Exosomes Derived from Squamous Head and Neck Cancer Promote Cell Survival after Ionizing Radiation

被引:142
作者
Mutschelknaus, Lisa [1 ]
Peters, Carsten [2 ]
Winkler, Klaudia [1 ]
Yentrapalli, Ramesh [1 ]
Heider, Theresa [1 ]
Atkinson, Michael John [1 ,3 ]
Moertl, Simone [1 ]
机构
[1] Helmholtz Zentrum mUNCHEN, German Res Ctr Environm Hlth, Inst Radiat Biol, Neuherberg, Germany
[2] Tech Univ Munich, Dept Chem, D-80290 Munich, Germany
[3] Tech Univ Munich, Radiat Biol, D-80290 Munich, Germany
来源
PLOS ONE | 2016年 / 11卷 / 03期
关键词
MESSENGER-RNAS; MICROVESICLES; MICRORNAS; MICROENVIRONMENT; PROLIFERATION; MECHANISM; THERAPY;
D O I
10.1371/journal.pone.0152213
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Exosomes are nanometer-sized extracellular vesicles that are believed to function as intercellular communicators. Here, we report that exosomes are able to modify the radiation response of the head and neck cancer cell lines BHY and FaDu. Exosomes were isolated from the conditioned medium of irradiated as well as non-irradiated head and neck cancer cells by serial centrifugation. Quantification using NanoSight technology indicated an increased exosome release from irradiated compared to non-irradiated cells 24 hours after treatment. To test whether the released exosomes influence the radiation response of other cells the exosomes were transferred to non-irradiated and irradiated recipient cells. We found an enhanced uptake of exosomes isolated from both irradiated and non-irradiated cells by irradiated recipient cells compared to non-irradiated recipient cells. Functional analyses by exosome transfer indicated that all exosomes (from non-irradiated and irradiated donor cells) increase the proliferation of non-irradiated recipient cells and the survival of irradiated recipient cells. The survival-promoting effects are more pronounced when exosomes isolated from irradiated compared to non-irradiated donor cells are transferred. A possible mechanism for the increased survival after irradiation could be the increase in DNA doublestrand break repair monitored at 6, 8 and 10 h after the transfer of exosomes isolated from irradiated cells. This is abrogated by the destabilization of the exosomes. Our results demonstrate that radiation influences both the abundance and action of exosomes on recipient cells. Exosomes transmit prosurvival effects by promoting the proliferation and radioresistance of head and neck cancer cells. Taken together, this study indicates a functional role of exosomes in the response of tumor cells to radiation exposure within a therapeutic dose range and encourages that exosomes are useful objects of study for a better understanding of tumor radiation response.
引用
收藏
页数:16
相关论文
共 32 条
[1]   Intergroup phase III comparison of standard radiation therapy and two schedules of concurrent chemoradiotherapy in patients with unresectable squamous cell head and neck cancer [J].
Adelstein, DJ ;
Li, Y ;
Adams, GL ;
Wagner, H ;
Kish, JA ;
Ensley, JF ;
Schuller, DE ;
Forastiere, AA .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (01) :92-98
[2]   The non-targeted effects of radiation are perpetuated by exosomes [J].
Al-Mayah, Ammar ;
Bright, Scott ;
Chapman, Kim ;
Irons, Sarah ;
Luo, Ping ;
Carter, David ;
Goodwin, Edwin ;
Kadhim, Munira .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2015, 772 :38-45
[3]   Possible Role of Exosomes Containing RNA in Mediating Nontargeted Effect of Ionizing Radiation [J].
Al-Mayah, Ammar H. J. ;
Irons, Sarah L. ;
Pink, Ryan C. ;
Carter, David R. F. ;
Kadhim, Munira A. .
RADIATION RESEARCH, 2012, 177 (05) :539-545
[4]   Intercellular transfer of the oncogenic receptor EGFrvIII by microvesicles derived from tumour cells [J].
Al-Nedawi, Khalid ;
Meehan, Brian ;
Micallef, Johann ;
Lhotak, Vladimir ;
May, Linda ;
Guha, Abhijit ;
Rak, Janusz .
NATURE CELL BIOLOGY, 2008, 10 (05) :619-U24
[5]   Ionizing Radiation and Glioblastoma Exosomes: Implications in Tumor Biology and Cell Migration [J].
Arscott, W. Tris ;
Tandle, Anita T. ;
Zhao, Shuping ;
Shabason, Jacob E. ;
Gordon, Ira K. ;
Schlaff, Cody D. ;
Zhang, Guofeng ;
Tofilon, Philip J. ;
Camphausen, Kevin A. .
TRANSLATIONAL ONCOLOGY, 2013, 6 (06) :638-U254
[6]   Tumour exosomes inhibit binding of tumour-reactive antibodies to tumour cells and reduce ADCC [J].
Battke, Christina ;
Ruiss, Romana ;
Welsch, Ulrich ;
Wimberger, Pauline ;
Lang, Stephan ;
Jochum, Simon ;
Zeidler, Reinhard .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 2011, 60 (05) :639-648
[7]   Exosomes from docetaxel-resistant breast cancer cells alter chemosensitivity by delivering microRNAs [J].
Chen, Wei-xian ;
Cai, Yan-qin ;
Lv, Meng-meng ;
Chen, Lin ;
Zhong, Shan-liang ;
Ma, Teng-fei ;
Zhao, Jian-hua ;
Tang, Jin-hai .
TUMOR BIOLOGY, 2014, 35 (10) :9649-9659
[8]   Exosomes secreted from human colorectal cancer cell lines contain mRNAs, microRNAs and natural antisense RNAs, that can transfer into the human hepatoma HepG2 and lung cancer A549 cell lines [J].
Chiba, Mitsuru ;
Kimura, Misako ;
Asari, Saya .
ONCOLOGY REPORTS, 2012, 28 (05) :1551-1558
[9]   Potential role of HER2-overexpressing exosomes in countering trastuzumab-based therapy [J].
Ciravolo, Valentina ;
Huber, Veronica ;
Ghedini, Gaia C. ;
Venturelli, Elisabetta ;
Bianchi, Francesca ;
Campiglio, Manuela ;
Morelli, Daniele ;
Villa, Antonello ;
Della Mina, Pamela ;
Menard, Sylvie ;
Filipazzi, Paola ;
Rivoltini, Licia ;
Tagliabue, Elda ;
Pupa, Serenella M. .
JOURNAL OF CELLULAR PHYSIOLOGY, 2012, 227 (02) :658-667
[10]   Docetaxel-Resistance in Prostate Cancer: Evaluating Associated Phenotypic Changes and Potential for Resistance Transfer via Exosomes [J].
Corcoran, Claire ;
Rani, Sweta ;
O'Brien, Keith ;
O'Neill, Amanda ;
Prencipe, Maria ;
Sheikh, Rizwan ;
Webb, Glenn ;
McDermott, Ray ;
Watson, William ;
Crown, John ;
O'Driscoll, Lorraine .
PLOS ONE, 2012, 7 (12)