Evidence map›Paper›PMID 32957515›Full record

ReviewCancers2020

Cancer-Associated Fibroblasts: Versatile Players in the Tumor Microenvironment.

Debolina Ganguly, Raghav Chandra, John Karalis, Martha Teke, Todd Aguilera, Ravikanth Maddipati, Megan B Wachsmann, Dario Ghersi, Giulia Siravegna, Herbert J Zeh and 3 more

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
6.0field-weighted citation impact, top 3% 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

75 citing papers in PubMed, 120 citations in OpenAlex.

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  20. Spatial microbiome-metabolic crosstalk drives CD8Frontiers in microbiology · 2025
    Article

15 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

13 authors at 4 institutions in 1 country.

Debolina GangulyDivision of Surgical Oncology, Department of Surgery, UT Southwestern (University of Texas Southwestern Medical Center), Dallas, TX 75390, USA.ORCID 0000-0002-7184-0053
Raghav ChandraDivision of Surgical Oncology, Department of Surgery, UT Southwestern (University of Texas Southwestern Medical Center), Dallas, TX 75390, USA.
John KaralisDivision of Surgical Oncology, Department of Surgery, UT Southwestern (University of Texas Southwestern Medical Center), Dallas, TX 75390, USA.ORCID 0000-0001-7601-5776
Martha TekeDivision of Surgical Oncology, Department of Surgery, UT Southwestern (University of Texas Southwestern Medical Center), Dallas, TX 75390, USA.
Todd AguileraDepartment of Radiation Oncology, UT Southwestern (University of Texas Southwestern Medical Center), Dallas, TX 75390, USA.
Ravikanth MaddipatiHarold C. Simmons Comprehensive Cancer Center, UT Southwestern (University of Texas Southwestern Medical Center), Dallas, TX 75390, USA.
Megan B WachsmannDepartment of Pathology, Veterans Affairs North Texas Health Care System, Dallas, TX 75216, USA.
Dario GhersiCollege of Information Science & Technology, University of Nebraska at Omaha, Omaha, NE 68182, USA.
Giulia SiravegnaMassachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA 02114, USA.ORCID 0000-0002-7132-6484
Herbert J ZehDivision of Surgical Oncology, Department of Surgery, UT Southwestern (University of Texas Southwestern Medical Center), Dallas, TX 75390, USA.
Rolf BrekkenDivision of Surgical Oncology, Department of Surgery, UT Southwestern (University of Texas Southwestern Medical Center), Dallas, TX 75390, USA.
David T TingMassachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA 02114, USA.ORCID 0000-0002-3261-2322
Matteo LigorioDivision of Surgical Oncology, Department of Surgery, UT Southwestern (University of Texas Southwestern Medical Center), Dallas, TX 75390, USA.ORCID 0000-0001-8865-0881
Southwestern University · USHarvard University · USUniversity of Nebraska at Omaha · USVA North Texas Health Care System · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer-associated fibroblasts (CAFs) are indispensable architects of the tumor microenvironment. They perform the essential functions of extracellular matrix deposition, stromal remodeling, tumor vasculature modulation, modification of tumor metabolism, and participation in crosstalk between cancer and immune cells. In this review, we discuss our current understanding of the principal differences between normal fibroblasts and CAFs, the origin of CAFs, their functions, and ultimately, highlight the intimate connection of CAFs to virtually all of the hallmarks of cancer. We address the remarkable degree of functional diversity and phenotypic plasticity displayed by CAFs and strive to stratify CAF biology among different tumor types into practical functional groups. Finally, we summarize the status of recent and ongoing trials of CAF-directed therapies and contend that the paucity of trials resulting in Food and Drug Administration (FDA) approvals thus far is a consequence of the failure to identify targets exclusive of pro-tumorigenic CAF phenotypes that are mechanistically linked to specific CAF functions. We believe that the development of a unified CAF nomenclature, the standardization of functional assays to assess the loss-of-function of CAF properties, and the establishment of rigorous definitions of CAF subpopulations and their mechanistic functions in cancer progression will be crucial to fully realize the promise of CAF-targeted therapies.

Indexed as

CAF therapeuticscancer-associated fibroblastschemoresistanceclinical trials targeting CAFshallmarks of cancerheterogeneityimmunomodulationtumor microenvironment

Identifiers

PMID32957515
PMCPMC7564346
OpenAlexW3086823661

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.