Home LiteratureArticle Details
PMID: 17957144 Published · ppublish English Comparative Study Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Let-7 prevents early cancer progression by suppressing expression of the embryonic gene HMGA2.

Cell cycle (Georgetown, Tex.) ·Vol. 6 ·No. 21 ·2007-11-01 ·Pages 2585-90

Park SM, Shell S, Radjabi AR, Schickel R, Feig C, Boyerinas B, Dinulescu DM, Lengyel E, Peter ME

Abstract

The microRNA let-7 regulates late embryonic development by suppressing expression of a number of genes such as c-myc and RAS as well as the embryonic gene high mobility group, A2 (HMGA2). We now demonstrate that HMGA2 is more efficiently targeted by let-7 than RAS. Its expression inversely correlates with the expression of let-7 in the NCI60 cells lines, and the expression of RAS does not change when amounts of let-7 that efficiently silence expression of HMGA2 are introduced into tumor cells. We did not find a difference in the expression of HMGA2 between primary ovarian cancer samples and matching metastases, suggesting that the expression of HMGA2 represents an early event during cancer progression. The late repression of HMGA2 by let-7 during embryonic development, and the early reexpression of HMGA2 during cancer development, is in line with the hypothesis that cancer development represents a case of reverse embryogenesis.

MeSH Terms
Cell Line, Tumor Disease Progression Female Gene Expression Regulation, Neoplastic/physiology HMGA2 Protein/antagonists & inhibitors,biosynthesis,genetics Humans MicroRNAs/physiology Ovarian Neoplasms/genetics,metabolism,prevention & control Suppression, Genetic
Chemicals
HMGA2 Protein MicroRNAs mirnlet7 microRNA, human
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Park Sun-Mi
The Ben May Department for Cancer Research, University of Chicago, Chicago, Illinois 60637, USA.
Shell Scott
Radjabi Amir Reza
Schickel Robert
Feig Christine
Boyerinas Ben
Dinulescu Daniela M
Lengyel Ernst
Peter Marcus E
Article Info
Journal
Cell cycle (Georgetown, Tex.)
Abbr.
Cell Cycle
ISSN
1551-4005
Published
2007-11-01
Epub
2007-00-06
Pages
2585-90
Language
English
Region
United States
NLM ID
101137841
Subset
IM
Grants
NIGMS NIH HHS · R01 GM61712 · United States
NCI NIH HHS · R01CA111882 · United States
Corrections
CommentIn
CommentIn
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com