Evidence map›Paper›PMID 38265973›Full record

ArticleAging2024

Potential prognosis and immunotherapy predictor TFAP2A in pan-cancer.

Chenxi Niu, Haixuan Wen, Shutong Wang, Guang Shu, Maonan Wang, Hanxi Yi, Ke Guo, Qiong Pan, Gang Yin

Open access · hybridAbstract read
In one paragraph

Article in Aging, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.6field-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

12 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Mechanistic study on the inhibition of triple-negative breast cancer progression by LncRNA TFAP2A-AS1 through the regulation of miR-6892/PHGDH.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2025
    Article
  10. Article
  11. Article
  12. 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

9 authors at 1 institution in 1 country.

Chenxi NiuDepartment of Pathology, Xiangya Hospital, School of Basic Medical Sciences, Central South University, Changsha, China.
Haixuan WenDepartment of Pathology, Xiangya Hospital, School of Basic Medical Sciences, Central South University, Changsha, China.
Shutong WangXiangya Medical School, Central South University, Changsha, China.
Guang ShuDepartment of Pathology, Xiangya Hospital, School of Basic Medical Sciences, Central South University, Changsha, China.
Maonan WangDepartment of Pathology, Xiangya Hospital, School of Basic Medical Sciences, Central South University, Changsha, China.
Hanxi YiDepartment of Pathology, Xiangya Hospital, School of Basic Medical Sciences, Central South University, Changsha, China.
Ke GuoDepartment of Neurology, The Third Xiangya Hospital of Central South University, Changsha, China.
Qiong PanDepartment of Obstetrics and Gynecology, The Third Xiangya Hospital of Central South University, Changsha, China.
Gang YinDepartment of Pathology, Xiangya Hospital, School of Basic Medical Sciences, Central South University, Changsha, China.
Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTFAP2A is critical in regulating the expression of various genes, affecting various biological processes and driving tumorigenesis and tumor development. However, the significance of TFAP2A in carcinogenesis processes remains obscure.

methodsIn our study, we explored multiple databases including TCGA, GTEx, HPA, cBioPortal, TCIA, and other well-established databases for further analysis to expound TFAP2A expression, genetic alternations, and their relationship with the prognosis and cellular signaling network alternations. GO term and KEGG pathway enrichment analysis as well as GSEA were conducted to examine the common functions of TFAP2A. RT-qPCR, Western Blot and Dual Luciferase Reporter assay were employed to perform experimental validation.

resultsTFAP2A mRNA expression level was upregulated and its genetic alternations were frequently present in most cancer types. The enrichment analysis results prompted us to investigate the changes in the tumor immune microenvironment further. We discovered that the expression of TFAP2A was significantly associated with the expression of immune checkpoint genes, immune subtypes, ESTIMATE scores, tumor-infiltrating immune cells, and the possible role of TFAP2A in predicting immunotherapy efficacy. In addition, high TFAP2A expression significantly correlated with several ICP genes, and promoted the expression of PD-L1 on mRNA and protein levels through regulating its expression at the transcriptional level. TFAP2A protein level was upregulated in fresh colon tumor tissue samples compared to that in the adjacent normal tissues, which essentially positively correlated with the expression of PD-L1.

conclusionsOur study suggests that targeting TFAP2A may provide a novel and effective strategy for cancer treatment.

Indexed as

B7-H1 AntigenColonic NeoplasmsTranscription Factor AP-2CarcinogenesisHumansImmunotherapyPrognosisRNA, MessengerTumor MicroenvironmentB7-H1 AntigenRNA, MessengerTFAP2A protein, humanTranscription Factor AP-2immunotherapypan-cancerPD-L1TFAP2Atumor microenvironment

Identifiers

PMID38265973
PMCPMC10866441
OpenAlexW4391126854

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.