A contrasting function for miR-137 in embryonic mammogenesis and adult breast carcinogenesis

Jong Min Lee, Kyoung Won Cho, Eun Jung Kim, Qinghuang Tang, Kye Seong Kim, Cheryll Tickle, Hansung Jung

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

MicroRNAs are differentially expressed in breast cancer cells and have been implicated in cancer formation, tumour invasion and metastasis. We investigated the miRNA expression profiles in the developing mammary gland. MiR-137 was expressed prominently in the developing mammary gland. When the miR-137 was over-expressed in the embryo, the mammary epithelium became thickened. Moreover, genes associated with mammary gland formation such as Tbx3 and Lef1 were not expressed. This suggests that miR-137 induces gland formation and invasion. When miR-137 was over-expressed in MDA-MB-231 cells, their ability to form tumours in adult mice was significantly reduced. These data support miR-137 decides epithelial cell behavior in the human breast cancer. It also suggests that miR-137 is a potential therapeutic target for amelioration of breast cancer progression.

Original languageEnglish
Pages (from-to)22048-22059
Number of pages12
JournalOncotarget
Volume6
Issue number26
DOIs
Publication statusPublished - 2015 Jan 1

Fingerprint

Human Mammary Glands
Carcinogenesis
Breast
Breast Neoplasms
MicroRNAs
Neoplasms
Aptitude
Embryonic Structures
Epithelium
Epithelial Cells
Neoplasm Metastasis
Genes
Therapeutics

All Science Journal Classification (ASJC) codes

  • Oncology

Cite this

Lee, Jong Min ; Cho, Kyoung Won ; Kim, Eun Jung ; Tang, Qinghuang ; Kim, Kye Seong ; Tickle, Cheryll ; Jung, Hansung. / A contrasting function for miR-137 in embryonic mammogenesis and adult breast carcinogenesis. In: Oncotarget. 2015 ; Vol. 6, No. 26. pp. 22048-22059.
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A contrasting function for miR-137 in embryonic mammogenesis and adult breast carcinogenesis. / Lee, Jong Min; Cho, Kyoung Won; Kim, Eun Jung; Tang, Qinghuang; Kim, Kye Seong; Tickle, Cheryll; Jung, Hansung.

In: Oncotarget, Vol. 6, No. 26, 01.01.2015, p. 22048-22059.

Research output: Contribution to journalArticle

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