Evidence map›Paper›PMID 37256381›Full record

ArticleJournal of cancer research and clinical oncology2023

Differences of genomic alterations and heavy metals in non-small cell lung cancer with different histological subtypes.

Die Mu, Hui Tang, Gen Teng, Xinyang Li, Yarui Zhang, Ge Gao, Dongjuan Wang, Lu Bai, Xiangyao Lian, Ming Wen and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Metal Ion Signaling in Biomedicine.Chemical reviews · 2025
    Review
  5. 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

14 authors at 3 institutions in 1 country.

Die Mu *Department of Oncology, Affiliated Hospital of Chengde Medical University, Chengde, 067000, China.
Hui Tang *Shanghai Zhangjiang Institute of Medical Innovation, Shanghai Biotecan Pharmaceuticals Co., Ltd., Shanghai, 200135, China.
Gen TengDepartment of Oncology, Affiliated Hospital of Chengde Medical University, Chengde, 067000, China.
Xinyang LiDepartment of Oncology, Affiliated Hospital of Chengde Medical University, Chengde, 067000, China.
Yarui ZhangDepartment of Oncology, Affiliated Hospital of Chengde Medical University, Chengde, 067000, China.
Ge GaoDepartment of Oncology, Affiliated Hospital of Chengde Medical University, Chengde, 067000, China.
Dongjuan WangDepartment of Oncology, Affiliated Hospital of Chengde Medical University, Chengde, 067000, China.
Lu BaiDepartment of Oncology, Affiliated Hospital of Chengde Medical University, Chengde, 067000, China.
Xiangyao LianDepartment of Oncology, Affiliated Hospital of Chengde Medical University, Chengde, 067000, China.
Ming WenShanghai Zhangjiang Institute of Medical Innovation, Shanghai Biotecan Pharmaceuticals Co., Ltd., Shanghai, 200135, China.
Lisha JiangShanghai Zhangjiang Institute of Medical Innovation, Shanghai Biotecan Pharmaceuticals Co., Ltd., Shanghai, 200135, China.
Shouxin WuShanghai Zhangjiang Institute of Medical Innovation, Shanghai Biotecan Pharmaceuticals Co., Ltd., Shanghai, 200135, China.
Huihui JiangShanghai Zhangjiang Institute of Medical Innovation, Shanghai Biotecan Pharmaceuticals Co., Ltd., Shanghai, 200135, China. jianghh@biotecan.com.
Cuimin ZhuDepartment of Oncology, Affiliated Hospital of Chengde Medical University, Chengde, 067000, China. minminzhu1006@163.com.
Chengde Medical University · CNShanghai Innovative Research Center of Traditional Chinese Medicine · CNShanghai Tenth People's Hospital · CN

Funding

Natural Science Foundation of Hebei Province No. H2020406050
6 · The paper itself

Abstract

purposeThis study aimed to explore the correlations among heavy metals concentration, histologic subtypes and molecular characteristics in patients with non-small cell lung cancer (NSCLC).

methodsIn this study, an NGS panel of 82 tumor-associated genes was used to identify genomic alternations in 180 newly diagnosed patients with NSCLC. The concentrations of 18 heavy metals in the serum samples were detected by inductively coupled plasma emission spectrometry (ICP-MS).

resultsA total of 243 somatic mutations of 25 mutant genes were identified in 115 of 148 patients with LUAD and 45 somatic mutations of 15 mutant genes were found in 24 of 32 patients with LUSC. The genomic alternations, somatic interactions, traditional serum biomarkers, and heavy metals were markedly different between patients with LUAD and LUSC. Moreover, patients with LUSC were significantly positively correlated with Ba, but not LUAD. Lastly, patients with EGFR mutations presented significant negative correlations with Cd and Sr, whereas patients with TP53 mutations showed a significant positive correlation with Pb.

conclusionThe genomic alternations, somatic interactions, traditional serum biomarkers, and heavy metals were different between patients with LUAC and LUSC, and heavy metals (e.g., Ba, Pb, and Cd) may contribute to the tumorigenesis of NSCLC with different histological and molecular subtypes.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsCadmiumGenomicsHumansLeadCadmiumLeadCirculating tumor DNAGenomic alterationsHeavy metalsLung adenocarcinomaLung squamous cell carcinomaTissue

Identifiers

PMID37256381
PMCPMC10423170
OpenAlexW4378783478

What OpenQuestion holds

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LicenceCC BY
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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.