Evidence map›Paper›PMID 39252643›Full record

ArticleACS applied materials & interfaces2024

Synergistic Enhancement of Photodynamic Cancer Therapy with Mesenchymal Stem Cells and Theranostic Nanoparticles.

Greta Butkiene, Aleja Marija Daugelaite, Vilius Poderys, Riccardo Marin, Simona Steponkiene, Evelina Kazlauske, Ilona Uzieliene, Dainius Daunoravicius, Daniel Jaque, Ricardas Rotomskis and 3 more

Abstract read
In one paragraph

Article in ACS applied materials & interfaces, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. 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

13 authors.

Greta ButkieneBiomedical Physics Laboratory of the National Cancer Institute, P. Baublio St. 3b, Vilnius LT-08406, Lithuania.ORCID 0000-0003-3244-4979
Aleja Marija DaugelaiteBiomedical Physics Laboratory of the National Cancer Institute, P. Baublio St. 3b, Vilnius LT-08406, Lithuania.ORCID 0009-0009-6921-8933
Vilius PoderysBiomedical Physics Laboratory of the National Cancer Institute, P. Baublio St. 3b, Vilnius LT-08406, Lithuania.ORCID 0000-0002-9504-3403
Riccardo MarinNano for Bioimaging Group (nanoBIG), Departamento de Física de Materiales, Facultad de Ciencias, Universidad Autónoma de Madrid, Madrid 28049, Spain.ORCID 0000-0003-3270-892X
Simona SteponkieneBiomedical Physics Laboratory of the National Cancer Institute, P. Baublio St. 3b, Vilnius LT-08406, Lithuania.ORCID 0000-0002-3469-0543
Evelina KazlauskeBiomedical Physics Laboratory of the National Cancer Institute, P. Baublio St. 3b, Vilnius LT-08406, Lithuania.ORCID 0000-0001-6088-9495
Ilona UzielieneDepartment of Regenerative Medicine, State Research Institute Centre for Innovative Medicine, Santariskiu g. 5, Vilnius LT-08406, Lithuania.ORCID 0000-0001-5484-9163
Dainius DaunoraviciusClinicus Vilnius, V. Grybo g. 17-135, Vilnius LT- 10318, Lithuania.ORCID 0000-0002-5711-5162
Daniel JaqueNano for Bioimaging Group (nanoBIG), Departamento de Física de Materiales, Facultad de Ciencias, Universidad Autónoma de Madrid, Madrid 28049, Spain.ORCID 0000-0002-3225-0667
Ricardas RotomskisBiomedical Physics Laboratory of the National Cancer Institute, P. Baublio St. 3b, Vilnius LT-08406, Lithuania.
Artiom SkripkaNano for Bioimaging Group (nanoBIG), Departamento de Física de Materiales, Facultad de Ciencias, Universidad Autónoma de Madrid, Madrid 28049, Spain.ORCID 0000-0003-4060-4290
Fiorenzo VetroneCentre Énergie, Matériaux et Télécommunications, Institut National de la Recherche Scientifique (INRS), Université du Québec, Varennes, Québec J3X 1P7, Canada.ORCID 0000-0002-3222-3052
Vitalijus KarabanovasBiomedical Physics Laboratory of the National Cancer Institute, P. Baublio St. 3b, Vilnius LT-08406, Lithuania.ORCID 0000-0002-5029-8840

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nanoparticles engineered to combat cancer and other life-threatening diseases may significantly improve patient outcomes. However, inefficient nanoparticle delivery to tumors limits their use and necessitates the development of complex delivery approaches. Here, we examine this issue by harnessing the tumor-homing abilities of human mesenchymal stem cells (MSCs) to deliver a decoupled theranostic complex of rare earth-doped nanoparticles (dNPs) and photosensitizer chlorin e6 (Ce6) to tumors. We show that both bone-marrow- and skin-derived MSCs can transport the dNP-Ce6 complex inside tumor spheroids, which is challenging to accomplish by passive delivery alone. MSCs deliver the dNP-Ce6 complex across the tumor spheroid, facilitating more effective photodynamic damage and tumor destruction than passively accumulated dNP-Ce6. The dNP-Ce6 complex also provides the built-in ability to monitor the MSC migration without causing undesired phototoxicity, which is essential for maximal and side-effect-free delivery of nanoparticles. Our results demonstrate how MSCs can be used as delivery vehicles for the transportation of the dNP-Ce6 complex, addressing the limitations of passive nanoparticle delivery and providing light-based theranostics.

Indexed as

ChlorophyllidesMesenchymal Stem CellsNanoparticlesPhotochemotherapyPhotosensitizing AgentsTheranostic NanomedicineAnimalsCell Line, TumorHumansMiceNeoplasmsPorphyrinsChlorophyllidesPhotosensitizing AgentsphytochlorinPorphyrinsdecoupled theranosticsdrug deliverymesenchymal stem cellsnanomedicinetumor homingupconverting nanoparticles

Identifiers

PMID39252643
PMCPMC11420871

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.