Department of Medical Oncology, Guangzhou First People's Hospital, School of Medicine, South China University of Technology, Guangzhou, Guangdong, China, 510180.
Department of Medical Oncology, Guangzhou First People's Hospital, Guangzhou Medical University, Guangzhou, Guangdong, China, 510180.
Int J Med Sci. 2020 May 18;17(9):1257-1268. doi: 10.7150/ijms.44285. eCollection 2020.
: IL-1β is reported to be involved in cancer development and distant metastasis. However, the underlying mechanism of IL-1β upon malignant behaviors remains largely unknown. In this study, we aimed to study whether IL-1β could enhance the stemness traits of tumor cells. : The concentrations of serum IL-1β in head and neck squamous cell carcinoma (HNSCC) and melanoma patients were detected using ELISA assay. The effect and mechanisms of IL-1β on tumor cell growth, migration, invasion and stemness characters were studied using HNSCC cell SCC7 and melanoma cell B16-F10. The underlying mechanisms were further explored. : Enhanced concentrations of IL-1β were positively correlated with advanced tumor stage in both HNSCC and melanoma patients. IL-1β treatment led to a significant increase in tumor growth both in vitro and in vivo. IL-1β stimulation promoted cell proliferation, colony formation and tumorigenicity. In addition, IL-1β-stimulated tumor cells gained enhanced capabilities on wounding healing and invasion capabilities. Moreover, IL-1β stimulation promoted the stem-like capabilities of both HNSCC cells and melanoma cells, including the enrichment of aldehyde dehydrogenase (ALDH) cells, up-regulation of stem cell related markers Nanog, OCT4, and SOX2, sphere formation and chemoresistance. Mechanistically, IL-1β treatment promoted the phosphorylation of Smad1/5/8 and activated its downstream target inhibitor of differentiation 1 (ID1). Silencing ID1 abrogated sphere formation and upregulated expression of stemness genes which were induced by IL-1β stimulation. : Our data demonstrates that IL-1β promotes the stemness of HNSCC and melanoma cells through activating Smad/ID1 signal pathway.
白细胞介素-1β(IL-1β)被报道参与癌症的发生和远处转移。然而,IL-1β 对恶性行为的潜在机制在很大程度上仍不清楚。在这项研究中,我们旨在研究 IL-1β 是否可以增强肿瘤细胞的干性特征。
采用 ELISA 法检测头颈部鳞状细胞癌(HNSCC)和黑色素瘤患者血清中 IL-1β 的浓度。采用 HNSCC 细胞 SCC7 和黑色素瘤细胞 B16-F10 研究 IL-1β 对肿瘤细胞生长、迁移、侵袭和干性特征的影响及其机制,并进一步探讨其潜在机制。
结果显示,HNSCC 和黑色素瘤患者中,增强的 IL-1β 浓度与肿瘤晚期阶段呈正相关。IL-1β 处理在体外和体内均显著促进肿瘤生长。IL-1β 刺激促进细胞增殖、集落形成和致瘤性。此外,IL-1β 刺激的肿瘤细胞在创伤愈合和侵袭能力方面获得了增强的能力。此外,IL-1β 刺激促进了 HNSCC 细胞和黑色素瘤细胞的干性特征,包括醛脱氢酶(ALDH)细胞的富集、干细胞相关标记物 Nanog、OCT4 和 SOX2 的上调、球体形成和化疗耐药性。
机制上,IL-1β 处理促进了 Smad1/5/8 的磷酸化,并激活了其下游靶基因分化抑制因子 1(ID1)。沉默 ID1 可阻断由 IL-1β 刺激诱导的球体形成,并上调干性基因的表达。
本研究表明,IL-1β 通过激活 Smad/ID1 信号通路促进 HNSCC 和黑色素瘤细胞的干性。