Li Li-Ting, Zhao Fang-Fang, Jia Zhi-Mei, Qi Li-Qing, Zhang Xi-Zhu, Zhang Lu, Li Ying-Ying, Yang Jiao-Jiao, Wang Shu-Juan, Lin Hui, Liu Chun-Hao, An Dong-Dong, Huang Ya-Qiong, Gao Xiao-Ling
Second School of Clinical Medicine, Shanxi Medical University, Taiyuan 030001, Shanxi Province, P.R. China.
School of Basic Medicine, Shanxi Medical University, Taiyuan 030001, Shanxi Province, P.R. China.
Mol Ther Oncolytics. 2021 Oct 1;23:220-230. doi: 10.1016/j.omto.2021.09.007. eCollection 2021 Dec 17.
The progression of breast cancer is closely related to obstructive sleep apnea-hypopnea syndrome (OSAHS). Low concentrations of cannabinoids promote tumor proliferation. However, the role of cannabinoid receptors (CBs) in chronic intermittent hypoxia (CIH)-induced breast cancer has not been reported. The migration and invasion of breast cancer cell lines (MCF-7 and T47D) were measured by scratch assay and transwell assay. Gene and protein expressions were analyzed by qPCR and western blotting. Tumor xenograft mice model were established to evaluate the function of CBs. We observed that chronic hypoxia (CH) and CIH increased CBs expression and promoted migration and invasion in breast cancer. Mice grafted with MCF-7 exhibited obvious tumor growth, angiogenesis, and lung metastasis in CIH compared with CH and control. In addition, CIH induced CBs expression, which subsequently activated insulin-like growth factor-1 receptor (IGF-1R)/AKT/glycogen synthase kinase-3β (GSK-3β) axis. Knockdown of CBs alleviated CIH-induced migration and invasion of breast cancer . Furthermore, CIH exaggerated the malignancy of breast cancer and silencing of CBs suppressed tumor growth and metastasis . Our study contributed to understanding the role of CIH in breast cancer development modulation.
乳腺癌的进展与阻塞性睡眠呼吸暂停低通气综合征(OSAHS)密切相关。低浓度的大麻素会促进肿瘤增殖。然而,大麻素受体(CBs)在慢性间歇性缺氧(CIH)诱导的乳腺癌中的作用尚未见报道。通过划痕试验和Transwell试验检测乳腺癌细胞系(MCF-7和T47D)的迁移和侵袭能力。采用qPCR和蛋白质印迹法分析基因和蛋白表达。建立肿瘤异种移植小鼠模型以评估CBs的功能。我们观察到慢性缺氧(CH)和CIH会增加CBs的表达,并促进乳腺癌的迁移和侵袭。与CH组和对照组相比,接种MCF-7的小鼠在CIH条件下表现出明显的肿瘤生长、血管生成和肺转移。此外,CIH诱导CBs表达,随后激活胰岛素样生长因子-1受体(IGF-1R)/AKT/糖原合酶激酶-3β(GSK-3β)轴。敲低CBs可减轻CIH诱导的乳腺癌迁移和侵袭。此外,CIH会加剧乳腺癌的恶性程度,而沉默CBs可抑制肿瘤生长和转移。我们的研究有助于理解CIH在乳腺癌发展调控中的作用。