Evidence map›Paper›PMID 39013086›Full record

ReviewMagyar onkologia2024

[Immunomodulation in the tumor microenvironment: Therapeutic potential of combined inhibition of tumor hypoxia and PD-1/ PD-L1].

Laura Svajda, Mihály Cserepes, Barbara Hegyi, Theodora Niczky, József Tóvári

Abstract readReviewEnglish Abstract
In one paragraph

Review in Magyar onkologia, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

5 authors.

Laura SvajdaKísérletes Farmakológiai Osztály, Országos Onkológiai Intézet, Budapest, Hungary. svajda.laura@ext.oncol.hu.
Mihály CserepesKísérletes Farmakológiai Osztály, Országos Onkológiai Intézet, Budapest, Hungary. svajda.laura@ext.oncol.hu.
Barbara HegyiNemzeti Tumorbiológiai Laboratórium, Országos Onkológiai Intézet, Budapest, Hungary.
Theodora NiczkyKísérletes Farmakológiai Osztály, Országos Onkológiai Intézet, Budapest, Hungary. svajda.laura@ext.oncol.hu.
József TóváriKísérletes Farmakológiai Osztály, Országos Onkológiai Intézet, Budapest, Hungary. svajda.laura@ext.oncol.hu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor hypoxia plays an important role in controlling tumor progression through signaling pathways related to the transcription factor HIF-1. In addition to enhancing migration, promoting angiogenesis and regulating metabolism, the hypoxic environment also affects immune function. In this hypoxic microenvironment an immunosuppressive milieu is established, where HIF-1 upregulates the expression of PD-L1, a key regulator of the immune response. We have found that elevated expression of PD-L1 correlates with increased HIF-1 levels in cancer cell lines and clinical samples. Thus, the co-inhibition of HIF-1 and PD-1/PD-L1 offers promising therapeutic possibilities. In this review we have examined the limitations of HIF-1 and PD-1/PD-L1 inhibition as monotherapy, explored their combined benefits and evaluated the feasibility of targeting PD-L1 with HIF-1 inhibitors.

Indexed as

B7-H1 AntigenNeoplasmsProgrammed Cell Death 1 ReceptorTumor HypoxiaTumor MicroenvironmentHumansHypoxia-Inducible Factor 1, alpha SubunitSignal TransductionB7-H1 AntigenCD274 protein, humanHypoxia-Inducible Factor 1, alpha SubunitPDCD1 protein, humanProgrammed Cell Death 1 Receptor

Identifiers

PMID39013086
PMCPMC11870698

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.