Evidence map›Paper›PMID 36720923›Full record

ArticleScientific reports2023

CENPF knockdown inhibits adriamycin chemoresistance in triple-negative breast cancer via the Rb-E2F1 axis.

Depeng Wang, Wei Xu, Minghua Huang, Wei Ma, Yulu Liu, Xingchen Zhou, Qingrui Yang, Kun Mu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.2field-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

19 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. The Prevalence and Clinical Significance of the Centromere Protein-F-Like Immunofluorescence Staining Pattern in a Large ANA-positive Cohort.Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2026
    Article
  4. Article
  5. Article
  6. Oncology research · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
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

8 authors at 5 institutions in 1 country.

Depeng Wang *Department of Pathology, School of Basic Medical Sciences, Shandong University, Wen Hua Xi Road 44, Jinan, 250012, China.
Wei Xu *Department of Rheumatology and Immunology, Shandong Provincial Hospital, Shandong University, Jingwu Road 324, Jinan, 250021, China.
Minghua HuangDepartment of Respiratory Medicine, Shandong Provincial Third Hospital, Shandong University, Jinan, 250132, China.
Wei MaDepartment of Pathology, School of Basic Medical Sciences, Shandong University, Wen Hua Xi Road 44, Jinan, 250012, China.
Yulu LiuDepartment of Pathology, School of Basic Medical Sciences, Shandong University, Wen Hua Xi Road 44, Jinan, 250012, China.
Xingchen ZhouDepartment of Pathology, The Second Hospital of Shandong University, Jinan, 250033, China.
Qingrui YangDepartment of Rheumatology and Immunology, Shandong Provincial Hospital, Shandong University, Jingwu Road 324, Jinan, 250021, China. qryang720@163.com.
Kun MuDepartment of Pathology, School of Basic Medical Sciences, Shandong University, Wen Hua Xi Road 44, Jinan, 250012, China. mukun@sdu.edu.cn.
Shandong University · CNQilu Hospital of Shandong University · CNSecond Hospital of Shandong University · CNShandong Provincial Hospital · CNWeifang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Drug resistance occurs frequently in triple-negative breast cancer (TNBC) and leads to early relapse and short survival. Targeting the DNA damage response (DDR) has become an effective strategy for overcoming TNBC chemoresistance. CENPF (centromere protein) is a key regulator of cell cycle progression, but its role in TNBC chemotherapy resistance remains unclear. Here, we found that CENPF, which is highly expressed in TNBC, is associated with a poor prognosis in patients receiving chemotherapy. In addition, in vitro CENPF knockdown significantly increased adriamycin (ADR)-induced cytotoxicity in MDA-MB-231 cells and ADR-resistant cells (MDA-MB-231/ADR). Then, we demonstrated that CENPF targets Chk1-mediated G2/M phase arrest and binds to Rb to compete with E2F1 in TNBC. Considering the crucial role of E2F1 in the DNA damage response and DNA repair, a novel mechanism by which CENPF regulates the Rb-E2F1 axis will provide new horizons to overcome chemotherapy resistance in TNBC.

Indexed as

Chromosomal Proteins, Non-HistoneDrug Resistance, NeoplasmTriple Negative Breast NeoplasmsCentromereDoxorubicinE2F1 Transcription FactorHumansMicrofilament ProteinsMitosiscentromere protein FChromosomal Proteins, Non-HistoneDoxorubicinE2F1 protein, humanE2F1 Transcription FactorMicrofilament Proteins

Identifiers

PMID36720923
PMCPMC9889717
OpenAlexW4318715179

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.