Evidence map›Paper›PMID 33046799›Full record

ArticleOncogene2021

Multi-color clonal tracking reveals intra-stage proliferative heterogeneity during mammary tumor progression.

Stefanie Tiede, Ravi Kiran Reddy Kalathur, Fabiana Lüönd, Luca von Allmen, Barbara Maria Szczerba, Mathias Hess, Tatjana Vlajnic, Benjamin Müller, James Canales Murillo, Nicola Aceto and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 16% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Breast cancers as ecosystems: a metabolic perspective.Cellular and molecular life sciences : CMLS · 2023
    Review
  4. Review
  5. Multidimensional Imaging of Breast Cancer.Cold Spring Harbor perspectives in medicine · 2023
    Review
  6. Article
  7. Review
  8. Review
  9. Beyond Genetics: Metastasis as an Adaptive Response in Breast Cancer.International journal of molecular sciences · 2022
    Review
  10. Review
  11. Review
  12. Article
  13. Review
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 3 institutions in 1 country.

Stefanie TiedeDepartment of Biomedicine, University of Basel, 4058, Basel, Switzerland. stefanie.tiede@unibas.ch.ORCID http://orcid.org/0000-0002-3763-7270
Ravi Kiran Reddy KalathurDepartment of Biomedicine, University of Basel, 4058, Basel, Switzerland.
Fabiana LüöndDepartment of Biomedicine, University of Basel, 4058, Basel, Switzerland.
Luca von AllmenDepartment of Biomedicine, University of Basel, 4058, Basel, Switzerland.
Barbara Maria SzczerbaDepartment of Biomedicine, University of Basel, 4058, Basel, Switzerland.
Mathias HessDepartment of Biomedicine, University of Basel, 4058, Basel, Switzerland.
Tatjana VlajnicInstitute of Pathology, University Hospital Basel, 4031, Basel, Switzerland.ORCID http://orcid.org/0000-0002-1067-6771
Benjamin MüllerDepartment of Biomedicine, University of Basel, 4058, Basel, Switzerland.
James Canales MurilloDepartment of Biomedicine, University of Basel, 4058, Basel, Switzerland.
Nicola AcetoDepartment of Biomedicine, University of Basel, 4058, Basel, Switzerland.
Gerhard ChristoforiDepartment of Biomedicine, University of Basel, 4058, Basel, Switzerland. Gerhard.christofori@unibas.ch.ORCID http://orcid.org/0000-0002-8696-9896
University of Basel · CHSIB Swiss Institute of Bioinformatics · CHUniversity Hospital of Basel · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite major progress in breast cancer research, the functional contribution of distinct cancer cell clones to malignant tumor progression and metastasis remains largely elusive. We have assessed clonal heterogeneity within individual primary tumors and metastases and also during the distinct stages of malignant tumor progression using clonal tracking of cancer cells in the MMTV-PyMT mouse model of metastatic breast cancer. Comparative gene expression analysis of clonal subpopulations reveals a substantial level of heterogeneity across and also within the various stages of breast carcinogenesis. The intra-stage heterogeneity is primarily manifested by differences in cell proliferation, also found within invasive carcinomas of luminal A-, luminal B-, and HER2-enriched human breast cancer. Surprisingly, in the mouse model of clonal tracing of cancer cells, chemotherapy mainly targets the slow-proliferative clonal populations and fails to efficiently repress the fast-proliferative populations. These insights may have considerable impact on therapy selection and response in breast cancer patients.

Indexed as

AnimalsBreast NeoplasmsCell Line, TumorCell ProliferationCell TrackingClonal EvolutionDisease ProgressionErb-b2 Receptor Tyrosine KinasesFemaleGene Expression ProfilingGene Regulatory NetworksHumansLaser Capture MicrodissectionMammary Neoplasms, ExperimentalMammary Tumor Virus, MouseMiceERBB2 protein, humanErb-b2 Receptor Tyrosine Kinases

Identifiers

PMID33046799
OpenAlexW3092365865

What OpenQuestion holds

Textmetadata
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.