OSCR

Tumor-derived GDF15 induces CCN3⁺ Schwann cells to promote cancer pain in pancreatic cancer.

Overview

Authors: Guojun Chen1, Weicheng Lu1, Meng Liu2, Qingqing Ye1, Yixin Xu1, Yanqun Zhang1, Xiangna Guo1, Yaqi Ye1, Xiaohua Yang1,3, Xiaolin Luo1, Wenjun Xin3,4, Jingdun Xie1
  1. Department of Anesthesiology, State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Sun Yat-sen University Cancer Center, Guangzhou, China
  2. Department of Anesthesia and Pain Medicine, Guangzhou First People’s Hospital, Guangzhou, China
  3. Guangdong Province Key Laboratory of Brain Function and Disease, Department of Physiology and Pain Research Center, Zhongshan Medical School, Sun Yat-sen University, Zhongshan Road 2, Guangzhou, China
  4. Key Laboratory for Molecular Genetic Mechanisms and Intervention Research on High Altitude Disease of Tibet Autonomous Region, School of Medicine, Xizang Minzu University, Xianyang, Shaanxi China
Journal: Nature communications, volume 17, issue 1, article 6328
Dates: received 9 August 2025; accepted 24 April 2026; published online 12 May 2026
Type: Research article · Language: English
License: CC BY-NC-ND
Identifiers: DOI 10.1038/s41467-026-72932-5 · PMID 42120379 · PMCID PMC13376396 · OpenAlex W7160938190
Open access: gold, a free copy (OpenAlex)
Status: data only
Categories: human (organism), mouse (organism), other condition (population), pain (population), cellular / molecular (subfield)
Methods: Statistics
Keywords: Neuroscience, Cancer
MeSH: Carcinoma, Pancreatic Ductal*, Pain*, Pancreatic Neoplasms*, Schwann Cells*, Animals, Cell Line, Tumor, Glial Cell Line-Derived Neurotrophic Factor Receptors, Glycolysis, Humans, Metabolic Reprogramming, Mice, Signal Transduction, Tumor Microenvironment (* major topic)
Topic: Connective Tissue Growth Factor Research (Molecular Biology, Biochemistry, Genetics and Molecular Biology), according to OpenAlex
Funding: National Natural Science Foundation of China (National Science Foundation of China) (82471238, 824B2028 and 82401446)
Citations: cited by 1 paper (Europe PMC); 87 references in the paper

Abstract

The abstract is not reproduced here: the paper's license (CC BY-NC-ND) does not allow it. Read it in the paper, at the publisher or on Europe PMC.

Code

The paper links to its data, not to its authors' code: see the Data section.

Tracing map

A tracing map links a paper to the code its authors published: this paper has none, so it has no map.

Data

Datasets cited

Data availability statement

The paper has a data availability statement. Its license (CC BY-NC-ND) does not allow reproducing it here; in short, from what the harvester recognized in it:

Read it in the paper: doi.org/10.1038/s41467-026-72932-5.

Versions

The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.

Version 1, 28 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 12 authors, 2 keywords, 13 MeSH terms, 1 funder, 86 references.

Cite

This paper

Chen, G., Lu, W., Liu, M., Ye, Q., Xu, Y., Zhang, Y., Guo, X., Ye, Y., Yang, X., Luo, X., Xin, W., & Xie, J. (2026). Tumor-derived GDF15 induces CCN3⁺ Schwann cells to promote cancer pain in pancreatic cancer. Nature communications, 17(1), 6328. https://doi.org/10.1038/s41467-026-72932-5

BibTeX

@article{chen2026tumor,
author = {Chen, Guojun and Lu, Weicheng and Liu, Meng and Ye, Qingqing and Xu, Yixin and Zhang, Yanqun and Guo, Xiangna and Ye, Yaqi and Yang, Xiaohua and Luo, Xiaolin and Xin, Wenjun and Xie, Jingdun},
title = {{Tumor-derived GDF15 induces CCN3⁺ Schwann cells to promote cancer pain in pancreatic cancer}},
journal = {Nature communications},
year = {2026},
month = may,
volume = {17},
number = {1},
pages = {6328},
publisher = {Nature Publishing Group},
issn = {2041-1723},
doi = {10.1038/s41467-026-72932-5},
url = {https://doi.org/10.1038/s41467-026-72932-5},
pmid = {42120379},
pmcid = {PMC13376396}
}

RIS

TY - JOUR
AU - Chen, Guojun
AU - Lu, Weicheng
AU - Liu, Meng
AU - Ye, Qingqing
AU - Xu, Yixin
AU - Zhang, Yanqun
AU - Guo, Xiangna
AU - Ye, Yaqi
AU - Yang, Xiaohua
AU - Luo, Xiaolin
AU - Xin, Wenjun
AU - Xie, Jingdun
TI - Tumor-derived GDF15 induces CCN3⁺ Schwann cells to promote cancer pain in pancreatic cancer
T2 - Nature communications
J2 - Nat Commun
PY - 2026
DA - 2026/05/12
VL - 17
IS - 1
SP - 6328
SN - 2041-1723
PB - Nature Publishing Group
DO - 10.1038/s41467-026-72932-5
UR - https://doi.org/10.1038/s41467-026-72932-5
LA - en
ER -

CSL-JSON

{
"id": "10.1038/s41467-026-72932-5",
"type": "article-journal",
"title": "Tumor-derived GDF15 induces CCN3⁺ Schwann cells to promote cancer pain in pancreatic cancer",
"container-title": "Nature communications",
"author": [
{
"family": "Chen",
"given": "Guojun"
},
{
"family": "Lu",
"given": "Weicheng"
},
{
"family": "Liu",
"given": "Meng"
},
{
"family": "Ye",
"given": "Qingqing"
},
{
"family": "Xu",
"given": "Yixin"
},
{
"family": "Zhang",
"given": "Yanqun"
},
{
"family": "Guo",
"given": "Xiangna"
},
{
"family": "Ye",
"given": "Yaqi"
},
{
"family": "Yang",
"given": "Xiaohua"
},
{
"family": "Luo",
"given": "Xiaolin"
},
{
"family": "Xin",
"given": "Wenjun"
},
{
"family": "Xie",
"given": "Jingdun"
}
],
"container-title-short": "Nat Commun",
"volume": "17",
"issue": "1",
"page": "6328",
"DOI": "10.1038/s41467-026-72932-5",
"PMID": "42120379",
"PMCID": "PMC13376396",
"ISSN": "2041-1723",
"publisher": "Nature Publishing Group",
"URL": "https://doi.org/10.1038/s41467-026-72932-5",
"language": "en",
"issued": {
"date-parts": [
[
2026,
5,
12
]
]
}
}

Similar papers

The papers with a page that share the most with this one: the tools found in their code, their categories, datasets, cited references and authors, the rarest counting most.

[1] doi:10.1038/s41392-026-02648-x
Prostaglandin E<sub>2</sub>-driven dedifferentiation of Schwann cells leads to perineural invasion in pancreatic ductal adenocarcinoma.
Journal: Signal transduction and targeted therapy
In common: other condition, cellular / molecular, 4 references
[2] doi:10.1158/0008-5472.can-25-2237 [code]
Extracellular Vesicle-Mediated O-GlcNAcase Transfer Drives Neuronal Necroptosis to Facilitate Gallbladder Cancer Perineural Invasion.
Journal: Cancer research
In common: other condition, mouse, cellular / molecular, 2 references
[3] doi:10.1016/j.celrep.2026.117314
GLIS3 marks a neural-like progenitor cell state that drives metastasis in pancreatic ductal adenocarcinoma.
Journal: Cell reports
In common: other condition, mouse, cellular / molecular, 1 reference
[4] doi:10.1016/j.xcrm.2026.102994
Targeting of tripartite neuron-cancer-immune cell crosstalk augments response to chemotherapy and immunotherapy.
Journal: Cell reports. Medicine
In common: other condition, mouse, cellular / molecular, 1 reference
[5] doi:10.1186/s12935-026-04243-0
LIS1 mediated Schwann cell reprogramming enhances perineural invasion by activating the serine/NMDAR/AKT signaling pathway in head and neck squamous carcinoma.
Journal: Cancer cell international
In common: other condition, mouse, cellular / molecular, 1 reference
[6] doi:10.1038/s41598-026-51848-6
SPARC is associated with tumor nerve stroma interactions and perineural invasion in pancreatic ductal adenocarcinoma.
Journal: Scientific reports
In common: other condition, mouse, 1 reference
[7] doi:10.1007/s10549-026-08050-z
Association of tumor Schwann cells with epithelial-mesenchymal transition and immune-suppressive microenvironment in triple-negative breast cancer.
Journal: Breast cancer research and treatment
In common: other condition, cellular / molecular, 1 reference
[8] doi:10.3389/ftox.2026.1783704
Modular <i>in vitro</i> evaluation of buparlisib-polymeric nanomedicines in 2D and 3D models of glioblastoma.
Journal: Frontiers in toxicology
In common: other condition, cellular / molecular, 1 reference
[9] doi:10.1016/j.isci.2026.115779
Propranolol alleviates cerebral infarction through the β2-AR-mediated ERK/NLRP3 pathway.
Journal: iScience
In common: mouse, cellular / molecular, 1 reference
[10] doi:10.1245/s10434-026-19666-2
Neuron-Associated Transcriptional Enrichment Is Associated with Distinct Biological States and Predicts Poor Prognosis in Gastric Cancer.
Journal: Annals of surgical oncology
In common: other condition, 1 reference

Contribute

The authors of this paper can claim it, correct its record and validate its tracing map, and the maintainers of its code (its owner, or a public member of its organization) correct what it says of their repository; anyone signed in can ask for its removal. Every request goes to OSCR's own machine, which answers it; your account page follows them.

Sign in with ORCID to claim this paper as one of its authors, correct its record or validate its tracing map: when the paper's metadata lists your ORCID iD, you are recognized at once. Maintainers of its code: sign in with GitHub, then claim the repository on your account page.

Request its removal

To ask OSCR to remove this record, the copies of its authors' scripts or its tracing map, use the removal request page: signed in, you say who you are, what to remove and why, then review and confirm the request. Published rules decide every request (how).

Discussion, reproductions, activity

Discussion: questions and error reports about this paper and its code, from signed-in readers and its authors. It opens with sign-in.

Reproductions: reports from readers who ran the authors' code: what they reproduced, with which environment, commit and data. It opens with sign-in.

Activity: what happens around this paper: new versions of its record, its map's validation, discussions and reproductions. It opens with sign-in.