Evidence map›Paper›PMID 33168016›Full record

ArticleJournal of nanobiotechnology2020

Elucidating the cellular response of silver nanoparticles as a potential combinatorial agent for cisplatin chemotherapy.

Renata Rank Miranda, Micaella Pereira da Fonseca, Barbara Korzeniowska, Lilian Skytte, Kaare Lund Rasmussen, Frank Kjeldsen

Open access · goldAbstract read
In one paragraph

Article in Journal of nanobiotechnology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Iranian journal of basic medical sciences · 2024
    Article
  5. Article
  6. Review
  7. Article
  8. 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

6 authors at 1 institution in 1 country.

Renata Rank MirandaDepartment of Biochemistry and Molecular Biology, University of Southern Denmark, Odense, 5230, Denmark. renatam.bio@gmail.com.ORCID http://orcid.org/0000-0001-8774-2418
Micaella Pereira da FonsecaDepartment of Biochemistry and Molecular Biology, University of Southern Denmark, Odense, 5230, Denmark.
Barbara KorzeniowskaDepartment of Biochemistry and Molecular Biology, University of Southern Denmark, Odense, 5230, Denmark.
Lilian SkytteDepartment of Physics, Chemistry and Pharmacy, University of Southern Denmark, Odense, 5230, Denmark.
Kaare Lund RasmussenDepartment of Physics, Chemistry and Pharmacy, University of Southern Denmark, Odense, 5230, Denmark.
Frank KjeldsenDepartment of Biochemistry and Molecular Biology, University of Southern Denmark, Odense, 5230, Denmark. frankk@bmb.sdu.dk.
University of Southern Denmark · DK

Funding

H2020 European Research Council 646603
6 · The paper itself

Abstract

backgroundCombination chemotherapy uses drugs that target different cancer hallmarks, resulting in synergistic or additive toxicity. This strategy enhances therapeutic efficacy as well as minimizes drug resistance and side effects. In this study, we investigated whether silver nanoparticles act as a combinatorial partner to cisplatin. In so doing, we compared post-exposure biological endpoints, intracellular drug accumulation, and changes in the proteome profile of tumoral and normal cell lines.

resultsCombinatorial exposure corresponded to cytotoxicity and oxidative stress in both cell lines, yet was substantially more effective against tumoral cells. Proteome analysis revealed that proteins related to energy metabolism pathways were upregulated in both cell lines, suggesting that combinatorial exposure corresponded to energetic modulation. However, proteins and upstream regulators involved in the cell cycle were downregulated, indicating reduced cell proliferation. The response to oxidative stress was markedly different in both cell lines; downregulation of antioxidant proteins in tumoral cells, yet upregulation of the antioxidant defense system in normal cells. These outcomes may have avoided higher cell death rates in normal cells.

conclusionsTaken together, our results indicate that combining silver nanoparticles with cisplatin increases the biological activity of the latter, and the combination warrants further exploration for future therapies.

Indexed as

AntioxidantsCell CycleCell LineCell ProliferationCell SurvivalCisplatinDrug TherapyEnergy MetabolismHep G2 CellsHumansMetal NanoparticlesOxidative StressProteomeSilverAntioxidantsCisplatinProteomeSilverCell viabilityCombination chemotherapyMetal uptakeProteomicsSilver nanoparticles

Identifiers

PMID33168016
PMCPMC7654574
OpenAlexW3099403067

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.