Evidence map›Paper›PMID 28341752›Full record

ReviewClinical cancer research : an official journal of the American Association for Cancer Research2017

The Promise of Targeting Macrophages in Cancer Therapy.

J Martin Brown, Lawrence Recht, Samuel Strober

Open access · bronzeAbstract readReview
In one paragraph

Review in Clinical cancer research : an official journal of the American Association for Cancer Research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 188 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
188citing papers in PubMed, 1 pooled it
17.2field-weighted citation impact, top 1% 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

188 citing papers in PubMed, 1 synthesis or guideline pooled it, 319 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. The authors respond to feedback onFrontiers in oncology · 2026
    Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. FOLR2Cell communication and signaling : CCS · 2025
    Review
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128 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

3 authors at 2 institutions in 1 country.

J Martin BrownDepartment of Radiation Oncology, Stanford University, Stanford, California. mbrown@stanford.edu.
Lawrence RechtDepartment of Neurology, Stanford University, Stanford, California.
Samuel StroberDepartment of Medicine, Stanford University, Stanford, California.
Stanford Medicine · USStanford University · US

Funding

Development of Clinical Strategies to Prevent GBM Recurrences After RadiotherapyR01CA149318 · NCI · STANFORD UNIVERSITY · PI BROWN, JOHN MARTIN · 2011 to 2015
$2.4M
Radiotherapy as Immunotherapy of TumorsR01CA163441 · NCI · STANFORD UNIVERSITY · PI STROBER, SAMUEL · 2012 to 2016
$2.2M
NCI NIH HHS R01 CA149318NCI NIH HHS R01 CA163441
6 · The paper itself

Abstract

Cancer therapy has developed around the concept of killing, or stopping the growth of, the cancer cells. Molecularly targeted therapy is the modern expression of this paradigm. Increasingly, however, the realization that the cancer has co-opted the normal cells of the stroma for its own survival has led to the concept that the tumor microenvironment (TME) could be targeted for effective therapy. In this review, we outline the importance of tumor-associated macrophages (TAM), a major component of the TME, in the response of tumors to cancer therapy. We discuss the normal role of macrophages in wound healing, the major phenotypes of TAMs, and their role in blunting the efficacy of cancer treatment by radiation and anticancer drugs, both by promoting tumor angiogenesis and by suppressing antitumor immunity. Finally, we review the many preclinical studies that have shown that the response of tumors to irradiation and anticancer drugs can be improved, sometimes markedly so, by depleting TAMs from tumors or by suppressing their polarization from an M1 to an M2 phenotype. The data clearly support the validity of clinical testing of combining targeting TAMs with conventional therapy.

Indexed as

Molecular Targeted TherapyAntineoplastic AgentsHumansMacrophagesNeoplasmsNeovascularization, PathologicTumor MicroenvironmentWound HealingAntineoplastic Agents

Identifiers

PMID28341752
PMCPMC5529121
OpenAlexW2600317738

What OpenQuestion holds

Textmetadata
LicenceTDM
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.