Evidence map›Paper›PMID 40725123›Full record

ArticleInternational journal of molecular sciences2025

PD-1/PD-L1 Inhibitors and Chemotherapy Synergy: Impact on Drug Resistance and PD-L1 Expression in Breast Cancer-Immune Cell Co-Cultures.

Güneş Özen Eroğlu, Ayşe Erol Bozkurt, İlhan Yaylım, Dürdane Serap Kuruca

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. 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

4 authors.

Güneş Özen EroğluDepartment of Molecular Medicine, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul 34093, Turkey.ORCID 0000-0003-3681-9336
Ayşe Erol BozkurtDepartment of Medical Biology, Faculty of Medicine, Istanbul University, Istanbul 34390, Turkey.
İlhan YaylımDepartment of Molecular Medicine, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul 34093, Turkey.
Dürdane Serap KurucaDepartment of Physiology, Faculty of Medicine, Istanbul Atlas University, Istanbul 34408, Turkey.ORCID 0000-0001-7878-9994

Funding

Istanbul University Scientifc Research Projects Unit Project No: 35486
6 · The paper itself

Abstract

Breast cancer is the most frequently diagnosed cancer among women. In recent years, immunotherapy, a key targeted treatment strategy, has gained prominence in the management of this disease. Immune cells within the tumor microenvironment can significantly affect treatment outcomes. Among immunotherapeutic approaches, or programmed death protein 1(PD-1) and programmed death-ligand 1(PD-L1)-targeted therapies are increasingly recognized for their role in modulating cancer-immune system interactions. This study investigated the impact of PD-1/PD-L1 pathway inhibition on the expression of drug resistance-related proteins in an in vitro breast cancer model incorporating immune cells. MDA-MB-231 and MCF-7 cell lines were used as breast cancer cells, while THP-1 and Jurkat cells represented monocytes and lymphocytes, respectively. The effects of paclitaxel (PTX), doxorubicin (Dox), and PD-1/PD-L1 inhibitors (BMS-1166 and Human PD-L1 Inhibitor IV (PI4)) on cell viability were evaluated using an MTT assay, and the IC

Indexed as

B7-H1 AntigenBreast NeoplasmsDrug Resistance, NeoplasmImmune Checkpoint InhibitorsProgrammed Cell Death 1 ReceptorCell Line, TumorCell SurvivalCoculture TechniquesDoxorubicinDrug SynergismFemaleGene Expression Regulation, NeoplasticHumansJurkat CellsMCF-7 CellsPaclitaxelB7-H1 AntigenCD274 protein, humanDoxorubicinImmune Checkpoint InhibitorsPaclitaxelPDCD1 protein, humanProgrammed Cell Death 1 Receptorbreast cancerchemotherapydrug resistanceimmunotherapyPD-L1

Identifiers

PMID40725123
PMCPMC12295165

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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.