Evidence map›Paper›PMID 36768935›Full record

ArticleInternational journal of molecular sciences2023

Synthesis and Biological Evaluation of Potential Oncoimmunomodulator Agents.

Raquel Gil-Edo, Sara Espejo, Eva Falomir, Miguel Carda

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. New Anticancer Agents: Design, Synthesis and Evaluation.International journal of molecular sciences · 2025
    Article
  3. Review
  4. 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.

Raquel Gil-EdoInorganic and Organic Chemistry Department, University Jaume I, E-12071 Castellón, Spain.ORCID 0000-0002-2977-7783
Sara EspejoInorganic and Organic Chemistry Department, University Jaume I, E-12071 Castellón, Spain.
Eva FalomirInorganic and Organic Chemistry Department, University Jaume I, E-12071 Castellón, Spain.ORCID 0000-0003-0329-6313
Miguel CardaInorganic and Organic Chemistry Department, University Jaume I, E-12071 Castellón, Spain.

Funding

Jaume I University UJI-B2018-38Jaume I University UJI-B2021-43Ministry of Economy, Industry and Competitiveness RTI2018-097345-B-100Ministry of science and innovation Spain PID2021-1262770B-100
6 · The paper itself

Abstract

Fourteen triazole-scaffold derivatives were synthetized and biologically evaluated as potential oncoimmunomodultator agents by targeting both PD-L1 and c-Myc. First, the antiproliferative activity of these molecules on the monocultures of several tumor cell lines (HT-29, A-549, and MCF-7) and on the non-tumor cell line HEK-293 was studied. Then, the effects on the mentioned biological targets were also evaluated. Finally, the effect on cancer cell viability when the molecules were co-cultured with immune cells (Jurkat T cells or THP-1) was also determined. Compounds bearing a bromoophenyl group were selected because of their excellent results, and their effect on IL-6 secretion was also studied. In conclusion, we found compounds that are capable of downregulating c-Myc, as well as influencing and altering the distribution of PD-L1 in tumor cells; the compounds are thus capable of influencing the behavior of defensive cells towards cancer cells.

Indexed as

B7-H1 AntigenInterleukin-6Cell Line, TumorHEK293 CellsHumansJurkat CellsB7-H1 AntigenInterleukin-6angiogenesisc-Mycco-culturesflow cytometryIL-6immunomodulationmultitarget inhibitorsPD-L1small molecules

Identifiers

PMID36768935
PMCPMC9917184

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.