Evidence map›Paper›PMID 34164589›Full record

ArticleAnnual review of cancer biology2020

Investigating Tumor Heterogeneity in Mouse Models.

Tuomas Tammela, Julien Sage

Abstract read
In one paragraph

Article in Annual review of cancer biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing 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

38 citing papers in PubMed.

  1. Article
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  11. Ancient Diseases in Vertebrates: Tumours through the Ages.Animals : an open access journal from MDPI · 2024
    Review
  12. Article
  13. Transplantable Subcutaneous Tumor Models.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Nanoceria: an innovative strategy for cancer treatment.Cellular and molecular life sciences : CMLS · 2023
    Review
  19. Robotic data acquisition with deep learning enables cell image-based prediction of transcriptomic phenotypes.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  20. 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

2 authors.

Tuomas TammelaCancer Biology and Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Julien SageDepartment of Pediatrics and Department of Genetics, Stanford University, Stanford, California 94305, USA.

Funding

Single-Cell Biology and Data Analysis Shared Resource (SCB-DA SR)U54CA217450 · NCI · VANDERBILT UNIVERSITY · PI WEAVER, ALISSA M · 2018 to 2022
$8.5M
Investigating molecular and cellular mechanisms of SCLC development to identify novel therapeutic strategiesR35CA231997 · NCI · STANFORD UNIVERSITY · PI SAGE, JULIEN · 2019 to 2025
$6.2M
Novel therapeutic approaches for enhancing anti-tumor immunity in SCLCU01CA213273 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BYERS, LAUREN AVERETT, HEYMACH, JOHN V. · 2017 to 2021
$3.0M
Molecular mechanisms of SCLC initiation and detection in mice and humansU01CA231851 · NCI · STANFORD UNIVERSITY · PI KRASNOW, MARK A · 2018 to 2022
$2.9M
Molecular and cellular mechanisms of SCLC metastasisR01CA206540 · NCI · STANFORD UNIVERSITY · PI SAGE, JULIEN · 2016 to 2019
$1.7M
Notch signaling in small cell lung carcinomaR01CA201513 · NCI · STANFORD UNIVERSITY · PI SAGE, JULIEN · 2016 to 2019
$1.5M
Investigating cellular heterogeneity in lung cancerR00CA187317 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI TAMMELA, TUOMAS · 2017 to 2019
$757k
Investigating Wnt and Lgr5 signaling as regulators of lung cancer heterogeneityK99CA187317 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI TAMMELA, TUOMAS · 2014 to 2015
$246k
NCI NIH HHS K99 CA187317NCI NIH HHS R00 CA187317NCI NIH HHS R01 CA201513NCI NIH HHS R01 CA206540NCI NIH HHS R35 CA231997NCI NIH HHS U01 CA213273NCI NIH HHS U01 CA231851NCI NIH HHS U54 CA217450
6 · The paper itself

Abstract

Cancer arises from a single cell through a series of acquired mutations and epigenetic alterations. Tumors gradually develop into a complex tissue comprised of phenotypically heterogeneous cancer cell populations, as well as noncancer cells that make up the tumor microenvironment. The phenotype, or state, of each cancer and stromal cell is influenced by a plethora of cell-intrinsic and cell-extrinsic factors. The diversity of these cellular states promotes tumor progression, enables metastasis, and poses a challenge for effective cancer treatments. Thus, the identification of strategies for the therapeutic manipulation of tumor heterogeneity would have significant clinical implications. A major barrier in the field is the difficulty in functionally investigating heterogeneity in tumors in cancer patients. Here we review how mouse models of human cancer can be leveraged to interrogate tumor heterogeneity and to help design better therapeutic strategies.

Indexed as

cancer stem cellsepigeneticsgeneticsmouse modelstumor heterogeneitytumor microenvironment

Identifiers

PMID34164589
PMCPMC8218894

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.