Xiao Ming Zhu, Fu Jin Yin, Bo Le Tao, Li Yi Dong, Lin Zhong Wei, Chen Zhe Sheng
Key Laboratory of Pharmaceutical Bioactive Substances, School of Traditional Chinese Medicine, Guangdong Pharmaceutical University, Guangzhou, China.
Department of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, St. John's University, Queens, NY, USA.
Discov Oncol. 2024 Dec 20;15(1):816. doi: 10.1007/s12672-024-01696-5.
As neoplastic cells proliferate, disseminate, and infiltrate, they undergo substantial alterations in their epigenetic configuration. Among the pivotal enzymes implicated in this phenomenon is the AlkB family of demethylases, notably AlkB homolog 1 (ALKBH1), which demonstrates conspicuous upregulation across various malignancies. The heightened expression of ALKBH1 renders it a compelling candidate for the development of multifaceted anticancer modalities. Despite the commendable progress achieved by investigators in elucidating the perturbations associated with ALKBH1 in malignant tissues, a comprehensive mechanism remains elusive. The present study endeavors to address this lacuna by synthesizing recent advancements pertaining to ALKBH1's involvement in oncogenesis over the preceding decade. Therefore, this research not only furnishes novel insights but also establishes a foundation for prospective initiatives aimed at cancer prophylaxis and therapeutics that exploit epigenetic regulatory mechanisms.
随着肿瘤细胞的增殖、扩散和浸润,它们的表观遗传构型会发生显著改变。参与这一现象的关键酶中包括去甲基化酶的AlkB家族,特别是AlkB同源物1(ALKBH1),它在各种恶性肿瘤中均表现出明显上调。ALKBH1的高表达使其成为开发多方面抗癌模式的有力候选对象。尽管研究人员在阐明恶性组织中与ALKBH1相关的扰动方面取得了值得称赞的进展,但全面的机制仍不清楚。本研究试图通过综合过去十年中有关ALKBH1参与肿瘤发生的最新进展来填补这一空白。因此,本研究不仅提供了新的见解,还为旨在利用表观遗传调控机制进行癌症预防和治疗的前瞻性举措奠定了基础。