Evidence map›Paper›PMID 31518642›Full record

ArticlePharmacological research2019

Macrophage activation by a substituted pyrimido[5,4-b]indole increases anti-cancer activity.

Joseph Hardie, Javier A Mas-Rosario, Siyoung Ha, Erik M Rizzo, Michelle E Farkas

Abstract read
In one paragraph

Article in Pharmacological research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

9 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Macrophage circadian rhythms are differentially affected based on stimuli.Integrative biology : quantitative biosciences from nano to macro · 2022
    Article
  8. Review
  9. Article
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

5 authors at 1 institution in 1 country.

Joseph HardieDepartment of Chemistry, University of Massachusetts Amherst, 710 North Pleasant Street, Amherst, MA, 01003, USA.
Javier A Mas-RosarioMolecular and Cellular Biology Graduate Program, University of Massachusetts, Amherst, MA, USA.
Siyoung HaDepartment of Chemistry, University of Massachusetts Amherst, 710 North Pleasant Street, Amherst, MA, 01003, USA.
Erik M RizzoDepartment of Biochemistry and Molecular Biology, University of Massachusetts, Amherst, MA, USA.
Michelle E FarkasDepartment of Chemistry, University of Massachusetts Amherst, 710 North Pleasant Street, Amherst, MA, 01003, USA; Molecular and Cellular Biology Graduate Program, University of Massachusetts, Amherst, MA, USA. Electronic address: farkas@chem.umass.edu.
University of Massachusetts Amherst · US

Funding

UMass Amherst PREP ProgramR25GM086264 · NIGMS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI PEYTON, SHELLY R., RICHARDSON, HEATHER NOËL · 2009 to 2023
$4.7M
CHEMISTRY-BIOLOGY INTERFACE PREDOCTORAL TRAINING GRANTST32GM008515 · NIGMS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI THOMPSON, LYNMARIE K. · 1995 to 2020
$4.3M
Intracellular Host-Guest Activation of Nanoparticle TherapeuticsR01EB014277 · NIBIB · UNIVERSITY OF MASSACHUSETTS AMHERST · PI ROTELLO, VINCENT M. · 2012 to 2014
$1.0M
NIBIB NIH HHS R01 EB014277NIGMS NIH HHS R25 GM086264NIGMS NIH HHS T32 GM008515
6 · The paper itself

Abstract

Immunotherapy has become a promising new approach for cancer treatment due to the immune system's ability to remove tumors in a safe and specific manner. Many tumors express anti-inflammatory factors that deactivate the local immune response or recruit peripheral macrophages into pro-tumor roles. Because of this, effective and specific ways of activating macrophages into anti-tumor phenotypes is highly desirable for immunotherapy purposes. Here, the use of a small molecule TLR agonist as a macrophage activator for anti-cancer therapy is reported. This compound, referred to as PBI1, demonstrated unique activation characteristics and expression patterns compared to treatment with LPS, through activation of TLR4. Furthermore, PBI1 treatment resulted in anti-tumor immune behavior, enhancing macrophage phagocytic efficiency five-fold versus non-treated macrophages. Additive effects were observed via use of a complementary strategy (anti-CD47 antibody), resulting in ∼10-fold enhancement of phagocytosis, suggesting this small molecule approach could be used in conjunction with other therapeutics.

Indexed as

AnimalsAntineoplastic AgentsCD47 AntigenCell LineImmunotherapyIndolesMacrophage ActivationMacrophagesMicePhagocytosisRAW 264.7 CellsSmall Molecule LibrariesAntineoplastic AgentsCD47 AntigenindoleIndolesSmall Molecule LibrariesAdjuvantCancerImmunotherapyInflammatoryMacrophagePhagocytosis

Identifiers

PMID31518642
PMCPMC6849472
OpenAlexW2972667717

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.