Literature DB >> 18674967

let-7 microRNAs in development, stem cells and cancer.

Ingo Büssing1, Frank J Slack, Helge Grosshans.   

Abstract

MicroRNAs (miRNAs) are small noncoding RNAs, approximately 22 nucleotides in length, that repress target messenger RNAs (mRNAs) through an antisense mechanism. The let-7 miRNA was originally discovered in the nematode Caenorhabditis elegans, where it regulates cell proliferation and differentiation, but subsequent work has shown that both its sequence and its function are highly conserved in mammals. Recent results have now linked decreased let-7 expression to increased tumorigenicity and poor patient prognosis. Moreover, during normal development, accumulation of let-7 can be prevented by LIN28, a promoter of pluripotency. Based on these findings, we propose that let-7 regulates 'stemness' by repressing self-renewal and promoting differentiation in both normal development and cancer. A more complete understanding of its function will thus provide insights into these processes and might yield diagnostic and therapeutic advances for cancer treatment.

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Year:  2008        PMID: 18674967     DOI: 10.1016/j.molmed.2008.07.001

Source DB:  PubMed          Journal:  Trends Mol Med        ISSN: 1471-4914            Impact factor:   11.951


  258 in total

1.  MUC1-C Induces the LIN28B→LET-7→HMGA2 Axis to Regulate Self-Renewal in NSCLC.

Authors:  Maroof Alam; Rehan Ahmad; Hasan Rajabi; Donald Kufe
Journal:  Mol Cancer Res       Date:  2014-11-03       Impact factor: 5.852

2.  microRNA-dependent temporal gene expression in the ureteric bud epithelium during mammalian kidney development.

Authors:  Vidya K Nagalakshmi; Volkhard Lindner; Andy Wessels; Jing Yu
Journal:  Dev Dyn       Date:  2014-11-23       Impact factor: 3.780

3.  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

4.  Structural basis of pre-let-7 miRNA recognition by the zinc knuckles of pluripotency factor Lin28.

Authors:  Fionna E Loughlin; Luca F R Gebert; Harry Towbin; Andreas Brunschweiger; Jonathan Hall; Frédéric H-T Allain
Journal:  Nat Struct Mol Biol       Date:  2011-12-11       Impact factor: 15.369

5.  Mechanical loading and TGF-β change the expression of multiple miRNAs in tendon fibroblasts.

Authors:  Christopher L Mendias; Jonathan P Gumucio; Evan B Lynch
Journal:  J Appl Physiol (1985)       Date:  2012-04-26

6.  Cross-analysis of gene and miRNA genome-wide expression profiles in human fibroblasts at different stages of transformation.

Authors:  Paola Ostano; Silvia Bione; Cristina Belgiovine; Ilaria Chiodi; Chiara Ghimenti; A Ivana Scovassi; Giovanna Chiorino; Chiara Mondello
Journal:  OMICS       Date:  2012 Jan-Feb

7.  MiR-181 mediates cell differentiation by interrupting the Lin28 and let-7 feedback circuit.

Authors:  X Li; J Zhang; L Gao; S McClellan; M A Finan; T W Butler; L B Owen; G A Piazza; Yaguang Xi
Journal:  Cell Death Differ       Date:  2011-10-07       Impact factor: 15.828

Review 8.  The role of miRNAs and endogenous siRNAs in maternal-to-zygotic reprogramming and the establishment of pluripotency.

Authors:  Petr Svoboda; Matyas Flemr
Journal:  EMBO Rep       Date:  2010-07-23       Impact factor: 8.807

9.  The Hippo pathway effectors TAZ/YAP regulate dicer expression and microRNA biogenesis through Let-7.

Authors:  Steven G Chaulk; Victoria J Lattanzi; Samantha E Hiemer; Richard P Fahlman; Xaralabos Varelas
Journal:  J Biol Chem       Date:  2013-12-09       Impact factor: 5.157

Review 10.  HMGA2, microRNAs, and stem cell aging.

Authors:  Scott M Hammond; Norman E Sharpless
Journal:  Cell       Date:  2008-12-12       Impact factor: 41.582

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