Evidence map›Paper›PMID 32982239›Full record

ArticleInternational journal of nanomedicine2020

Nanomicellar Lenalidomide-Fenretinide Combination Suppresses Tumor Growth in an

Isabella Orienti, Giovanna Farruggia, Ferro Nguyen, Peng Guan, Natalia Calonghi, Venkatadri Kolla, Michael Chorny, Garrett M Brodeur

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2020. 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
0.4field-weighted citation impact, top 35% 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

11 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Fenretinide in Cancer and Neurological Disease: A Two-Face Janus Molecule.International journal of molecular sciences · 2022
    Review
  10. Article
  11. Targeting Sphingolipids for Cancer Therapy.Frontiers in oncology · 2021
    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

8 authors at 2 institutions in 2 countries.

Isabella OrientiDepartment of Pharmacy and Biotechnology, University of Bologna, Bologna 40127, Italy.ORCID 0000-0003-1972-2807
Giovanna FarruggiaDepartment of Pharmacy and Biotechnology, University of Bologna, Bologna 40127, Italy.ORCID 0000-0003-3599-7034
Ferro NguyenDivisions of Oncology and Cardiology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.ORCID 0000-0001-6640-8445
Peng GuanDivisions of Oncology and Cardiology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Natalia CalonghiDepartment of Pharmacy and Biotechnology, University of Bologna, Bologna 40127, Italy.
Venkatadri KollaDivisions of Oncology and Cardiology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.ORCID 0000-0002-2385-3407
Michael ChornyDivisions of Oncology and Cardiology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.ORCID 0000-0002-8243-9089
Garrett M BrodeurDivisions of Oncology and Cardiology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.ORCID 0000-0002-6721-122X
Children's Hospital of Philadelphia · USUniversity of Bologna · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeIn a previous study, we demonstrated that the combination of fenretinide with lenalidomide, administered by a novel nanomicellar formulation (FLM), provided a strong antitumor effect in a neuroblastoma TrkB-expressing tumor. In this study, we tested the nanomicellar combination in an EXPERIMENTAL

designFLM was administered to mice bearing human NLF xenografts to evaluate its efficacy in comparison with the nanomicelles containing fenretinide alone (FM). Confocal laser-scanning fluorescence microscopy images of the NLF cells treated with FLM and FM allowed us to estimate the nanomicelle ability to transport the encapsulated drugs inside the tumor cells. Flow cytometric analysis of the cells from treated tumors was performed to assess the effect of treatment on GD2 expression and NK cell infiltration.

resultsFLM and FM decreased the growth of NLF xenografts at comparable extents during the treatment period. Afterwards, FLM induced a progressive tumor regression without regrowth, while FM treatment was followed by regrowth within 15-20 days after the end of treatment. Both FLM and FM were able to penetrate the tumor cells transporting the encapsulated drugs. FLM transported higher amount of fenretinide inside the cells. Also, FLM treatment strongly increased GD2 expression in treated tumors and slightly decreased the NK infiltration compared to FM.

conclusionFLM treatment induced a superior antitumor response than FM in NLF xenografts, presumably due to the combined effects of fenretinide cytotoxicity and lenalidomide antiangiogenic activity. The ability of FLM to penetrate tumor cells, transporting the encapsulated drugs, substantially improved the therapeutic efficiency of this system. Moreover, the enhancement of GD2 expression in FLM treated tumors offers the possibility to further increase the antitumor effect by the use of anti-GD2 CAR-T cells and anti-GD2 antibodies in combination with FLM in multimodal therapies.

Indexed as

AnimalsAntineoplastic Combined Chemotherapy ProtocolsCell Line, TumorDrug Delivery SystemsFemaleFenretinideGene Expression Regulation, NeoplasticHumansKiller Cells, NaturalLenalidomideMicellesMice, NudeMicroscopy, ConfocalNanostructuresNeuroblastomaN-Myc Proto-Oncogene ProteinFenretinideLenalidomideMicellesMYCN protein, humanN-Myc Proto-Oncogene Proteinantitumor activityfenretinide–lenalidomide combinationGD2 increased expression.nanomicelle penetration in tumor cellsnanomicellesneuroblastoma

Identifiers

PMID32982239
PMCPMC7502401
OpenAlexW3086052470

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.