Evidence map›Paper›PMID 31085701›Full record

ArticleCancer research2019

Disruption of the Scaffolding Function of mLST8 Selectively Inhibits mTORC2 Assembly and Function and Suppresses mTORC2-Dependent Tumor Growth

Yoonha Hwang, Laura C Kim, Wenqiang Song, Deanna N Edwards, Rebecca S Cook, Jin Chen

Open access · greenAbstract read
In one paragraph

Article in Cancer research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

25 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. UsingCells · 2023
    Review
  13. Article
  14. mTOR: A Potential New Target in Nonalcoholic Fatty Liver Disease.International journal of molecular sciences · 2022
    Review
  15. Review
  16. Review
  17. Article
  18. New mechanistic insights into the RAS-SIN1 interaction at the membrane.Frontiers in cell and developmental biology · 2022
    Article
  19. Article
  20. Review
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

6 authors at 2 institutions in 1 country.

Yoonha Hwang *Veterans Affairs Medical Center, Tennessee Valley Healthcare System, Nashville, Tennessee.ORCID 0000-0001-7420-4477
Laura C Kim *Program in Cancer Biology, Vanderbilt University, Nashville, Tennessee.
Wenqiang SongVeterans Affairs Medical Center, Tennessee Valley Healthcare System, Nashville, Tennessee.
Deanna N EdwardsVeterans Affairs Medical Center, Tennessee Valley Healthcare System, Nashville, Tennessee.ORCID 0000-0001-5481-5879
Rebecca S CookProgram in Cancer Biology, Vanderbilt University, Nashville, Tennessee.
Jin ChenVeterans Affairs Medical Center, Tennessee Valley Healthcare System, Nashville, Tennessee. jin.chen@vanderbilt.edu.ORCID 0000-0002-5557-2079
Vanderbilt University · USVA Tennessee Valley Healthcare System · US

Funding

MULTIDISCIPLINARY BASIC RESEARCH TRAINING IN CANCERT32CA009592 · NCI · VANDERBILT UNIVERSITY · PI Justin M Balko, Julie A Rhoades (Sterling) · 1987 to 2026
$10.4M
Ephrin-A1 in Tumor-Endothelial Interaction During MetastasisR01CA095004 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI CHEN, JIN · 2003 to 2019
$4.6M
ephrin-A1 in lipogenesis and breast cancer metastatic progressionR01CA177681 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BRANTLEY-SIEDERS, DANA M, CHEN, JIN · 2014 to 2019
$1.9M
EphA2 Receptor Tyrosine Kinase in Malignant Tumor CellR01CA114301 · NCI · VANDERBILT UNIVERSITY · PI CHEN, JIN · 2005 to 2009
$1.5M
Targeting mLST8 in mTORC2-dependent lung cancerF31CA220804 · NCI · VANDERBILT UNIVERSITY · PI KIM, LAURA C · 2017 to 2019
$88k
Targeting mTORC2 in lung squamous cancerI01BX000134 · VA · VETERANS HEALTH ADMINISTRATION · PI Jin Chen · 2009 to 2026
–
BLRD VA I01 BX000134NCI NIH HHS F31 CA220804NCI NIH HHS R01 CA095004NCI NIH HHS R01 CA114301NCI NIH HHS R01 CA177681NCI NIH HHS T32 CA009592
6 · The paper itself

Abstract

mTOR is a serine/threonine kinase that acts in two distinct complexes, mTORC1 and mTORC2, and is dysregulated in many diseases including cancer. mLST8 is a shared component of both mTORC1 and mTORC2, yet little is known regarding how mLST8 contributes to assembly and activity of the mTOR complexes. Here we assessed mLST8 loss in a panel of normal and cancer cells and observed little to no impact on assembly or activity of mTORC1. However, mLST8 loss blocked mTOR association with mTORC2 cofactors RICTOR and SIN1, thus abrogating mTORC2 activity. Similarly, a single pair of mutations on mLST8 with a corresponding mutation on mTOR interfered with mTORC2 assembly and activity without affecting mTORC1. We also discovered a direct interaction between mLST8 and the NH

Indexed as

AnimalsApoptosisBiomarkers, TumorCell ProliferationGene Expression Regulation, NeoplasticHumansMaleMechanistic Target of Rapamycin Complex 1Mechanistic Target of Rapamycin Complex 2MiceMice, NudemTOR Associated Protein, LST8 HomologPhosphorylationProstatic NeoplasmsProto-Oncogene Proteins c-aktSignal TransductionBiomarkers, TumorMechanistic Target of Rapamycin Complex 1Mechanistic Target of Rapamycin Complex 2MLST8 protein, humanmTOR Associated Protein, LST8 HomologProto-Oncogene Proteins c-akt

Identifiers

PMID31085701
PMCPMC6606357
OpenAlexW2945448086

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.