Mesenchymal stem cells enhance lung cancer initiation through activation of IL-6/JAK2/STAT3 pathway

被引:72
作者
Hsu, Han-Shui [1 ,2 ]
Lin, Jiun-Han [1 ]
Hsu, Tien-Wei [1 ]
Su, Kelly [1 ]
Wang, Cheng-Wien [3 ]
Yang, Kuang-Yao [4 ]
Chiou, Shih-Hwa [5 ,6 ]
Hung, Shih-Chieh [5 ,6 ,7 ]
机构
[1] Natl Yang Ming Univ, Sch Med, Inst Emergency & Crit Care Med, Taipei 112, Taiwan
[2] Taipei Vet Gen Hosp, Dept Surg, Div Thorac Surg, Taipei, Taiwan
[3] Ton Yen Gen Hosp, Dept Orthoped, Hsinchu, Taiwan
[4] Natl Yang Ming Univ, Sch Med, Taipei Vet Gen Hosp, Dept Chest Med, Taipei 112, Taiwan
[5] Natl Yang Ming Univ, Sch Med, Inst Clin Med, Taipei 112, Taiwan
[6] Taipei Vet Gen Hosp, Dept Med Res & Educ, Stem Cell Lab, Taipei, Taiwan
[7] Natl Yang Ming Univ, Sch Med, Inst Pharmacol, Taipei 112, Taiwan
关键词
IL6; JAK2; STAT3; Lung cancer; Mesenchymal stem cell; Tumor initiation; STAT3; ACTIVATION; STROMAL CELLS; INTERLEUKIN-6; FIBROBLASTS; IL-6; DIFFERENTIATION; CARCINOMA; CONTRIBUTES; RECRUITMENT; TRANSITION;
D O I
10.1016/j.lungcan.2011.07.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The role of mesenchymal stem cells (MSCs) and IL-6 in lung cancer has not been well-addressed. We aimed to determine if MSCs can enhance the ability of tumor initiation of lung cancer cells, and link MSCs with activation of the IL-6/JAK2/STAT3 signaling pathway. Materials and methods: Lung cancer cell lines A549 and CL1-5 were directly or indirectly cocultured with MSCs. Spheres were defined as cell colonies with >50% area showing 3-dimensional structure and blurred cell margins. Cells without and with MSCs were injected into NOD/SCID mice. The percentage of tumor formation was determined. The influence of the IL-6/JAK2/STAT3 signaling pathway in cancer cell sphere formation and tumor growth were investigated. Results: A very small number of lung cancer cells, when mixed with otherwise non-tumorigenic MSCs, obtained de novo tumorigenicity when injected subcutaneously and allowed to form a tumor xenograft. Secretion of IL-6 from MSCs increased activation of the JAK2/STAT3 pathway in cancer cells, and enhanced sphere formation and tumor initiation. A reduced capacity of tumor formation of A549 and CL1-5 lung cancer cells when IL-6 was inhibited in MSCs or STAT3 was silenced in A549 and CL1-5 admixed with MSCs. Conclusions: Culture of A549 or CL1-5 lung cancer cells with MSCs increased sphere formation, drug resistance, and overexpression of pluripotency markers through activation of the IL-6/JAK2/STAT3 pathway. MSCs enhanced the capability of A549 and CL1-5 lung cancer cells to form tumors in immunodeficient mice. Blockade of the IL-6/JAK2/STAT3 pathway attenuated the capability of A549 and CL1-5 cells to form tumors. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:167 / 177
页数:11
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