Evidence map›Paper›PMID 27105503›Full record

ArticleOncotarget2016

ANXA1 inhibits miRNA-196a in a negative feedback loop through NF-kB and c-Myc to reduce breast cancer proliferation.

Yi Yuan, Durkeshwari Anbalagan, Lay Hoon Lee, Ramar Perumal Samy, Muthu K Shanmugam, Alan Prem Kumar, Gautam Sethi, Peter E Lobie, Lina H K Lim

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
5.4field-weighted citation impact, top 4% 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

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 64 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. The role and application prospects of ANXA1 in gastric cancer cells.Medical oncology (Northwood, London, England) · 2025
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  17. Ad- and AAV8-mediatedMolecular therapy. Methods & clinical development · 2021
    Article
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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

9 authors at 3 institutions in 3 countries.

Yi YuanDepartment of Physiology, Yong Loo Lin School of Medicine, National University Health System (NUHS), National University of Singapore (NUS), Singapore.
Durkeshwari AnbalaganDepartment of Physiology, Yong Loo Lin School of Medicine, National University Health System (NUHS), National University of Singapore (NUS), Singapore.
Lay Hoon LeeDepartment of Physiology, Yong Loo Lin School of Medicine, National University Health System (NUHS), National University of Singapore (NUS), Singapore.
Ramar Perumal SamyDepartment of Physiology, Yong Loo Lin School of Medicine, National University Health System (NUHS), National University of Singapore (NUS), Singapore.
Muthu K ShanmugamDepartment of Pharmacology, Yong Loo Lin School of Medicine, NUHS, National University of Singapore, Singapore.
Alan Prem KumarDepartment of Pharmacology, Yong Loo Lin School of Medicine, NUHS, National University of Singapore, Singapore.
Gautam SethiDepartment of Pharmacology, Yong Loo Lin School of Medicine, NUHS, National University of Singapore, Singapore.
Peter E LobieDepartment of Pharmacology, Yong Loo Lin School of Medicine, NUHS, National University of Singapore, Singapore.
Lina H K LimDepartment of Physiology, Yong Loo Lin School of Medicine, National University Health System (NUHS), National University of Singapore (NUS), Singapore.
National University of Singapore · SGNational University Health System · SGCurtin University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MiRNAs are endogenous ~22 nt RNAs which play critical regulatory roles in a wide range of biological and pathological processes, which can act as oncogenes or tumor suppressor genes depending on their target genes. We have recently shown that ANXA1 inhibits the expression of miRNAs including miR196a. Here, we show that miR196a was highly expressed in ER+ MCF-7 breast cancer cells when compared to normal mammary gland cells, with expression levels negatively correlating to ANXA1. ANXA1 inhibits the biogenesis of oncogenic miR-196a by suppressing primary-miR196a indirectly through the stimulation of c-myc and NFkB expression and activity in breast cancer cells. In a negative feedback loop, miR-196a directly inhibits ANXA1 and enhances breast cancer cell proliferation in vitro. Finally, miR196a promotes breast tumor growth in vivo. This study reports a novel regulatory circuit between ANXA1, NF-kB, c-myc and miR-196a which regulates breast cancer cell proliferation and tumor growth.

Indexed as

AnimalsAnnexin A1Breast NeoplasmsCell Line, TumorCell ProliferationFeedback, PhysiologicalFemaleGene Expression Regulation, NeoplasticHumansMCF-7 CellsMice, Inbred BALB CMice, NudeMicroRNAsNF-kappa BProto-Oncogene Proteins c-mycRNA InterferenceAnnexin A1MicroRNAsMIRN196 microRNA, humanMYC protein, humanNF-kappa BProto-Oncogene Proteins c-mycannexin 1breast cancerc-mycImmune responseImmunityImmunology and Microbiology SectionmicroRNAspri-miR-196a

Identifiers

PMID27105503
PMCPMC5053628
OpenAlexW2341433383

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.