Evidence map›Paper›PMID 32016810›Full record

ReviewPathology oncology research : POR2020

mTOR in Lung Neoplasms.

Ildiko Krencz, Anna Sebestyen, Andras Khoor

Abstract readReview
PubMed Publisher
In one paragraph

Review in Pathology oncology research : POR, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

19 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Pathology oncology research : POR · 2024
    Article
  8. mTOR hyperactivity andPathology oncology research : POR · 2024
    Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. The Importance ofDiagnostics (Basel, Switzerland) · 2021
    Review
  19. 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

3 authors at 2 institutions in 2 countries.

Ildiko Krencz1st Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.
Anna Sebestyen1st Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.
Andras KhoorDepartment of Laboratory Medicine and Pathology, Mayo Clinic, 4500 San Pablo Road, Jacksonville, FL, 32224, USA. Khoor.Andras@mayo.edu.
Semmelweis University · HUMayo Clinic in Florida · US

Funding

Nemzeti Kutatási, Fejlesztési és Innovaciós Alap ED_17-1-2017-0009Nemzeti Kutatási Fejlesztési és Innovációs Hivatal NKFI-FK-128404Nemzeti Kutatási Fejlesztési és Innovációs Hivatal NVKP_16-1-2016-0004
6 · The paper itself

Abstract

With the discovery of rapamycin 45 years ago, studies in the mechanistic target of rapamycin (mTOR) field started 2 decades before the identification of the mTOR kinase. Over the years, studies revealed that the mTOR signaling is a master regulator of homeostasis and integrates a variety of environmental signals to regulate cell growth, proliferation, and metabolism. Deregulation of mTOR signaling, particularly hyperactivation, frequently occurs in human tumors. Recent advances in molecular profiling have identified mutations or amplification of certain genes coding proteins involved in the mTOR pathway (eg, PIK3CA, PTEN, STK11, and RICTOR) as the most common reasons contributing to mTOR hyperactivation. These genetic alterations of the mTOR pathway are frequently observed in lung neoplasms and may serve as a target for personalized therapy. mTOR inhibitor monotherapy has met limited clinical success so far; however, rational drug combinations are promising to improve efficacy and overcome acquired resistance. A better understanding of mTOR signaling may have the potential to help translation of mTOR pathway inhibitors into the clinical setting.

Indexed as

Antineoplastic AgentsBiomarkers, TumorHumansLung NeoplasmsMechanistic Target of Rapamycin Complex 1Mechanistic Target of Rapamycin Complex 2Protein Kinase InhibitorsSignal TransductionTOR Serine-Threonine KinasesAntineoplastic AgentsBiomarkers, TumorMechanistic Target of Rapamycin Complex 1Mechanistic Target of Rapamycin Complex 2MTOR protein, humanProtein Kinase InhibitorsTOR Serine-Threonine KinasesLung neoplasmsmTORC1mTORC2mTOR inhibitorsmTOR signaling

Identifiers

PMID32016810
OpenAlexW3005216907

What OpenQuestion holds

Textmetadata
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.