Evidence map›Paper›PMID 38282415›Full record

ArticleClinical and translational medicine2024

Molecular features of luminal breast cancer defined through spatial and single-cell transcriptomics.

Ryohei Yoshitake, Hitomi Mori, Desiree Ha, Xiwei Wu, Jinhui Wang, Xiaoqiang Wang, Kohei Saeki, Gregory Chang, Hyun Jeong Shim, Yin Chan and 1 more

Open access · goldAbstract read
In one paragraph

Article in Clinical and translational medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
5.1field-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

25 citing papers in PubMed, 22 citations in OpenAlex.

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  19. Advancements in the Application of scRNA-Seq in Breast Research: A Review.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

11 authors at 2 institutions in 2 countries.

Ryohei YoshitakeDepartment of Cancer Biology and Molecular Medicine, Beckman Research Institute of City of Hope, Duarte, California, USA.
Hitomi MoriDepartment of Cancer Biology and Molecular Medicine, Beckman Research Institute of City of Hope, Duarte, California, USA.
Desiree HaDepartment of Cancer Biology and Molecular Medicine, Beckman Research Institute of City of Hope, Duarte, California, USA.
Xiwei WuIntegrative Genomics Core, Beckman Research Institute of City of Hope, Monrovia, California, USA.
Jinhui WangIntegrative Genomics Core, Beckman Research Institute of City of Hope, Monrovia, California, USA.
Xiaoqiang WangDepartment of Cancer Biology and Molecular Medicine, Beckman Research Institute of City of Hope, Duarte, California, USA.
Kohei SaekiDepartment of Cancer Biology and Molecular Medicine, Beckman Research Institute of City of Hope, Duarte, California, USA.
Gregory ChangDepartment of Cancer Biology and Molecular Medicine, Beckman Research Institute of City of Hope, Duarte, California, USA.
Hyun Jeong ShimDepartment of Cancer Biology and Molecular Medicine, Beckman Research Institute of City of Hope, Duarte, California, USA.
Yin ChanDepartment of Cancer Biology and Molecular Medicine, Beckman Research Institute of City of Hope, Duarte, California, USA.
Shiuan ChenDepartment of Cancer Biology and Molecular Medicine, Beckman Research Institute of City of Hope, Duarte, California, USA.ORCID 0000-0002-4482-6926
City Of Hope National Medical Center · USCity of Hope · US

Funding

Transgenic Mouse FacilityP30CA033572 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI John Charles Williams · 1985 to 2026
$86.3M
Menopausal transition - a window of susceptibility for the promotion of breast cancer by environmental exposuresU01ES026137 · NIEHS · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI CHEN, SHIUAN, NEUHAUSEN, SUSAN L. · 2015 to 2019
$4.8M
NCI NIH HHS P30 CA033572NIEHS NIH HHS U01 ES026137NIH HHS P30CA033572NIH HHS U01ES026137
6 · The paper itself

Abstract

backgroundIntratumour heterogeneity is a hallmark of most solid tumours, including breast cancers. We applied spatial transcriptomics and single-cell RNA-sequencing on patient-derived xenografts (PDXs) to profile spatially resolved cell populations within oestrogen receptor-positive (ER

methodsTwo PDXs of 'ER-high' breast cancers with opposite oestrogen-mediated growth responses were investigated: oestrogen-suppressed GS3 (80-100% ER) and oestrogen-dependent SC31 (40-90% ER) models. The observation was validated via single-cell analyses on an 'ER-low' PDX, GS1 (5% ER). The results from our spatial and single-cell analyses were further supported by a public ER

resultsOur space-gene-function study revealed four spatially distinct compartments within ER

conclusionsOur study identified the gene signature in our 'proliferative' compartment as an important determinant of luminal cancer subtypes. This 'proliferative' cell population is a causative feature of luminal B breast cancer, contributing toward its aggressive behaviours.

Indexed as

Breast NeoplasmsEstrogensFemaleGene Expression ProfilingHumansHypoxiaInflammationKi-67 AntigenReceptors, EstrogenEstrogensKi-67 AntigenReceptors, Estrogenbreast cancerintratumour heterogeneityoestrogen receptorsingle-cell RNA-sequencingspatial transcriptomics

Identifiers

PMID38282415
PMCPMC10823285
OpenAlexW4391326191

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.