Evidence map›Paper›PMID 32333246›Full record

ReviewMolecular biology reports2020

Role of PI3K/AKT pathway in cancer: the framework of malignant behavior.

Ningni Jiang, Qijie Dai, Xiaorui Su, Jianjiang Fu, Xuancheng Feng, Juan Peng

Open access · hybridAbstract readReview
In one paragraph

Review in Molecular biology reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 331 papers.

0numbers the graph read from it
0cells of the map it votes in
331citing papers in PubMed
30.1field-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

331 citing papers in PubMed, 563 citations in OpenAlex.

  1. Article
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  3. Recent advances in hormone-based biopharmaceuticals for cancer therapy.Journal of the Egyptian National Cancer Institute · 2026
    Review
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  15. Role ofTranslational cancer research · 2026
    Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Review

271 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 2 countries.

Ningni Jiang *Department of Pathology, The Third Affiliated Hospital of Guangzhou Medical University, 63 Duobao Road, Guangzhou, 510150, China.ORCID http://orcid.org/0000-0002-6851-8928
Qijie Dai *Department of Pathology, The Third Affiliated Hospital of Guangzhou Medical University, 63 Duobao Road, Guangzhou, 510150, China.ORCID http://orcid.org/0000-0001-7583-7196
Xiaorui Su *Department of Pathology, The Third Affiliated Hospital of Guangzhou Medical University, 63 Duobao Road, Guangzhou, 510150, China.ORCID http://orcid.org/0000-0001-5847-1794
Jianjiang FuDepartment of Pathology, The Third Affiliated Hospital of Guangzhou Medical University, 63 Duobao Road, Guangzhou, 510150, China.ORCID http://orcid.org/0000-0002-3952-9898
Xuancheng FengDepartment of Pathology, The Third Affiliated Hospital of Guangzhou Medical University, 63 Duobao Road, Guangzhou, 510150, China. 2816924339@qq.com.ORCID http://orcid.org/0000-0002-8722-6306
Juan PengDepartment of Pathology, The Third Affiliated Hospital of Guangzhou Medical University, 63 Duobao Road, Guangzhou, 510150, China. pengjuan1979@yahoo.com.ORCID http://orcid.org/0000-0001-6308-3040
Guangdong University of Education · CNThird Affiliated Hospital of Guangzhou Medical University · CN

Funding

Guangzhou Medical University C195015021Natural Science Foundation of Guangdong Province 2016A030310280The National Natural Science Foundation of China 81602631The Third Affiliated Hospital of Guangzhou Medical Uiversity 2019A008
6 · The paper itself

Abstract

Given that the PI3K/AKT pathway has manifested its compelling influence on multiple cellular process, we further review the roles of hyperactivation of PI3K/AKT pathway in various human cancers. We state the abnormalities of PI3K/AKT pathway in different cancers, which are closely related with tumorigenesis, proliferation, growth, apoptosis, invasion, metastasis, epithelial-mesenchymal transition, stem-like phenotype, immune microenvironment and drug resistance of cancer cells. In addition, we investigated the current clinical trials of inhibitors against PI3K/AKT pathway in cancers and found that the clinical efficacy of these inhibitors as monotherapy has so far been limited despite of the promising preclinical activity, which means combinations of targeted therapy may achieve better efficacies in cancers. In short, we hope to feature PI3K/AKT pathway in cancers to the clinic and bring the new promising to patients for targeted therapies.

Indexed as

ApoptosisCell Line, TumorCell ProliferationCell Transformation, NeoplasticEpithelial-Mesenchymal TransitionHumansNeoplasmsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSignal TransductionTumor MicroenvironmentPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktAKTCancerPI3KPTENTargeted therapy

Identifiers

PMID32333246
PMCPMC7295848
OpenAlexW3017786087

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.