The State Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei- MOST) & Key Laboratory of Oral Biomedicine Ministry of Education, School & Hospital of Stomatology, Wuhan University, Wuhan, China.
Department of Oral Maxillofacial-Head Neck Oncology, School and Hospital of Stomatology, Wuhan University, Wuhan, China.
Oral Dis. 2021 Mar;27(2):204-214. doi: 10.1111/odi.13540. Epub 2020 Jul 30.
Ribonucleotide reductase M2 (RRM2) is a rate-limiting enzyme involved in DNA repair and synthesis. This study aimed to investigate the expression level, clinicopathological significance, and prognostic value of RRM2 in oral squamous cell carcinoma (OSCC).
Human OSCC tissue microarrays were used to detect the expression of RRM2, cancer stem cell (CSC) markers CD44 and aldehyde dehydrogenase 1 (ALDH1), and the epithelial-mesenchymal transition (EMT) marker Slug. The correlation of RRM2 expression with clinicopathological parameters was evaluated. The effects of RRM2 on cell proliferation, migration, and apoptosis were investigated.
Compared with normal and dysplastic tissues, the expression of RRM2 in human primary OSCC was significantly increased, and its overexpression was correlated with advanced pathological grade. The overall survival rate of patients with high RRM2 expression was lower than that of patients with low RRM2 expression. The overexpression of RRM2 was significantly associated with OSCC recurrence, and its overexpression was correlated with the CSC markers CD44 and ALDH1 and the EMT marker Slug. The expression of RRM2 promotes the proliferation and migration of human OSCC cells and inhibits apoptosis.
Ribonucleotide reductase M2 may be a novel target in the diagnosis, prognosis, and therapy of OSCC.
核苷酸还原酶 M2(RRM2)是一种参与 DNA 修复和合成的限速酶。本研究旨在探讨 RRM2 在口腔鳞状细胞癌(OSCC)中的表达水平、临床病理意义和预后价值。
使用人类 OSCC 组织微阵列检测 RRM2、癌症干细胞(CSC)标志物 CD44 和醛脱氢酶 1(ALDH1)以及上皮-间充质转化(EMT)标志物 Slug 的表达。评估 RRM2 表达与临床病理参数的相关性。研究 RRM2 对细胞增殖、迁移和凋亡的影响。
与正常和发育不良组织相比,RRM2 在人类原发性 OSCC 中的表达明显增加,其过表达与高级别病理相关。高 RRM2 表达患者的总生存率低于低 RRM2 表达患者。RRM2 的过表达与 OSCC 复发显著相关,其过表达与 CSC 标志物 CD44 和 ALDH1 以及 EMT 标志物 Slug 相关。RRM2 的表达促进了人类 OSCC 细胞的增殖和迁移,并抑制了细胞凋亡。
核苷酸还原酶 M2 可能是 OSCC 诊断、预后和治疗的新靶点。