KMT2D: A key emerging epigenetic regulator in head and neck diseases and tumors

被引:0
作者
Wang, Kexin [1 ,2 ]
Zhan, Fang [1 ]
Yang, Xiaochen [2 ]
Jiao, Mengyu [1 ,3 ]
Wang, Peiyan [1 ,3 ]
Zhang, Hui [1 ,3 ]
Shang, Wei [2 ,3 ]
Deng, Jing [1 ,3 ,4 ]
Wang, Lin [2 ,3 ]
机构
[1] Qingdao Univ, Dept Oral Med, Affiliated Hosp, Qingdao 266000, Shandong, Peoples R China
[2] Qingdao Univ, Dept Oral & Maxillofacial Surg, Affiliated Hosp, Qingdao 266000, Shandong, Peoples R China
[3] Qingdao Univ, Sch Stomatol, Qingdao 266023, Peoples R China
[4] Dent Digital Med & 3D Printing Engn Lab Qingdao, Qingdao 266003, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
KMT2D; Histone; Kabuki syndrome; Cancer; PD-L1; Review; CANCER; DIFFERENTIATION; TRANSCRIPTION; METHYLATION; DISRUPTION; ENHANCERS; KDM6A;
D O I
10.1016/j.lfs.2025.123523
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Histone modifications are critical determinants of chromatin accessibility and gene expression, both of which are intrinsically linked to human development and disease. Lysine methyltransferase 2D (KMT2D), a prominent member of the H3K4 methyltransferase family, is ubiquitously expressed across human tissues. Recent studies have found that it can regulate gene expression and signal pathway opening and closing in more than one way, playing an important role in cell proliferation and cell cycle homeostasis. Although previous studies have identified KMT2D as a potentially pivotal factor in the development and pathology of head and neck tissues, the regulatory networks associated with KMT2D in various complex head and neck diseases remain incompletely elucidated. This review seeks to consolidate recent findings on KMT2D's involvement in head and neck diseases, thereby laying the groundwork for future research into its mechanistic role in disease progression. A deeper understanding of KMT2D's functions and regulatory mechanisms is essential for advancing our comprehension of histone modifications and for the development of diagnostic tools and targeted therapeutic strategies for head and neck diseases.
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页数:11
相关论文
共 98 条
  • [1] KMT2D Deficiency Impairs Super-Enhancers to Confer a Glycolytic Vulnerability in Lung Cancer
    Alam, Hunain
    Tang, Ming
    Maitituoheti, Mayinuer
    Dhar, Shilpa S.
    Kumar, Manish
    Han, Chae Young
    Ambati, Chandrashekar R.
    Amin, Samir B.
    Gu, Bingnan
    Chen, Tsai-Yu
    Lin, Yu-Hsi
    Chen, Jichao
    Muller, Florian L.
    Putluri, Nagireddy
    Flores, Elsa R.
    DeMayo, Francesco J.
    Baseler, Laura
    Rai, Kunal
    Lee, Min Gyu
    [J]. CANCER CELL, 2020, 37 (04) : 599 - +
  • [2] Alves L.D.F., 2015, J, Oncol. Rep., V33, P2017
  • [3] Cancer immunotherapy: the quest for better biomarkers
    不详
    [J]. NATURE MEDICINE, 2022, 28 (12) : 2437 - 2437
  • [4] [Anonymous], 2022, J. Cancer Med., V12, P7234
  • [5] [Anonymous], 2013, Clin. Genet., V84, P539
  • [6] [Anonymous], 2015, Hum. Mol. Genet., V24, P4443
  • [7] MLL4 is required after implantation, whereas MLL3 becomes essential during late gestation
    Ashokkumar, Deepthi
    Zhang, Qinyu
    Much, Christian
    Bledau, Anita S.
    Naumann, Ronald
    Alexopoulou, Dimitra
    Dahl, Andreas
    Goveas, Neha
    Fu, Jun
    Anastassiadis, Konstantinos
    Stewart, A. Francis
    Kranz, Andrea
    [J]. DEVELOPMENT, 2020, 147 (12):
  • [8] Genetic heterogeneity and enrichment of variants in DNA-repair genes in ameloblastoma
    Awotoye, Waheed
    Whitt, Joseph Craig
    Yoo, Byunggil
    Farooqi, Midhat S.
    Farrow, Emily G.
    Allareddy, Veerasathpurush
    Amendt, Brad A.
    Venugopalan, Shankar Rengasamy
    [J]. JOURNAL OF ORAL PATHOLOGY & MEDICINE, 2023, 52 (03) : 263 - 270
  • [9] Liquid biopsy epigenomic profiling for cancer subtyping
    Baca, Sylvan C.
    Seo, Ji-Heui
    Davidsohn, Matthew P.
    Fortunato, Brad
    Semaan, Karl
    Sotudian, Shahabbedin
    Lakshminarayanan, Gitanjali
    Diossy, Miklos
    Qiu, Xintao
    El Zarif, Talal
    Savignano, Hunter
    Canniff, John
    Madueke, Ikenna
    Saliby, Renee Maria
    Zhang, Ziwei
    Li, Rong
    Jiang, Yijia
    Taing, Len
    Awad, Mark
    Chau, Cindy H.
    Decaprio, James A.
    Figg, William D.
    Greten, Tim F.
    Hata, Aaron N.
    Hodi, F. Stephen
    Hughes, Melissa E.
    Ligon, Keith L.
    Lin, Nancy
    Ng, Kimmie
    Oser, Matthew G.
    Meador, Catherine
    Parsons, Heather A.
    Pomerantz, Mark M.
    Rajan, Arun
    Ritz, Jerome
    Thakuria, Manisha
    Tolaney, Sara M.
    Wen, Patrick Y.
    Long, Henry
    Berchuck, Jacob E.
    Szallasi, Zoltan
    Choueiri, Toni K.
    Freedman, Matthew L.
    [J]. NATURE MEDICINE, 2023, 29 (11) : 2737 - 2741
  • [10] Novel KDM6A (UTX) mutations and a clinical and molecular review of the X-linked Kabuki syndrome (KS2)
    Banka, S.
    Lederer, D.
    Benoit, V.
    Jenkins, E.
    Howard, E.
    Bunstone, S.
    Kerr, B.
    McKee, S.
    Lloyd, I. C.
    Shears, D.
    Stewart, H.
    White, S. M.
    Savarirayan, R.
    Mancini, G. M. S.
    Beysen, D.
    Cohn, R. D.
    Grisart, B.
    Maystadt, I.
    Donnai, D.
    [J]. CLINICAL GENETICS, 2015, 87 (03) : 252 - 258