MicroRNAs as mediators and communicators between cancer cells and the tumor microenvironment

被引:170
作者
Kohlhapp, F. J. [1 ]
Mitra, A. K. [2 ]
Lengyel, E. [3 ]
Peter, M. E. [1 ]
机构
[1] Northwestern Univ, Div Hematol Oncol, Feinberg Sch Med, Chicago, IL 60611 USA
[2] Indiana Univ, Indiana Univ Sch Med, Med Sci Program, Bloomington, IN USA
[3] Univ Chicago, Dept Gynecol & Obstet, Gynecol Oncol Sect, Chicago, IL 60637 USA
关键词
MESENCHYMAL STEM-CELLS; REGULATORY T-CELLS; GROWTH-FACTOR; HEPATOCELLULAR-CARCINOMA; STROMAL FIBROBLASTS; SUPPRESSOR-CELLS; DOWN-REGULATION; HUMAN BREAST; OVARIAN-CANCER; DUAL ROLE;
D O I
10.1038/onc.2015.89
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cancer cells grow in an environment comprised of multiple components that support tumor growth and contribute to therapy resistance. Major cell types in the tumor microenvironment are fibroblasts, endothelial cells and infiltrating immune cells all of which communicate with cancer cells. One way that these cell types promote cancer progression is by altering the expression of microRNAs (miRNAs), small noncoding RNAs that negatively regulate protein expression, either in the cancer cells or in the associated normal cells. Changes in miRNA expression can be brought about by direct interaction between the stromal cells and cancer cells, by paracrine factors secreted by any of the cell types or even through direct communication between cells through secreted miRNAs. Understanding the role of miRNAs in the complex interactions between the tumor and cells in its microenvironment is necessary if we are to understand tumor progression and devise new treatments.
引用
收藏
页码:5857 / 5868
页数:12
相关论文
共 116 条
[1]   The chemokine SDF-1 is a chemoattractant for human CD34(+) hematopoietic progenitor cells and provides a new mechanism to explain the mobilization of CD34(+) progenitors to peripheral blood [J].
Aiuti, A ;
Webb, IJ ;
Bleul, C ;
Springer, T ;
GutierrezRamos, JC .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (01) :111-120
[2]   Consensus Micro RNAs Governing the Switch of Dormant Tumors to the Fast-Growing Angiogenic Phenotype [J].
Almog, Nava ;
Ma, Lili ;
Schwager, Christian ;
Brinkmann, Bastian G. ;
Beheshti, Afshin ;
Vajkoczy, Peter ;
Folkman, Judah ;
Hlatky, Lynn ;
Abdollahi, Amir .
PLOS ONE, 2012, 7 (08)
[3]   Silencing of miR-148a in cancer-associated fibroblasts results in WNT10B-mediated stimulation of tumor cell motility [J].
Aprelikova, O. ;
Palla, J. ;
Hibler, B. ;
Yu, X. ;
Greer, Y. E. ;
Yi, M. ;
Stephens, R. ;
Maxwell, G. L. ;
Jazaeri, A. ;
Risinger, J. I. ;
Rubin, J. S. ;
Niederhuber, J. .
ONCOGENE, 2013, 32 (27) :3246-3253
[4]   The role of miR-31 and its target gene SATB2 in cancer-associated fibroblasts [J].
Aprelikova, Olga ;
Yu, Xiang ;
Palla, John ;
Wei, Bih-Rong ;
John, Simone ;
Yi, Ming ;
Stephens, Robert ;
Simpson, R. Mark ;
Risinger, John I. ;
Jazaeri, Amir ;
Niederhuber, John .
CELL CYCLE, 2010, 9 (21) :4387-4398
[5]   MicroRNAs Transfer from Human Macrophages to Hepato-Carcinoma Cells and Inhibit Proliferation [J].
Aucher, Anne ;
Rudnicka, Dominika ;
Davis, Daniel M. .
JOURNAL OF IMMUNOLOGY, 2013, 191 (12) :6250-6260
[6]   Embryonic Stem Cell-Specific miR302-367 Cluster: Human Gene Structure and Functional Characterization of Its Core Promoter [J].
Barroso-delJesus, Alicia ;
Romero-Lopez, Cristina ;
Lucena-Aguilar, Gema ;
Melen, Gustavo J. ;
Sanchez, Laura ;
Ligero, Gertrudis ;
Berzal-Herranz, Alfredo ;
Menendez, Pablo .
MOLECULAR AND CELLULAR BIOLOGY, 2008, 28 (21) :6609-6619
[7]   Reprogramming of the tumour microenvironment by stromal PTEN-regulated miR-320 [J].
Bronisz, A. ;
Godlewski, J. ;
Wallace, J. A. ;
Merchant, A. S. ;
Nowicki, M. O. ;
Mathsyaraja, H. ;
Srinivasan, R. ;
Trimboli, A. J. ;
Martin, C. K. ;
Li, F. ;
Yu, L. ;
Fernandez, S. A. ;
Pecot, T. ;
Rosol, T. J. ;
Cory, S. ;
Hallett, M. ;
Park, M. ;
Piper, M. G. ;
Marsh, C. B. ;
Yee, L. D. ;
Jimenez, R. E. ;
Nuovo, G. ;
Lawler, S. E. ;
Chiocca, E. A. ;
Leone, G. ;
Ostrowski, M. C. .
NATURE CELL BIOLOGY, 2012, 14 (02) :159-167
[8]   Extracellular Vesicles Modulate the Glioblastoma Microenvironment via a Tumor Suppression Signaling Network Directed by miR-1 [J].
Bronisz, Agnieszka ;
Wang, Yan ;
Nowicki, Michal O. ;
Peruzzi, Pierpaolo ;
Ansari, Khairul I. ;
Ogawa, Daisuke ;
Balaj, Leonora ;
De Rienzo, Gianluca ;
Mineo, Marco ;
Nakano, Ichiro ;
Ostrowski, Michael C. ;
Hochberg, Fred ;
Weissleder, Ralph ;
Lawler, Sean E. ;
Chiocca, E. Antonio ;
Godlewski, Jakub .
CANCER RESEARCH, 2014, 74 (03) :738-750
[9]   Pleiotropic actions of miR-21 highlight the critical role of deregulated stromal microRNAs during colorectal cancer progression [J].
Bullock, M. D. ;
Pickard, K. M. ;
Nielsen, B. S. ;
Sayan, A. E. ;
Jenei, V. ;
Mellone, M. ;
Mitter, R. ;
Primrose, J. N. ;
Thomas, G. J. ;
Packham, G. K. ;
Mirenzami, A. H. .
CELL DEATH & DISEASE, 2013, 4 :e684-e684
[10]   Re-polarization of tumor-associated macrophages to pro-inflammatory M1 macrophages by microRNA-155 [J].
Cai, Xing ;
Yin, Yuan ;
Li, Ningzhu ;
Zhu, Dihan ;
Zhang, Junfeng ;
Zhang, Chen-Yu ;
Zen, Ke .
JOURNAL OF MOLECULAR CELL BIOLOGY, 2012, 4 (05) :341-343