Evidence map›Paper›PMID 38439112›Full record

ArticleBMC nutrition2024

Docosahexaenoic acid (DHA) impairs hypoxia-induced cellular and exosomal overexpression of immune-checkpoints and immunomodulatory molecules in different subtypes of breast cancer cells.

Sepideh Maralbashi, Cynthia Aslan, Houman Kahroba, Milad Asadi, Mohammad Sadegh Soltani-Zangbar, Navideh Haghnavaz, Farhad Jadidi, Farhad Salari, Tohid Kazemi

Open access · goldAbstract read
In one paragraph

Article in BMC nutrition, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 7% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
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  3. Article
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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 5 institutions in 4 countries.

Sepideh MaralbashiApplied drug research center, Tabriz University of Medical Sciences, Tabriz, Iran.
Cynthia AslanImmunology Research Center, Tabriz University of Medical Science, Tabriz, Iran.
Houman KahrobaDepartment of Toxicogenomics, GROW School for Oncology and Developmental Biology, Maastricht University, Maastricht, the Netherlands.
Milad AsadiDepartment of Basic Oncology, Health Institute of Ege University, Izmir, Turkey.
Mohammad Sadegh Soltani-ZangbarDepartment of Immunology, Faculty of Medicine, Tabriz University of Medical Science, Tabriz, Iran.
Navideh HaghnavazDepartment of Immunology, Faculty of Medicine, Tabriz University of Medical Science, Tabriz, Iran.
Farhad JadidiDepartment of Immunology, Faculty of Medicine, Tabriz University of Medical Science, Tabriz, Iran.
Farhad SalariDepartment of Immunology, Faculty of Medicine, Kermanshah University of Medical Science, Kermanshah, Iran. f.salari@kums.ac.ir.
Tohid KazemiImmunology Research Center, Tabriz University of Medical Science, Tabriz, Iran. kazemit@tbzmed.ac.ir.ORCID http://orcid.org/0000-0002-8583-1270
Tabriz University of Medical Sciences · IRUniversity of Tabriz · IREge University · TRKermanshah University of Medical Sciences · IRMaastricht University · NL

Funding

Farhad Salari 97143Tohid Kazemi 95-011
6 · The paper itself

Abstract

backgroundTumor cells express immune-checkpoint molecules to suppress anti-tumor immune responses. In part, immune evasion takes place by secreting exosomes bearing immune-checkpoint and immunomodulatory molecules and their inducing and/or regulating agents e.g., microRNAs (miRs). This study aimed to evaluate the effects of omega-3 fatty acid, docosahexaenoic acid (DHA), on the expression of some selected immune-checkpoint and immunomodulatory molecules and their regulating miRs under both normoxic and hypoxic conditions in triple negative (TNBC) invasive and triple positive non-invasive breast cancer cell lines.

methodsMDA-MB-231 and BT-474 cells were treated with 100 µM DHA under hypoxic and normoxic conditions for 24 h. Exosomes were isolated by ultracentrifuge and confirmed by electron microscope and anti-CD9, -CD63, -CD81 immunoblotting. Total RNA from cells and exosomes were extracted and expression of CD39, CD73, CD47, CD80, PD-L1, B7-H3, B7-H4 genes and their related miRs were evaluated by quantitative Real-time PCR.

resultsThis study showed significant over-expression of immune-checkpoint and immunomodulatory molecules under hypoxic condition. Treatment with DHA resulted in a significant decrease in immune-checkpoint and immunomodulatory molecule expression as well as an upregulation of their regulatory miRNA expression.

conclusionDHA supplementation may be utilized in breast cancer therapy for down-regulation of cellular and exosomal immune escape-related molecules.

Indexed as

Breast cancerDocosahexaenoic acidExosomeImmune-checkpointsMicroRNA

Identifiers

PMID38439112
PMCPMC10910708
OpenAlexW4392369885

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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.