Evidence map›Paper›PMID 39266299›Full record

ArticleLife science alliance2024

Crosstalk between bone metastatic cancer cells and sensory nerves in bone metastatic progression.

Sun H Park, Shunsuke Tsuzuki, Kelly F Contino, Jenna Ollodart, Matthew R Eber, Yang Yu, Laiton R Steele, Hiroyuki Inaba, Yuko Kamata, Takahiro Kimura and 10 more

Abstract read
In one paragraph

Article in Life science alliance, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
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  11. Not Just Neurons: Pain Is Orchestrated in Partnership with Many Non-neuronal Cells.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Review
  12. 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

20 authors.

Sun H ParkDepartment of Cancer Biology and Atrium Health Wake Forest Baptist Comprehensive Cancer Center, Wake Forest University School of Medicine, Winston-Salem, NC, USA.ORCID 0009-0009-3859-9120
Shunsuke TsuzukiDepartment of Cancer Biology and Atrium Health Wake Forest Baptist Comprehensive Cancer Center, Wake Forest University School of Medicine, Winston-Salem, NC, USA.ORCID 0000-0001-6164-4684
Kelly F ContinoDepartment of Cancer Biology and Atrium Health Wake Forest Baptist Comprehensive Cancer Center, Wake Forest University School of Medicine, Winston-Salem, NC, USA.ORCID 0000-0002-7690-5012
Jenna OllodartDepartment of Cancer Biology and Atrium Health Wake Forest Baptist Comprehensive Cancer Center, Wake Forest University School of Medicine, Winston-Salem, NC, USA.ORCID 0000-0003-4837-4194
Matthew R EberDepartment of Cancer Biology and Atrium Health Wake Forest Baptist Comprehensive Cancer Center, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
Yang YuDepartment of Cancer Biology and Atrium Health Wake Forest Baptist Comprehensive Cancer Center, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
Laiton R SteeleDepartment of Cancer Biology and Atrium Health Wake Forest Baptist Comprehensive Cancer Center, Wake Forest University School of Medicine, Winston-Salem, NC, USA.ORCID 0000-0001-6861-7398
Hiroyuki InabaDepartment of Urology, Jikei University School of Medicine, Tokyo, Japan.
Yuko KamataDepartment of Oncology, Jikei University School of Medicine, Tokyo, Japan.
Takahiro KimuraDepartment of Urology, Jikei University School of Medicine, Tokyo, Japan.
Ilsa ColemanDivision of Human Biology, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Peter S NelsonDivision of Human Biology, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Enriqueta Muñoz-IslasUnidad Académica Multidisciplinaria Reynosa Aztlán, Universidad Autónoma de Tamaulipas, Reynosa, Mexico.
Juan Miguel Jiménez-AndradeUnidad Académica Multidisciplinaria Reynosa Aztlán, Universidad Autónoma de Tamaulipas, Reynosa, Mexico.
Thomas J MartinDepartment of Anesthesiology, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
Kimberly D MackenzieTeva Pharmaceuticals, Redwood City, CA, USA.
Jennifer R StrattonTeva Pharmaceuticals, Redwood City, CA, USA.
Fang-Chi HsuDepartment of Biostatistics and Data Science Wake Forest University School of Medicine, Winston-Salem, NC, USA.
Christopher M PetersDepartment of Anesthesiology, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
Yusuke ShiozawaDepartment of Cancer Biology and Atrium Health Wake Forest Baptist Comprehensive Cancer Center, Wake Forest University School of Medicine, Winston-Salem, NC, USA yshiozaw@wakehealth.edu.ORCID 0000-0001-9814-9230

Funding

TRANSCRIPTOME AND PROTEOME STRATIFICATION OF PROSTATE ADENOCARCINOMA PHENOTYPESP50CA097186 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PETER S NELSON · 2002 to 2026
$58.1M
Tumor Tissue CoreP30CA012197 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Ruben A. Mesa · 1985 to 2026
$55.4M
Defining and Targeting Lineage Transition Programs Operative in AR Pathway Independent Prostate CancerR01CA234715 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI NELSON, PETER S · 2020 to 2024
$2.0M
Targeting Vulnerabilities Exposed by Cancer Treatment-Induced Lineage PlasticityR01CA266452 · NCI · FRED HUTCHINSON CANCER CENTER · PI PETER S NELSON · 2022 to 2026
$2.0M
The contributions of sensory nerves to bone metastasis and associated bone painR01CA238888 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI SHIOZAWA, YUSUKE · 2020 to 2024
$1.8M
Dissecting Neural Circuits Involved in Musculoskeletal PainR21AR078366 · NIAMS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI PETERS, CHRISTOPHER MICHAEL · 2021 to 2022
$367k
NCI NIH HHS P30 CA012197NCI NIH HHS P50 CA097186NCI NIH HHS R01 CA234715NCI NIH HHS R01 CA238888NCI NIH HHS R01 CA266452NIAMS NIH HHS R21 AR078366
6 · The paper itself

Abstract

Although the role of peripheral nerves in cancer progression has been appreciated, little is known regarding cancer/sensory nerve crosstalk and its contribution to bone metastasis and associated pain. In this study, we revealed that the cancer/sensory nerve crosstalk plays a crucial role in bone metastatic progression. We found that (i) periosteal sensory nerves expressing calcitonin gene-related peptide (CGRP) are enriched in mice with bone metastasis; (ii) cancer patients with bone metastasis have elevated CGRP serum levels; (iii) bone metastatic patient tumor samples express elevated calcitonin receptor-like receptor (CRLR, a CGRP receptor component); (iv) higher CRLR levels in cancer patients are negatively correlated with recurrence-free survival; (v) CGRP induces cancer cell proliferation through the CRLR/p38/HSP27 pathway; and (vi) blocking sensory neuron-derived CGRP reduces cancer cell proliferation in vitro and bone metastatic progression in vivo. This suggests that CGRP-expressing sensory nerves are involved in bone metastatic progression and that the CGRP/CRLR axis may serve as a potential therapeutic target for bone metastasis.

Indexed as

Bone NeoplasmsCalcitonin Gene-Related PeptideCell ProliferationDisease ProgressionSensory Receptor CellsAnimalsCalcitonin Receptor-Like ProteinCell Line, TumorFemaleHumansMaleMiceSignal TransductionCalcitonin Gene-Related PeptideCalcitonin Receptor-Like Protein

Identifiers

PMID39266299
PMCPMC11393574

What Socratic 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 Socratic graph.