates with poor differentiation and unfavorable prognosis
- Authors:
- Fu, Jia
Qiu, Huijuan
Cai, Muyan
Pan, Yinghua
Cao, Yun
Liu, Lili
Yun, Jingping
Zhang, Chris Zhiyi - Abstract:
- <abstract abstract-type="main" xml:lang="en" id="cas12100-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Cyclin F, capable of forming Skp1‐Cul1‐F‐box protein ubiquitin ligase complex, is implicated in controlling centrosome duplication and preventing genome instability. Cyclin F oscillates during cell cycle with a similar pattern to cyclin A. However, its expression and significance in cancer remain obscure. In this study, we showed that cyclin F was noticeably decreased in 16 pairs of tissue samples of hepatocellular carcinoma (HCC) compared to paracarcinoma tissues, at both mRNA and protein levels. Immunohistochemical staining data revealed that in 71.8% (176/245) of HCC cases, cyclin F expression in tumor tissue was much lower than that in nontumorous tissue. Low cyclin F expression, defined by receiver operating characteristic curve analysis, was present in 69.0% of HCC patients. Low expression of cyclin F was significantly correlated with tumor size, clinical stage, serum alpha‐fetoprotein level and tumor multiplicity. Further study showed that cyclin F expression was reversely associated with tumor differentiation in HCC. Kaplan<bold>–</bold>Meier analysis indicated that low cyclin F expression was related to poor overall survival and recurrence‐free survival. The prognostic impact of cyclin F was further confirmed by stratified survival analysis. Importantly, multivariate analysis revealed that low cyclin F expression was an independent poor<abstract abstract-type="main" xml:lang="en" id="cas12100-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Cyclin F, capable of forming Skp1‐Cul1‐F‐box protein ubiquitin ligase complex, is implicated in controlling centrosome duplication and preventing genome instability. Cyclin F oscillates during cell cycle with a similar pattern to cyclin A. However, its expression and significance in cancer remain obscure. In this study, we showed that cyclin F was noticeably decreased in 16 pairs of tissue samples of hepatocellular carcinoma (HCC) compared to paracarcinoma tissues, at both mRNA and protein levels. Immunohistochemical staining data revealed that in 71.8% (176/245) of HCC cases, cyclin F expression in tumor tissue was much lower than that in nontumorous tissue. Low cyclin F expression, defined by receiver operating characteristic curve analysis, was present in 69.0% of HCC patients. Low expression of cyclin F was significantly correlated with tumor size, clinical stage, serum alpha‐fetoprotein level and tumor multiplicity. Further study showed that cyclin F expression was reversely associated with tumor differentiation in HCC. Kaplan<bold>–</bold>Meier analysis indicated that low cyclin F expression was related to poor overall survival and recurrence‐free survival. The prognostic impact of cyclin F was further confirmed by stratified survival analysis. Importantly, multivariate analysis revealed that low cyclin F expression was an independent poor prognostic marker for overall survival. We conclude that cyclin F is downregulated in HCC and is a promising prognostic marker for patients suffering from this deadly disease.</p> </abstract> … (more)
- Is Part Of:
- Cancer science. Volume 104:Issue 4(2013:Apr.)
- Journal:
- Cancer science
- Issue:
- Volume 104:Issue 4(2013:Apr.)
- Issue Display:
- Volume 104, Issue 4 (2013)
- Year:
- 2013
- Volume:
- 104
- Issue:
- 4
- Issue Sort Value:
- 2013-0104-0004-0000
- Page Start:
- 508
- Page End:
- 515
- Publication Date:
- 2013-02-17
- Subjects:
- Cancer -- Periodicals
Neoplasms -- Periodicals
Research -- Periodicals
Electronic journals
616.994005 - Journal URLs:
- http://firstsearch.oclc.org ↗
http://firstsearch.oclc.org/journal=1347-9032;screen=info;ECOIP ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1349-7006 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/cas.12100 ↗
- Languages:
- English
- ISSNs:
- 1347-9032
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3046.603000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3905.xml