Literature DB >> 19477633

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.

Lingeng Lu1, Dionyssios Katsaros, Khvaramze Shaverdashvili, Biyun Qian, Yixing Wu, Irene A Rigault de la Longrais, Mario Preti, Guido Menato, Herbert Yu.   

Abstract

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.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19477633     DOI: 10.1016/j.ejca.2009.05.003

Source DB:  PubMed          Journal:  Eur J Cancer        ISSN: 0959-8049            Impact factor:   9.162


  47 in total

1.  Molecular basis for interaction of let-7 microRNAs with Lin28.

Authors:  Yunsun Nam; Casandra Chen; Richard I Gregory; James J Chou; Piotr Sliz
Journal:  Cell       Date:  2011-11-10       Impact factor: 41.582

Review 2.  The mammalian ovary from genesis to revelation.

Authors:  Mark A Edson; Ankur K Nagaraja; Martin M Matzuk
Journal:  Endocr Rev       Date:  2009-09-23       Impact factor: 19.871

3.  MYC protein inhibits transcription of the microRNA cluster MC-let-7a-1~let-7d via noncanonical E-box.

Authors:  Zifeng Wang; Sheng Lin; Julia Jun Li; Zhenhua Xu; Hong Yao; Xiao Zhu; Dan Xie; Zan Shen; Johnny Sze; Kui Li; Gang Lu; Danny Tat-Ming Chan; Wai Sang Poon; Hsiang-fu Kung; Marie Chia-mi Lin
Journal:  J Biol Chem       Date:  2011-09-08       Impact factor: 5.157

4.  LIN28B polymorphisms influence susceptibility to epithelial ovarian cancer.

Authors:  Jennifer Permuth-Wey; Donghwa Kim; Ya-Yu Tsai; Hui-Yi Lin; Y Ann Chen; Jill Barnholtz-Sloan; Michael J Birrer; Gregory Bloom; Stephen J Chanock; Zhihua Chen; Daniel W Cramer; Julie M Cunningham; Getachew Dagne; Judith Ebbert-Syfrett; David Fenstermacher; Brooke L Fridley; Montserrat Garcia-Closas; Simon A Gayther; William Ge; Aleksandra Gentry-Maharaj; Jesus Gonzalez-Bosquet; Ellen L Goode; Edwin Iversen; Heather Jim; William Kong; John McLaughlin; Usha Menon; Alvaro N A Monteiro; Steven A Narod; Paul D P Pharoah; Catherine M Phelan; Xiaotao Qu; Susan J Ramus; Harvey Risch; Joellen M Schildkraut; Honglin Song; Heather Stockwell; Rebecca Sutphen; Kathryn L Terry; Jonathan Tyrer; Robert A Vierkant; Nicolas Wentzensen; Johnathan M Lancaster; Jin Q Cheng; Thomas A Sellers
Journal:  Cancer Res       Date:  2011-04-11       Impact factor: 12.701

5.  Lin28A and Lin28B inhibit let-7 microRNA biogenesis by distinct mechanisms.

Authors:  Elena Piskounova; Christos Polytarchou; James E Thornton; Robert J LaPierre; Charalabos Pothoulakis; John P Hagan; Dimitrios Iliopoulos; Richard I Gregory
Journal:  Cell       Date:  2011-11-23       Impact factor: 41.582

6.  LIN28A Modulates Splicing and Gene Expression Programs in Breast Cancer Cells.

Authors:  Jun Yang; Brian D Bennett; Shujun Luo; Kaoru Inoue; Sara A Grimm; Gary P Schroth; Pierre R Bushel; H Karimi Kinyamu; Trevor K Archer
Journal:  Mol Cell Biol       Date:  2015-07-06       Impact factor: 4.272

Review 7.  Signaling of miRNAs-FOXM1 in cancer and potential targeted therapy.

Authors:  Min Shi; Jiujie Cui; Keping Xie
Journal:  Curr Drug Targets       Date:  2013-09       Impact factor: 3.465

8.  Lin28 regulates BMP4 and functions with Oct4 to affect ovarian tumor microenvironment.

Authors:  Wei Ma; Jing Ma; Jie Xu; Chong Qiao; Adam Branscum; Andres Cardenas; Andre T Baron; Peter Schwartz; Nita J Maihle; Yingqun Huang
Journal:  Cell Cycle       Date:  2012-12-19       Impact factor: 4.534

Review 9.  Stem cells in aged mammalian ovaries.

Authors:  Irma Virant-Klun; Thomas Skutella
Journal:  Aging (Albany NY)       Date:  2010-01-26       Impact factor: 5.682

10.  SIRT6 Suppresses Pancreatic Cancer through Control of Lin28b.

Authors:  Sita Kugel; Carlos Sebastián; Julien Fitamant; Kenneth N Ross; Supriya K Saha; Esha Jain; Adrianne Gladden; Kshitij S Arora; Yasutaka Kato; Miguel N Rivera; Sridhar Ramaswamy; Ruslan I Sadreyev; Alon Goren; Vikram Deshpande; Nabeel Bardeesy; Raul Mostoslavsky
Journal:  Cell       Date:  2016-05-12       Impact factor: 41.582

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.