Evidence map›Paper›PMID 24568338›Full record

ArticleMolecular pharmaceutics2014

Enhancing targeted tumor treatment by near IR light-activatable photodynamic-photothermal synergistic therapy.

Zhen Fan, Xuemei Dai, Yuefeng Lu, Eugene Yu, Nupur Brahmbatt, NaTasha Carter, Christine Tchouwou, Anant Kumar Singh, Yolanda Jones, Hongtao Yu and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular pharmaceutics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

13 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Article
  3. Photodynamic therapy reduces cell viability, migration and triggers necroptosis in prostate tumor cells.Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology · 2023
    Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Nanomaterials as photothermal therapeutic agents.Progress in materials science · 2019
    Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. 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

11 authors at 3 institutions in 1 country.

Zhen FanDepartment of Chemistry, Jackson State University , Jackson, Mississippi 39217, United States.
Xuemei Dai
Yuefeng Lu
Eugene Yu
Nupur Brahmbatt
NaTasha Carter
Christine Tchouwou
Anant Kumar Singh
Yolanda Jones
Hongtao Yu
Paresh Chandra Ray
Jackson State University · USAlcorn State University · USUniversity of Mississippi Medical Center · US

Funding

TRANSCRIPTOMICS OF GIARDIA LAMBLIAG12RR013459 · NCRR · JACKSON STATE UNIVERSITY · PI TCHOUNWOU, PAUL B. · 1998 to 2011
$18.0M
Undergraduate Biomedical Research Training at Jackson State UniversityT34GM007672 · NIGMS · JACKSON STATE UNIVERSITY · PI STEVENS, JACQUELINE JEANETTE · 1985 to 2015
$5.1M
NCRR NIH HHS 5G12RR013459NCRR NIH HHS G12 RR013459NIGMS NIH HHS 5-T34-GM007672-28NIGMS NIH HHS T34 GM007672
6 · The paper itself

Abstract

For several decades, cancer has been one of the most life-threatening diseases. For enhancing anticancer efficiency with minimum side effects, combination therapy is envisioned. The current manuscript reports for the first time the development of a methylene blue (MB) bound nanoplatform, which is capable of delivering targeted diagnostic and combined synergistic photothermal and photodynamic treatment of cancer. Experimental data found that, once the nanoparticle binds with the target cell surface, it can detect LNCaP human prostate cancer cell selectively using fluorescence imaging. Our result shows that the therapeutic actions can be controlled with external NIR light. No cytotoxicity was observed in the absence of NIR light. Targeted photodynamic and photothermal treatment using 785 nm NIR light indicates that the multimodal treatment enhances the possibility of destroying LNCaP prostate cancer cells in vitro dramatically. We discuss the operating principle for the targeted imaging and possible mechanisms for combined therapeutic actions. Our experimental data show that NIR light activated combined therapy for cancer may become a highly effective treatment procedure in clinical settings.

Indexed as

PhototherapyCell Line, TumorCombined Modality TherapyHumansMaleMethylene BlueMolecular Targeted TherapyNanostructuresPhotochemotherapyProstatic NeoplasmsReactive Oxygen SpeciesMethylene BlueReactive Oxygen Species

Identifiers

PMID24568338
PMCPMC3983349
OpenAlexW2060830935

What OpenQuestion holds

Textmetadata
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.