Evidence map›Paper›PMID 37129253›Full record

ReviewACS nano2023

Photodynamic and Photothermal Therapies: Synergy Opportunities for Nanomedicine.

Marta Overchuk, Robert A Weersink, Brian C Wilson, Gang Zheng

Open access · bronzeAbstract readReview
In one paragraph

Review in ACS nano, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 378 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
378citing papers in PubMed, 1 pooled it
118.6field-weighted citation impact, top 1% 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

378 citing papers in PubMed, 1 synthesis or guideline pooled it, 1,081 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Linking In Vivo Imaging to Therapeutic Outcome withInternational journal of molecular sciences · 2026
    Review
  11. Sulfur Vacancy-Enriched CuAngewandte Chemie (International ed. in English) · 2026
    Article
  12. NIR-Assisted Multimodal Strategies for Enhanced Antibacterial Therapy.Small (Weinheim an der Bergstrasse, Germany) · 2026
    Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Article

318 more citing papers are in PubMed but not listed here.

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 at 2 institutions in 2 countries.

Marta OverchukPrincess Margaret Cancer Centre, University Health Network, Toronto, Ontario M5G 1L7, Canada.
Robert A WeersinkPrincess Margaret Cancer Centre, University Health Network, Toronto, Ontario M5G 1L7, Canada.
Brian C WilsonPrincess Margaret Cancer Centre, University Health Network, Toronto, Ontario M5G 1L7, Canada.
Gang ZhengPrincess Margaret Cancer Centre, University Health Network, Toronto, Ontario M5G 1L7, Canada.ORCID 0000-0002-0705-7398
University Health Network · CAUniversity of North Carolina at Chapel Hill · US

Funding

CIHR FDN154326
6 · The paper itself

Abstract

Tumoricidal photodynamic (PDT) and photothermal (PTT) therapies harness light to eliminate cancer cells with spatiotemporal precision by either generating reactive oxygen species or increasing temperature. Great strides have been made in understanding biological effects of PDT and PTT at the cellular, vascular and tumor microenvironmental levels, as well as translating both modalities in the clinic. Emerging evidence suggests that PDT and PTT may synergize due to their different mechanisms of action, and their nonoverlapping toxicity profiles make such combination potentially efficacious. Moreover, PDT/PTT combinations have gained momentum in recent years due to the development of multimodal nanoplatforms that simultaneously incorporate photodynamically- and photothermally active agents. In this review, we discuss how combining PDT and PTT can address the limitations of each modality alone and enhance treatment safety and efficacy. We provide an overview of recent literature featuring dual PDT/PTT nanoparticles and analyze the strengths and limitations of various nanoparticle design strategies. We also detail how treatment sequence and dose may affect cellular states, tumor pathophysiology and drug delivery, ultimately shaping the treatment response. Lastly, we analyze common experimental design pitfalls that complicate preclinical assessment of PDT/PTT combinations and propose rational guidelines to elucidate the mechanisms underlying PDT/PTT interactions.

Indexed as

NanoparticlesNeoplasmsPhotochemotherapyCell Line, TumorHumansNanomedicinePhotosensitizing AgentsPhototherapyPhotothermal TherapyPhotosensitizing Agentscancercombination therapiesdrug deliverymultimodal nanoparticlesPDTphotodynamic therapyphotomedicinephotothermal therapyPTTtheranostics

Identifiers

PMID37129253
PMCPMC10173698
OpenAlexW4367180472

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.