Evidence map›Paper›PMID 29155146›Full record

ArticleBiochemical pharmacology2018

HDAC inhibitor suppresses proliferation and invasion of breast cancer cells through regulation of miR-200c targeting CRKL.

Xuehai Bian, Zhongxing Liang, Amber Feng, Eric Salgado, Hyunsuk Shim

Abstract read
In one paragraph

Article in Biochemical pharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
–field-weighted citation impact
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

34 citing papers in PubMed.

  1. Article
  2. Article
  3. Decoding the Epigenome of Breast Cancer.International journal of molecular sciences · 2025
    Review
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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

5 authors.

Xuehai BianDepartment of Radiation Oncology, Emory University, Atlanta GA30322, USA; Department of Thyroid Surgery, China-Japan Union Hospital of Jilin University, Jilin Provincial Key Laboratory of Surgical Translational Medicine, Changchun, China.
Zhongxing LiangDepartment of Radiation Oncology, Emory University, Atlanta GA30322, USA; Winship Cancer Institute, Emory University, Atlanta GA30322, USA. Electronic address: zliang@emory.edu.
Amber FengDepartment of Radiation Oncology, Emory University, Atlanta GA30322, USA.
Eric SalgadoDepartment of Radiation Oncology, Emory University, Atlanta GA30322, USA.
Hyunsuk ShimDepartment of Radiation Oncology, Emory University, Atlanta GA30322, USA; Winship Cancer Institute, Emory University, Atlanta GA30322, USA. Electronic address: hshim@emory.edu.

Funding

Graduate Training in the Pharmacological StudiesT32GM008602 · NIGMS · EMORY UNIVERSITY · PI HALL, RANDY A. · 1996 to 2021
$5.1M
Development of anti-CXCR4 compounds to block breast cancer metastasisR01CA165306 · NCI · EMORY UNIVERSITY · PI SHIM, HYUNSUK · 2012 to 2016
$1.7M
Development of anti-CXCR4 compounds as anti-metastatic, angiogenic drugR01CA109366 · NCI · EMORY UNIVERSITY · PI SHIM, HYUNSUK · 2006 to 2010
$1.3M
NCI NIH HHS R01 CA109366NCI NIH HHS R01 CA165306NIGMS NIH HHS T32 GM008602
6 · The paper itself

Abstract

Although histone deacetylase (HDAC) inhibitors have been shown to effectively induce the inhibition of proliferation and migration in breast cancer, the anticancer mechanism remains poorly understood. Our studies show that miR-200c was significantly downregulated in breast cancer cell lines compared to normal cell lines and inversely correlated with the levels of class IIa HDACs and CRKL. HDAC inhibitors and the ectopic expression of miR-200c as tumor suppressors inhibited the proliferation, invasion, and migration of breast cancer cells by downregulating CRKL. These results indicate that the anticancer mechanism of HDAC inhibitor was realized partially by regulating miR-200c via CRKL targeting. Our findings suggest that the HDAC-miR200c-CRKL signaling axis could be a novel diagnostic marker and potential therapeutic target in breast cancer.

Indexed as

Adaptor Proteins, Signal TransducingBreast NeoplasmsCell ProliferationFemaleGene TargetingHistone Deacetylase InhibitorsHumansMCF-7 CellsMicroRNAsNeoplasm InvasivenessNuclear ProteinsAdaptor Proteins, Signal TransducingCRKL proteinHistone Deacetylase InhibitorsMicroRNAsMIRN200 microRNA, humanNuclear ProteinsBreast cancerCRKLHDAC inhibitorMiR-200cSAHA

Identifiers

PMID29155146
PMCPMC5733635

What OpenQuestion holds

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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.