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Pluripotent factor lin-28 and its homologue lin-28b in epithelial ovarian cancer and their associations with disease outcomes and expression of let-7a and IGF-II
被引:100
作者:
Lu, Lingeng
[1
]
Katsaros, Dionyssios
[2
]
Shaverdashvili, Khvaramze
[1
]
Qian, Biyun
[1
,3
]
Wu, Yixing
[1
]
de la Longrais, Irene A. Rigault
[2
]
Preti, Mario
[2
]
Menato, Guido
[2
]
Yu, Herbert
[1
]
机构:
[1] Yale Univ, Sch Med, Yale Canc Ctr, Dept Epidemiol & Publ Hlth, New Haven, CT 06520 USA
[2] Univ Turin, Dept Obstet & Gynecol, Gynecol Oncol & Breast Canc Unit, Turin, Italy
[3] Tianjin Med Univ Canc Inst & Hosp, Dept Epidemiol, Tianjin, Peoples R China
基金:
美国国家卫生研究院;
关键词:
Epithelial ovarian cancer;
Lin-28;
Let-7;
IGF-II;
Prognosis;
GROWTH-FACTOR-II;
FACTOR BINDING PROTEIN-3;
SELF-RENEWAL;
GENE;
RNA;
TRANSLATION;
PROGRESSION;
REPRESSION;
MICRORNAS;
LIN28;
D O I:
10.1016/j.ejca.2009.05.003
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Lin-28 and lin-28B are RNA-binding proteins which can block microRNA let-7 maturation and affect the differentiation and proliferation of embryonic stem cells. Lin-28 may also regulate the expression of insulin-like growth factor II (IGF-II). As one of the pluripotent factors involved in making induced pluripotent stem cells (iPS), lin-28 is considered a potential therapeutic target for cancer treatment. To further understand the role of lin-28 in cancer, we analysed the expression of lin-28 and its homologue lin-28B in tumour samples, and evaluated their associations with let-7a maturation, IGF-II expression, disease features and outcomes in 211 patients with primary epithelial ovarian cancer. The analysis showed that both lin-28 and lin-28B were positively correlated with primary and pre-let-7a-3; lin-28B, not lin-28, was inversely correlated with mature let-7a. A positive correlation was also observed between lin-28B and IGF-II expression, while no association was found between lin-28B and IGF-I or IGFBP-3. The study further demonstrated that lin-28B expression was associated with the risk of disease progression and death; patients with high lin-28B had shorter progression-free and overall survival than those with low lin-28B. These results seem to support the findings of recent in vitro experiments, showing that lin-28 blocks the process of let-7a maturation. Our study also suggests that lin-28B may promote ovarian cancer progression and serve as an unfavourable prognostic marker for the disease. The correlation between lin-28B and IGF-II indicates that the growth factor may mediate the effect of lin-28B on tumour growth. (C) 2009 Elsevier Ltd. All rights reserved.
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页码:2212 / 2218
页数:7
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