Tunicamycin-induced endoplasmic reticulum stress inhibits chemoresistance of FaDu hypopharyngeal carcinoma cells in 3D collagen I cultures and in vivo

被引:8
作者
Gu, Cuirong [1 ]
Zhang, Yue [2 ]
Chen, Dan [1 ]
Liu, Huifen [1 ]
Mi, Kun [1 ]
机构
[1] Univ Elect Sci & Technol China, Sichuan Canc Hosp & Inst, Sichuan Canc Ctr, Sch Med,Radiat Oncol Key Lab Sichuan Prov, Chengdu, Peoples R China
[2] Univ Elect Sci & Technol China, Sichuan Canc Hosp & Inst, Sichuan Canc Ctr, Sch Med,Clin Lab, Chengdu, Peoples R China
基金
中国国家自然科学基金;
关键词
3D collagen I culture; Chemoresistance; Tunicamycin; Endoplasmic reticulum stress; FaDu hypopharyngeal carcinoma cell; CANCER STEM-CELL; GLYCOSYLATION; INTEGRIN; HEAD; PHENOTYPE; THERAPY; VITRO;
D O I
10.1016/j.yexcr.2021.112725
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The prognosis in patients with advanced head and neck squamous cell carcinoma (HNSCC) is widely affected by the resistance to chemotherapy. As a culture scaffold, collagen I was showed to promote CSC (cancer stem cell) properties of cancer cells which could be used as in vitro models to study the chemoresistance in HNSCC. Endoplasmic reticulum (ER) stress is a cellular stress condition which could affect tumor progression and promote the anti-tumor effects of certain drugs. However, the impact of ER stress on collagen I induced CSC properties and chemoresistance of HNSCC cells has not been addressed. In this study we investigated the effects of tunicamycin (TM) induced ER stress on the stemness and sensitivity to chemotherapeutic drugs of FaDu hypopharyngeal carcinoma cells in 3D (three-dimensional) collagen I cultures and mouse xenograft models. Our study revealed that Collagen I scaffold promoted CSC properties and increased G1 population of FaDu cells in 3D cultures, accompanied by maturation of integrin beta 1 and enhanced activated TGF-beta 1 concentration. Compared to 2D (two-dimensional) cultured cells, cells in 3D Collagen I scaffold exhibited significantly increased resistance to chemotherapeutic drugs of cisplatin and paclitaxel. Further analysis revealed that TM induced ER stress preferentially attenuated chemoresistance of FaDu cells in 3D collagen I, downregulated their CSC properties and TGF-beta 1 concentration and resulted in deglycosylation of integrin beta 1. TM was further evaluated in the mouse xenograft models and showed significant tumor growth inhibition in combination with paclitaxel than either TM or paclitaxel alone. Taken together, Our findings suggest that TM-induced ER stress potentiates anticancer efficacy of FaDu cells in 3D cultures and in vivo, and highlight implications for targeting chemotherapy-resistant cancer stem cells under ER stress conditions.
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页数:9
相关论文
共 44 条
[1]  
Bellis SL, 1999, J CELL PHYSIOL, V181, P33, DOI 10.1002/(SICI)1097-4652(199910)181:1<33::AID-JCP4>3.0.CO
[2]  
2-#
[3]   Variant glycosylation:: an underappreciated regulatory mechanism for β1 integrins [J].
Bellis, SL .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2004, 1663 (1-2) :52-60
[4]   Integrin β1 signaling is necessary for transforming growth factor-β activation of p38MAPK and epithelial plasticity [J].
Bhowmick, NA ;
Zent, R ;
Ghiassi, M ;
McDonnell, M ;
Moses, HL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (50) :46707-46713
[5]   β1 integrin function in vivo:: Adhesion, migration and more [J].
Brakebusch, C ;
Fässler, R .
CANCER AND METASTASIS REVIEWS, 2005, 24 (03) :403-411
[6]   Could 3D models of cancer enhance drug screening? [J].
Brancato, Virginia ;
Oliveira, Joaquim Miguel ;
Correlo, Vitor Manuel ;
Reis, Rui Luis ;
Kundu, Subhas C. .
BIOMATERIALS, 2020, 232
[7]  
Bray F, 2018, CA-CANCER J CLIN, V68, P394, DOI [10.3322/caac.21492, 10.3322/caac.21609]
[8]   Perspectives in chemosensitivity and chemoresistance assays and their implementation in head and neck cancer [J].
Bussmann, Lara ;
Busch, Chia-Jung ;
Loerincz, Balazs B. ;
Rieckmann, Thorsten ;
Block, Andreas ;
Knecht, Rainald .
EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY, 2016, 273 (12) :4073-4080
[9]   The enhancement of cancer stem cell properties of MCF-7 cells in 3D collagen scaffolds for modeling of cancer and anti-cancer drugs [J].
Chen, Lei ;
Xiao, Zhifeng ;
Meng, Yue ;
Zhao, Yannan ;
Han, Jin ;
Su, Guannan ;
Chen, Bing ;
Dai, Jianwu .
BIOMATERIALS, 2012, 33 (05) :1437-1444
[10]   Characterization of FaDu-R, a radioresistant head and neck cancer cell line, and cancer stem cells [J].
Cho, Kwang-Jae ;
Park, Eun-Ji ;
Kim, Min-Sik ;
Joo, Young-Hoon .
AURIS NASUS LARYNX, 2018, 45 (03) :566-573