Evidence map›Paper›PMID 31757040›Full record

ArticleInternational journal of molecular sciences2019

Significant Benefits of Nanoparticles Containing a Necrosis Inhibitor on Mice Testicular Tissue Autografts Outcomes.

Federico Del Vento, Maxime Vermeulen, Bernard Ucakar, Jonathan Poels, Anne des Rieux, Christine Wyns

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. 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
3.0field-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

12 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Programmed cell death in triple-negative breast cancer.Cellular & molecular biology letters · 2025
    Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. 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

6 authors at 2 institutions in 1 country.

Federico Del VentoGynecology-Andrology Unit, Medical School, Institute of Experimental and Clinical Research, Catholic University of Louvain, UCLouvain, 1200 Brussels, Belgium.
Maxime VermeulenGynecology-Andrology Unit, Medical School, Institute of Experimental and Clinical Research, Catholic University of Louvain, UCLouvain, 1200 Brussels, Belgium.ORCID 0000-0003-4021-4225
Bernard UcakarAdvanced Drug Delivery and Biomaterials Unit, Louvain Drug Research Institute, Catholic University of Louvain, UCLouvain, 1200 Brussels, Belgium.
Jonathan PoelsGynecology-Andrology Unit, Medical School, Institute of Experimental and Clinical Research, Catholic University of Louvain, UCLouvain, 1200 Brussels, Belgium.
Anne des RieuxAdvanced Drug Delivery and Biomaterials Unit, Louvain Drug Research Institute, Catholic University of Louvain, UCLouvain, 1200 Brussels, Belgium.ORCID 0000-0001-9953-3816
Christine WynsGynecology-Andrology Unit, Medical School, Institute of Experimental and Clinical Research, Catholic University of Louvain, UCLouvain, 1200 Brussels, Belgium.ORCID 0000-0002-6581-5003
UCLouvain · BECliniques Universitaires Saint-Luc · BE

Funding

Fondation contre le cancer 2016-141 FAF-C/2016/745
6 · The paper itself

Abstract

Fertility preservation for prepubertal boys relies exclusively on cryopreservation of immature testicular tissue (ITT) containing spermatogonia as the only cells with reproductive potential. Preclinical studies that used a nude mice model to evaluate the development of human transplanted ITT were characterized by important spermatogonial loss. We hypothesized that the encapsulation of testicular tissue in an alginate matrix supplemented with nanoparticles containing a necrosis inhibitor (NECINH-NPS) would improve tissue integrity and germ cells' survival in grafts. We performed orthotopic autotransplantation of 1 mm³ testicular tissue fragments recovered form mice (aged 4-5 weeks). Fragments were either non-encapsulated, encapsulated in an alginate matrix, or encapsulated in an alginate matrix containing NECINH-NPs. Grafts were recovered 5- and 21-days post-transplantation. We evaluated tissue integrity (hematoxylin-eosin staining), germ cells survival (immunohistochemistry for promyelocytic leukemia zinc-finger, VASA, and protein-boule-like), apoptosis (immunohistochemistry for active-caspase 3), and lipid peroxidation (immunohistochemistry for malondialdehyde). NECINH-NPs significantly improved testicular tissue integrity and germ cells' survival after 21 days. Oxidative stress was reduced after 5 days, regardless of nanoparticle incorporation. No effect on caspase-dependent apoptosis was observed. In conclusion, NECINH-NPs in an alginate matrix significantly improved tissue integrity and germ cells' survival in grafts with the perspective of higher reproductive outcomes.

Indexed as

AlginatesAnimalsApoptosisCell SurvivalFertility PreservationLipid PeroxidationMaleMiceNanoparticlesSpermatogoniaTestisTumor Necrosis Factor InhibitorsAlginatesTumor Necrosis Factor Inhibitorsfertility preservationmale fertilitynanoparticlesnecrosisnecrosis inhibitorprepubertal boysprepubertal testicular tissuespermatogoniatissue engineeringtransplantation

Identifiers

PMID31757040
PMCPMC6929043
OpenAlexW2989596229

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.