Evidence map›Paper›PMID 35250965›Full record

ReviewFrontiers in immunology2021

mTOR-Mediated Regulation of Immune Responses in Cancer and Tumor Microenvironment.

Sahar Mafi, Behzad Mansoori, Shahram Taeb, Hossein Sadeghi, Reza Abbasi, William C Cho, Davoud Rostamzadeh

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 144 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
144citing papers in PubMed, 4 pooled it
15.7field-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

144 citing papers in PubMed, 4 syntheses or guidelines pooled it, 200 citations in OpenAlex.

  1. Pooled it
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  13. Autophagy in Melanoma: Molecular Mechanisms and Therapeutic Perspectives.International journal of molecular sciences · 2026
    Review
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  17. Role of Ferredoxin 1Cancer pathogenesis and therapy · 2026
    Review
  18. Review
  19. WTAP-mediated mMolecular genetics and genomics : MGG · 2026
    Article
  20. Article

84 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

7 authors at 4 institutions in 3 countries.

Sahar MafiDepartment of Clinical Biochemistry, Yasuj University of Medical Sciences, Yasuj, Iran.
Behzad MansooriThe Wistar Institute, Molecular & Cellular Oncogenesis Program, Philadelphia, PA, United States.
Shahram TaebDepartment of Radiology, School of Paramedical Sciences, Guilan University of Medical Sciences, Rasht, Iran.
Hossein SadeghiMedicinal Plants Research Center, Yasuj University of Medical Sciences, Yasuj, Iran.
Reza AbbasiMedicinal Plants Research Center, Yasuj University of Medical Sciences, Yasuj, Iran.
William C ChoDepartment of Clinical Oncology, Queen Elizabeth Hospital, Hong Kong, Hong Kong SAR, China.
Davoud RostamzadehDepartment of Clinical Biochemistry, Yasuj University of Medical Sciences, Yasuj, Iran.
Yasuj University of Medical Sciences · IRGuilan University of Medical Sciences · IRQueen Elizabeth Hospital · CNThe Wistar Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The mechanistic/mammalian target of rapamycin (mTOR) is a downstream mediator in the phosphatidylinositol 3-kinase (PI3K)/Akt signaling pathways, which plays a pivotal role in regulating numerous cellular functions including cell growth, proliferation, survival, and metabolism by integrating a variety of extracellular and intracellular signals in the tumor microenvironment (TME). Dysregulation of the mTOR pathway is frequently reported in many types of human tumors, and targeting the PI3K/Akt/mTOR signaling pathway has been considered an attractive potential therapeutic target in cancer. The PI3K/Akt/mTOR signaling transduction pathway is important not only in the development and progression of cancers but also for its critical regulatory role in the tumor microenvironment. Immunologically, mTOR is emerging as a key regulator of immune responses. The mTOR signaling pathway plays an essential regulatory role in the differentiation and function of both innate and adaptive immune cells. Considering the central role of mTOR in metabolic and translational reprogramming, it can affect tumor-associated immune cells to undergo phenotypic and functional reprogramming in TME. The mTOR-mediated inflammatory response can also promote the recruitment of immune cells to TME, resulting in exerting the anti-tumor functions or promoting cancer cell growth, progression, and metastasis. Thus, deregulated mTOR signaling in cancer can modulate the TME, thereby affecting the tumor immune microenvironment. Here, we review the current knowledge regarding the crucial role of the PI3K/Akt/mTOR pathway in controlling and shaping the immune responses in TME.

Indexed as

NeoplasmsTOR Serine-Threonine KinasesTumor MicroenvironmentHumansImmunityPhosphatidylinositol 3-KinasePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktMTOR protein, humanPhosphatidylinositol 3-KinasePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTOR Serine-Threonine Kinasescancerimmune responsemTORPI3K/Akt/mTOR signaling pathwayT cellTumor microenvironment

Identifiers

PMID35250965
PMCPMC8894239
OpenAlexW4213121631

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.