Evidence map›Paper›PMID 31727629›Full record

ArticleCancer research2020

Prophylactic

Chang Li, Meredith M Course, Iain A McNeish, Charles W Drescher, Paul N Valdmanis, André Lieber

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Molecular therapy. Methods & clinical development · 2025
    Article
  2. Article
  3. Article
  4. Article
  5. Human gene therapy · 2022
    Article
  6. Safe and efficientMolecular therapy. Methods & clinical development · 2022
    Article
  7. Article
  8. Review
  9. Article
  10. In Vivo HSC Gene Therapy Using a Bi-modular HDAd5/35++ Vector Cures Sickle Cell Disease in a Mouse Model.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
    Article
  11. Article
  12. Article
  13. 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 4 institutions in 2 countries.

Chang LiDivision of Medical Genetics, Department of Medicine, University of Washington, Seattle, Washington.
Meredith M CourseDivision of Medical Genetics, Department of Medicine, University of Washington, Seattle, Washington.ORCID 0000-0002-6412-4438
Iain A McNeishImperial College, London, United Kingdom.ORCID 0000-0002-9387-7586
Charles W DrescherFred Hutchinson Cancer Research Center, Seattle, Washington.
Paul N ValdmanisDivision of Medical Genetics, Department of Medicine, University of Washington, Seattle, Washington.
André LieberDivision of Medical Genetics, Department of Medicine, University of Washington, Seattle, Washington. lieber00@uw.edu.
University of Washington Medical Center · USFred Hutch Cancer Center · USThe London College · GBUniversity of Washington · US

Funding

In Vivo Hematopoietic Stem Cell Gene Therapy of Beta-Thalassemia and Sickle Cell DiseaseR01HL130040 · NHLBI · UNIVERSITY OF WASHINGTON · PI LIEBER, ANDRE MICHAEL · 2016 to 2024
$4.3M
Approach for in vivo gene delivery into hematopoietic stem cells for hemophilia A therapyR01HL141781 · NHLBI · UNIVERSITY OF WASHINGTON · PI LIEBER, ANDRE MICHAEL · 2018 to 2021
$2.3M
Hematopoietic stem cell based gene therapy of breast cancerR21CA193077 · NCI · UNIVERSITY OF WASHINGTON · PI LIEBER, ANDRE MICHAEL · 2015 to 2016
$370k
NCI NIH HHS R21 CA193077NHLBI NIH HHS R01 HL130040NHLBI NIH HHS R01 HL141781
6 · The paper itself

Abstract

Population-wide testing for cancer-associated mutations has established that more than one-fifth of ovarian and breast carcinomas are associated with inherited risk. Salpingo-oophorectomy and/or mastectomy are currently the only effective options offered to women with high-risk germline mutations. Our goal here is to develop a long-lasting approach that provides immunoprophylaxis for mutation carriers. Our approach leverages the fact that at early stages, tumors recruit hematopoietic stem/progenitor cells (HSPC) from the bone marrow and differentiate them into tumor-supporting cells. We developed a technically simple technology to genetically modify HSPCs

Indexed as

Genetic TherapyHematopoietic Stem Cell TransplantationAnimalsApoptosisB7-H1 AntigenCell ProliferationCombined Modality TherapyFemaleHematopoietic Stem CellsHumansMammary Neoplasms, AnimalMiceMice, Inbred C57BLMice, TransgenicMicroRNAsOvarian NeoplasmsB7-H1 AntigenCd274 protein, mouseMicroRNAsMirn423 microRNA, mouse

Identifiers

PMID31727629
PMCPMC7002220
OpenAlexW2987917474

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.