Second School of Clinical Medicine, Southern Medical University, Guangzhou, Guangdong, China.
Department of Otorhinolaryngology, Guangdong Provincial People's Hospital & Guangdong Academy of Medical Sciences, No.106, Zhongshan Er Road, Guangzhou, 510080, Guangdong Province, China.
BMC Cancer. 2019 Aug 27;19(1):840. doi: 10.1186/s12885-019-6029-y.
Advanced stage laryngeal squamous cell carcinoma (LSCC) presents a poor prognosis; thus, there is a great need to identify novel prognostic molecular markers. Procollagen-lysine, 2-oxoglutarate 5-dioxygenase 2 (PLOD2) is thought to be a novel prognostic factor in several cancers, but its role in LSCC remains unknown. Cancer stem cells (CSCs) are responsible for most instances of tumor recurrence and the development of drug resistance and have been proven to be present in head and neck cancers. Our preliminary study indicated that PLOD2 was elevated in LSCC tissues; therefore, we hypothesized that PLOD2 is related to the prognosis of LSCC patients and aimed to explore the role and underlying mechanism of PLOD2 in LSCC.
We validated the prognostic role of PLOD2 in 114 LSCC patients by immunohistochemistry. Stable PLOD2-overexpressing Hep-2 and FaDu cells were established and assessed by molecular biology and biochemistry methods both in vitro and in vivo.
We confirmed that PLOD2 overexpression was correlated with poor prognosis in LSCC patients. PLOD2 overexpression strengthened the CSC-like properties of Hep-2 and FaDu cells, activated the Wnt signaling pathway and conferred drug resistance in LSCC in vitro and in vivo.
We found that PLOD2 could serve as a prognostic marker in patients with LSCC and confer drug resistance in LSCC by increasing CSC-like traits; in addition, a Wnt-responsive CSC pathway was identified.
晚期喉鳞状细胞癌(LSCC)预后较差;因此,迫切需要鉴定新的预后分子标志物。脯氨酰-赖氨酸,2-氧戊二酸 5-双加氧酶 2(PLOD2)被认为是几种癌症的新型预后因素,但它在 LSCC 中的作用尚不清楚。癌症干细胞(CSCs)是导致大多数肿瘤复发和耐药性发展的原因,并且已被证明存在于头颈部癌症中。我们的初步研究表明 PLOD2 在 LSCC 组织中升高;因此,我们假设 PLOD2 与 LSCC 患者的预后有关,并旨在探讨 PLOD2 在 LSCC 中的作用及其潜在机制。
我们通过免疫组织化学验证了 PLOD2 在 114 例 LSCC 患者中的预后作用。通过分子生物学和生物化学方法,在体外和体内稳定过表达 PLOD2 的 Hep-2 和 FaDu 细胞进行了评估。
我们证实 PLOD2 的过表达与 LSCC 患者的不良预后相关。PLOD2 的过表达增强了 Hep-2 和 FaDu 细胞的 CSC 样特性,激活了 Wnt 信号通路,并在体外和体内赋予了 LSCC 耐药性。
我们发现 PLOD2 可作为 LSCC 患者的预后标志物,并通过增加 CSC 样特征赋予 LSCC 耐药性;此外,还确定了一个 Wnt 反应性 CSC 途径。