Evidence map›Paper›PMID 36133617›Full record

ArticleNanoscale advances2019

Selective photothermal killing of cancer cells using LED-activated nucleus targeting fluorescent carbon dots.

Stephen A Hill, Sadiyah Sheikh, Qiaoyu Zhang, Lorena Sueiro Ballesteros, Andrew Herman, Sean A Davis, David J Morgan, Monica Berry, David Benito-Alifonso, M Carmen Galan

Abstract read
In one paragraph

Article in Nanoscale advances, 2019. 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
–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

11 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Carbon Dots as an Emergent Class of Antimicrobial Agents.Nanomaterials (Basel, Switzerland) · 2021
    Review
  9. Article
  10. Article
  11. Review
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

10 authors.

Stephen A HillSchool of Chemistry, University of Bristol Cantock's Close Bristol UK M.C.Galan@bristol.ac.uk.ORCID https://orcid.org/0000-0001-5395-6426
Sadiyah SheikhSchool of Chemistry, University of Bristol Cantock's Close Bristol UK M.C.Galan@bristol.ac.uk.ORCID https://orcid.org/0000-0003-2079-7566
Qiaoyu ZhangSchool of Chemistry, University of Bristol Cantock's Close Bristol UK M.C.Galan@bristol.ac.uk.
Lorena Sueiro BallesterosSchool of Cellular and Molecular Medicine, Faculty of Life Sciences Flow Cytometry Facility University Walk Bristol UK.
Andrew HermanSchool of Cellular and Molecular Medicine, Faculty of Life Sciences Flow Cytometry Facility University Walk Bristol UK.
Sean A DavisSchool of Chemistry, University of Bristol Cantock's Close Bristol UK M.C.Galan@bristol.ac.uk.
David J MorganCardiff Catalysis Institute, School of Chemistry, Cardiff University Park Place Cardiff UK.ORCID https://orcid.org/0000-0002-6571-5731
Monica BerrySchool of Chemistry, University of Bristol Cantock's Close Bristol UK M.C.Galan@bristol.ac.uk.
David Benito-AlifonsoSchool of Chemistry, University of Bristol Cantock's Close Bristol UK M.C.Galan@bristol.ac.uk.
M Carmen GalanSchool of Chemistry, University of Bristol Cantock's Close Bristol UK M.C.Galan@bristol.ac.uk.ORCID https://orcid.org/0000-0001-7307-2871

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of effective theranostic probes in cancer therapy is hampered due to issues with selectivity and off-target toxicity. We report the selective LED-photothermal ablation of cervical (HeLa) cancer cells over human dermal fibroblasts (HDF) using a new class of green-emissive fluorescent carbon dots (FCDs). The FCDs can be easily prepared in one pot using cheap and commercial starting materials. Physico-chemical characterization revealed that a surface coating of 2,5-deoxyfructosazine on a robust amorphous core gives rise to the nanomaterial's unique properties. We show that intracellular uptake mostly involves passive mechanisms in combination with intracellular DNA interactions to target the nucleus and that cancer cell selective killing is likely due to an increase in intracellular temperature in combination with ATP depletion, which is not observed upon exposure to either the "naked" core FCDs or the surface components individually. The selectivity of these nanoprobes and the lack of apparent production of toxic metabolic byproducts make these new nanomaterials promising agents in cancer therapy.

Identifiers

PMID36133617
PMCPMC9417209

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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.