Evidence map›Paper›PMID 31733040›Full record

ReviewCancer medicine2020

Advances in IKBKE as a potential target for cancer therapy.

Min Yin, Xin Wang, Jie Lu

Open access · goldAbstract readReview
In one paragraph

Review in Cancer medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

36 citing papers in PubMed, 63 citations in OpenAlex.

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  11. Substituted 1,4-naphthoquinones for potential anticancer therapeutics:Computational and structural biotechnology journal · 2025
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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 3 institutions in 1 country.

Min YinDepartment of Oncology, Jinan Fifth People's Hospital, Jinan, PR China.
Xin WangDepartment of Oncology, Renmin Hospital of Wuhan University, Hubei Province, Wuhan, PR China.
Jie LuDepartment of Neurosurgery, The First Affiliated Hospital of Shandong First Medical University, Jinan, PR China.ORCID 0000-0002-8164-1402
Jinan City People's Hospital · CNShandong First Medical University · CNShandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

IKBKE (inhibitor of nuclear factor kappa-B kinase subunit epsilon), a member of the nonclassical IKK family, plays an important role in the regulation of inflammatory reactions, activation and proliferation of immune cells, and metabolic diseases. Recent studies have demonstrated that IKBKE plays a crucial regulatory role in malignant tumor development. In recent years, IKBKE, an important oncoprotein in several kinds of tumors, has been widely found to regulate a variety of cytokines and signaling pathways. IKBKE promotes the growth, proliferation, invasion, and drug resistance of various cancers. This paper makes a detailed review that focuses on the recent discoveries of IKBKE in the malignant tumors, and puts forward that IKBKE is becoming an important therapeutic target for clinical treatment, which has been more and more realized.

Indexed as

AnimalsAntineoplastic Combined Chemotherapy ProtocolsCarcinogenesisCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticHumansI-kappa B KinaseNeoplasmsNF-kappaB-Inducing KinaseProtein Kinase InhibitorsProtein Serine-Threonine KinasesProto-Oncogene ProteinsSignal TransductionXenograft Model Antitumor AssaysI-kappa B KinaseIKBKE protein, humanNF-kappaB-Inducing KinaseProtein Kinase InhibitorsProtein Serine-Threonine KinasesProto-Oncogene ProteinsIKBKENF-κBsignaling pathwaysmall molecule inhibitors

Identifiers

PMID31733040
PMCPMC6943080
OpenAlexW2988838247

What OpenQuestion holds

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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.