Evidence map›Paper›PMID 26431183›Full record

ArticleCell stem cell2015

Circulating IGF-I and IGFBP3 Levels Control Human Colonic Stem Cell Function and Are Disrupted in Diabetic Enteropathy.

Francesca D'Addio, Stefano La Rosa, Anna Maestroni, Peter Jung, Elena Orsenigo, Moufida Ben Nasr, Sara Tezza, Roberto Bassi, Giovanna Finzi, Alessandro Marando and 13 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell stem cell, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 1 pooled it
6.7field-weighted citation impact, top 2% 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

47 citing papers in PubMed, 1 synthesis or guideline pooled it, 81 citations in OpenAlex.

  1. Pooled it
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  11. The role of IGF/IGF-1R signaling in the regulation of cancer stem cells.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors at 7 institutions in 4 countries.

Francesca D'Addio *Nephrology Division, Boston Children's Hospital, Harvard Medical School, Boston 02115, MA, USA.
Stefano La Rosa *Department of Pathology, Ospedale di Circolo, Varese 21100, Italy.
Anna MaestroniTransplant Medicine, IRCCS Ospedale San Raffaele, Milan 20132, Italy.
Peter JungInstitute for Research in Biomedicine (IRB Barcelona), Barcelona 08028, Spain.
Elena OrsenigoSurgery, Protein Microsequencing Facility, IRCCS Ospedale San Raffaele, Milan 20132, Italy.
Moufida Ben NasrNephrology Division, Boston Children's Hospital, Harvard Medical School, Boston 02115, MA, USA.
Sara TezzaNephrology Division, Boston Children's Hospital, Harvard Medical School, Boston 02115, MA, USA.
Roberto BassiNephrology Division, Boston Children's Hospital, Harvard Medical School, Boston 02115, MA, USA.
Giovanna FinziDepartment of Pathology, Ospedale di Circolo, Varese 21100, Italy.
Alessandro MarandoDepartment of Pathology, Ospedale di Circolo, Varese 21100, Italy.
Andrea VerganiNephrology Division, Boston Children's Hospital, Harvard Medical School, Boston 02115, MA, USA.
Roberto FregoGastroenterology, Protein Microsequencing Facility, IRCCS Ospedale San Raffaele, Milan 20132, Italy.
Luca AlbarelloPathology Unit, Protein Microsequencing Facility, IRCCS Ospedale San Raffaele, Milan 20132, Italy.
Annapaola AndolfoProMiFa, Protein Microsequencing Facility, IRCCS Ospedale San Raffaele, Milan 20132, Italy.
Roberta ManuguerraDepartment of Biomedical, Biotechnological and Translational Sciences, Unit of Pathology, University of Parma, Parma 43121, Italy.
Edi VialeGastroenterology, Protein Microsequencing Facility, IRCCS Ospedale San Raffaele, Milan 20132, Italy.
Carlo StaudacherSurgery, Protein Microsequencing Facility, IRCCS Ospedale San Raffaele, Milan 20132, Italy.
Domenico CorradiDepartment of Biomedical, Biotechnological and Translational Sciences, Unit of Pathology, University of Parma, Parma 43121, Italy.
Eduard BatlleInstitute for Research in Biomedicine (IRB Barcelona), Barcelona 08028, Spain.
David BreaultDivision of Endocrinology, Boston Children's Hospital, Harvard Medical School, Boston 02115, MA, USA.
Antonio SecchiTransplant Medicine, IRCCS Ospedale San Raffaele, Milan 20132, Italy.
Franco FolliDepartment of Medicine, Division of Diabetes, University of Texas Health Science Center at San Antonio, San Antonio 78229, Texas, USA.
Paolo FiorinaNephrology Division, Boston Children's Hospital, Harvard Medical School, Boston 02115, MA, USA.
Boston Children's Hospital · USIRCCS Ospedale San Raffaele · ITUniversity of Parma · ITInstitució Catalana de Recerca i Estudis Avançats · ESInstitute for Research in Biomedicine · ESThe University of Texas Health Science Center at San Antonio · USVita-Salute San Raffaele University · IT

Funding

STRUCTURE-FUNCTION RELATIONSHIPS IN THE ALIMENTARY TRACTP30DK034854 · NIDDK · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI WAYNE I LENCER · 1986 to 2026
$32.4M
Characterization of Telomerase Expressing Intestinal Stem CellsR01DK084056 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI BREAULT, DAVID T · 2010 to 2015
$2.2M
NIDDK NIH HHS P30 DK034854NIDDK NIH HHS P30DK034854NIDDK NIH HHS R01 DK084056NIDDK NIH HHS R01DK084056
6 · The paper itself

Abstract

The role of circulating factors in regulating colonic stem cells (CoSCs) and colonic epithelial homeostasis is unclear. Individuals with long-standing type 1 diabetes (T1D) frequently have intestinal symptoms, termed diabetic enteropathy (DE), though its etiology is unknown. Here, we report that T1D patients with DE exhibit abnormalities in their intestinal mucosa and CoSCs, which fail to generate in vitro mini-guts. Proteomic profiling of T1D+DE patient serum revealed altered levels of insulin-like growth factor 1 (IGF-I) and its binding protein 3 (IGFBP3). IGFBP3 prevented in vitro growth of patient-derived organoids via binding its receptor TMEM219, in an IGF-I-independent manner, and disrupted in vivo CoSC function in a preclinical DE model. Restoration of normoglycemia in patients with long-standing T1D via kidney-pancreas transplantation or in diabetic mice by treatment with an ecto-TMEM219 recombinant protein normalized circulating IGF-I/IGFBP3 levels and reestablished CoSC homeostasis. These findings demonstrate that peripheral IGF-I/IGFBP3 controls CoSCs and their dysfunction in DE.

Indexed as

AnimalsColonDiabetes ComplicationsDiabetes Mellitus, ExperimentalHumansInsulin-Like Growth Factor Binding Protein 3Insulin-Like Growth Factor IIntestinal MucosaMembrane ProteinsMiceProteomicsStem CellsIGF1 protein, humanIGFBP3 protein, humanInsulin-Like Growth Factor Binding Protein 3Insulin-Like Growth Factor IMembrane Proteinscolonic stem cellsdiabetic enteropathydiabetic nephropathyhyperglycemiaIGFBP3IGF-Ikidney transplantationpancreas transplantationtype 1 diabetestype 2 diabetesuremia

Identifiers

PMID26431183
PMCPMC4826279
OpenAlexW2158381262

What OpenQuestion holds

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Registered trials

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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.