Evidence map›Paper›PMID 34068643›Full record

ReviewCells2021

Emerging Roles of SKP2 in Cancer Drug Resistance.

Ting Wu, Xinsheng Gu, Hongmei Cui

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

22 citing papers in PubMed, 44 citations in OpenAlex.

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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 2 institutions in 1 country.

Ting WuInstitute of Toxicology, School of Public Health, Lanzhou University, Lanzhou 730000, China.
Xinsheng GuDepartment of Pharmacology, College of Basic Medical Sciences, Hubei University of Medicine, Shiyan 442000, China.
Hongmei CuiInstitute of Toxicology, School of Public Health, Lanzhou University, Lanzhou 730000, China.
Lanzhou University · CNHubei University of Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

More than half of all cancer patients receive chemotherapy, however, some of them easily acquire drug resistance. Resistance to chemotherapy has become a massive obstacle to achieve high rates of pathological complete response during cancer therapy. S-phase kinase-associated protein 2 (Skp2), as an E3 ligase, was found to be highly correlated with drug resistance and poor prognosis. In this review, we summarize the mechanisms that Skp2 confers to drug resistance, including the Akt-Skp2 feedback loop, Skp2-p27 pathway, cell cycle and mitosis regulation, EMT (epithelial-mesenchymal transition) property, enhanced DNA damage response and repair, etc. We also addressed novel molecules that either inhibit Skp2 expression or target Skp2-centered interactions, which might have vast potential for application in clinics and benefit cancer patients in the future.

Indexed as

Drug Resistance, NeoplasmAnimalsCell CycleCell Line, TumorDNA DamageDNA RepairEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticHumansIn Vitro TechniquesMiceMitosisNeoplasmsPhosphorylationProtein BindingSignal TransductionSKP2 protein, humanS-Phase Kinase-Associated ProteinsUbiquitin-Protein LigasesAktcell cycleDNA damage response and repairdrug resistanceEMTinhibitorsmitosisp27Skp2

Identifiers

PMID34068643
PMCPMC8150781
OpenAlexW3162214391

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.