Evidence map›Paper›PMID 32385408›Full record

ArticleCommunications biology2020

Heat shock protein 90-targeted photodynamic therapy enables treatment of subcutaneous and visceral tumors.

Kensuke Kaneko, Takuya Osada, Michael A Morse, William R Gwin, Joshua D Ginzel, Joshua C Snyder, Xiao-Yi Yang, Cong-Xiao Liu, Márcio A Diniz, Khaldon Bodoor and 3 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.0field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Mitochondria-Targeted Nanomotor: HAdvanced materials (Deerfield Beach, Fla.) · 2026
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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

13 authors at 4 institutions in 1 country.

Kensuke KanekoDepartment of Surgery, Duke University Medical Center, Durham, NC, 27710, USA.ORCID 0000-0003-0510-4602
Takuya OsadaDepartment of Surgery, Duke University Medical Center, Durham, NC, 27710, USA.
Michael A MorseDepartment of Surgery, Duke University Medical Center, Durham, NC, 27710, USA.
William R GwinDepartment of Medicine, University of Washington, Seattle, WA, 98195, USA.ORCID 0000-0001-6314-0965
Joshua D GinzelDepartment of Cell Biology, Duke University, Durham, NC, 27710, USA.ORCID 0000-0001-5635-7314
Joshua C SnyderDepartment of Surgery, Duke University Medical Center, Durham, NC, 27710, USA.ORCID 0000-0002-9787-3371
Xiao-Yi YangDepartment of Surgery, Duke University Medical Center, Durham, NC, 27710, USA.
Cong-Xiao LiuDepartment of Surgery, Duke University Medical Center, Durham, NC, 27710, USA.
Márcio A DinizBiostatistics and Bioinformatics Research Center, Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA, 90048, USA.ORCID 0000-0002-2427-7843
Khaldon BodoorDepartment of Pharmacology and Cancer Biology, Duke University, Durham, NC, 27710, USA.
Philip F HughesDepartment of Pharmacology and Cancer Biology, Duke University, Durham, NC, 27710, USA.ORCID 0000-0002-2217-455X
Timothy Aj HaysteadDepartment of Pharmacology and Cancer Biology, Duke University, Durham, NC, 27710, USA. timothy.haystead@dm.duke.edu.
H Kim LyerlyDepartment of Surgery, Duke University Medical Center, Durham, NC, 27710, USA. kim.lyerly@duke.edu.ORCID 0000-0002-0063-4770
Duke University · USDuke Medical Center · USCedars-Sinai Medical Center · USUniversity of Washington · US

Funding

Training Program in Developmental & Stem Cell BiologyT32HD040372 · NICHD · DUKE UNIVERSITY · PI Terry H Lechler · 2001 to 2026
$8.9M
NICHD NIH HHS T32 HD040372
6 · The paper itself

Abstract

Photodynamic therapy (PDT) ablates malignancies by applying focused near-infrared (nIR) light onto a lesion of interest after systemic administration of a photosensitizer (PS); however, the accumulation of existing PS is not tumor-exclusive. We developed a tumor-localizing strategy for PDT, exploiting the high expression of heat shock protein 90 (Hsp90) in cancer cells to retain high concentrations of PS by tethering a small molecule Hsp90 inhibitor to a PS (verteporfin, VP) to create an Hsp90-targeted PS (HS201). HS201 accumulates to a greater extent than VP in breast cancer cells both in vitro and in vivo, resulting in increased treatment efficacy of HS201-PDT in various human breast cancer xenografts regardless of molecular and clinical subtypes. The therapeutic index achieved with Hsp90-targeted PDT would permit treatment not only of localized tumors, but also more diffusely infiltrating processes such as inflammatory breast cancer.

Indexed as

Antineoplastic AgentsCell Line, TumorHSP90 Heat-Shock ProteinsHumansMCF-7 CellsPhotochemotherapyPhotosensitizing AgentsVerteporfinAntineoplastic AgentsHSP90 Heat-Shock ProteinsPhotosensitizing AgentsVerteporfin

Identifiers

PMID32385408
PMCPMC7210113
OpenAlexW3021622390

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.