Evidence map›Paper›PMID 36014530›Full record

ReviewMolecules (Basel, Switzerland)2022

Overview of Research into mTOR Inhibitors.

Beibei Mao, Qi Zhang, Li Ma, Dong-Sheng Zhao, Pan Zhao, Peizheng Yan

Open access · goldAbstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
12.2field-weighted citation impact, top 1% 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

75 citing papers in PubMed, 147 citations in OpenAlex.

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15 more citing papers are in PubMed but not listed here.

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.

Beibei MaoCollege of Pharmacy, Shandong University of Traditional Chinese Medicine, Jinan 250355, China.
Qi ZhangCollege of Pharmacy, Shandong University of Traditional Chinese Medicine, Jinan 250355, China.
Li MaShandong Provincial Key Laboratory of Molecular Engineering, State Key Laboratory of Biobased Material and Green Papermaking, School of Chemistry and Chemical Engineering, Qilu University of Technology (Shandong Academy of Sciences), Jinan 250353, China.ORCID 0000-0003-3458-7754
Dong-Sheng ZhaoCollege of Pharmacy, Shandong University of Traditional Chinese Medicine, Jinan 250355, China.ORCID 0000-0003-3265-5442
Pan ZhaoCollege of Pharmacy, Shandong University of Traditional Chinese Medicine, Jinan 250355, China.
Peizheng YanCollege of Pharmacy, Shandong University of Traditional Chinese Medicine, Jinan 250355, China.ORCID 0000-0002-1955-4412
Shandong University of Traditional Chinese Medicine · CNQilu University of Technology · CN

Funding

National Natural Science Foundation of China 81903780National Natural Science Foundation of China 82004233Shandong Provincial Natural Science Foundation ZR2019BB031Shandong Provincial Natural Science Foundation ZR2020QB114
6 · The paper itself

Abstract

The mammalian target of rapamycin (mTOR) is a serine/threonine kinase that belongs to the phosphoinositide 3-kinase (PI3K)-related kinase (PIKK) family. The kinase exists in the forms of two complexes, mTORC1 and mTORC2, and it participates in cell growth, proliferation, metabolism, and survival. The kinase activity is closely related to the occurrence and development of multiple human diseases. Inhibitors of mTOR block critical pathways to produce antiviral, anti-inflammatory, antiproliferative and other effects, and they have been applied to research in cancer, inflammation, central nervous system diseases and viral infections. Existing mTOR inhibitors are commonly divided into mTOR allosteric inhibitors, ATP-competitive inhibitors and dual binding site inhibitors, according to their sites of action. In addition, there exist several dual-target mTOR inhibitors that target PI3K, histone deacetylases (HDAC) or ataxia telangiectasia mutated and Rad-3 related (ATR) kinases. This review focuses on the structure of mTOR protein and related signaling pathways as well as the structure and characteristics of various mTOR inhibitors. Non-rapalog allosteric inhibitors will open new directions for the development of new therapeutics specifically targeting mTORC1. The applications of ATP-competitive inhibitors in central nervous system diseases, viral infections and inflammation have laid the foundation for expanding the indications of mTOR inhibitors. Both dual-binding site inhibitors and dual-target inhibitors are beneficial in overcoming mTOR inhibitor resistance.

Indexed as

MTOR InhibitorsPhosphatidylinositol 3-KinasesAdenosine TriphosphateHumansInflammationMechanistic Target of Rapamycin Complex 1Protein Kinase InhibitorsProto-Oncogene Proteins c-aktSirolimusTOR Serine-Threonine KinasesAdenosine TriphosphateMechanistic Target of Rapamycin Complex 1MTOR InhibitorsMTOR protein, humanPhosphatidylinositol 3-KinasesProtein Kinase InhibitorsProto-Oncogene Proteins c-aktSirolimusTOR Serine-Threonine Kinasesdual inhibitorshuman diseasesmTORmTOR inhibitors

Identifiers

PMID36014530
PMCPMC9413691
OpenAlexW4292566549

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.