Evidence map›Paper›PMID 35618790›Full record

ArticleBritish journal of cancer2022

Stepwise evolutionary genomics of early-stage lung adenocarcinoma manifesting as pure, heterogeneous and part-solid ground-glass nodules.

Hao Li, Zewen Sun, Rongxin Xiao, Qingyi Qi, Xiao Li, Haiyan Huang, Xuan Wang, Jian Zhou, Zhenfan Wang, Ke Liu and 3 more

Open access · greenAbstract read
In one paragraph

Article in British journal of cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 24% of its field
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

11 citing papers in PubMed, 12 citations in OpenAlex.

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

13 authors at 2 institutions in 1 country.

Hao Li *Department of Thoracic Surgery, Peking University People's Hospital, Beijing, China.ORCID http://orcid.org/0000-0001-9426-9446
Zewen Sun *Department of Thoracic Surgery, Peking University People's Hospital, Beijing, China.
Rongxin Xiao *Department of Thoracic Surgery, Peking University People's Hospital, Beijing, China.ORCID http://orcid.org/0000-0002-0880-093X
Qingyi Qi *Department of Radiology, Peking University People's Hospital, Beijing, China.
Xiao LiDepartment of Thoracic Surgery, Peking University People's Hospital, Beijing, China. dr.lixiao@163.com.ORCID http://orcid.org/0000-0002-0455-0355
Haiyan HuangBerry Oncology Corporation, No. 4 Science Park Road, Changping District, Beijing, China.
Xuan WangDepartment of Cardiac Surgery, Peking University People's Hospital, Beijing, China.
Jian ZhouDepartment of Thoracic Surgery, Peking University People's Hospital, Beijing, China.
Zhenfan WangDepartment of Thoracic Surgery, Peking University People's Hospital, Beijing, China.
Ke LiuBerry Oncology Corporation, No. 4 Science Park Road, Changping District, Beijing, China.
Ping YinDepartment of Radiology, Peking University People's Hospital, Beijing, China.
Fan YangDepartment of Thoracic Surgery, Peking University People's Hospital, Beijing, China.
Jun WangDepartment of Thoracic Surgery, Peking University People's Hospital, Beijing, China. wangjun@pkuph.edu.cn.ORCID http://orcid.org/0000-0002-7033-5012
Peking University · CNBerry Oncology (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study was designed to unravel the genomic landscape and evolution of early-stage subsolid lung adenocarcinomas (SSN-LUADs) manifesting as pure ground-glass nodules (pGGNs), heterogeneous ground-glass nodules (HGGNs) and part-solid nodules (PSNs).

methodsSamples subjected to either broad-panel next-generation sequencing (NGS) or whole-exome sequencing (WES) were included. Clinicopathologic and genomic features were compared among pGGN, HGGN and PSN, while tumour evolutionary trajectories and mutational signatures were evaluated in the entire cohort.

resultsIn total, 247 SSN-LUAD samples subjected to broad-panel NGS and 125 to WES were identified. Compared with PSNs, HGGNs had significantly lower tumour mutation count (P < 0.001), genomic alteration count (P < 0.001), and intra-tumour heterogeneity (P = 0.005). Statistically significant upward trends were observed in alterations involving driver mutations and oncogenic pathways from pGGNs to HGGNs to PSNs. EGFR mutation was proved to be a key early event in the progression of SSN-LUADs, with subsequently two evolutionary trajectories involving either RBM10 or TP53 mutation in the cancer-evolution models.

conclusionsThis study provided evidence for unravelling the previously unknown genomic underpinnings associated with SSN-LUAD evolution from pGGN to HGGN to PSN, proving that HGGN was an intermediate SSN form between pGGN and PSN genetically.

Indexed as

Adenocarcinoma of LungLung NeoplasmsPrecancerous ConditionsGenomicsHumansRetrospective StudiesRNA-Binding ProteinsTomography, X-Ray ComputedRBM10 protein, humanRNA-Binding Proteins

Identifiers

PMID35618790
PMCPMC9381762
OpenAlexW4281556836

What OpenQuestion holds

Textmetadata
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.