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Erschienen in: Medical Oncology 4/2013

01.12.2013 | Original Paper

Elevated expression of tumor miR-222 in pancreatic cancer is associated with Ki67 and poor prognosis

verfasst von: ChongLek Lee, Hang He, Yongjian Jiang, Yang Di, Feng Yang, Ji Li, Chen Jin, Deliang Fu

Erschienen in: Medical Oncology | Ausgabe 4/2013

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Abstract

Pancreatic cancer is known for its bad prognosis. Micro-RNAs mis-expressions are associated with various human cancers and offer new candidate targets for diagnostic and therapeutic strategies. Micro-RNA-222 has been shown to play a crucial role in cancer cell proliferation in recent studies. However, its correlations with the clinicopathological characters of pancreatic cancer still remain unclear. Through a prospective study of 60 pairs of pancreatic cancer tissues, adjacent normal tissues were examined by quantitative reverse-transcription polymerase chain reaction. The correlation between the expression of micro-RNA-222 and clinico-pathological characters was performed using the two-sample Student’s t test. The survival correlations were analyzed by the Kaplan–Meier method and the Cox’s proportional hazards model. Results showed that the expression levels of micro-RNA-222 were significantly elevated in the pancreatic cancer tissue compared with that in adjacent normal tissue. In addition, the overexpression of the tissue micro-RNA-222 strongly related to the expression level of Ki67. Finally, Cox’s proportional hazards model analysis confirmed that micro-RNA-222 high expression level was an independent predictor of poor prognosis. This study provides the first evidence of a potential link between Ki67 and micro-RNA-222, which are both relevant to cell proliferation. Our data suggest the potential of micro-RNA-222 as a prognostic biomarker for the pancreatic cancer.
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Metadaten
Titel
Elevated expression of tumor miR-222 in pancreatic cancer is associated with Ki67 and poor prognosis
verfasst von
ChongLek Lee
Hang He
Yongjian Jiang
Yang Di
Feng Yang
Ji Li
Chen Jin
Deliang Fu
Publikationsdatum
01.12.2013
Verlag
Springer US
Erschienen in
Medical Oncology / Ausgabe 4/2013
Print ISSN: 1357-0560
Elektronische ISSN: 1559-131X
DOI
https://doi.org/10.1007/s12032-013-0700-y

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