Evidence map›Paper›PMID 39414944›Full record

ArticleScientific reports2024

Bidirectional effects of morphine on pancreatic cancer progression via the p38/JNK pathway.

Jing Ning, Xiubing Chen, Qing Li, Dan Yang, Chunxiao Xie, Shanyu Qin, Haixing Jiang

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Targeting the MAPK Pathway in Cancer.International journal of molecular sciences · 2025
    Review
  4. Article
  5. 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

7 authors.

Jing Ning *Department of Gastroenterology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Xiubing Chen *Department of Gastroenterology, The Fifth Affiliated Hospital of Guangxi Medical University, Nanning, China.
Qing Li *Department of Gastroenterology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Dan YangDepartment of Gastroenterology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Chunxiao XieDepartment of Gastroenterology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Shanyu QinDepartment of Gastroenterology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China. qinshanyu@gxmu.edu.cn.
Haixing JiangDepartment of Gastroenterology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China. Jianghaixing@gxmu.edu.cn.

Funding

National Natural Science Foundation of China 81960119Natural Science Foundation of Guangxi Zhuang Autonomous Region 2018GXNSFAA281221Scientific Research Project of Guangxi Health Commission Z20190717
6 · The paper itself

Abstract

Cancer patients commonly use morphine to alleviate advanced pain. Studies have shown that morphine may influence and intervene in the malignancy of various cancers, but its role and effects on pancreatic cancer are less studied. This study aims to examine how morphine affects pancreatic cancer and its possible mechanisms. In vitro experiments were conducted using the CCK-8 experiment, colony formation experiment, EdU test, wound healing experiment, and transwell migration and invasion experiment. Tumor xenograft tests were employed to investigate the in vivo impact of morphine on pancreatic cancer. The Western blot (WB) assay was used to detect possible changes in key proteins of the related signaling pathway. Our experimental results showed that low concentrations of morphine (25 µM) promoted the progression of pancreatic cancer, while high concentrations of morphine (100 µM) inhibited its progression. Further, we demonstrated that morphine may interfere with the progression of pancreatic cancer by acting on the p38/JNK signaling pathway. Morphine may affect pancreatic cancer progression through the p38/JNK pathway in a bidirectional manner at different concentrations.

Indexed as

MAP Kinase Signaling SystemMorphinePancreatic NeoplasmsAnimalsCell Line, TumorCell MovementCell ProliferationDisease ProgressionHumansMaleMiceMice, Nudep38 Mitogen-Activated Protein KinasesXenograft Model Antitumor AssaysMorphinep38 Mitogen-Activated Protein Kinases

Identifiers

PMID39414944
PMCPMC11484833

What OpenQuestion holds

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Registered trials

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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.