Evidence map›Paper›PMID 34579762›Full record

ArticleBreast cancer research : BCR2021

Transcriptome analysis of heterogeneity in mouse model of metastatic breast cancer.

Anastasia A Ionkina, Gabriela Balderrama-Gutierrez, Krystian J Ibanez, Steve Huy D Phan, Angelique N Cortez, Ali Mortazavi, Jennifer A Prescher

Open access · goldAbstract read
In one paragraph

Article in Breast cancer research : BCR, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.9field-weighted citation impact, top 11% 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

27 citing papers in PubMed, 36 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

7 authors at 1 institution in 1 country.

Anastasia A IonkinaDepartment of Molecular Biology and Biochemistry, University of California Irvine, Irvine, CA, 92697, USA.
Gabriela Balderrama-GutierrezDepartment of Developmental and Cell Biology, University of California Irvine, Irvine, CA, 92697, USA.
Krystian J IbanezDepartment of Developmental and Cell Biology, University of California Irvine, Irvine, CA, 92697, USA.
Steve Huy D PhanDepartment of Molecular Biology and Biochemistry, University of California Irvine, Irvine, CA, 92697, USA.
Angelique N CortezDepartment of Developmental and Cell Biology, University of California Irvine, Irvine, CA, 92697, USA.
Ali MortazaviDepartment of Developmental and Cell Biology, University of California Irvine, Irvine, CA, 92697, USA. ali.mortazavi@uci.edu.
Jennifer A PrescherDepartment of Molecular Biology and Biochemistry, University of California Irvine, Irvine, CA, 92697, USA. jpresche@uci.edu.ORCID 0000-0002-9250-4702
University of California, Irvine · US

Funding

CARCINOGENESIST32CA009054 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI EDINGER, AIMEE L, FRUMAN, DAVID ALEXANDER · 1985 to 2025
$8.6M
purchase of an All-in-One Fluorescence MicroscopeR01GM107630 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI PRESCHER, JENNIFER · 2013 to 2021
$2.6M
NCI NIH HHS T32 CA009054NCI NIH HHS T32-CA009054NIGMS NIH HHS GM107630NIGMS NIH HHS R01 GM107630
6 · The paper itself

Abstract

backgroundCancer metastasis is a complex process involving the spread of malignant cells from a primary tumor to distal organs. Understanding this cascade at a mechanistic level could provide critical new insights into the disease and potentially reveal new avenues for treatment. Transcriptome profiling of spontaneous cancer models is an attractive method to examine the dynamic changes accompanying tumor cell spread. However, such studies are complicated by the underlying heterogeneity of the cell types involved. The purpose of this study was to examine the transcriptomes of metastatic breast cancer cells using the well-established MMTV-PyMT mouse model.

methodsOrgan-derived metastatic cell lines were harvested from 10 female MMTV-PyMT mice. Cancer cells were isolated and sorted based on the expression of CD44

resultsComparison of RNA sequencing data across all cell populations produced distinct gene clusters. Differential gene expression patterns related to CD44 expression, organ tropism, and immunomodulatory signatures were observed. scRNA-seq identified expression profiles based on tissue-dependent niches and clonal heterogeneity. These cohorts of data were narrowed down to identify subsets of genes with high expression and known metastatic propensity. Dot plot analyses further revealed clusters expressing cancer stem cell and cancer dormancy markers. Changes in relevant genes were investigated across pseudo-time and tissue origin using Monocle2. These data revealed transcriptomes that may contribute to sub-clonal evolution and treatment evasion during cancer progression.

conclusionsWe performed a comprehensive transcriptome analysis of tumor heterogeneity and organ tropism during breast cancer metastasis. These data add to our understanding of metastatic progression and highlight targets for breast cancer treatment. These markers could also be used to image the impact of tumor heterogeneity on metastases.

Indexed as

AnimalsBreast NeoplasmsCell ProliferationCluster AnalysisDisease Models, AnimalDisease ProgressionEpithelial-Mesenchymal TransitionFemaleGene Expression ProfilingGenetic HeterogeneityHyaluronan ReceptorsMiceNeoplastic Stem CellsOrgan SpecificitySingle-Cell AnalysisCd44 protein, mouseHyaluronan ReceptorsBreast cancerMetastasisMMTV-PyMT modelOrgan tropismSingle-cell RNA sequencingTumor heterogeneity

Identifiers

PMID34579762
PMCPMC8477508
OpenAlexW3203803698

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.