Cited by 8Cellular transport and secretionAutophagy in Disease and TherapyPI3K/AKT/mTOR signaling in cancer

Folliculin – A tumor suppressor at the intersection of metabolic signaling and membrane traffic

Open access
Dodding, Mark P.·2017·Small GTPases

Abstract

The Birt-Hoge-Dubé syndrome tumor suppressor Folliculin is a regulator of metabolism and has as a wide range of cellular and organismal phenotypes associated with its disruption. However, the molecular mechanisms which underlie its functions are poorly understood. Folliculin has been described to associate with lysosomes in response to nutrient depletion and form a key part of the signaling network that controls the activity of mTORC1. We recently reported that Folliculin can control the nutrient dependent cytoplasmic distribution of lysosomes by promoting the formation of a complex with the Golgi-associated small GTPase Rab34 and its effector RILP. We thus define a mechanistic connection between the lysosomal nutrient signaling network and the transport machinery that controls the distribution and dynamics of this organelle. Here we summarise the main conclusions from that study, attempt to integrate our findings with other recent studies on lysosome distribution/dynamics, and discuss the potential consequences of the dysregulation of this processes caused by Folliculin loss for Birt-Hoge-Dubé syndrome and normal cell function.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1080/21541248.2016.1204808

Cites

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • A growing body of work supports an intrinsic role of FLCN and its associated interacting proteins in regulating lysosome positioning in response to cellular metabolism.

    “It is intriguing to note that a growing body of work also supports the intrinsic role of FLCN and its associated interacting proteins in regulating lysosome positioning in response to cellular metabolism (Starling et al., 2016; Dodding, 2017).”

    From Signal integration in the (m)TORC1 growth pathway (2018) · cites this paper as Dodding, 2017

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

The citation lists haven’t been fetched yet

References 50 · Cited by 8

Authors
Dodding, M. P.
Affiliations
King's College London (GB)
Corresponding author
Dodding, Mark P.
Venue
Small GTPases
Published
2016-06-29
Volume
8
Issue
2
Pages
100-105
ISSN
  • 2154-1248 (ISSN-L)
  • 2154-1256
OpenAlex
W2460743054
Cited by
8
References
50
Citations by year
2024: 1 · 2023: 1 · 2021: 2 · 2020: 2 · 2019: 1 · 2018: 1
Type
journal article
Language
en
Open access
Locations
  • Small GTPases (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • Explore Bristol Research (acceptedVersion, other-oa)
  • Bristol Research (University of Bristol) (submittedVersion, other-oa)
  • Research Portal (King's College London) (submittedVersion)
Funders
  • Wellcome Trust (097316/Z/11/Z, /Z/11/Z, 097316)
  • Directorate for Biological Sciences
  • Biotechnology and Biological Sciences Research Council (BB/L006774/1)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
  • Health Sciences › Medicine › Epidemiology › Autophagy in Disease and Therapy
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › PI3K/AKT/mTOR signaling in cancer
Keywords
folliculin, Birt-Hogg-Dubé syndrome, tumor suppressor, Rab34, RILP, mTORC1 signaling, nutrient signaling, membrane trafficking, metabolic signaling
MeSH terms
Cell Membrane, Humans, Lysosomes, Signal Transduction, Protein Transport, Tumor Suppressor Proteins

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review