Evidence map›Paper›PMID 31467126›Full record

ArticleHaematologica2020

Dissecting molecular mechanisms of resistance to NOTCH1-targeted therapy in T-cell acute lymphoblastic leukemia xenografts.

Valentina Agnusdei, Sonia Minuzzo, Marica Pinazza, Alessandra Gasparini, Laura Pezzè, Adriana Agnese Amaro, Lorenza Pasqualini, Paola Del Bianco, Martina Tognon, Chiara Frasson and 6 more

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Targeting Notch in oncology: the path forward.Nature reviews. Drug discovery · 2021
    Review
  7. Review
  8. Review
  9. 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

16 authors at 8 institutions in 2 countries.

Valentina AgnusdeiIstituto Oncologico Veneto IOV - IRCCS, Padova.
Sonia MinuzzoDepartment of Surgery, Oncology and Gastroenterology, University of Padova, Padova.
Marica PinazzaIstituto Oncologico Veneto IOV - IRCCS, Padova.
Alessandra GaspariniIstituto Oncologico Veneto IOV - IRCCS, Padova.
Laura PezzèLaboratory of Molecular Cancer Genetics, Department of Cellular, Computational and Integrative Biology (CIBIO), University of Trento.
Adriana Agnese AmaroTumor Epigenetics, IRCCS Ospedale Policlinico San Martino, Genova.
Lorenza PasqualiniTumor Epigenetics, IRCCS Ospedale Policlinico San Martino, Genova.
Paola Del BiancoIstituto Oncologico Veneto IOV - IRCCS, Padova.
Martina TognonIstituto Oncologico Veneto IOV - IRCCS, Padova.
Chiara FrassonIstituto di Ricerca Pediatrica, Fondazione Città della Speranza, Padova.
Pietro PalumboMedical Genetics Unit, Fondazione IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, Italy.
Yari CiribilliLaboratory of Molecular Cancer Genetics, Department of Cellular, Computational and Integrative Biology (CIBIO), University of Trento.
Ulrich PfefferTumor Epigenetics, IRCCS Ospedale Policlinico San Martino, Genova.
Massimo CarellaMedical Genetics Unit, Fondazione IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, Italy.
Alberto AmadoriIstituto Oncologico Veneto IOV - IRCCS, Padova.
Stefano IndraccoloIstituto Oncologico Veneto IOV - IRCCS, Padova stefano.indraccolo@unipd.it.
Istituto Oncologico Veneto · ITOspedale Policlinico San Martino · ITCasa Sollievo della Sofferenza · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITUniversity of Padua · ITCancer Genetics (United States) · USCittà della Speranza Foundation · ITUniversity of Trento · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite substantial progress in treatment of T-cell acute lymphoblastic leukemia (T-ALL), mortality remains relatively high, mainly due to primary or acquired resistance to chemotherapy. Further improvements in survival demand better understanding of T-ALL biology and development of new therapeutic strategies. The Notch pathway has been involved in the pathogenesis of this disease and various therapeutic strategies are currently under development, including selective targeting of NOTCH receptors by inhibitory antibodies. We previously demonstrated that the NOTCH1-specific neutralizing antibody OMP52M51 prolongs survival in TALL patient-derived xenografts bearing

Indexed as

Precursor T-Cell Lymphoblastic Leukemia-LymphomaAnimalsHumansMice, Inbred NODMice, SCIDReceptor, Notch1Signal TransductionT-LymphocytesXenograft Model Antitumor AssaysNOTCH1 protein, humanReceptor, Notch1

Identifiers

PMID31467126
PMCPMC7193477
OpenAlexW2971058467

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.