Evidence map›Paper›PMID 36536517›Full record

ArticleThe Korean journal of pain2023

A positive feedback loop of heparanase/syndecan1/nerve growth factor regulates cancer pain progression.

Xiaohu Su, Bingwu Wang, Zhaoyun Zhou, Zixian Li, Song Tong, Simin Chen, Nan Zhang, Su Liu, Maoyin Zhang

Open access · diamondAbstract read
In one paragraph

Article in The Korean journal of pain, 2023. 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
0.2field-weighted citation impact, top 50% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  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

9 authors at 2 institutions in 1 country.

Xiaohu SuDepartment of Anesthesiology, Suqian First People's Hospital, Suqian City, Jiangsu Province, China.ORCID https://orcid.org/0000-0001-7060-7025
Bingwu WangCancer Institute, The Second Affiliated Hospital of Xuzhou Medical University, Xuzhou City, Jiangsu Province, China.ORCID https://orcid.org/0000-0002-6446-9671
Zhaoyun ZhouDepartment of Anesthesiology, Tai'an Central Hospital, Tai'an City, Shandong Province, China.ORCID https://orcid.org/0000-0003-3185-2495
Zixian LiDepartment of Anesthesiology, Graduate School of Xuzhou Medical University, Xuzhou City, Jiangsu Province, China.ORCID https://orcid.org/0000-0002-0692-0460
Song TongDepartment of Anesthesiology, Graduate School of Xuzhou Medical University, Xuzhou City, Jiangsu Province, China.ORCID https://orcid.org/0000-0002-8153-6426
Simin ChenDepartment of Anesthesiology, Graduate School of Xuzhou Medical University, Xuzhou City, Jiangsu Province, China.ORCID https://orcid.org/0000-0001-7395-0275
Nan ZhangDepartment of Anesthesiology, Graduate School of Xuzhou Medical University, Xuzhou City, Jiangsu Province, China.ORCID https://orcid.org/0000-0003-1055-6152
Su LiuDepartment of Anesthesiology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou City, Jiangsu Province, China.ORCID https://orcid.org/0000-0001-5177-5218
Maoyin ZhangDepartment of Anesthesiology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou City, Jiangsu Province, China.ORCID https://orcid.org/0000-0001-7629-6010
Xuzhou Medical College · CNTaian City Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The purpose of this research was to assess the role of heparanase (HPSE)/syndecan1 (SDC1)/nerve growth factor (NGF) on cancer pain from melanoma. Methods: The influence of HPSE on the biological function of melanoma cells and cancer pain in a mouse model was evaluated. Immunohistochemical staining was used to analyze HPSE and SDC1. HPSE, NGF, and SDC1 were detected using western blot. Inflammatory factors were detected using ELISA assay. Results: HPSE promoted melanoma cell viability, proliferation, migration, invasion, and tumor growth, as well as cancer pain, while SST0001 treatment reversed the promoting effect of HPSE. HPSE up-regulated NGF, and NGF feedback promoted HPSE. High expression of NGF reversed the inhibitory effect of HPSE down-regulation on melanoma cell phenotype deterioration, including cell viability, proliferation, migration, and invasion. SST0001 down-regulated SDC1 expression. SDC1 reversed the inhibitory effect of SST0001 on cancer pain. Conclusions: The results showed that HPSE promoted melanoma development and cancer pain by interacting with NGF/SDC1. It provides new insights to better understand the role of HPSE in melanoma and also provides a new direction for cancer pain treatment.

Indexed as

Cancer PainCell ProliferationCell SurvivalFeedbackMelanomaNerve Growth FactorPain ManagementSyndecan-1.

Identifiers

PMID36536517
PMCPMC9812689
OpenAlexW4313312195

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.