Evidence map›Paper›PMID 26215676›Full record

ArticleOncotarget2015

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, Han-Sung Jung

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 28% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Role of T-box transcription factor 3 in gastric cancers.World journal of gastrointestinal pathophysiology · 2023
    Review
  3. MicroRNAs: A Link between Mammary Gland Development and Breast Cancer.International journal of molecular sciences · 2022
    Review
  4. Review
  5. Article
  6. Article
  7. microRNA-137 is downregulated in thyroid cancer and inhibits proliferation and invasion by targeting EGFR.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  8. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 5 institutions in 3 countries.

Jong-Min LeeDivision in Anatomy and Developmental Biology, Department of Oral Biology, Oral Science Research Center, BK21 PLUS Project, Yonsei University College of Dentistry, Seoul, Korea.
Kyoung-Won ChoDepartment of Radiology, Seoul National University Hospital, Seoul, Korea.
Eun-Jung KimDivision in Anatomy and Developmental Biology, Department of Oral Biology, Oral Science Research Center, BK21 PLUS Project, Yonsei University College of Dentistry, Seoul, Korea.
Qinghuang TangDivision in Anatomy and Developmental Biology, Department of Oral Biology, Oral Science Research Center, BK21 PLUS Project, Yonsei University College of Dentistry, Seoul, Korea.
Kye-Seong KimGraduate School of Biomedical Science and Engineering, College of Medicine, Hanyang University, Seoul, Korea.
Cheryll TickleDepartment of Biology and Biochemistry, University of Bath, Bath, UK.
Han-Sung JungDivision in Anatomy and Developmental Biology, Department of Oral Biology, Oral Science Research Center, BK21 PLUS Project, Yonsei University College of Dentistry, Seoul, Korea.
Yonsei University · KRYonsei University College of DentistryHanyang University · KRSeoul National University Hospital · KRUniversity of Bath · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

AnimalsBreast NeoplasmsCarcinogenesisFemaleHEK293 CellsHeterograftsHumansMammary Glands, AnimalMammary Neoplasms, ExperimentalMiceMice, Inbred BALB CMice, NudeMicroRNAsPregnancyMicroRNAsMIRN137 microRNA, humanMIRN137 microRNA, mousebreast cancermammary gland developmentmiR-137tachykinin-1tumour suppressor

Identifiers

PMID26215676
PMCPMC4673145
OpenAlexW1837485140

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.