Evidence map›Paper›PMID 31092827›Full record

ArticleNature communications2019

Evaluating cell lines as models for metastatic breast cancer through integrative analysis of genomic data.

Ke Liu, Patrick A Newbury, Benjamin S Glicksberg, William Z D Zeng, Shreya Paithankar, Eran R Andrechek, Bin Chen

Abstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing 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

69 citing papers in PubMed.

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  11. Targeting triple-negative breast cancer: apoptotic and antitumor effects of Artemisia sieberi Besser extracts.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2025
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9 more citing papers are in PubMed but not listed here.

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

7 authors.

Ke LiuDepartment of Pediatrics and Human Development, College of Human Medicine, Michigan State University, Grand Rapids, 49503, MI, USA.ORCID http://orcid.org/0000-0003-3190-1656
Patrick A NewburyDepartment of Pediatrics and Human Development, College of Human Medicine, Michigan State University, Grand Rapids, 49503, MI, USA.ORCID http://orcid.org/0000-0002-3756-1747
Benjamin S GlicksbergBakar Computational Health Sciences Institute, University of California San Francisco, San Francisco, 94158, CA, USA.
William Z D ZengBakar Computational Health Sciences Institute, University of California San Francisco, San Francisco, 94158, CA, USA.
Shreya PaithankarHealth Informatics and Bioinformatics, School of Computing and Information Systems, Grand Valley State University, Grand Rapids, 49504, MI, USA.
Eran R AndrechekDepartment of Physiology, Michigan State University, East Lansing, 48824, MI, USA.
Bin ChenDepartment of Pediatrics and Human Development, College of Human Medicine, Michigan State University, Grand Rapids, 49503, MI, USA. Bin.Chen@hc.msu.edu.ORCID http://orcid.org/0000-0001-8858-874X

Funding

Integrating transcriptomic, proteomic and pharmacogenomic data to inform individualized therapy in cancersK01ES028047 · NIEHS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CHEN, BIN · 2017 to 2020
$682k
Targeting glucose metabolism for the treatment of Hepatocellular CarcinomaR21TR001743 · NCATS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CHEN, BIN · 2017 to 2018
$560k
NCATS NIH HHS R21 TR001743NIEHS NIH HHS K01 ES028047
6 · The paper itself

Abstract

Cell lines are widely-used models to study metastatic cancer although the extent to which they recapitulate the disease in patients remains unknown. The recent accumulation of genomic data provides an unprecedented opportunity to evaluate the utility of them for metastatic cancer research. Here, we reveal substantial genomic differences between breast cancer cell lines and metastatic breast cancer patient samples. We also identify cell lines that more closely resemble the different subtypes of metastatic breast cancer seen in the clinic and show that surprisingly, MDA-MB-231 cells bear little genomic similarities to basal-like metastatic breast cancer patient samples. Further comparison suggests that organoids more closely resemble the transcriptome of metastatic breast cancer samples compared to cell lines. Our work provides a guide for cell line selection in the context of breast cancer metastasis and highlights the potential of organoids in these studies.

Indexed as

BreastBreast NeoplasmsCell Culture TechniquesCell Line, TumorDatasets as TopicFemaleGene Expression ProfilingGenomicsHumansOrganoids

Identifiers

PMID31092827
PMCPMC6520398

What OpenQuestion holds

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Registered trials

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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.