Mesenchymal stem/stromal cells-derived IL-6 promotes nasopharyngeal carcinoma growth and resistance to cisplatin via upregulating CD73 expression

被引:41
作者
Zeng, Jincheng [1 ,2 ,3 ]
Chen, Shasha [1 ]
Li, Caihong [1 ,2 ]
Ye, Ziyu [1 ]
Lin, Bihua [1 ,2 ]
Liang, Yanfang [4 ]
Wang, Bin [1 ]
Ma, Yan [1 ]
Chai, Xingxing [6 ]
Zhang, Xin [1 ,5 ]
Zhou, Keyuan [1 ,2 ]
Zhang, Qunzhou [3 ]
Zhang, Haitao [1 ,2 ]
机构
[1] Guangdong Med Univ, Dongguan Key Lab Med Bioact Mol Dev & Translat Re, Guangdong Prov Key Lab Med Mol Diagnost, Dongguan 523808, Peoples R China
[2] Guangdong Med Univ, Dept Biochem & Mol Biol, Zhanjiang, Peoples R China
[3] Univ Penn, Sch Dent Med, Dept Oral & Maxillofacial Surg & Pharmacol, Philadelphia, PA 19104 USA
[4] Jinan Univ, Peoples Hosp Dongguan 1, Dongguan Hosp, Dept Pathol, Dongguan 523905, Peoples R China
[5] Guangdong Med Univ, Lab Anim Ctr, Zhanjiang 524023, Peoples R China
[6] Sun Yat Sen Univ, Affiliated Jiangmen Hosp, Jiangmen Cent Hosp, Clin Expt Ctr, Jiangmen 529030, Peoples R China
基金
中国国家自然科学基金;
关键词
nasopharyngeal carcinoma; mesenchymal stem/stromal cells; tumor microenvironment; IL-6; CD73; EPSTEIN-BARR-VIRUS; INTERLEUKIN-6; PROMOTES; TUMOR MICROENVIRONMENT; DIFFERENTIATION; MODULATION; SURVIVAL; RELEASE; CANCER; AXIS;
D O I
10.7150/jca.37932
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Previous studies have implicated the important role of mesenchymal stem/stromal cells (MSCs) within tumor microenvironment (TME) in the pathogenesis and progression of nasopharyngeal carcinoma (NPC), but the potential mechanisms are still unclear. Herein, we showed that an elevated IL-6 level was positively correlated with elevated expression of CD73 in TME of NPC. NPC specimens with an IL-6(high)CD73(high) phenotype showed higher expression levels of gp80, gp130, p-STAT3, MMP-9 and alpha-SMA, and clinically, a poorer prognosis than those with an IL-6(low)CD73(low) phenotype. We found that stimulation with conditioned media derived from IL-6 gene knocked out MSC (MSCIL6KO-CM) down-regulated the expression of CD73, IL-6, gp80, p-STAT3, and proliferative cell nuclear antigen (PCNA) in CNE-2 NPC cells. Meanwhile, NPC cells co-cultured with MSCIL6KO-CM were more sensitive to cisplatin than those co-cultured with MSC-CM. Additionally, MSC-derived IL-6 transcriptionally upregulated CD73 expression via activating STAT3 signaling pathway in NPC cells. In summary, our findings suggest that MSCs promote NPC progression and chemoresistance by upregulation of CD73 expression via activating STAT3 signaling pathway.
引用
收藏
页码:2068 / 2079
页数:12
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