Evidence map›Paper›PMID 42325112›Full record

ArticlePain research & management2026

High-Dose Tramadol Enhances the Proliferative and Invasive Potential of Pancreatic Ductal Adenocarcinoma in Mice Through Microenvironmental Alteration.

Tomoya Kuramochi, Tomoaki Itaya, Makoto Sano, Yukino Oshima, Jinsuk Kim, Osamu Kitajima, Hideaki Ijichi, Takahiro Suzuki

Abstract read
In one paragraph

Article in Pain research & management, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

8 authors.

Tomoya KuramochiDepartment of Obstetrics and Gynecology, Juntendo University, Urayasu Hospital 2-1-1 Tomioka, Urayasu Chiba, 279-0021, Japan, juntendo.ac.jp.ORCID https://orcid.org/0009-0001-0185-7941
Tomoaki ItayaDepartment of Anesthesiology, Nihon University School of Medicine, 30-1 Oyaguchi-Kamimachi Itabashi-ku, Tokyo 173-8610, Japan, nihon-u.ac.jp.ORCID https://orcid.org/0000-0001-9679-9395
Makoto SanoDepartment of Anesthesiology, Nihon University School of Medicine, 30-1 Oyaguchi-Kamimachi Itabashi-ku, Tokyo 173-8610, Japan, nihon-u.ac.jp.
Yukino OshimaDepartment of Anesthesiology, Nihon University School of Medicine, 30-1 Oyaguchi-Kamimachi Itabashi-ku, Tokyo 173-8610, Japan, nihon-u.ac.jp.
Jinsuk KimDepartment of Anesthesiology, Nihon University School of Medicine, 30-1 Oyaguchi-Kamimachi Itabashi-ku, Tokyo 173-8610, Japan, nihon-u.ac.jp.
Osamu KitajimaDepartment of Anesthesiology, Nihon University School of Medicine, 30-1 Oyaguchi-Kamimachi Itabashi-ku, Tokyo 173-8610, Japan, nihon-u.ac.jp.
Hideaki IjichiDepartment of Gastroenterology, The University of Tokyo, 7-3-1 Hongo Bunkyo ku, Tokyo 113-0033, Japan, u-tokyo.ac.jp.
Takahiro SuzukiDepartment of Anesthesiology, Nihon University School of Medicine, 30-1 Oyaguchi-Kamimachi Itabashi-ku, Tokyo 173-8610, Japan, nihon-u.ac.jp.

Funding

Japan Society for the Promotion of Science JP24K12060
6 · The paper itself

Abstract

purposeOpioids are known to have various effects on cancer depending on the type and dose. Tramadol, a weak opioid used for mild cancer pain, exhibits antitumor effects, whereas strong opioids demonstrate protumor effects. We previously reported that 10 mg/kg/day of tramadol (low dose) improves cancer pain and exerts antitumor effects in mice with pancreatic cancer. However, the effects of high-dose tramadol on pancreatic cancer remain unknown. Therefore, the effect of high-dose tramadol on pancreatic cancer was investigated in mice using the pancreatic cancer model mouse KPPC (LSL - Kras

methodsHigh-dose tramadol (50 mg/kg/day) was orally administered to 6-week-old KPPC mice bearing pancreatic ductal adenocarcinoma until a humane endpoint (n = 10). Cancer-related pain was assessed using the mouse grimace scale, and tumor status was determined histopathologically. Plasma cytokine concentrations were assessed using a cytokine array. The effects of tramadol on the invasive potential of murine pancreatic ductal adenocarcinoma cell lines were investigated in vitro.

resultsHigh-dose tramadol improved mouse grimace scale scores but increased tumor size (1734.2 vs. 907.1 mm

conclusionThese results suggest that high-dose tramadol improves cancer-associated pain but enhances the tumor volume of pancreatic ductal adenocarcinoma by decreasing anti-tumor CD8

Indexed as

Analgesics, OpioidCarcinoma, Pancreatic DuctalCell ProliferationPancreatic NeoplasmsTramadolTumor MicroenvironmentAnimalsCancer PainCell Line, TumorCytokinesDisease Models, AnimalDose-Response Relationship, DrugMaleMiceMice, Inbred C57BLMice, TransgenicAnalgesics, OpioidCytokinesTramadolCD8+T lymphocytesKPPC mouseM2-like tumor-associated macrophagespancreatic cancertramadolweak opioid

Identifiers

PMID42325112
PMCPMC13284832

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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.