Evidence map›Paper›PMID 31059026›Full record

ArticleMolecular medicine reports2019

Curcumin reverses doxorubicin resistance via inhibition the efflux function of ABCB4 in doxorubicin‑resistant breast cancer cells.

Chunjie Wen, Lijuan Fu, Jiafeng Huang, Yi Dai, Bin Wang, Ge Xu, Lanxiang Wu, Honghao Zhou

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 3 pooled it
3.7field-weighted citation impact, top 5% 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

56 citing papers in PubMed, 3 syntheses or guidelines pooled it, 92 citations in OpenAlex.

  1. Pooled it
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  3. Frontiers in oncology · 2021
    Pooled it
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  18. Curcumin Administration Routes in Breast Cancer Treatment.International journal of molecular sciences · 2024
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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

8 authors at 1 institution in 1 country.

Chunjie WenInstitute of Life Sciences, Chongqing Medical University, Yuzhong, Chongqing 400016, P.R. China.
Lijuan FuInstitute of Traditional Chinese Medicine, Chongqing Medical University, Yuzhong, Chongqing 400016, P.R. China.
Jiafeng HuangInstitute of Life Sciences, Chongqing Medical University, Yuzhong, Chongqing 400016, P.R. China.
Yi DaiInstitute of Life Sciences, Chongqing Medical University, Yuzhong, Chongqing 400016, P.R. China.
Bin WangInstitute of Life Sciences, Chongqing Medical University, Yuzhong, Chongqing 400016, P.R. China.
Ge XuInstitute of Life Sciences, Chongqing Medical University, Yuzhong, Chongqing 400016, P.R. China.
Lanxiang WuInstitute of Life Sciences, Chongqing Medical University, Yuzhong, Chongqing 400016, P.R. China.
Honghao ZhouInstitute of Life Sciences, Chongqing Medical University, Yuzhong, Chongqing 400016, P.R. China.
Chongqing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Doxorubicin is one of the most widely used chemotherapy agents for the treatment of breast cancer. However, the development of doxorubicin resistance limits the long‑term treatment benefits in patients with breast cancer. Curcumin, a well‑known dietary polyphenol derived from the rhizomes of turmeric (Curcuma longa), enhances the sensitivity of breast cancer cells to chemotherapeutic agents; however, the mechanisms underlying this phenomenon remain unclear. The aim of the present study was to evaluate the effect of curcumin on chemoresistance in doxorubicin‑resistant breast cancerMCF‑7/DOX and MDA‑MB‑231/DOX cell lines. Cell Counting Kit‑8, monolayer transport, western blot and ATPase activity assays were performed during the study. The results revealed that curcumin significantly enhanced the effect of doxorubicin in doxorubicin‑resistant breast cancer cells. The intracellular accumulation of doxorubicin was substantially increased following curcumin treatment in doxorubicin‑resistant breast cancer cells, in a manner that was inversely dependent on the activity of ATP binding cassette subfamily B member 4 (ABCB4). Treatment with a combination of curcumin and doxorubicin decreases the efflux of doxorubicin in ABCB4‑overexpressing cells. Furthermore, curcumin inhibited the ATPase activity of ABCB4 without altering its protein expression. In conclusion, curcumin reversed doxorubicin resistance in human breast cancer MCF‑7/DOX and MDA‑MB‑231/DOX cells by inhibiting the ATPase activity of ABCB4. The study highlights the promising use of curcumin as a chemosensitizer in the treatment of breast cancer.

Indexed as

Adenosine TriphosphatasesAnimalsATP Binding Cassette Transporter, Subfamily B, Member 1Breast NeoplasmsCell SurvivalCurcuminDogsDoxorubicinDrug Resistance, NeoplasmFemaleHumansMadin Darby Canine Kidney CellsMCF-7 CellsAdenosine TriphosphatasesATP Binding Cassette Transporter, Subfamily B, Member 1CurcuminDoxorubicin

Identifiers

PMID31059026
PMCPMC6522915
OpenAlexW2937212472

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.