Evidence map›Paper›PMID 27477490›Full record

ReviewNature reviews. Nephrology2016

Roles of mTOR complexes in the kidney: implications for renal disease and transplantation.

Daniel Fantus, Natasha M Rogers, Florian Grahammer, Tobias B Huber, Angus W Thomson

Open access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Nephrology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 116 papers.

0numbers the graph read from it
0cells of the map it votes in
116citing papers in PubMed
13.1field-weighted citation impact, top 1% 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

116 citing papers in PubMed, 197 citations in OpenAlex.

  1. Trial
  2. Mechanistic target of rapamycin complex-1 plays a role in inhibiting kidney KAmerican journal of physiology. Renal physiology · 2026
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56 more citing papers are in PubMed but not listed here.

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

5 authors at 3 institutions in 2 countries.

Daniel FantusStarzl Transplantation Institute, Department of Surgery, University of Pittsburgh School of Medicine, 200 Lothrop Street, W1540 BST, Pittsburgh, Pennsylvania 15261, USA.
Natasha M RogersStarzl Transplantation Institute, Department of Surgery, University of Pittsburgh School of Medicine, 200 Lothrop Street, W1540 BST, Pittsburgh, Pennsylvania 15261, USA.
Florian GrahammerDepartment of Medicine IV, Medical Center-Faculty of Medicine, University of Freiburg, Hugstetter Strasse 55, Freiburg 79106, Germany.
Tobias B HuberDepartment of Medicine IV, Medical Center-Faculty of Medicine, University of Freiburg, Hugstetter Strasse 55, Freiburg 79106, Germany.
Angus W ThomsonStarzl Transplantation Institute, Department of Surgery, University of Pittsburgh School of Medicine, 200 Lothrop Street, W1540 BST, Pittsburgh, Pennsylvania 15261, USA.
University of Pittsburgh · USUniversity Medical Center Freiburg · DEUniversity of Freiburg · DE

Funding

Tomotherapy and Hematopoietic Stem Cells For Tolerance to Kidney TransplantsU01AI102456 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI KAUFMAN, DIXON B · 2012 to 2022
$19.2M
Alemtuzumab and Regulatory T Cells for Heart Transplant Tolerance in MonkeysU01AI091197 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI THOMSON, ANGUS W · 2010 to 2016
$4.3M
Regulation of Liver DC Function and Transplant ToleranceR56AI118777 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI THOMSON, ANGUS W · 2015 to 2015
$381k
NIAID NIH HHS R56 AI118777NIAID NIH HHS U01 AI091197NIAID NIH HHS U01 AI102456
6 · The paper itself

Abstract

The mTOR pathway has a central role in the regulation of cell metabolism, growth and proliferation. Studies involving selective gene targeting of mTOR complexes (mTORC1 and mTORC2) in renal cell populations and/or pharmacologic mTOR inhibition have revealed important roles of mTOR in podocyte homeostasis and tubular transport. Important advances have also been made in understanding the role of mTOR in renal injury, polycystic kidney disease and glomerular diseases, including diabetic nephropathy. Novel insights into the roles of mTORC1 and mTORC2 in the regulation of immune cell homeostasis and function are helping to improve understanding of the complex effects of mTOR targeting on immune responses, including those that impact both de novo renal disease and renal allograft outcomes. Extensive experience in clinical renal transplantation has resulted in successful conversion of patients from calcineurin inhibitors to mTOR inhibitors at various times post-transplantation, with excellent long-term graft function. Widespread use of this practice has, however, been limited owing to mTOR-inhibitor- related toxicities. Unique attributes of mTOR inhibitors include reduced rates of squamous cell carcinoma and cytomegalovirus infection compared to other regimens. As understanding of the mechanisms by which mTORC1 and mTORC2 drive the pathogenesis of renal disease progresses, clinical studies of mTOR pathway targeting will enable testing of evolving hypotheses.

Indexed as

AnimalsEndothelial CellsEpithelial CellsFibrosisGraft RejectionHumansIschemiaKidneyKidney DiseasesKidney GlomerulusKidney TransplantationKidney TubulesMechanistic Target of Rapamycin Complex 1Mechanistic Target of Rapamycin Complex 2Multiprotein ComplexesPodocytesMechanistic Target of Rapamycin Complex 1Mechanistic Target of Rapamycin Complex 2Multiprotein ComplexesTOR Serine-Threonine Kinases

Identifiers

PMID27477490
PMCPMC6553645
OpenAlexW2497334009

What Socratic 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 Socratic graph.