Evidence map›Paper›PMID 28583723›Full record

ReviewCytokine & growth factor reviews2017

Control of B lymphocyte development and functions by the mTOR signaling pathways.

Terri N Iwata, Julita A Ramírez-Komo, Heon Park, Brian M Iritani

Abstract readReview
In one paragraph

Review in Cytokine & growth factor reviews, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

44 citing papers in PubMed, 66 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

4 authors at 1 institution in 1 country.

Terri N IwataThe Department of Comparative Medicine, University of Washington, Seattle, WA 98195, USA.
Julita A Ramírez-KomoThe Department of Comparative Medicine, University of Washington, Seattle, WA 98195, USA.
Heon ParkThe Department of Comparative Medicine, University of Washington, Seattle, WA 98195, USA.
Brian M IritaniThe Department of Comparative Medicine, University of Washington, Seattle, WA 98195, USA. Electronic address: biritani@uw.edu.
University of Washington · US

Funding

Targeting Fnip1 to disrupt B cell development, metabolism, and transformationR01AI114556 · NIAID · UNIVERSITY OF WASHINGTON · PI IRITANI, BRIAN M · 2015 to 2019
$2.0M
Laboratory Animal Medicine and Translational Research Training for VeterinariansR25OD010450 · OD · UNIVERSITY OF WASHINGTON · PI BRABB, THEA, IRITANI, BRIAN M · 2012 to 2015
$634k
mTOR signaling in B cell development, function, and metabolismK01OD021421 · OD · UNIVERSITY OF WASHINGTON · PI IWATA, TERRI · 2016 to 2019
$484k
Folliculin Interacting Proteins in Lymphocyte Development and AutoimmunityR21AI109020 · NIAID · UNIVERSITY OF WASHINGTON · PI IRITANI, BRIAN M · 2014 to 2015
$425k
Loss of EBF1 Expression: A Novel Murine Model for Human B-ALLK01OD010554 · OD · UNIVERSITY OF WASHINGTON · PI RAMIREZ, JULITA A · 2012 to 2016
$400k
Fnip1 Function in Lymphocyte Development, Activation and MetabolismR56AI092093 · NIAID · UNIVERSITY OF WASHINGTON · PI IRITANI, BRIAN M · 2013 to 2013
$353k
NIAID NIH HHS R01 AI114556NIAID NIH HHS R21 AI109020NIAID NIH HHS R56 AI092093NIH HHS K01 OD010554NIH HHS K01 OD021421NIH HHS R25 OD010450
6 · The paper itself

Abstract

Mechanistic target of rapamycin (mTOR) is a serine/threonine kinase originally discovered as the molecular target of the immunosuppressant rapamycin. mTOR forms two compositionally and functionally distinct complexes, mTORC1 and mTORC2, which are crucial for coordinating nutrient, energy, oxygen, and growth factor availability with cellular growth, proliferation, and survival. Recent studies have identified critical, non-redundant roles for mTORC1 and mTORC2 in controlling B cell development, differentiation, and functions, and have highlighted emerging roles of the Folliculin-Fnip protein complex in regulating mTOR and B cell development. In this review, we summarize the basic mechanisms of mTOR signaling; describe what is known about the roles of mTORC1, mTORC2, and the Folliculin/Fnip1 pathway in B cell development and functions; and briefly outline current clinical approaches for targeting mTOR in B cell neoplasms. We conclude by highlighting a few salient questions and future perspectives regarding mTOR in B lineage cells.

Indexed as

Signal TransductionAnimalsB-LymphocytesCarrier ProteinsCell ProliferationEstroneHumansMechanistic Target of Rapamycin Complex 1Mechanistic Target of Rapamycin Complex 2MicePhosphorylationTOR Serine-Threonine KinasesCarrier ProteinsEstroneFNIP1 protein, mouseMechanistic Target of Rapamycin Complex 1Mechanistic Target of Rapamycin Complex 2TOR Serine-Threonine KinasesB lymphocyte developmentFnip1FolliculinmTOR

Identifiers

PMID28583723
PMCPMC5559228
OpenAlexW2618398235

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.