Evidence map›Paper›PMID 38764053›Full record

ArticleCancer cell international2024

EZH2 G553C significantly increases the risk of brain metastasis from lung cancer due to salt bridge instability.

Hanjun Wang, Ling Wang, Sheng Zhang, Qicai Liu, Feng Gao

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Article in Cancer cell international, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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1 citing paper in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Hanjun Wang *Department of Pathology, The First Affiliated Hospital, Fujian Medical University, Fuzhou, 350004, People's Republic of China.
Ling Wang *Department of Pathology, The First Affiliated Hospital, Fujian Medical University, Fuzhou, 350004, People's Republic of China.
Sheng ZhangDepartment of Pathology, The First Affiliated Hospital, Fujian Medical University, Fuzhou, 350004, People's Republic of China.
Qicai LiuDepartment of Reproductive Medicine Centre, 1st Affiliated Hospital, Fujian Medical University, 20 Chazhong Road, Fuzhou, 350005, China. lqc673673673@163.com.
Feng GaoDepartment of Pathology, The First Affiliated Hospital, Fujian Medical University, Fuzhou, 350004, People's Republic of China. fengfang77777@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe incidence and mortality of lung cancer is the highest in China and the world. Brain is the most common distant metastasis site of lung cancer. Its transfer mechanism and predictive biomarkers are still unclear. EZH2 participates in the catalysis of transcriptional inhibition complex, mediates chromatin compactness, leads to the silencing of its downstream target genes, participates in the silencing of multiple tumor suppressor genes, and is related to cell proliferation, apoptosis and cycle regulation. In physiology, EZH2 has high activity in stem cells or progenitor cells, inhibits genes related to cell cycle arrest and promotes self-renewal. To detect the expression and mutation of EZH2 gene in patients with brain metastasis of lung cancer, and provide further theoretical basis for exploring the pathogenesis of brain metastasis of lung cancer and finding reliable biomarkers to predict brain metastasis of lung cancer.

methodsThis study investigated susceptible genes for brain metastasis of lung cancer. The second-generation sequencing technology was applied to screen the differential genes of paired samples (brain metastasis tissues, lung cancer tissues and adjacent tissues) of lung cancer patients with brain metastasi.

resultsIt revealed that there was a significant difference in the G553C genotype of EZH2 between lung cancer brain metastasis tissues and lung cancer tissues (p = 0.045). The risk of lung cancer brain metastasis in G allele carriers was 2.124 times higher than that in C allele carriers. Immunohistochemistry showed that compared with lung cancer patients and lung cancer patients with brain metastasis, the expression level of EZH2 in lung cancer tissues of lung cancer patients was significantly higher than that in adjacent lung tissues (p < 0.0001), and higher than that in brain metastasis tissues (p = 0.0309). RNA in situ immunohybridization showed that EZH2 mRNA expression was gradually high in lung cancer adjacent tissues, lung cancer tissues and lung cancer brain metastasis tissues.

conclusionsEZH2 G553C polymorphism contributes to the prediction of brain metastasis of lung cancer, in which G allele carriers are more prone to brain metastasis.

Indexed as

EZH2ForecastGene polymorphismLung cancer brain metastasisNGS

Identifiers

PMID38764053
PMCPMC11103815

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