Evidence map›Paper›PMID 40066091›Full record

ReviewFrontiers in oncology2025

Advances in targeting protein S-palmitoylation in tumor immunity and therapy.

Miaomiao Han, Yuanhao Lv, Yiyang Chen, Zhaoyi Li, Jiaqi Tian, Hongyan Zhou, Yunlong Wang, Wei Su, Jiateng Zhong

Abstract readReview
In one paragraph

Review in Frontiers in oncology, 2025. 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
–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

12 citing papers in PubMed.

  1. Article
  2. ProteinJournal of pharmaceutical analysis · 2026
    Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. The Roles of ProteinCancer communications (London, England) · 2026
    Review
  10. Review
  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.

Miaomiao Han *Department of Pathology, School of Basic Medical Sciences, Xinxiang Medical University, Xinxiang, China.
Yuanhao Lv *Department of Pathology, School of Basic Medical Sciences, Xinxiang Medical University, Xinxiang, China.
Yiyang ChenDepartment of Pathology, The First Affiliated Hospital of Xinxiang Medical University, Xinxiang, China.
Zhaoyi LiDepartment of Pathology, The First Affiliated Hospital of Xinxiang Medical University, Xinxiang, China.
Jiaqi TianDepartment of Pathology, School of Basic Medical Sciences, Xinxiang Medical University, Xinxiang, China.
Hongyan ZhouHenan Bioengineering Technology Research Center, Zhengzhou, China.
Yunlong WangXinxiang Key Laboratory of Precision Diagnosis and Treatment for Colorectal Cancer, Xinxiang First People's Hospital, Xinxiang, China.
Wei SuDepartment of Pathology, The First Affiliated Hospital of Xinxiang Medical University, Xinxiang, China.
Jiateng ZhongDepartment of Pathology, School of Basic Medical Sciences, Xinxiang Medical University, Xinxiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

S-palmitoylation is a reversible and dynamic post-translational modification of proteins. A palmitoyl group is covalently attached to a cysteine residue of the protein by a thioester link. It regulates the transcription and expression of downstream target genes and cell signaling, influencing cellular functions. Research indicates a substantial correlation between S-palmitoylation and tumorigenesis and immunotherapy, where it plays a pivotal role in modulating T cell activation, cytokine signaling, autophagy, phagocytosis, and death. Moreover, palmitoylation contributes to drug resistance and immunological evasion in tumor cells, enabling them to circumvent the effects of chemotherapeutic drugs and immune surveillance. Inhibitors that target S-palmitoylation have demonstrated significant potential in enhancing the efficacy of tumor immunotherapy, offering a novel strategy for cancer treatment. Nonetheless, obstacles such as inhibitor specificity and efficacy persist, requiring more extensive investigations into the exact mechanisms of S-palmitoylation to develop more effective targeted therapeutics. This article summarizes recent developments in S-palmitoylation concerning tumor immunity and treatment. The article examines the regulatory function of S-palmitoylation, its modifying enzymes in tumor cell signaling, and novel tumor immunotherapies that target S-palmitoylation.

Indexed as

drug resistanceimmune escapeimmunotherapyS-palmitoylationT cellstumor

Identifiers

PMID40066091
PMCPMC11891048

What Socratic 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 Socratic graph.