Evidence map›Paper›PMID 36964635›Full record

ArticleHereditas2023

CCNE1 is a predictive and immunotherapeutic indicator in various cancers including UCEC: a pan-cancer analysis.

Xingyu Zheng, Lingli Chen, Wenlu Liu, Shuangshuang Zhao, Ye Yan, Jianzhen Zhao, Wenyan Tian, Yingmei Wang

Open access · goldFull text read
In one paragraph

Article in Hereditas, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

17 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Ethanol extract fromNarra J · 2025
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
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 1 institution in 1 country.

Xingyu Zheng *Department of Gynecology and Obstetrics, Tianjin Medical University General Hospital, Tianjin, China.ORCID http://orcid.org/0000-0002-5995-4058
Lingli Chen *Department of Gynecology and Obstetrics, Tianjin Medical University General Hospital, Tianjin, China.
Wenlu Liu *Department of Gynecology and Obstetrics, Tianjin Medical University General Hospital, Tianjin, China.
Shuangshuang ZhaoDepartment of Gynecology and Obstetrics, Tianjin Medical University General Hospital, Tianjin, China.
Ye YanDepartment of Gynecology and Obstetrics, Tianjin Medical University General Hospital, Tianjin, China.
Jianzhen ZhaoDepartment of Gynecology and Obstetrics, Tianjin Medical University General Hospital, Tianjin, China.
Wenyan TianDepartment of Gynecology and Obstetrics, Tianjin Medical University General Hospital, Tianjin, China.
Yingmei WangDepartment of Gynecology and Obstetrics, Tianjin Medical University General Hospital, Tianjin, China. wangyingmei@tmu.edu.cn.
Tianjin Medical University General Hospital · CN

Funding

Key Rerearch Program of Tianjin Health Commission TJWJ2022XK009National Natural Science Foundation of China 82172626Tianjin Municipal Science and Technology Bureau 20JCZDJC00330
6 · The paper itself

Abstract

backgroundCCNE1 plays an important oncogenic role in several tumors, especially high-stage serous ovarian cancer and endometrial cancer. Nevertheless, the fundamental function of CCNE1 has not been explored in multiple cancers. Therefore, bioinformatics analyses of pan-cancer datasets were carried out to explore how CCNE1 regulates tumorigenesis.

methodsA variety of online tools and cancer databases, including GEPIA2, SangerBox, LinkedOmics and cBioPortal, were applied to investigate the expression of CCNE1 across cancers. The pan-cancer datasets were used to search for links between CCNE1 expression and prognosis, DNA methylation, m6A level, genetic alterations, CCNE1-related genes, and tumor immunity. We verified that CCNE1 has biological functions in UCEC cell lines using CCK-8, EdU, and Transwell assays.

resultsIn patients with different tumor types, a high mRNA expression level of CCNE1 was related to a poor prognosis. Genes related to CCNE1 were connected to the cell cycle, metabolism, and DNA damage repair, according to GO and KEGG enrichment analyses. Genetic alterations of CCNE1, including duplications and deep mutations, have been observed in various cancers. Immune analysis revealed that CCNE1 had a strong correlation with TMB, MSI, neoantigen, and ICP in a variety of tumor types, and this correlation may have an impact on the sensitivity of various cancers to immunotherapy. CCK-8, EdU and Transwell assays suggested that CCNE1 knockdown can suppress UCEC cell proliferation, migration and invasion.

conclusionOur study demonstrated that CCNE1 is upregulated in multiple cancers in the TCGA database and may be a promising predictive biomarker for the immunotherapy response in some types of cancers. Moreover, CCNE1 knockdown can suppress the proliferation, migration and invasion of UCEC cells.

Indexed as

Cyclin ENeoplasmsOncogene ProteinsCell DivisionCell LineCell ProliferationHumansCCNE1 protein, humanCyclin EOncogene ProteinsCCNE1ImmunePancancerPrognosisUCEC

Identifiers

PMID36964635
PMCPMC10037856
OpenAlexW4360863116

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read64
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.