Role and potential therapeutic value of histone methyltransferases in drug resistance mechanisms in lung cancer

被引:3
作者
Zhang, Linxiang [1 ,2 ]
Zhang, Xueying [1 ,2 ]
Shi, Yan [1 ,2 ]
Ni, Yuhan [1 ,2 ]
Fei, Jiaojiao [1 ,2 ]
Jin, Zhixin [1 ,2 ]
Li, Wenjuan [1 ,2 ]
Wang, Xiaojing [1 ,2 ]
Wu, Nan [1 ,2 ]
机构
[1] First Affiliated Hosp, Affiliated Hosp 1, Dept Pulm Crit Care Med, Mol Diag Ctr ,Key Lab Clin & Preclin Res Resp Dis, Bengbu, Anhui, Peoples R China
[2] First Affiliated Hosp, Affiliated Hosp 1, Bengbu Med Coll, Bengbu, Peoples R China
基金
中国国家自然科学基金;
关键词
lung cancer; histone methyltransferases; epigenetics; drug resistance; cancer therapy; LYSINE METHYLTRANSFERASES; EZH2; METHYLATION; PROMOTES; SENSITIVITY; EXPRESSION; INHIBITORS; GEFITINIB; CELLS; H3R2;
D O I
10.3389/fonc.2024.1376916
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Lung cancer, ranking second globally in both incidence and high mortality among common malignant tumors, presents a significant challenge with frequent occurrences of drug resistance despite the continuous emergence of novel therapeutic agents. This exacerbates disease progression, tumor recurrence, and ultimately leads to poor prognosis. Beyond acquired resistance due to genetic mutations, mounting evidence suggests a critical role of epigenetic mechanisms in this process. Numerous studies have indicated abnormal expression of Histone Methyltransferases (HMTs) in lung cancer, with the abnormal activation of certain HMTs closely linked to drug resistance. HMTs mediate drug tolerance in lung cancer through pathways involving alterations in cellular metabolism, upregulation of cancer stem cell-related genes, promotion of epithelial-mesenchymal transition, and enhanced migratory capabilities. The use of HMT inhibitors also opens new avenues for lung cancer treatment, and targeting HMTs may contribute to reversing drug resistance. This comprehensive review delves into the pivotal roles and molecular mechanisms of HMTs in drug resistance in lung cancer, offering a fresh perspective on therapeutic strategies. By thoroughly examining treatment approaches, it provides new insights into understanding drug resistance in lung cancer, supporting personalized treatment, fostering drug development, and propelling lung cancer therapy into novel territories.
引用
收藏
页数:11
相关论文
共 118 条
[81]  
Siegel RL, 2018, CA-CANCER J CLIN, V68, P7, DOI [10.3322/caac.21442, 10.3322/caac.21551]
[82]   G9a Promotes Invasion and Metastasis of Non-Small Cell Lung Cancer through Enhancing Focal Adhesion Kinase Activation via NF-κB Signaling Pathway [J].
Sun, Ting ;
Zhang, Keqiang ;
Pangeni, Rajendra P. ;
Wu, Jun ;
Li, Wendong ;
Du, Yong ;
Guo, Yuming ;
Chaurasiya, Shyambabu ;
Arvanitis, Leonidas ;
Raz, Dan J. .
MOLECULAR CANCER RESEARCH, 2021, 19 (03) :429-440
[83]   Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries [J].
Sung, Hyuna ;
Ferlay, Jacques ;
Siegel, Rebecca L. ;
Laversanne, Mathieu ;
Soerjomataram, Isabelle ;
Jemal, Ahmedin ;
Bray, Freddie .
CA-A CANCER JOURNAL FOR CLINICIANS, 2021, 71 (03) :209-249
[84]   Targeting cell-cycle machinery in cancer [J].
Suski, Jan M. ;
Braun, Marcin ;
Strmiska, Vladislav ;
Sicinski, Piotr .
CANCER CELL, 2021, 39 (06) :759-778
[85]   Histone Methylases and Demethylases Regulating Antagonistic Methyl Marks: Changes Occurring in Cancer [J].
Taylor-Papadimitriou, Joyce ;
Burchell, Joy M. .
CELLS, 2022, 11 (07)
[86]   Chromatin remodeling by the histone methyltransferase EZH2 drives lung pre-malignancy and is a target for cancer prevention [J].
Tellez, Carmen S. ;
Picchi, Maria A. ;
Juri, Daniel ;
Do, Kieu ;
Desai, Dhimant H. ;
Amin, Shantu G. ;
Hutt, Julie A. ;
Filipczak, Piotr T. ;
Belinsky, Steven A. .
CLINICAL EPIGENETICS, 2021, 13 (01)
[87]   Mechanism-driven biomarkers to guide immune checkpoint blockade in cancer therapy [J].
Topalian, Suzanne L. ;
Taube, Janis M. ;
Anders, Robert A. ;
Pardoll, Drew M. .
NATURE REVIEWS CANCER, 2016, 16 (05) :275-287
[88]  
Tulpule A., 2020, Annu Rev Cancer Biol, V24, DOI [10.3389/fgene.2023.1120815, DOI 10.3389/FGENE.2023.1120815]
[89]   Histone H3K9 methyltransferase SETDB1 augments invadopodia formation to promote tumor metastasis [J].
Ueshima, Shuhei ;
Fang, Jia .
ONCOGENE, 2022, 41 (24) :3370-3380
[90]   2nd ESMO Consensus Conference on Lung Cancer: early-stage non-small-cell lung cancer consensus on diagnosis, treatment and follow-up [J].
Vansteenkiste, J. ;
Crino, L. ;
Dooms, C. ;
Douillard, J. Y. ;
Faivre-Finn, C. ;
Lim, E. ;
Rocco, G. ;
Senan, S. ;
Van Schil, P. ;
Veronesi, G. ;
Stahel, R. ;
Peters, S. ;
Felip, E. .
ANNALS OF ONCOLOGY, 2014, 25 (08) :1462-1474