Evidence map›Paper›PMID 25906254›Full record

ArticlePloS one2015

mLST8 Promotes mTOR-Mediated Tumor Progression.

Kyoko Kakumoto, Jun-Ichiro Ikeda, Masato Okada, Eiichi Morii, Chitose Oneyama

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

32 citing papers in PubMed, 62 citations in OpenAlex.

  1. Gene model for the ortholog ofbioRxiv : the preprint server for biology · 2026
    Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. 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

5 authors at 1 institution in 1 country.

Kyoko KakumotoDepartment of Oncogene Research, Research Institute for Microbial Disease, Osaka, University, Suita, Osaka, Japan.
Jun-Ichiro IkedaDepartment of Pathology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Masato OkadaDepartment of Oncogene Research, Research Institute for Microbial Disease, Osaka, University, Suita, Osaka, Japan.
Eiichi MoriiDepartment of Pathology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Chitose OneyamaDepartment of Oncogene Research, Research Institute for Microbial Disease, Osaka, University, Suita, Osaka, Japan.
Osaka University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The activity of the mechanistic target of rapamycin (mTOR) is elevated in various types of human cancers, implicating a role in tumor progression. However, the molecular mechanisms underlying mTOR upregulation remain unclear. In this study, we found that the expression of mLST8, a required subunit of both mTOR complex 1 (mTORC1) and complex 2 (mTORC2), was upregulated in several human colon and prostate cancer cell lines and tissues. Knockdown of mLST8 significantly suppressed mTORC1 and mTORC2 complex formation, and it also inhibited tumor growth and invasiveness in human colon carcinoma (HCT116) and prostate cancer (LNCaP) cells. Overexpression of mLST8 induced anchorage-independent cell growth in normal epithelial cells (HaCaT), although mLST8 knockdown had no effect on normal cell growth. mLST8 knockdown reduced mTORC2-mediated phosphorylation of AKT in both cancer and normal cells, whereas it potently inhibited mTORC1-mediated phosphorylation of 4E-BP1 specifically in cancer cells. These results suggest that mLST8 plays distinct roles in normal and cancer cells, depending upon its expression level, and that mLST8 upregulation may contribute to tumor progression by constitutively activating both the mTORC1 and mTORC2 pathways.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsCarcinomaCell Cycle ProteinsCell LineCell Line, TumorCell ProliferationColonic NeoplasmsDisease ProgressionEpithelial CellsHCT116 CellsHT29 CellsHumansMaleMechanistic Target of Rapamycin Complex 1Mechanistic Target of Rapamycin Complex 2Adaptor Proteins, Signal TransducingCell Cycle ProteinsEIF4EBP1 protein, humanMechanistic Target of Rapamycin Complex 1Mechanistic Target of Rapamycin Complex 2MLST8 protein, humanmTOR Associated Protein, LST8 HomologMultiprotein ComplexesPhosphoproteinsProto-Oncogene Proteins c-aktTOR Serine-Threonine Kinases

Identifiers

PMID25906254
PMCPMC4408021
OpenAlexW1993517337

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.