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Pluripotency factors Lin28 and Oct4 identify a sub-population of stem cell-like cells in ovarian cancer

  • S. Peng
    ,
  • N. J. Maihle
    ,
  • Y. Huang(corresponding author)
*Corresponding author for this work
  • Central South University
    ,
  • Yale University
Scholary Output:
Contribution to journal
Article
Research
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Lin28 and Oct4 are highly expressed in human embryonic stem (ES) cells and, along with two other stem cell marker proteins (Nanog and Sox2), together can convert human somatic cells to pluripotency. As an RNA-binding protein, Lin28 acts to stimulate the translation of a specific subset of mRNAs, and to inhibit the biogenesis of a group of microRNAs. Oct4 is a transcription factor essential for the maintenance of pluripotency and survival of ES cells. In this study, we report that a sub-population of epithelial ovarian cancer (EOC) cells co-expresses Lin28 and Oct4 as demonstrated in the analyses of both cell lines and patient tumor samples. We also observe that the combined expression of these proteins in tumor samples is correlated with advanced tumor grade. Intriguingly, when the expression of these two proteins is repressed in the same cells using RNA interference, there is significant reduction in cell growth and survival. We thus propose that Lin28 and Oct4 may have important roles in the initiation and/or progression of EOC, and consequently may serve as important molecular diagnostics and/or therapeutic targets for the development of novel treatment strategies in EOC patients.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Research
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 2153-2159 (7 pages)

Journal (Volume, Issue Number)

Oncogene (Volume 29, Issue 14)

Publication milestones

  • Published - 04/2010

Publication status

Published - 04/2010

ISSN

0950-9232

Publication IDs

  • Scopus: 77950794030
  • PubMed: 20101213

Publication metrics

Metrics

Scopus
citations
Fractional count
1
Fractional count
0.33
Fractional count
2
Fractional count
0.67
Fractional count
1
Fractional count
1
SciVal
citations
203
SciVal
FWCI
6.13
SciVal
Author count
3
SciVal
Paper percentile
98
SciVal
Top percentile
5

PlumX, opens in new tab

Captures
121
Citation count
238

Funding Details

We thank Jianyu Jin for technical assistance, Jill Reiter for extracts from ovarian cancer cells and insightful scientific discussions, Philip Low and Gil Mor for cell lines and Jason Wilken for critical discussions and reading of this paper. This study was supported by the Fannie E Rippel Foundation and a CT Stem Cell Grant 09SCAYALE14 to YH, and a Yale School of Medicine ‘Senior Women in Medicine’ Professorship, and NIH CA 79808 to NJM.
FundersFunding numbers
NIH
-
NCI
R01CA079808
Fannie E. Rippel Foundation
09SCAYALE14
YSM
-