Evidence map›Paper›PMID 32386594›Full record

ArticleCell chemical biology2020

Blockade of Oncogenic NOTCH1 with the SERCA Inhibitor CAD204520 in T Cell Acute Lymphoblastic Leukemia.

Matteo Marchesini, Andrea Gherli, Anna Montanaro, Laura Patrizi, Claudia Sorrentino, Luca Pagliaro, Chiara Rompietti, Samuel Kitara, Sabine Heit, Claus E Olesen and 18 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell chemical biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

31 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Notch Inhibitors and BH3 Mimetics in T-Cell Acute Lymphoblastic Leukemia.International journal of molecular sciences · 2024
    Review
  9. Article
  10. Review
  11. Acute lymphoblastic leukaemia.Nature reviews. Disease primers · 2024
    Review
  12. CAD204520 TargetsInternational journal of molecular sciences · 2024
    Article
  13. Article
  14. Uncovering NOTCH1 as a Promising Target in the Treatment ofInternational journal of molecular sciences · 2023
    Article
  15. Review
  16. Article
  17. Frontiers in oncology · 2023
    Article
  18. Article
  19. Article
  20. 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

28 authors at 6 institutions in 4 countries.

Matteo MarchesiniUniversity of Parma, Department of Medicine and Surgery, Parma 43126, Italy.
Andrea GherliUniversity of Parma, Department of Medicine and Surgery, Parma 43126, Italy.
Anna MontanaroUniversity of Parma, Department of Medicine and Surgery, Parma 43126, Italy.
Laura PatriziUniversity of Perugia, Department of Medicine, Hematology and Clinical Immunology, Perugia 06123, Italy.
Claudia SorrentinoUniversity of Parma, Department of Medicine and Surgery, Parma 43126, Italy.
Luca PagliaroUniversity of Parma, Department of Medicine and Surgery, Parma 43126, Italy.
Chiara RompiettiUniversity of Perugia, Department of Medicine, Hematology and Clinical Immunology, Perugia 06123, Italy.
Samuel KitaraDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02215, USA.
Sabine HeitUniversity of Oxford, Department of Biochemistry, Oxford OX1 3QU, UK.
Claus E OlesenAarhus University, Department of Biomedicine, 8000 Aarhus C, Denmark.
Jesper V MøllerAarhus University, Department of Biomedicine, 8000 Aarhus C, Denmark.
Monia SaviUniversity of Parma, Department of Chemistry, Life Sciences and Environmental Sustainability, Parma 43124, Italy.
Leonardo BocchiUniversity of Parma, Department of Chemistry, Life Sciences and Environmental Sustainability, Parma 43124, Italy.
Rocchina VilellaUniversity of Parma, Department of Chemistry, Life Sciences and Environmental Sustainability, Parma 43124, Italy.
Federica RizziUniversity of Parma, Department of Medicine and Surgery, Parma 43126, Italy; INBB - Biostructures and Biosystems National Institute, Rome 00136, Italy.
Marilena BaglioneUniversity of Parma, Department of Medicine and Surgery, Parma 43126, Italy.
Giorgia RastelliUniversity of Parma, Department of Medicine and Surgery, Parma 43126, Italy.
Caterina LoiaconoUniversity of Parma, Department of Medicine and Surgery, Parma 43126, Italy.
Roberta La StarzaUniversity of Perugia, Department of Medicine, Hematology and Clinical Immunology, Perugia 06123, Italy.
Cristina MecucciUniversity of Perugia, Department of Medicine, Hematology and Clinical Immunology, Perugia 06123, Italy.
Kimberly StegmaierDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02215, USA; The Broad Institute, Cambridge, MA 02142, USA.
Franco AversaUniversity of Parma, Department of Medicine and Surgery, Parma 43126, Italy.
Donatella StilliUniversity of Parma, Department of Chemistry, Life Sciences and Environmental Sustainability, Parma 43124, Italy.
Anne-Marie Lund WintherCado Biotechnology IvS, Copenhagen, Denmark.
Paolo SportolettiUniversity of Perugia, Department of Medicine, Hematology and Clinical Immunology, Perugia 06123, Italy.
Maike BublitzUniversity of Oxford, Department of Biochemistry, Oxford OX1 3QU, UK.
William Dalby-BrownCado Biotechnology IvS, Copenhagen, Denmark.
Giovanni RotiUniversity of Parma, Department of Medicine and Surgery, Parma 43126, Italy. Electronic address: giovanni.roti@unipr.it.
University of Parma · ITUniversity of Perugia · ITAarhus University · DKUniversity of Oxford · GBBroad Institute · USHarvard University · US

Funding

Integrating Transforming Approaches to Identify and Target New Vulnerabilities in CancerR35CA210030 · NCI · DANA-FARBER CANCER INST · PI STEGMAIER, KIMBERLY · 2016 to 2022
$7.3M
NCI NIH HHS R35 CA210030
6 · The paper itself

Abstract

The identification of SERCA (sarco/endoplasmic reticulum calcium ATPase) as a target for modulating gain-of-function NOTCH1 mutations in Notch-dependent cancers has spurred the development of this compound class for cancer therapeutics. Despite the innate toxicity challenge associated with SERCA inhibition, we identified CAD204520, a small molecule with better drug-like properties and reduced off-target Ca

Indexed as

AnimalsAntineoplastic AgentsCell Line, TumorCell ProliferationDrug Screening Assays, AntitumorEnzyme InhibitorsFemaleHumansMaleMiceMice, Inbred BALB CMice, Inbred ICRMice, Inbred NODMice, SCIDMolecular StructureMutationAntineoplastic AgentsEnzyme InhibitorsNOTCH1 protein, humanReceptor, Notch1CAD204520crystal structuremantle cell lymphoma (MCL)NOTCH1NOTCH1 mutationPEST mutationP-type ATPases screeningSERCAT cell acute lymphoblastic leukemia (T-ALL)thapsigargin

Identifiers

PMID32386594
PMCPMC7305996
OpenAlexW3022320566

What OpenQuestion holds

Textmetadata
LicenceTDM
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.