Evidence map›Paper›PMID 38536720›Full record

ArticleeLife2024

Exploration of drug resistance mechanisms in triple negative breast cancer cells using a microfluidic device and patient tissues.

Wanyoung Lim, Inwoo Hwang, Jiande Zhang, Zhenzhong Chen, Jeonghun Han, Jaehyung Jeon, Bon-Kyoung Koo, Sangmin Kim, Jeong Eon Lee, Youngkwan Kim and 5 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 14% 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

10 citing papers in PubMed, 7 citations in OpenAlex.

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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

15 authors at 4 institutions in 3 countries.

Wanyoung Lim *Department of Biomedical Engineering, Sungkyunkwan University, Suwon, Republic of Korea.
Inwoo Hwang *Department of Molecular Cell Biology, Sungkyunkwan University School of Medicine, Suwon, Republic of Korea.ORCID https://orcid.org/0000-0002-1162-1449
Jiande ZhangSchool of Mechanical Engineering, Sungkyunkwan University, Suwon, Republic of Korea.
Zhenzhong ChenSchool of Mechanical Engineering, Sungkyunkwan University, Suwon, Republic of Korea.
Jeonghun HanSchool of Mechanical Engineering, Sungkyunkwan University, Suwon, Republic of Korea.
Jaehyung JeonSchool of Mechanical Engineering, Sungkyunkwan University, Suwon, Republic of Korea.
Bon-Kyoung KooInstitute of Molecular Biotechnology of the Austrian Academy of Sciences (IMBA), Vienna Biocenter (VBC), Vienna, Austria.
Sangmin KimDepartment of Breast Cancer Center, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Jeong Eon LeeDivision of Breast Surgery, Department of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Youngkwan KimDepartment of Molecular Cell Biology, Sungkyunkwan University School of Medicine, Suwon, Republic of Korea.
Kenneth J PientaThe Cancer Ecology Center at the James Buchanan Brady Urological Institute, Johns Hopkins School of Medicine, Baltimore, United States.ORCID https://orcid.org/0000-0002-4138-2186
Sarah R AmendThe Cancer Ecology Center at the James Buchanan Brady Urological Institute, Johns Hopkins School of Medicine, Baltimore, United States.
Robert H AustinDepartment of Physics, Princeton University, Princeton, United States.
Jee-Yin AhnDepartment of Molecular Cell Biology, Sungkyunkwan University School of Medicine, Suwon, Republic of Korea.ORCID https://orcid.org/0000-0003-0002-008X
Sungsu ParkDepartment of Biomedical Engineering, Sungkyunkwan University, Suwon, Republic of Korea.ORCID https://orcid.org/0000-0003-3062-1302
Sungkyunkwan University · KRSamsung Medical Center · KRInstitute of Molecular Biotechnology · ATPrinceton University · US

Funding

Korea Dementia Research Center HU21C0157Korea Institute for Advancement of Technology P0008746Ministry of Trade, Industry and Energy 20008413
6 · The paper itself

Abstract

Chemoresistance is a major cause of treatment failure in many cancers. However, the life cycle of cancer cells as they respond to and survive environmental and therapeutic stress is understudied. In this study, we utilized a microfluidic device to induce the development of doxorubicin-resistant (DOXR) cells from triple negative breast cancer (TNBC) cells within 11 days by generating gradients of DOX and medium. In vivo chemoresistant xenograft models, an unbiased genome-wide transcriptome analysis, and a patient data/tissue analysis all showed that chemoresistance arose from failed epigenetic control of the nuclear protein-1 (NUPR1)/histone deacetylase 11 (HDAC11) axis, and high

Indexed as

Triple Negative Breast NeoplasmsCell Line, TumorDoxorubicinDrug Resistance, NeoplasmGene Expression Regulation, NeoplasticHumansLab-On-A-Chip DevicesNuclear ProteinsDoxorubicinNuclear Proteinscancer biologyhistone deacetylase 11humanmicrofluidic chipnuclear protein 1polyaneuploid cancer cellsresistancetriple negative breast cancer

Identifiers

PMID38536720
PMCPMC10972559
OpenAlexW4387310194

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.