Evidence map›Paper›PMID 39820491›Full record

ArticleCell death & disease2025

Targeting EGFR-binding protein SLC7A11 enhancing antitumor immunity of T cells via inducing MHC-I antigen presentation in nasopharyngeal carcinoma.

Haihua Wang, Songqing Fan, Yuting Zhan, Yue Xu, Yao Du, Jiadi Luo, Hongjing Zang, Shuping Peng, Weiyuan Wang

Abstract read
In one paragraph

Article in Cell death & disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Open life sciences · 2026
    Article
  12. Article
  13. Article
  14. 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.

Haihua Wang *Department of Pathology, The Second Xiangya Hospital, Central South University, 410011, Changsha, Hunan, China.
Songqing Fan *Department of Pathology, The Second Xiangya Hospital, Central South University, 410011, Changsha, Hunan, China.ORCID 0000-0002-1486-9909
Yuting ZhanDepartment of Pathology, The Second Xiangya Hospital, Central South University, 410011, Changsha, Hunan, China.
Yue XuDepartment of Pathology, The Second Xiangya Hospital, Central South University, 410011, Changsha, Hunan, China.
Yao DuDepartment of Pathology, The Second Xiangya Hospital, Central South University, 410011, Changsha, Hunan, China.
Jiadi LuoDepartment of Pathology, The Second Xiangya Hospital, Central South University, 410011, Changsha, Hunan, China.
Hongjing ZangDepartment of Pathology, The Second Xiangya Hospital, Central South University, 410011, Changsha, Hunan, China.
Shuping PengCancer Research Institute, School of Basic Medical Science, Central South University, 410078, Changsha, Hunan, China.ORCID 0000-0001-9567-9295
Weiyuan WangDepartment of Pathology, The Xiangya Hospital, Central South University, 410008, Changsha, Hunan, China. weiyuanwang@csu.edu.cn.ORCID 0000-0002-2336-3301

Funding

National Natural Science Foundation of China (National Science Foundation of China) 81802791National Natural Science Foundation of China (National Science Foundation of China) 81972838National Natural Science Foundation of China (National Science Foundation of China) 82102805National Natural Science Foundation of China (National Science Foundation of China) 82200019Natural Science Foundation of Hunan Province (Hunan Provincial Natural Science Foundation) 2020JJ4122Natural Science Foundation of Hunan Province (Hunan Provincial Natural Science Foundation) 2022JJ30966
6 · The paper itself

Abstract

Approximately 80% of nasopharyngeal carcinoma (NPC) patients exhibit EGFR overexpression. The overexpression of EGFR has been linked to its potential role in modulating major histocompatibility complex class I (MHC-I) molecules. We discovered that EGFR, operating in a kinase-independent manner, played a role in stabilizing the expression of SLC7A11, which subsequently inhibited MHC-I antigen presentation. This mechanism, in turn, provided protection to NPC cells against T cell-mediated cytotoxicity. The underlying molecular processes revealed that the high and stable expression of SLC7A11 hindered the nuclear entry of GR, thereby suppressing TAP1 transcription and the presentation of MHC-I molecules. Additionally, elevated SLC7A11 expression led to an increase in FAF2 expression and triggered ERAD-dependent degradation of MHC-I, resulting in a reduction of MHC-I molecules on the cell membrane. The NPC patients exhibiting high EGFR and low MHC-I expression, combined with a scarcity of CD8

Indexed as

Amino Acid Transport System y+Antigen PresentationHistocompatibility Antigens Class INasopharyngeal CarcinomaNasopharyngeal NeoplasmsT-LymphocytesAnimalsATP Binding Cassette Transporter, Subfamily B, Member 2CD8-Positive T-LymphocytesCell Line, TumorErbB ReceptorsFemaleHumansMiceAmino Acid Transport System y+ATP Binding Cassette Transporter, Subfamily B, Member 2EGFR protein, humanErbB ReceptorsHistocompatibility Antigens Class ISLC7A11 protein, humanTAP1 protein, human

Identifiers

PMID39820491
PMCPMC11739652

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.