详细信息

CA3 bridges dietary restriction to glioblastoma suppression and tumor progression as a key downstream effector  ( SCI-EXPANDED收录)  

文献类型:期刊文献

英文题名:CA3 bridges dietary restriction to glioblastoma suppression and tumor progression as a key downstream effector

作者:Mao, Junxiang[1,2];Cai, Zhibiao[3];Xie, Dong[4];Guo, Man[4];Gao, Yu[4];Zhao, Guohui[4];Zhou, Jie[1,2]

第一作者:Mao, Junxiang

通信作者:Zhou, J[1];Zhou, J[2]

机构:[1]Lanzhou Univ, Hosp 2, 82 Cuiyingmen,Linxia Rd, Lanzhou City 730000, Gansu Province, Peoples R China;[2]Lanzhou Univ, Clin Med Sch, 82 Cuiyingmen,Linxia Rd, Lanzhou City 730000, Gansu Province, Peoples R China;[3]940 Th Hosp Joint Logist Support Force Chinese Peo, Dept Neurosurg, 333 Nanbinhe Rd, Lanzhou City 730000, Gansu Province, Peoples R China;[4]Gansu Univ Tradit Chinese Med, Dept Clin 1, Coll Med, 35 Dingxi East Rd, Lanzhou City 730000, Gansu Province, Peoples R China

第一机构:Lanzhou Univ, Hosp 2, 82 Cuiyingmen,Linxia Rd, Lanzhou City 730000, Gansu Province, Peoples R China

通信机构:[1]corresponding author), Lanzhou Univ, Hosp 2, 82 Cuiyingmen,Linxia Rd, Lanzhou City 730000, Gansu Province, Peoples R China;[2]corresponding author), Lanzhou Univ, Clin Med Sch, 82 Cuiyingmen,Linxia Rd, Lanzhou City 730000, Gansu Province, Peoples R China.

年份:2025

卷号:15

期号:1

外文期刊名:SCIENTIFIC REPORTS

收录:;Scopus(收录号:2-s2.0-105006835342);WOS:【SCI-EXPANDED(收录号:WOS:001498767900016)】;

基金:Not applicable.

语种:英文

外文关键词:Dietary restriction; Glioblastoma multiforme; CA3; Single-cell transcriptome; Biomarker

摘要:Dietary restriction (DR) is recognized as a health-promoting, non-pharmacological intervention with demonstrated inhibitory effects on the initiation and progression of cancer. The molecular mechanisms underpinning DR's anticancer activity are pivotal, with documented evidence of its suppressive role across a spectrum of cancers. Glioblastoma multiforme (GBM) represents an aggressively malignant intracranial neoplasm, and despite incremental therapeutic and managerial advancements, the clinical outcomes remain suboptimal. Consequently, the discovery of novel molecular markers to augment diagnostic accuracy and therapeutic efficacy is imperative. Employing an array of bioinformatics strategies, we conducted an exhaustive analysis of molecules associated with DR, culminating in the identification of CA3 as a novel molecular marker for GBM. We evaluated its diagnostic and therapeutic potential within GBM. Our data indicate that the DR-associated molecule CA3 may exhibit correlations with multiple GBM phenotypes, including the immune contexture, with particular emphasis on the tumor's invasive and migratory capacities. Subsequent inquiries confirmed that modulating CA3 expression can effectively curb the genesis and progression of GBM. Our research substantiates that DR can mitigate the onset and development of GBM via the gene CA3, thereby validating a novel GBM marker and proposing a non-pharmacological interventional approach for this life-threatening condition.

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