Evidence map›Paper›PMID 40207224›Full record

ArticleFrontiers in immunology2025

Exploring the possible mechanism of low-dose naloxone exposure improving the immune microenvironment of gastric cancer tumors.

Xiangzhen Min, Yan Ma, Mingyue Lv, Xiaoxi Li, Renjun Lv, Xiaoyong Zhao, Yufang Leng

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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.

Xiangzhen MinThe First School of Clinical Medicine, Lanzhou University, Lanzhou, China.
Yan Ma *Department of Anesthesiology, Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China.
Mingyue LvDepartment of Pharmacy, Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China.
Xiaoxi LiThe First School of Clinical Medicine, Lanzhou University, Lanzhou, China.
Renjun LvThe First School of Clinical Medicine, Lanzhou University, Lanzhou, China.
Xiaoyong ZhaoDepartment of Anesthesiology, Shandong Cancer Hospital and Institute Affiliated to Shandong First Medical University (Shandong Academy of Medical Science), Jinan, Shandong, China.
Yufang Leng *Department of Anesthesiology, The First Hospital of Lanzhou University, Lanzhou, Gansu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Gastric cancer, one of the most common cancers of the digestive tract, has high incidence and mortality rates. Until recently, surgery has been the most effective method of treatment for gastric cancer. Surgery, however, inevitably results in dysfunction of the autonomic nervous system, entry of tumor cells into the bloodstream, and immunosuppression during the perioperative period, all of which increase the risk of complications in patients with gastric cancer. Opioid receptors play an important role in the proliferation and secretion of cytotoxic factors by immune cells. Opiate usage inhibits immune cell function, reduces the release of cytotoxic factors, and enables tumor cells to evade the immune system, thereby increasing the risk of perioperative complications. Opioid antagonists may reverse opioid-mediated immunosuppression in several ways. However, studies on the molecular biology of opioid receptor antagonists in relation to their ability to improve immune function in patients with gastric cancer are limited. Methods: We first analyzed the cancer genome atlas stomach adenocarcinoma (TCGA-STAD) dataset to determine the correlation between changes in immune function and toll-like receptor 4 (TLR4) expression in patients with gastric cancer. A transwell co-culture system was established using CD8 Results: We found that changes in perioperative immune function strongly correlated with TLR4 expression on the surface of immune cells in patients with gastric cancer. Low-dose naloxone (LDN) increased CD8 Conclusion: LDN improved the ability of CD8

Indexed as

NaloxoneNarcotic AntagonistsStomach NeoplasmsTumor MicroenvironmentAnimalsCD8-Positive T-LymphocytesCell Line, TumorFemaleHumansMaleMiceSignal TransductionToll-Like Receptor 4NaloxoneNarcotic AntagonistsTLR4 protein, humanToll-Like Receptor 4CD8+T cellsimmune checkpointimmune functionlow-dose naloxoneopioid receptors

Identifiers

PMID40207224
PMCPMC11979148

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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.