Bring along your friends: Homotypic and heterotypic circulating tumor cell clustering to accelerate metastasis

被引:67
作者
Aceto, Nicola [1 ,2 ]
机构
[1] Univ Basel, Dept Biomed, Canc Metastasis Lab, Basel, Switzerland
[2] Univ Hosp Basel, Spitalstr 21, CH-4031 Basel, Switzerland
基金
欧洲研究理事会; 瑞士国家科学基金会;
关键词
Circulating tumor cells; Circulating tumor cell clusters; Metastasis; Cell-cell interactions; Liquid biopsy; BREAST-CANCER; CLINICAL-SIGNIFICANCE; PERIPHERAL-BLOOD; E-CADHERIN; TRANSITION; EMBOLISM; ROUTE; SIZE;
D O I
10.1016/j.bj.2019.11.002
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
Metastasis formation is a hallmark of invasive cancers and it is achieved through the shedding of circulating tumor cells (CTCs) from the primary site into the blood circulation. There, CTCs are found as single cells or as multicellular clusters, with clusters carrying an elevated ability to survive within the bloodstream and initiate new metastatic lesions at distant sites. Clusters of CTCs include homotypic clusters made of cancer cells only, as well as heterotypic clusters that incorporate stromal or immune cells along with cancer cells. Both homotypic and heterotypic CTC clusters are characterized by a high metastasis-forming capability, high proliferation rate and by distinct molecular features compared to single CTCs, and their presence in the peripheral circulation of cancer patients is generally associated with a poor prognosis. In this short review, we summarize the current literature that describes homotypic and heterotypic CTC clusters, both in the context of their molecular characteristics as well as their value in the clinical setting. While CTC clusters have only recently emerged as key players in the metastatic process and many aspects of their biology remain to be investigated, a detailed understanding of their vulnerabilities may pave the way towards the generation of new metastasis-suppressing agents.
引用
收藏
页码:18 / 23
页数:6
相关论文
共 51 条
[1]   En Route to Metastasis: Circulating Tumor Cell Clusters and Epithelial-to-Mesenchymal Transition [J].
Aceto, Nicola ;
Toner, Mehmet ;
Maheswaran, Shyamala ;
Haber, Daniel A. .
TRENDS IN CANCER, 2015, 1 (01) :44-52
[2]   Circulating Tumor Cell Clusters Are Oligoclonal Precursors of Breast Cancer Metastasis [J].
Aceto, Nicola ;
Bardia, Aditya ;
Miyamoto, David T. ;
Donaldson, Maria C. ;
Wittner, Ben S. ;
Spencer, Joel A. ;
Yu, Min ;
Pely, Adam ;
Engstrom, Amanda ;
Zhu, Huili ;
Brannigan, Brian W. ;
Kapur, Ravi ;
Stott, Shannon L. ;
Shioda, Toshi ;
Ramaswamy, Sridhar ;
Ting, David T. ;
Lin, Charles P. ;
Toner, Mehmet ;
Haber, Daniel A. ;
Maheswaran, Shyamala .
CELL, 2014, 158 (05) :1110-1122
[3]   Clusters of circulating tumor cells traverse capillary-sized vessels [J].
Au, Sam H. ;
Storey, Brian D. ;
Moore, John C. ;
Tang, Qin ;
Chen, Yeng-Long ;
Javaid, Sarah ;
Sarioglu, A. Fatih ;
Sullivan, Ryan ;
Madden, Marissa W. ;
O'Keefe, Ryan ;
Haber, Daniel A. ;
Maheswaran, Shyamala ;
Langenau, David M. ;
Stott, Shannon L. ;
Toner, Mehmet .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2016, 113 (18) :4947-4952
[4]  
Brandt B, 1996, CANCER RES, V56, P4556
[5]  
Chan C K, 1987, J Thorac Imaging, V2, P4, DOI 10.1097/00005382-198710000-00004
[6]   A collective route to metastasis: Seeding by tumor cell clusters [J].
Cheung, Kevin J. ;
Ewald, Andrew J. .
SCIENCE, 2016, 352 (6282) :167-169
[7]   Polyclonal breast cancer metastases arise from collective dissemination of keratin 14-expressing tumor cell clusters [J].
Cheung, Kevin J. ;
Padmanaban, Veena ;
Silvestri, Vanesa ;
Schipper, Koen ;
Cohen, Joshua D. ;
Fairchild, Amanda N. ;
Gorin, Michael A. ;
Verdone, James E. ;
Pienta, Kenneth J. ;
Bader, Joel S. ;
Ewald, Andrew J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2016, 113 (07) :E854-E863
[8]   Characterization of circulating tumor cell aggregates identified in patients with epithelial tumors [J].
Cho, Edward H. ;
Wendel, Marco ;
Luttgen, Madelyn ;
Yoshioka, Craig ;
Marrinucci, Dena ;
Lazar, Daniel ;
Schram, Ethan ;
Nieva, Jorge ;
Bazhenova, Lyudmila ;
Morgan, Alison ;
Ko, Andrew H. ;
Korn, W. Michael ;
Kolatkar, Anand ;
Bethel, Kelly ;
Kuhn, Peter .
PHYSICAL BIOLOGY, 2012, 9 (01)
[9]   Microfluidic technologies for circulating tumor cell isolation [J].
Cho, Hyungseok ;
Kim, Jinho ;
Song, Hanjung ;
Sohn, Keun Yong ;
Jeon, MinHyon ;
Han, Ki-Ho .
ANALYST, 2018, 143 (13) :2936-2970
[10]   Clinical evaluation of a novel microfluidic device for epitope-independent enrichment of circulating tumour cells in patients with small cell lung cancer [J].
Chudziak, Jakub ;
Burt, Deborah J. ;
Mohan, Sumitra ;
Rothwell, Dominic G. ;
Mesquita, Barbara ;
Antonello, Jenny ;
Dalby, Suzanne ;
Ayub, Mahmood ;
Priest, Lynsey ;
Carter, Louise ;
Krebs, Matthew G. ;
Blackhall, Fiona ;
Dive, Caroline ;
Brady, Ged .
ANALYST, 2016, 141 (02) :669-678