Evidence map›Paper›PMID 39183755›Full record

ArticleJournal of bone oncology2024

Pharmacologic Hedgehog inhibition modulates the cytokine profile of osteolytic breast cancer cells.

Natalie E Bennett, Dominique V Parker, Rachel S Mangano, Jennifer E Baum, Logan A Northcutt, Jade S Miller, Erik P Beadle, Julie A Rhoades

Abstract read
In one paragraph

Article in Journal of bone oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

8 authors.

Natalie E BennettProgram in Cancer Biology, Vanderbilt University, Nashville, TN, United States.
Dominique V ParkerProgram in Cancer Biology, Vanderbilt University, Nashville, TN, United States.
Rachel S ManganoCenter for Bone Biology, Vanderbilt University Medical Center, Nashville, TN, United States.
Jennifer E BaumCenter for Bone Biology, Vanderbilt University Medical Center, Nashville, TN, United States.
Logan A NorthcuttProgram in Cancer Biology, Vanderbilt University, Nashville, TN, United States.
Jade S MillerCenter for Bone Biology, Vanderbilt University Medical Center, Nashville, TN, United States.
Erik P BeadleCenter for Bone Biology, Vanderbilt University Medical Center, Nashville, TN, United States.
Julie A RhoadesProgram in Cancer Biology, Vanderbilt University, Nashville, TN, United States.

Funding

Vanderbilt Diabetes Research CenterP30DK020593 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI DAVID H WASSERMAN · 2012 to 2026
$29.3M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007347 · NIGMS · VANDERBILT UNIVERSITY · PI WILLIAMS, CHRISTOPHER S. · 1985 to 2023
$26.3M
Vanderbilt Mouse Metabolic Physiology CenterU24DK059637 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2001 to 2015
$14.9M
Medical Scientist Training ProgramT32GM152284 · NIGMS · VANDERBILT UNIVERSITY · PI Christopher S. Williams · 2024 to 2026
$4.8M
NRSA Training CoreTL1TR002244 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Julie A. Bastarache · 2017 to 2026
$4.6M
Next Gen Targeted nanoparticles for Inhibiting Gli2 in Bone Metastatic TumorsR01CA264508 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Craig Lewis Duvall, Julie A Rhoades (Sterling) · 2023 to 2026
$2.6M
Targeting the Bone Microenvironment to Reduce Tumor-induced Bone DiseaseI01BX001957 · VA · VETERANS HEALTH ADMINISTRATION · PI RHOADES (STERLING), JULIE A · 2013 to 2025
–
BLRD VA I01 BX001957BLRD VA IK6 BX006476NCATS NIH HHS TL1 TR002244NCI NIH HHS R01 CA264508NIDDK NIH HHS P30 DK020593NIDDK NIH HHS U24 DK059637NIGMS NIH HHS T32 GM007347NIGMS NIH HHS T32 GM152284
6 · The paper itself

Abstract

The establishment and progression of bone metastatic breast cancer is supported by immunosuppressive myeloid populations that enable tumor growth by dampening the innate and adaptive immune response. Much work remains to understand how to target these tumor-myeloid interactions to improve treatment outcomes. Noncanonical Hedgehog signaling is an essential component of bone metastatic tumor progression, and prior literature suggests a potential role for Hedgehog signaling and its downstream effector Gli2 in modulating immune responses. In this work, we sought to identify if inhibition of noncanonical Hedgehog signaling alters the cytokine profile of osteolytic breast cancer cells and the subsequent communication between the tumor cells and myeloid cells. Examination of large patient databases revealed significant relationships between Gli2 expression and expression of markers of myeloid maturation and activation as well as cytokine expression. We found that treatment with HPI-1 reduced tumor cell expression of numerous cytokine genes, including

Indexed as

Bone metastasisBreast cancerCytokineM−CSFMonocyteMyeloid

Identifiers

PMID39183755
PMCPMC11342115

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.