Overexpression of the RNA-binding proteins Lin28B and IGF2BP3 (IMP3) is associated with chemoresistance and poor disease outcome in ovarian cancer

被引:105
作者
Hsu, K-F [1 ]
Shen, M-R [2 ]
Huang, Y-F [1 ]
Cheng, Y-M [1 ]
Lin, S-H [3 ]
Chow, N-H [4 ]
Cheng, S-W [4 ]
Chou, C-Y [1 ]
Ho, C-L [4 ]
机构
[1] Natl Cheng Kung Univ, Natl Cheng Kung Univ Hosp, Dept Obstet & Gynecol, Coll Med, Tainan 70101, Taiwan
[2] Natl Cheng Kung Univ, Natl Cheng Kung Univ Hosp, Dept Pharmacol, Coll Med, Tainan 70101, Taiwan
[3] Natl Cheng Kung Univ, Natl Cheng Kung Univ Hosp, Inst Clin Med, Coll Med, Tainan 70101, Taiwan
[4] Natl Cheng Kung Univ, Natl Cheng Kung Univ Hosp, Dept Pathol, Coll Med, Tainan 70101, Taiwan
关键词
ovarian cancer; chemoresistance; Lin28B; IMP3; ANTICANCER DRUG CISPLATIN; MESSENGER-RNA; UNFAVORABLE PROGNOSIS; CELLULAR ACCUMULATION; COPPER-HISTIDINE; TRANSPORTER CTR1; EXPRESSION; MARKER; PLATINUM; FAMILY;
D O I
10.1038/bjc.2015.254
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: RNA-binding proteins have an important role in messenger RNA (mRNA) regulation during tumour development and carcinogenesis. In the present study, we examined the insulin-like growth factor 2 mRNA-binding proteins (IGF2BPs; hereafter refered to as IMPs) and Lin28 family expressions in epithelial ovarian carcinoma (EOC) patients and correlated their expression levels with the response to chemotherapy, hCTR1 expression and patient survival. Methods: Patients clinical information, real-time RT-PCR, immunohistochemistry, western blot, Transwell migration invasion assays, and cytotoxicity assays were used. Results: From 140 EOC patients, high expression of IMP3 or Lin28B was associated with poor survival, and women diagnosed at advanced stages with elevated IMP3 and Lin28B were at higher risk of developing chemoresistance. High IMP3 levels combined with high Lin28B levels significantly correlated with the poorest 5-year survival rates. Knockdown of IMP3 or Lin28B decreased cell proliferation, migration, and invasion, and increased the platinum sensitivity, but not taxol sensitivity, of ovarian cancer cells through increased expression of hCTR1, a copper transporter involved in platinum uptake. High expression of hCTR1 correlated with low expression of IMP3/Lin28B and better progression-free survival in advanced-stage EOC patients. Conclusion: Testing for a combination of elevated IMP3 and Lin28B levels could further facilitate the identification of a patient subgroup with the worst prognosis.
引用
收藏
页码:414 / 424
页数:11
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