Evidence map›Paper›PMID 30693031›Full record

ArticleJournal of oncology2019

UBE2C Induces Cisplatin Resistance via ZEB1/2-Dependent Upregulation of ABCG2 and ERCC1 in NSCLC Cells.

Yan Wu, Dan Jin, Xiaohong Wang, Jing Du, Weihua Di, Jiajia An, Cuijie Shao, Jiwei Guo

RetractedErratum issuedOpen access · hybridAbstract readRetracted Publication
In one paragraph

Article in Journal of oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

25 citing papers in PubMed, 36 citations in OpenAlex.

  1. ERCC1/NGFR affects prognosis in basal-like breast cancer.European journal of medical research · 2025
    Article
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  6. Role of UBE2C in Brain Cancer Invasion and Dissemination.International journal of molecular sciences · 2023
    Review
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  8. Article
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  14. New Insights into Therapy-Induced Progression of Cancer.International journal of molecular sciences · 2020
    Review
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  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Yan WuCancer Research Institute, Binzhou Medical University Hospital, Binzhou 256603, China.
Dan JinDepartment of Pain Medicine, Binzhou Medical University Hospital, Binzhou 256603, China.
Xiaohong WangDepartment of Thyroid and Breast Surgery, Binzhou Medical University Hospital, Binzhou 256603, China.
Jing DuCancer Research Institute, Binzhou Medical University Hospital, Binzhou 256603, China.
Weihua DiDepartment of Pain Medicine, Binzhou Medical University Hospital, Binzhou 256603, China.
Jiajia AnDepartment of Clinical Laboratory, Binzhou Medical University Hospital, Binzhou 256603, China.
Cuijie ShaoDepartment of Pain Medicine, Binzhou Medical University Hospital, Binzhou 256603, China.
Jiwei GuoCancer Research Institute, Binzhou Medical University Hospital, Binzhou 256603, China.ORCID 0000-0003-1636-6499
Binzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesCisplatin (DDP) is one of the most commonly used chemotherapeutic drugs for several cancers, including non-small-cell lung cancer (NSCLC). However, resistance to DDP eventually develops, limiting its further application. New therapy targets are urgently needed to reverse DDP resistance.

methodsThe mRNA expression of

resultsIn this study, we examined the effect of UBE2C and ZEB1/2 expression levels in DDP-resistant cells of NSCLC. We confirmed that aberrant expression of UBE2C and ZEB1/2 plays a critical role in repressing the DDP sensitivity to NSCLC cells. Additionally, knockdown of UBE2C significantly sensitized resistant cells to DDP by repressing the expression of ZEB1/2. Mechanistic investigations indicated that UBE2C transcriptionally regulated ZEB1/2 by accelerating promoter activity. This study revealed that ZEB1/2 promotes the epithelial mesenchymal transition and expression of ABCG2 and ERCC1 to participate in UBE2C-mediated NSCLC DDP-resistant cell progression, metastasis, and invasion.

conclusionUBE2C may be a novel therapy target for NSCLC for sensitizing cells to the chemotherapeutic agent DDP.

Identifiers

PMID30693031
PMCPMC6333017
OpenAlexW2908049419

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.