Evidence map›Paper›PMID 41226687›Full record

ArticleInternational journal of molecular sciences2025

Naltrexone Has Variable and Schedule-Dependent Effects on Oral Squamous Cell Carcinoma Cells.

Sahar Kazmi, Erica Sanford, Zaid A Rammaha, Ethan J Bengson, Feng Gao, Linda Sangalli, Cai M Roberts

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Sahar KazmiCollege of Dental Medicine-Illinois, Midwestern University, Downers Grove, IL 60515, USA.
Erica SanfordCollege of Dental Medicine-Illinois, Midwestern University, Downers Grove, IL 60515, USA.
Zaid A RammahaBiomedical Sciences Program, Midwestern University, Downers Grove, IL 60515, USA.
Ethan J BengsonBiomedical Sciences Program, Midwestern University, Downers Grove, IL 60515, USA.
Feng GaoCollege of Dental Medicine-Illinois, Midwestern University, Downers Grove, IL 60515, USA.ORCID 0000-0001-9956-6087
Linda SangalliCollege of Dental Medicine-Illinois, Midwestern University, Downers Grove, IL 60515, USA.ORCID 0000-0002-1386-5594
Cai M RobertsDepartment of Pharmacology, Midwestern University, Downers Grove, IL 60515, USA.ORCID 0000-0001-6545-5792

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oral squamous cell carcinoma (OSCC) is marked by profound differences in survival between the localized and disseminated disease, estimated to result in a 70% and less than a 40% five-year survival rate with surgical and/or radiation approaches (in localized cases) and chemotherapy (in metastatic cases), respectively. Given the suboptimal efficacy of current management options, new therapeutic approaches are needed to supplement existing chemotherapies and improve outcomes. One emerging therapeutic option is naltrexone (NTX), an opioid antagonist that has shown promising outcomes at low doses in other forms of cancer. This study sought to determine the effectiveness of intermittent dosing of naltrexone on oral cancer cell survival, either as a single agent or in combination with traditional chemotherapy. Two human OSCC lines (locally invasive SCC-25 and metastatic Detroit 562) were cultured. Cells were exposed to 1 µM and 10 µM NTX alone, using intermittent (5 h once, 5 h daily, 5 h every other day) or constant 72 h exposure. Cells were exposed to combination therapy with cisplatin or docetaxel under three NTX regimens (5 h, 24 h, and continuous). Cell viability was determined using Sulphorhodamine B (SRB) assay and Cell Counting Kit-8 (CCK-8). Differences across treatments were assessed using ANOVA (

Indexed as

Antineoplastic AgentsCarcinoma, Squamous CellMouth NeoplasmsNaltrexoneCell Line, TumorCell ProliferationCell SurvivalCisplatinDocetaxelHumansAntineoplastic AgentsCisplatinDocetaxelNaltrexonechemotherapynaltrexoneopioid growth factor receptororal squamous cell carcinoma

Identifiers

PMID41226687
PMCPMC12609663

What OpenQuestion holds

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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.