Fibroblast-Derived Exosomes Contribute to Chemoresistance through Priming Cancer Stem Cells in Colorectal Cancer

被引:292
作者
Hu, Yibing [1 ,2 ]
Yan, Chang [1 ,2 ]
Mu, Lei [1 ,2 ]
Huang, Kaiyu [1 ,2 ]
Li, Xiaolan [2 ]
Tao, Deding [2 ]
Wu, Yaqun [1 ]
Qin, Jichao [1 ,2 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Tongji Hosp, Dept Surg, Wuhan 430074, Peoples R China
[2] Huazhong Univ Sci & Technol, Tongji Med Coll, Tongji Hosp, Mol Med Ctr, Wuhan 430074, Peoples R China
基金
中国国家自然科学基金;
关键词
DRUG-RESISTANCE; BETA-CATENIN; ACTIVATION PROTEIN; TUMOR-GROWTH; CHEMOTHERAPY; POPULATION; EXPRESSION; PHENOTYPE; MECHANISM; EXCHANGE;
D O I
10.1371/journal.pone.0125625
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
Chemotherapy resistance observed in patients with colorectal cancer (CRC) may be related to the presence of cancer stem cells (CSCs), but the underlying mechanism(s) remain unclear. Carcinoma-associated fibroblasts (CAFs) are intimately involved in tumor recurrence, and targeting them increases chemo-sensitivity. We investigated whether fibroblasts might increase CSCs thus mediating chemotherapy resistance. CSCs were isolated from either patient-derived xenografts or CRC cell lines based on expression of CD133. First, CSCs were found to be inherently resistant to cell death induced by chemotherapy. In addition, fibroblast-derived conditioned medium (CM) promoted percentage, clonogenicity and tumor growth of CSCs (i.e., CD133+ and TOP-GFP+) upon treatment with 5-fluorouracil (5-Fu) or oxaliplatin (OXA). Further investigations exhibited that exosomes, isolated from CM, similarly took the above effects. Inhibition of exosome secretion decreased the percentage, clonogenicity and tumor growth of CSCs. Altogether, our findings suggest that, besides targeting CSCs, new therapeutic strategies blocking CAFs secretion even before chemotherapy shall be developed to gain better clinical benefits in advanced CRCs.
引用
收藏
页数:17
相关论文
共 43 条
[1]  
[Anonymous], 2020, CA Cancer J Clin, DOI DOI 10.3322/CAAC.21590
[2]   Exosome Transfer from Stromal to Breast Cancer Cells Regulates Therapy Resistance Pathways [J].
Boelens, Mirjam C. ;
Wu, Tony J. ;
Nabet, Barzin Y. ;
Xu, Bihui ;
Qiu, Yu ;
Yoon, Taewon ;
Azzam, Diana J. ;
Victor, Christina Twyman-Saint ;
Wiemann, Brianne Z. ;
Ishwaran, Hemant ;
ter Brugge, Petra J. ;
Jonkers, Jos ;
Slingerland, Joyce ;
Minn, Andy J. .
CELL, 2014, 159 (03) :499-513
[3]   Variable β-catenin expression in colorectal cancers indicates tumor progression driven by the tumor environment [J].
Brabletz, T ;
Jung, A ;
Reu, S ;
Porzner, M ;
Hlubek, F ;
Kunz-Schughart, LA ;
Knuechel, R ;
Kirchner, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (18) :10356-10361
[4]   Targeting Carcinoma-Associated Fibroblasts Within the Tumor Stroma With a Fibroblast Activation Protein-Activated Prodrug [J].
Brennen, W. Nathaniel ;
Rosen, D. Marc ;
Wang, Hao ;
Isaacs, John T. ;
Denmeade, Samuel R. .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2012, 104 (17) :1320-1334
[5]   Exosome release of β-catenin: a novel mechanism that antagonizes Wnt signaling [J].
Chairoungdua, Arthit ;
Smith, Danielle L. ;
Pochard, Pierre ;
Hull, Michael ;
Caplan, Michael J. .
JOURNAL OF CELL BIOLOGY, 2010, 190 (06) :1079-1091
[6]   Chemoresistant Colorectal Cancer Cells, the Cancer Stem Cell Phenotype, and Increased Sensitivity to Insulin-like Growth Factor-I Receptor Inhibition [J].
Dallas, Nikolaos A. ;
Xia, Ling ;
Fan, Fan ;
Gray, Michael J. ;
Gaur, Puja ;
van Buren, George, II ;
Samuel, Shaija ;
Kim, Michael P. ;
Lim, Sherry J. ;
Ellis, Lee M. .
CANCER RESEARCH, 2009, 69 (05) :1951-1957
[7]   Chemotherapy Alters Monocyte Differentiation to Favor Generation of Cancer-Supporting M2 Macrophages in the Tumor Microenvironment [J].
Dijkgraaf, Eveline M. ;
Heusinkveld, Moniek ;
Tummers, Bart ;
Vogelpoel, Lisa T. C. ;
Goedemans, Renske ;
Jha, Veena ;
Nortier, Johan W. R. ;
Welters, Marij J. P. ;
Kroep, Judith R. ;
van der Burg, Sjoerd H. .
CANCER RESEARCH, 2013, 73 (08) :2480-2492
[8]   Colorectal Cancer Stem Cells Are Enriched in Xenogeneic Tumors Following Chemotherapy [J].
Dylla, Scott J. ;
Beviglia, Lucia ;
Park, In-Kyung ;
Chartier, Cecile ;
Raval, Janak ;
Ngan, Lucy ;
Pickell, Kellie ;
Aguilar, Jorge ;
Lazetic, Sasha ;
Smith-Berdan, Stephanie ;
Clarke, Michael F. ;
Hoey, Tim ;
Lewicki, John ;
Gurney, Austin L. .
PLOS ONE, 2008, 3 (06)
[9]   The Stem Cell Marker CD133 Associates with Enhanced Colony Formation and Cell Motility in Colorectal Cancer [J].
Elsaba, Tarek M. A. ;
Martinez-Pomares, Luisa ;
Robins, Adrian R. ;
Crook, Simon ;
Seth, Rashmi ;
Jackson, Darryl ;
McCart, Amy ;
Silver, Andrew R. ;
Tomlinson, Ian P. M. ;
Ilyas, Mohammad .
PLOS ONE, 2010, 5 (05)
[10]   The requirement for freshly isolated human colorectal cancer (CRC) cells in isolating CRC stem cells [J].
Fan, F. ;
Bellister, S. ;
Lu, J. ;
Ye, X. ;
Boulbes, D. R. ;
Tozzi, F. ;
Sceusi, E. ;
Kopetz, S. ;
Tian, F. ;
Xia, L. ;
Zhou, Y. ;
Bhattacharya, R. ;
Ellis, L. M. .
BRITISH JOURNAL OF CANCER, 2015, 112 (03) :539-546