Evidence map›Paper›PMID 27923030›Full record

ArticleNature medicine2016

Patient-derived induced pluripotent stem cells in cancer research and precision oncology.

Eirini P Papapetrou

Erratum issued Registry-linked trialAbstract read
In one paragraph

Article in Nature medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT03894852 (SRSF2 Gene Mutation in Patients With Therapy Related Myelodysplastic Syndromes / Acute Myeloid Leukemia), which is not on this map. Cited by 102 papers.

0numbers the graph read from it
0cells of the map it votes in
102citing papers in PubMed
–field-weighted citation impact
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.

NCT03894852 completednot on this mapstarted 2019, after this paper: background citation

SRSF2 Gene Mutation in Patients With Therapy Related Myelodysplastic Syndromes / Acute Myeloid Leukemia

TypeobservationalSponsorZeinab Albadry Mohammed ZahranRan2019 to 2020Enrolled139ConditionsTherapy Related Myelodysplastic Syndrome and Therapy Related Acute Myeloid LeukemiaArmsPCR and cytogenetics
3 · Its place in the literature

Who cites it

102 citing papers in PubMed.

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42 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

1 author.

Eirini P PapapetrouDepartment of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, New York, USA.ORCID 0000-0001-7002-417X

Funding

Modeling chromosome 7 loss in Myelodysplasia-iPSCsR01HL121570 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI PAPAPETROU, EIRINI · 2014 to 2018
$2.1M
Genetic correction of human beta-thalassemic induced pluripotent stem cellsR00DK087923 · NIDDK · UNIVERSITY OF WASHINGTON · PI PAPAPETROU, EIRINI · 2013 to 2015
$760k
NHLBI NIH HHS R01 HL121570NIDDK NIH HHS R00 DK087923
6 · The paper itself

Abstract

Together with recent advances in the processing and culture of human tissue, bioengineering, xenotransplantation and genome editing, Induced pluripotent stem cells (iPSCs) present a range of new opportunities for the study of human cancer. Here we discuss the main advantages and limitations of iPSC modeling, and how the method intersects with other patient-derived models of cancer, such as organoids, organs-on-chips and patient-derived xenografts (PDXs). We highlight the opportunities that iPSC models can provide beyond those offered by existing systems and animal models and present current challenges and crucial areas for future improvements toward wider adoption of this technology.

Indexed as

Induced Pluripotent Stem CellsNeoplasmsNeoplastic Stem CellsPrecision MedicineTranslational Research, BiomedicalAnimalsBiomedical ResearchCell DifferentiationCellular ReprogrammingDrug Resistance, NeoplasmHumansMedical OncologyNeoplasm TransplantationOrganoidsTransplantation, Heterologous

Identifiers

PMID27923030
PMCPMC5233709

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Registered trials

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.