Evidence map›Paper›PMID 33786735›Full record

ArticleJournal of assisted reproduction and genetics2021

Disease-inducing potential of two leukemic cell lines in a xenografting model.

D D Manavella, Sonia Herraiz, M Soares, A Buigues, A Pellicer, J Donnez, C Díaz-García, M M Dolmans

Open access · greenAbstract read
In one paragraph

Article in Journal of assisted reproduction and genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 36% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

8 authors at 5 institutions in 5 countries.

D D ManavellaPôle de Recherche en Gynécologie, Institut de Recherche Expérimentale et Clinique, Université Catholique de Louvain, Avenue Mounier 52, bte. B1.52.02, 1200, Brussels, Belgium.
Sonia HerraizIVI Foundation-Instituto de Investigación Sanitaria Hospital La Fe (IIS La Fe), Valencia, Spain. sonia.herraiz@ivirma.com.ORCID http://orcid.org/0000-0003-0703-6922
M SoaresPôle de Recherche en Gynécologie, Institut de Recherche Expérimentale et Clinique, Université Catholique de Louvain, Avenue Mounier 52, bte. B1.52.02, 1200, Brussels, Belgium.
A BuiguesIVI Foundation-Instituto de Investigación Sanitaria Hospital La Fe (IIS La Fe), Valencia, Spain.
A PellicerIVI Foundation-Instituto de Investigación Sanitaria Hospital La Fe (IIS La Fe), Valencia, Spain.
J DonnezSociety for Research into Infertility, Brussels, Belgium.
C Díaz-GarcíaIVI Foundation-Instituto de Investigación Sanitaria Hospital La Fe (IIS La Fe), Valencia, Spain.
M M DolmansPôle de Recherche en Gynécologie, Institut de Recherche Expérimentale et Clinique, Université Catholique de Louvain, Avenue Mounier 52, bte. B1.52.02, 1200, Brussels, Belgium.
Instituto de Investigación Sanitaria La Fe · ESCliniques Universitaires Saint-Luc · BEGuyra Paraguay · PYUCLouvain · BEValencian Infertility Institute · ES

Funding

Conselleria d'Educació, Investigació, Cultura i Esport PROMETEO/2018/137Fonds De La Recherche Scientifique - FNRS 5/4/150/5Fonds De La Recherche Scientifique - FNRS FNRS-PDR Convention T.0077.14, Télévie grant No. 7.6515.16FMinisterio de Ciencia, Innovación y Universidades CP19-00141
6 · The paper itself

Abstract

purposeCryopreserved ovarian tissue transplant restores ovarian function in young cancer patients after gonadotoxic treatment. However, leukemia is associated with increased risk of malignant cell transmission. We aimed to assess the tumor-inducing potential of two different leukemic cell lines when xenografted to immunodeficient mice.

methodsFifty-four female immunodeficient mice were grafted with either 100, 200, 500, 1000, and 10,000 chronic myeloid leukemia in blast crisis (BV-173) cells or relapsed acute lymphoblastic leukemia (RCH-ACV) cells, embedded inside a fibrin scaffold along with 50,000 human ovarian stromal cells. Two mice per cell line received the fibrin matrix without leukemic cells as negative controls. Clinical signs of disease were monitored for 20 weeks. Grafts, liver tissue, and masses were collected for macroscopic analysis and gene expression of BCR-ABL1 and E2A-PBX fusion transcripts present in BV-173 and RCH-ACV respectively.

resultsBV-173 cells: Mice grafted with 100, 200, or 500 cells showed no sign of disease after and were negative for BCR-ABL1 expression. Three of the 5 animals grafted with 1000 cells and all mice with 10,000 cells developed disease and showed BCR-ABL1-positive expression. RCH-ACV cells: Two out of 4 mice grafted with 100 cells developed disease and were E2A-PBX1-positive. All the animals grafted with higher cell doses showed signs of disease and all but one were E2A-PBX1-positive.

conclusionThe present work proves that the disease-inducing potential of BV-173 and RCH-ACV leukemic cells xenografted to SCID mouse peritoneum differs between cell lines, depending on cell number, type, status, and cytogenetic disease profile when ovarian tissue is harvested.

Indexed as

Transplantation, HeterologousAnimalsCell Line, TumorCryopreservationDisease Models, AnimalFemaleFertility PreservationFusion Proteins, bcr-ablGene Expression Regulation, NeoplasticHeterograftsHomeodomain ProteinsHumansLeukemia, Myelogenous, Chronic, BCR-ABL PositiveMiceOncogene Proteins, FusionOvarian FollicleBCR-ABL1 fusion protein, humanE2A-Pbx1 fusion proteinFusion Proteins, bcr-ablHomeodomain ProteinsOncogene Proteins, FusionFertility preservationLeukemiaLeukemic cell engraftmentOvarian tissue cryopreservationOvarian tissue transplantation

Identifiers

PMID33786735
PMCPMC8266930
OpenAlexW3148124838

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.