Mesgari Hassan, Esmaelian Samar, Nasiri Kamyar, Ghasemzadeh Shabnam, Doroudgar Parisa, Payandeh Zahra
Oral and Maxillofacial Surgery Department, Faculty of Dentistry, Islamic Azad University Tehran Branch, Tehran 1148963537, Iran.
Faculty of Dentistry, Islamic Azad University Tehran Branch, Tehran 1148963537, Iran.
Cancers (Basel). 2023 Nov 27;15(23):5600. doi: 10.3390/cancers15235600.
Oral squamous cell carcinoma (OSCC) is a prevalent and significant type of oral cancer that has far-reaching health implications worldwide. Epigenetics, a field focused on studying heritable changes in gene expression without modifying DNA sequence, plays a pivotal role in OSCC. Epigenetic changes, encompassing DNA methylation, histone modifications, and miRNAs, exert control over gene activity and cellular characteristics. In OSCC, aberrant DNA methylation of tumor suppressor genes (TSG) leads to their inactivation, subsequently facilitating tumor growth. As a result, distinct patterns of gene methylation hold promise as valuable biomarkers for the detection of OSCC. Oral cancer treatment typically involves surgery, radiation therapy, and chemotherapy, but even with these treatments, cancer cells cannot be effectively targeted and destroyed. Researchers are therefore exploring new methods to target and eliminate cancer cells. One promising approach is the use of epigenetic modifiers, such as DNA methyltransferase (DNMT) inhibitors and histone deacetylase (HDAC) inhibitors, which have been shown to modify abnormal epigenetic patterns in OSCC cells, leading to the reactivation of TSGs and the suppression of oncogenes. As a result, epigenetic-targeted therapies have the potential to directly alter gene expression and minimize side effects. Several studies have explored the efficacy of such therapies in the treatment of OSCC. Although studies have investigated the efficacy of epigenetic therapies, challenges in identifying reliable biomarkers and developing effective combination treatments are acknowledged. Of note, epigenetic mechanisms play a significant role in drug resistance in OSCC and other cancers. Aberrant DNA methylation can silence tumor suppressor genes, while alterations in histone modifications and chromatin remodeling affect gene expression related to drug metabolism and cell survival. Thus, understanding and targeting these epigenetic processes offer potential strategies to overcome drug resistance and improve the efficacy of cancer treatments in OSCC. This comprehensive review focuses on the complex interplay between epigenetic alterations and OSCC cells. This will involve a deep dive into the mechanisms underlying epigenetic modifications and their impact on OSCC, including its initiation, progression, and metastasis. Furthermore, this review will present the role of epigenetics in the treatment and diagnosis of OSCC.
口腔鳞状细胞癌(OSCC)是一种常见且严重的口腔癌类型,在全球范围内对健康有着深远影响。表观遗传学是一个专注于研究基因表达的可遗传变化而不改变DNA序列的领域,在OSCC中起着关键作用。表观遗传变化包括DNA甲基化、组蛋白修饰和微小RNA(miRNA),它们控制着基因活性和细胞特征。在OSCC中,肿瘤抑制基因(TSG)的异常DNA甲基化导致其失活,进而促进肿瘤生长。因此,不同的基因甲基化模式有望成为检测OSCC的有价值生物标志物。口腔癌治疗通常包括手术、放射治疗和化疗,但即使采用这些治疗方法,癌细胞也无法被有效靶向和摧毁。因此,研究人员正在探索新的方法来靶向和消除癌细胞。一种有前景的方法是使用表观遗传修饰剂,如DNA甲基转移酶(DNMT)抑制剂和组蛋白去乙酰化酶(HDAC)抑制剂,这些已被证明可改变OSCC细胞中异常的表观遗传模式,导致TSG重新激活并抑制癌基因。因此,表观遗传靶向疗法有可能直接改变基因表达并将副作用降至最低。多项研究探讨了此类疗法在治疗OSCC中的疗效。尽管已有研究调查了表观遗传疗法的疗效,但人们认识到在确定可靠的生物标志物和开发有效的联合治疗方面仍存在挑战。值得注意的是,表观遗传机制在OSCC和其他癌症的耐药性中起重要作用。异常的DNA甲基化可使肿瘤抑制基因沉默,而组蛋白修饰和染色质重塑的改变会影响与药物代谢和细胞存活相关的基因表达。因此,了解并靶向这些表观遗传过程为克服耐药性和提高OSCC癌症治疗疗效提供了潜在策略。这篇综述聚焦于表观遗传改变与OSCC细胞之间的复杂相互作用。这将深入探究表观遗传修饰的潜在机制及其对OSCC的影响,包括其发生、发展和转移。此外,本综述还将阐述表观遗传学在OSCC治疗和诊断中的作用。