Clinical implications of epithelial cell plasticity in cancer progression

被引:55
作者
Aparicio, Luis A. [1 ]
Blanco, Moises [2 ]
Castosa, Raquel [2 ]
Concha, Angel [3 ]
Valladares, Manuel [1 ]
Calvo, Lourdes [1 ]
Figueroa, Angelica [2 ]
机构
[1] CHUAC, Serv Oncol Med, INIB1C, Sergas,UDC, La Coruna, Spain
[2] Univ Coruna UDC, Grp Invest Traslac Canc, Inst Invest Biomed Coruna INIBIC, Complexo Hosp Univ Coruna CHUAC Sergas, As Xubias 15006, A Coruna, Spain
[3] CHUAC, Serv Anat Patolog, INIBIC, Sergas,UDC, La Coruna, Spain
关键词
Cancer stem cells; Circulating tumour cells; Drug resistance; Epithelial plasticity; Medical perspective; CIRCULATING TUMOR-CELLS; TO-MESENCHYMAL TRANSITION; E-CADHERIN EXPRESSION; BETA-CATENIN EXPRESSION; BREAST-CANCER; STEM-CELL; IMMUNOHISTOCHEMICAL EXPRESSION; PROGNOSTIC-SIGNIFICANCE; COLORECTAL-CANCER; LUNG-CANCER;
D O I
10.1016/j.canlet.2015.06.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
In the last few years, the role of epithelial cell plasticity in cancer biology research has gained increasing attention. This concept refers to the ability of the epithelial cells to dynamically switch between different phenotypic cellular states. This programme is particularly relevant during the epithelial-to-mesenchymal transition (EMT) in cancer progression. During colonization, epithelial cells first activate the EMT programme to disseminate from a primary tumour to reach a distant tissue site. During this process, cells are transported into the circulation and are able to escape the immune system of the host. Then, a reverse process called mesenchymal-to-epithelial transition (MET) occurs on cells that settle in the distant organs. Although epithelial cell plasticity has an important impact on tumour biology, the clinical relevance of this concept remains to be recapitulated. In this review, we will update the current state of epithelial cell plasticity in cancer progression and its clinical implications for the design of therapeutic strategies, the acquisition of multidrug resistance, and future perspectives for the management of cancer patients. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:1 / 10
页数:10
相关论文
共 119 条
[1]
miR-203 Regulates Cell Proliferation through Its Influence on Hakai Expression [J].
Abella, Vanessa ;
Valladares, Manuel ;
Rodriguez, Teresa ;
Haz, Mar ;
Blanco, Moises ;
Tarrio, Nuria ;
Iglesias, Pilar ;
Aparicio, Luis A. ;
Figueroa, Angelica .
PLOS ONE, 2012, 7 (12)
[2]
Stem cell and epithelial-mesenchymal transition markers are frequently overexpressed in circulating tumor cells of metastatic breast cancer patients [J].
Aktas, Bahriye ;
Tewes, Mitra ;
Fehm, Tanja ;
Hauch, Siegfried ;
Kimmig, Rainer ;
Kasimir-Bauer, Sabine .
BREAST CANCER RESEARCH, 2009, 11 (04)
[3]
Epithelial Plasticity: A Common Theme in Embryonic and Cancer Cells [J].
Angela Nieto, M. .
SCIENCE, 2013, 342 (6159) :708-+
[4]
The epithelial-mesenchymal transition under control: Global programs to regulate epithelial plasticity [J].
Angela Nieto, M. ;
Cano, Amparo .
SEMINARS IN CANCER BIOLOGY, 2012, 22 (5-6) :361-368
[5]
The ins and Outs of the Epithelial to Mesenchymal Transition in Health and Disease [J].
Angela Nieto, M. .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, VOL 27, 2011, 27 :347-376
[6]
Circulating miR-200c and miR-141 and outcomes in patients with breast cancer [J].
Antolin, Silvia ;
Calvo, Lourdes ;
Blanco-Calvo, Moises ;
Paz Santiago, Maria ;
Jose Lorenzo-Patino, Maria ;
Haz-Conde, Mar ;
Santamarina, Isabel ;
Figueroa, Angelica ;
Miguel Anton-Aparicio, Luis ;
Valladares-Ayerbes, Manuel .
BMC CANCER, 2015, 15
[7]
Posttranscriptional regulation by RNA-binding proteins during epithelial-to-mesenchymal transition [J].
Aparicio, Luis A. ;
Abella, Vanessa ;
Valladares, Manuel ;
Figueroa, Angelica .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2013, 70 (23) :4463-4477
[8]
Biological influence of Hakai in cancer: a 10-year review [J].
Aparicio, Luis A. ;
Valladares, Manuel ;
Blanco, Moises ;
Alonso, Guillermo ;
Figueroa, Angelica .
CANCER AND METASTASIS REVIEWS, 2012, 31 (1-2) :375-386
[9]
Epithelial to Mesenchymal Transition Contributes to Drug Resistance in Pancreatic Cancer [J].
Arumugam, Thiruvengadam ;
Ramachandran, Vijaya ;
Fournier, Keith F. ;
Wang, Huamin ;
Marquis, Lauren ;
Abbruzzese, James L. ;
Gallick, Gary E. ;
Logsdon, Craig D. ;
McConkey, David J. ;
Choi, Woonyoung .
CANCER RESEARCH, 2009, 69 (14) :5820-5828
[10]
Glioma stem cells promote radioresistance by preferential activation of the DNA damage response [J].
Bao, Shideng ;
Wu, Qiulian ;
McLendon, Roger E. ;
Hao, Yueling ;
Shi, Qing ;
Hjelmeland, Anita B. ;
Dewhirst, Mark W. ;
Bigner, Darell D. ;
Rich, Jeremy N. .
NATURE, 2006, 444 (7120) :756-760