Evidence map›Paper›PMID 40506490›Full record

ReviewZhongguo fei ai za zhi = Chinese journal of lung cancer2025

[Research and Therapeutic Advances of 26S Proteasome Subunit 
in Non-small Cell Lung Cancer].

Chenrui Mou, Shaotong Zou, Chao Ren, Zihan Yi, Jianlin Shi

Abstract readReviewEnglish Abstract
In one paragraph

Review in Zhongguo fei ai za zhi = Chinese journal of lung cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Chenrui MouDepartment of Chest Surgery, The Third Affiliated Hospital of Kunming Medical University, Yunnan Tumor Hospital, 
Kunming 650118, China.
Shaotong ZouKunming Medical University, Kunming 650032, China.
Chao RenDepartment of Chest Surgery, The Third Affiliated Hospital of Kunming Medical University, Yunnan Tumor Hospital, 
Kunming 650118, China.
Zihan YiDepartment of Chest Surgery, The Third Affiliated Hospital of Kunming Medical University, Yunnan Tumor Hospital, 
Kunming 650118, China.
Jianlin ShiDepartment of Chest Surgery, The Third Affiliated Hospital of Kunming Medical University, Yunnan Tumor Hospital, 
Kunming 650118, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung cancer is one of the most common cancers worldwide and is the leading cause of cancer deaths. Lung adenocarcinoma is the most common type of lung cancer. Due to the lack of effective biomarkers and therapeutic targets in the proliferation and metastasis of lung adenocarcinoma, the overall treatment of lung adenocarcinoma is not optimistic. Therefore, there is a need to find new ideas and methods for lung adenocarcinoma treatment. The 26S proteasome is a multiprotein complex responsible for degrading misfolded proteins and maintaining intracellular protein homeostasis. During the development of non-small cell lung cancer (NSCLC), the regulatory granule subunit of the 26S proteasome promotes the malignant progression of tumours by regulating tumour-associated proteins, immune cells, and related signalling pathways. The proteasome core particle is a key subunit for degrading proteins, and its inhibitors have shown promising anti-tumour effects when combined with conventional chemotherapeutic agents. However, limited by toxic side effects and tumour heterogeneity, targeted inhibitors against the 26S proteasome are still not widely used in NSCLC treatment. This article reviews the mechanism of action and related therapeutic research of 26S proteasome regulatory particle subunits and core particle subunits in NSCLC, and explores the potential of these inhibitors in clinical application.
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Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsProteasome Endopeptidase ComplexAnimalsAntineoplastic AgentsHumansProteasome InhibitorsAntineoplastic AgentsATP dependent 26S proteaseProteasome Endopeptidase ComplexProteasome Inhibitors19S regulatory particle20S core particle26S proteasome subunitsLung neoplasms

Identifiers

PMID40506490
PMCPMC12171614

What OpenQuestion holds

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Registered trials

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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.