Evidence map›Paper›PMID 40681687›Full record

ArticleNPJ precision oncology2025

Integrative multi-omics and machine learning reveal critical functions of proliferating cells in prognosis and personalized treatment of lung adenocarcinoma.

Shun Wang, Dingtao Hu, Ruohuang Wang, Jie Huang, Baoqing Wang

Abstract read
In one paragraph

Article in NPJ precision oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. 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

5 authors.

Shun Wang *Department of Respiratory Medicine, Shanghai Xuhui Central Hospital, Zhongshan-Xuhui Hospital, Fudan University, Shanghai, China.
Dingtao Hu *Department of Oncology, The First Affiliated Hospital of Anhui Medical University, Hefei, China.
Ruohuang Wang *Department of Otolaryngology, The Second Affiliated Hospital of the Naval Military Medical University (Shanghai Changzheng Hospital), Shanghai, China.
Jie HuangDepartment of Respiratory Medicine, Shanghai Xuhui Central Hospital, Zhongshan-Xuhui Hospital, Fudan University, Shanghai, China. syarhuang@163.com.
Baoqing WangDepartment of Respiratory Medicine, Shanghai Xuhui Central Hospital, Zhongshan-Xuhui Hospital, Fudan University, Shanghai, China. Wang.baoqing@zs-hospital.sh.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung adenocarcinoma (LUAD) is a major cause of cancer-related mortality globally. Proliferating cells, crucial components of the tumor immune microenvironment (TIME), play a significant role in cancer progression and immunotherapy response. Herein, we utilized multi-omics data and employed a multifaceted approach to delineate the proliferating cell landscape in LUAD. The Scissor algorithm was applied to identify Scissor+ proliferating cell genes associated with prognosis. An integrative machine learning program, comprising 111 algorithms, was developed to construct a Scissor+ proliferating cell risk score (SPRS). The SPRS model demonstrated superior performance in predicting prognosis and clinical outcomes compared to 30 previously published models. The role of SPRS and five pivotal genes in immunotherapy response was evaluated, and their expression was experimentally verified. Multifactorial analysis confirmed SPRS as an independent prognostic factor affecting LUAD patient survival. High- and low-SPRS groups exhibited different biological functions and immune cell infiltration in the TIME. High SPRS patients showed resistance to immunotherapy but increased sensitivity to chemotherapeutic and targeted therapeutic agents. Our study elucidates the dynamics of proliferating cells in LUAD, enhancing prognostic accuracy and highlighting the potential of SPRS and its constituent genes for personalized therapeutic interventions.

Identifiers

PMID40681687
PMCPMC12274462

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.