Evidence map›Paper›PMID 23270413›Full record

ArticleBMC genomics2012

An integrative analysis of cellular contexts, miRNAs and mRNAs reveals network clusters associated with antiestrogen-resistant breast cancer cells.

Seungyoon Nam, Xinghua Long, Changhyuk Kwon, Sun Kim, Kenneth P Nephew

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 17% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. The Emerging Roles of miR-125b in Cancers.Cancer management and research · 2020
    Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. The novel role of miRNAs for tamoxifen resistance in human breast cancer.Cellular and molecular life sciences : CMLS · 2015
    Review
  11. Article
  12. miRNA clusters as therapeutic targets for hormone-resistant breast cancer.Expert review of endocrinology & metabolism · 2015
    Article
  13. Article
  14. 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

5 authors at 4 institutions in 3 countries.

Seungyoon NamCancer Genomics Branch, National Cancer Center, Goyang-si, Gyeonggi-do, 410-769, Korea. seungyoon.nam@ncc.re.kr
Xinghua Long
Changhyuk Kwon
Sun Kim
Kenneth P Nephew
National Cancer Center · KRIndiana University School of MedicineSeoul National University · KRWuhan University · CN

Funding

DNA Methylation and Ovarian CancerR01CA085289 · NCI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI NEPHEW, KENNETH P · 2002 to 2012
$2.4M
NCI NIH HHS CA085289NCI NIH HHS CA113001
6 · The paper itself

Abstract

backgroundA major goal of the field of systems biology is to translate genome-wide profiling data (e.g., mRNAs, miRNAs) into interpretable functional networks. However, employing a systems biology approach to better understand the complexities underlying drug resistance phenotypes in cancer continues to represent a significant challenge to the field. Previously, we derived two drug-resistant breast cancer sublines (tamoxifen- and fulvestrant-resistant cell lines) from the MCF7 breast cancer cell line and performed genome-wide mRNA and microRNA profiling to identify differential molecular pathways underlying acquired resistance to these important antiestrogens. In the current study, to further define molecular characteristics of acquired antiestrogen resistance we constructed an "integrative network". We combined joint miRNA-mRNA expression profiles, cancer contexts, miRNA-target mRNA relationships, and miRNA upstream regulators. In particular, to reduce the probability of false positive connections in the network, experimentally validated, rather than prediction-oriented, databases were utilized to obtain connectivity. Also, to improve biological interpretation, cancer contexts were incorporated into the network connectivity.

resultsBased on the integrative network, we extracted "substructures" (network clusters) representing the drug resistant states (tamoxifen- or fulvestrant-resistance cells) compared to drug sensitive state (parental MCF7 cells). We identified un-described network clusters that contribute to antiestrogen resistance consisting of miR-146a, -27a, -145, -21, -155, -15a, -125b, and let-7s, in addition to the previously described miR-221/222.

conclusionsBy integrating miRNA-related network, gene/miRNA expression and text-mining, the current study provides a computational-based systems biology approach for further investigating the molecular mechanism underlying antiestrogen resistance in breast cancer cells. In addition, new miRNA clusters that contribute to antiestrogen resistance were identified, and they warrant further investigation.

Indexed as

Molecular Targeted TherapyBreast NeoplasmsCluster AnalysisComputational BiologyDrug Resistance, NeoplasmEstrogensHumansMCF-7 CellsMicroRNAsRNA, MessengerEstrogensMicroRNAsRNA, Messenger

Identifiers

PMID23270413
PMCPMC3560207
OpenAlexW2156818392

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.