Evidence map›Paper›PMID 32238950›Full record

ArticleNature protocols2020

Cloning of ground-state intestinal stem cells from endoscopic biopsy samples.

Marcin Duleba, Yusuke Yamamoto, Rahul Neupane, Wei Rao, Jingzhong Xie, Yutao Qi, Audrey-Ann Liew, Suchan Niroula, Yanting Zhang, Rajasekaran Mahalingam and 11 more

Abstract readEvaluation Study
PubMed Publisher
In one paragraph

Article in Nature protocols, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 20% 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

6 citing papers in PubMed, 12 citations in OpenAlex.

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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

21 authors at 8 institutions in 2 countries.

Marcin Duleba *Stem Cell Center, Department of Biology and Biochemistry, University of Houston, Houston, Texas, USA.
Yusuke Yamamoto *Division of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.
Rahul NeupaneStem Cell Center, Department of Biology and Biochemistry, University of Houston, Houston, Texas, USA.
Wei RaoStem Cell Center, Department of Biology and Biochemistry, University of Houston, Houston, Texas, USA.
Jingzhong XieStem Cell Center, Department of Biology and Biochemistry, University of Houston, Houston, Texas, USA.ORCID http://orcid.org/0000-0002-5838-9632
Yutao QiStem Cell Center, Department of Biology and Biochemistry, University of Houston, Houston, Texas, USA.
Audrey-Ann LiewStem Cell Center, Department of Biology and Biochemistry, University of Houston, Houston, Texas, USA.
Suchan NiroulaStem Cell Center, Department of Biology and Biochemistry, University of Houston, Houston, Texas, USA.
Yanting ZhangStem Cell Center, Department of Biology and Biochemistry, University of Houston, Houston, Texas, USA.
Rajasekaran MahalingamStem Cell Center, Department of Biology and Biochemistry, University of Houston, Houston, Texas, USA.
Shan WangStem Cell Center, Department of Biology and Biochemistry, University of Houston, Houston, Texas, USA.
Kristina GollerStem Cell Center, Department of Biology and Biochemistry, University of Houston, Houston, Texas, USA.
Jaffer A AjaniDepartment of Gastrointestinal Medical Oncology, Division of Cancer Medicine, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Matthew VincentTract Pharmaceuticals, Inc., Marlborough, Massachusetts, USA.
Khek Yu HoDepartments of Medicine and Pathology, National University of Singapore, Singapore, Singapore.
Jason K HouDivision of Gastroenterology, Baylor College of Medicine, Houston, Texas, USA.
Jeffrey S HyamsDivision of Digestive Diseases, Hepatology, and Nutrition, Connecticut Children's Medical Center, Hartford, Connecticut, USA.
Francisco A SylvesterDivision of Gastroenterology, Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Christopher P CrumDepartment of Pathology, Harvard Medical School and Brigham and Women's Hospital, Boston, Massachusetts, USA.
Frank McKeonStem Cell Center, Department of Biology and Biochemistry, University of Houston, Houston, Texas, USA. fdmckeon@uh.edu.ORCID http://orcid.org/0000-0002-7747-9983
Wa XianStem Cell Center, Department of Biology and Biochemistry, University of Houston, Houston, Texas, USA. wxian@uh.edu.ORCID http://orcid.org/0000-0001-6315-8858
University of Houston · USBaylor College of Medicine · USBrigham and Women's Hospital · USConnecticut Children's Medical Center · USNational University of Singapore · SGPhio Pharmaceuticals (United States) · USThe University of Texas MD Anderson Cancer Center · USUniversity of North Carolina at Chapel Hill · US

Funding

Predicting Response to Standardized Pediatric Colitis Therapy: PROTECT StudyU01DK095745 · NIDDK · CONNECTICUT CHILDREN'S MEDICAL CENTER · PI DENSON, LEE ARMISTEAD, HYAMS, JEFFREY SAMUEL · 2012 to 2016
$10.4M
Pathogenic Heterogeneity in Mucosal Stem Cells in Pediatric Crohn's DiseaseR01DK115445 · NIDDK · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI XIAN, WA · 2018 to 2021
$2.6M
Clonal Reconstruction and Targeting of the Correa SequenceR01CA241600 · NCI · UNIVERSITY OF HOUSTON · PI MCKEON, FRANK D. · 2019 to 2023
$2.3M
Patient-Matched Stem Cells of the Barrett's-Dysplasia-Adenocarcinoma SequenceU24CA228550 · NCI · UNIVERSITY OF HOUSTON · PI MCKEON, FRANK D. · 2017 to 2022
$1.0M
NCI NIH HHS R01 CA241600NCI NIH HHS U24 CA228550NIDDK NIH HHS R01 DK115445NIDDK NIH HHS U01 DK095745
6 · The paper itself

Abstract

'Adult' or 'somatic' stem cells harbor an intrinsic ability to regenerate tissues. Heterogeneity of such stem cells along the gastrointestinal tract yields the known segmental specificity of this organ and may contribute to the pathology of certain enteric conditions. Here we detail technology for the generation of 'libraries' of clonogenic cells from 1-mm-diamter endoscopic biopsy samples from the human gastrointestinal tract. Each of the 150-300 independent clones in a typical stem cell library can be clonally expanded to billions of cells in a few weeks while maintaining genomic stability and the ability to undergo multipotent differentiation to the specific epithelia from which the sample originated. The key to this methodology is the intrinsic immortality of normal intestinal stem cells (ISCs) and culture systems that maintain them as highly immature, ground-state ISCs marked by a single-cell clonogenicity of 70% and a corresponding 250-fold proliferative advantage over spheroid technologies. Clonal approaches such as this enhance the resolution of molecular genetics, make genome editing easier, and may be useful in regenerative medicine, unravelling heterogeneity in disease, and facilitating drug discovery.

Indexed as

Cell Culture Techniques3T3 CellsAdult Stem CellsAnimalsBiopsyEndoscopy, GastrointestinalHumansIntestinal MucosaMice

Identifiers

PMID32238950
OpenAlexW3014523009

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.