Evidence map›Paper›PMID 39021279›Full record

ArticleJournal of cellular and molecular medicine2024

Prognostic heterogeneity of Ki67 in non-small cell lung cancer: A comprehensive reappraisal on immunohistochemistry and transcriptional data.

Yujing Yang, Xinye Shao, Zhi Li, Lingyun Zhang, Bowen Yang, Bo Jin, Xuejun Hu, Xiujuan Qu, Xiaofang Che, Yunpeng Liu

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

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

10 authors.

Yujing YangDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang, China.
Xinye ShaoDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang, China.
Zhi LiDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang, China.
Lingyun ZhangDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang, China.
Bowen YangDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang, China.
Bo JinDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang, China.
Xuejun HuDepartment of Respiratory and Infectious Disease of Geriatrics, The First Hospital of China Medical University, Shenyang, China.
Xiujuan QuDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang, China.
Xiaofang CheDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang, China.
Yunpeng LiuDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang, China.ORCID 0000-0002-9645-7990

Funding

China Medical University High-level Talent Introduction Support Project 36003Key Research and Development Program of Liaoning Province 2018225060National Natural Science Foundation of China 81972197Technological Special Project of Liaoning Province of China 2019020176-JH1/103
6 · The paper itself

Abstract

In the present study, the debatable prognostic value of Ki67 in patients with non-small cell lung cancer (NSCLC) was attributed to the heterogeneity between lung adenocarcinoma (LUAD) and lung squamous carcinoma (LUSC). Based on meta-analyses of 29 studies, a retrospective immunohistochemical cohort of 1479 patients from our center, eight transcriptional datasets and a single-cell datasets with 40 patients, we found that high Ki67 expression suggests a poor outcome in LUAD, but conversely, low Ki67 expression indicates worse prognosis in LUSC. Furthermore, low proliferation in LUSC is associated with higher metastatic capacity, which is related to the stronger epithelial-mesenchymal transition potential, immunosuppressive microenvironment and angiogenesis. Finally, nomogram model incorporating clinical risk factors and Ki67 expression outperformed the basic clinical model for the accurate prognostic prediction of LUSC. With the largest prognostic assessment of Ki67 from protein to mRNA level, our study highlights that Ki67 also has an important prognostic value in NSCLC, but separate evaluation of LUAD and LUSC is necessary to provide more valuable information for clinical decision-making in NSCLC.

Indexed as

Carcinoma, Non-Small-Cell LungImmunohistochemistryKi-67 AntigenLung NeoplasmsAgedBiomarkers, TumorCarcinoma, Squamous CellEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticHumansMaleMiddle AgedNomogramsPrognosisRetrospective StudiesBiomarkers, TumorKi-67 AntigenKi67non‐small cell lung cancerprognosistumour microenvironmenttumour proliferation

Identifiers

PMID39021279
PMCPMC11255407

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.