Evidence map›Paper›PMID 35706338›Full record

ArticleChemical research in toxicology2022

Biological Impacts of Reduced Graphene Oxide Affected by Protein Corona Formation.

Roxana Coreas, Carmen Castillo, Zongbo Li, Dong Yan, Ziting Gao, Junyi Chen, Dimitrios Bitounis, Dorsa Parviz, Michael S Strano, Philip Demokritou and 1 more

Open access · greenAbstract read
In one paragraph

Article in Chemical research in toxicology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

11 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. 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

11 authors at 3 institutions in 1 country.

Roxana CoreasEnvironmental Toxicology Graduate Program, University of California, Riverside, California 92521, United States.ORCID 0000-0001-6057-4717
Carmen CastilloDepartment of Biochemistry, University of California, Riverside, California 92521, United States.
Zongbo LiDepartment of Chemistry, University of California, Riverside, California 92521, United States.
Dong YanNanofabrication Facility, University of California, Riverside, California 92521, United States.
Ziting GaoDepartment of Chemistry, University of California, Riverside, California 92521, United States.
Junyi ChenEnvironmental Toxicology Graduate Program, University of California, Riverside, California 92521, United States.ORCID 0000-0001-7453-6623
Dimitrios BitounisCenter for Nanotechnology and Nanotoxicology, HSPH-NIEHS Nanosafety Center, Department of Environmental Health, Harvard T. H. Chan School of Public Health Initiative for Sustainable Nanotechnology, Harvard University, Boston, Massachusetts 02115, United States.ORCID 0000-0002-9739-3300
Dorsa ParvizDepartment of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States.
Michael S StranoDepartment of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States.ORCID 0000-0003-2944-808X
Philip DemokritouCenter for Nanotechnology and Nanotoxicology, HSPH-NIEHS Nanosafety Center, Department of Environmental Health, Harvard T. H. Chan School of Public Health Initiative for Sustainable Nanotechnology, Harvard University, Boston, Massachusetts 02115, United States.ORCID 0000-0002-2484-9143
Wenwan ZhongEnvironmental Toxicology Graduate Program, University of California, Riverside, California 92521, United States.ORCID 0000-0002-3317-3464
University of California, Riverside · USHarvard University · USMassachusetts Institute of Technology · US

Funding

UC Riverside MARC U* Star Undergraduate Research ProgramT34GM062756 · NIGMS · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI MARTINEZ, ERNEST · 2001 to 2022
$8.7M
Research Training in Environmental ToxicologyT32ES018827 · NIEHS · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI Yinsheng Wang · 2010 to 2026
$5.3M
Engineered Nanomaterial Synthesis, Characterization and Method Development Center for Nano-safety ResearchU24ES026946 · NIEHS · HARVARD SCHOOL OF PUBLIC HEALTH · PI DEMOKRITOU, PHILIP · 2016 to 2020
$3.8M
MARC at University of California RiversideT34GM149470 · NIGMS · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI ERNEST MARTINEZ · 2023 to 2026
$2.1M
Nano-response: Immune stimulation, microbiome perturbation, and impacts from protein coronaU01ES027293 · NIEHS · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI ZHONG, WENWAN · 2016 to 2020
$996k
An LTQ-Orbitrap Elite with ETD for the Keck Proteomics FacilityS10OD010669 · OD · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI WANG, YINSHENG · 2013 to 2013
$600k
NIEHS NIH HHS T32 ES018827NIEHS NIH HHS U01 ES027293NIEHS NIH HHS U24 ES026946NIGMS NIH HHS T34 GM062756NIGMS NIH HHS T34 GM149470NIH HHS S10 OD010669
6 · The paper itself

Abstract

Applications of reduced graphene oxide (rGO) in many different areas have been gradually increasing owing to its unique physicochemical characteristics, demanding more understanding of their biological impacts. Herein, we assessed the toxicological effects of rGO in mammary epithelial cells. Because the as-synthesized rGO was dissolved in sodium cholate to maintain a stable aqueous dispersion, we hypothesize that changing the cholate concentration in the dispersion may alter the surface property of rGO and subsequently affect its cellular toxicity. Thus, four types of rGO were prepared and compared: rGO dispersed in 4 and 2 mg/mL sodium cholate, labeled as rGO and concentrated-rGO (c-rGO), respectively, and rGO and c-rGO coated with a protein corona through 1 h incubation in culture media, correspondingly named pro-rGO and pro-c-rGO. Notably, c-rGO and pro-c-rGO exhibited higher toxicity than rGO and pro-rGO and also caused higher reactive oxygen species production, more lipid membrane peroxidation, and more significant disruption of mitochondrial-based ATP synthesis. In all toxicological assessments, pro-c-rGO induced more severe adverse impacts than c-rGO. Further examination of the material surface, protein adsorption, and cellular uptake showed that the surface of c-rGO was coated with a lower content of surfactant and adsorbed more proteins, which may result in the higher cellular uptake observed with pro-c-rGO than pro-rGO. Several proteins involved in cellular redox mediation were also more enriched in pro-c-rGO. These results support the strong correlation between dispersant coating and corona formation and their subsequent cellular impacts. Future studies in this direction could reveal a deeper understanding of the correlation and the specific cellular pathways involved and help gain knowledge on how the toxicity of rGO could be modulated through surface modification, guiding the sustainable applications of rGO.

Indexed as

GraphiteProtein CoronaReactive Oxygen SpeciesSodium Cholategraphene oxideGraphiteProtein CoronaReactive Oxygen SpeciesSodium Cholate

Identifiers

PMID35706338
PMCPMC9842398
OpenAlexW4282962492

What OpenQuestion holds

Textmetadata
LicenceTDM
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.