Evidence map›Paper›PMID 27487127›Full record

ArticleOncotarget2016

miR-145 sensitizes breast cancer to doxorubicin by targeting multidrug resistance-associated protein-1.

Man Gao, Lingling Miao, Mingxia Liu, Chenggang Li, Cunzhi Yu, Hong Yan, Yongxiang Yin, Yizheng Wang, Xinming Qi, Jin Ren

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 52 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 2 pooled it
4.6field-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

52 citing papers in PubMed, 2 syntheses or guidelines pooled it, 93 citations in OpenAlex.

  1. Pooled it
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  4. miR-145 restoration overcomes oxaliplatin resistance via ABCC1 in colorectal cancer.Journal of the Egyptian National Cancer Institute · 2026
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  9. MiRNAs: main players of cancer drug resistance target ABC transporters.Naunyn-Schmiedeberg's archives of pharmacology · 2025
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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

10 authors at 3 institutions in 1 country.

Man GaoCenter for Drug Safety Evaluation and Research, Shanghai Institute of Materia Medica, CAS., Shanghai, China.
Lingling MiaoCenter for Drug Safety Evaluation and Research, Shanghai Institute of Materia Medica, CAS., Shanghai, China.
Mingxia LiuCenter for Drug Safety Evaluation and Research, Shanghai Institute of Materia Medica, CAS., Shanghai, China.
Chenggang LiCenter for Drug Safety Evaluation and Research, Shanghai Institute of Materia Medica, CAS., Shanghai, China.
Cunzhi YuCenter for Drug Safety Evaluation and Research, Shanghai Institute of Materia Medica, CAS., Shanghai, China.
Hong YanCenter for Drug Safety Evaluation and Research, Shanghai Institute of Materia Medica, CAS., Shanghai, China.
Yongxiang YinDepartment of Pathology, Wuxi Maternity and Children Health Hospital Affiliated Nanjing Medical University, Wuxi, China.
Yizheng WangThe Brain Science Center, Beijing Institute of Basic Medical Sciences, Beijing, China.
Xinming QiCenter for Drug Safety Evaluation and Research, Shanghai Institute of Materia Medica, CAS., Shanghai, China.
Jin RenCenter for Drug Safety Evaluation and Research, Shanghai Institute of Materia Medica, CAS., Shanghai, China.
Shanghai Institute of Materia Medica · CNInstitute of Basic Medical Sciences of the Chinese Academy of Medical SciencesNanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multidrug resistance-associated protein 1 (MRP1) is an important efflux transporter and overexpression of MRP1 usually leads to chemoresistance in breast cancer. Here, we found MRP1 overexpressed in human breast cancer tissues and breast cancer cell lines (compared with normal breast tissues and cell line, respectively). And MRP1 level increased in doxorubicin resistant MCF-7 cells compared with parental MCF-7 cells. Increasing evidences suggest microRNAs (miRNAs) influence chemotherapy response. We found miR-145 level decreased in human breast cancer tissues, breast cancer cell lines and doxorubicin resistant MCF-7 cells, and inversely correlated with MRP1 expression level. In the process of constructing MCF-7 doxorubicin resistant cell line, escalating doxorubicin markedly decreased miR-145 level, following by increased MRP1 level. Further study showed, miR-145 suppressed MRP1 expression by directly targeting MRP1 3'-untranslated regions. Overexpression of miR-145 sensitized breast cancer cells to doxorubicin in vitro and enhanced to doxorubicin chemotherapy in vivo through inducing intracellular doxorubicin accumulation via inhibiting MRP1. Taken together, our study revealed miR-145 sensitizes breast cancer to doxorubicin by targeting MRP1 and indicated the potential application in developing MRP1 inhibitor.

Indexed as

3' Untranslated RegionsAnimalsAntibiotics, AntineoplasticATP-Binding Cassette, Sub-Family C ProteinsBreast NeoplasmsCell Line, TumorCell SurvivalDoxorubicinDrug Resistance, MultipleFemaleGene Expression Regulation, NeoplasticHumansMCF-7 CellsMice, Inbred BALB CMice, NudeMicroRNAs3' Untranslated RegionsAntibiotics, AntineoplasticATP-Binding Cassette, Sub-Family C ProteinsDoxorubicinMicroRNAsMIRN145 microRNA, humanmultidrug resistance-associated protein 1breast cancerchemoresistancedoxorubicinmiRNAMRP1

Identifiers

PMID27487127
PMCPMC5312343
OpenAlexW2507115513

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.