Vimentin and Epithelial-Mesenchymal Transition in Human Breast Cancer – Observations in vitro and in vivo

Cells Tissues Organs - Tập 185 Số 1-3 - Trang 191-203 - 2007
Maria I. Kokkinos1, Razan Wafai2, M. K. Wong2, Donald F. Newgreen3, Erik W. Thompson2,4, Mark Waltham2,4
1Department of Surgery, St Vincent’s Hospital, University of Melbourne, Melbourne, Australia
2University of Melbourne
3Royal Children’s Hospital, Melbourne
4Victorian Breast Cancer Research Consortium

Tóm tắt

Breast cancer is a highly prevalent disease among women worldwide. While the expression of certain proteins within these tumours is used for prognosis and selection of therapies, there is a continuing need for additional markers to be identified. A considerable amount of current literature, based predominantly on cell culture systems, suggests that a major mechanism responsible for the progression of breast cancer is due to tumour cells losing their epithelial features and gaining mesenchymal properties. These events are proposed to be very similar to the epithelial-mesenchymal transition (EMT) process that has been well characterised in embryonic development. For the developmental and putative cancer EMT, the cell intermediate filament status changes from a keratin-rich network which connects to adherens junctions and hemidesmosomes, to a vimentin-rich network connecting to focal adhesions. This review summarises observations of vimentin expression in breast cancer model systems, and discusses the potential role of EMT in human breast cancer progression, and the prognostic usefulness of vimentin expression.

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Tài liệu tham khảo

10.1002%2Fpath.1711470407

10.1530%2Fjrf.0.1140307

10.1074%2Fjbc.M005912200

10.1083%2Fjcb.109.4.1653

10.1016%2Fj.transproceed.2004.12.043

10.1038%2Fnrc1231

10.1262%2Fjrd.17099

10.1111%2Fj.1582-4934.2005.tb00350.x

10.1046%2Fj.1365-2184.2003.00265.x

10.1242%2Fjcs.00906

10.1002%2F%28SICI%291521-1878%28199801%2920%3A1%3C79%3A%3AAID-BIES11%3E3.0.CO%3B2-5

10.1016%2FS0012-1606%2889%2980017-X

10.1111%2Fj.1432-0436.1982.tb01266.x

10.1083%2Fjcb.133.4.853

10.1016%2FS0248-4900%2899%2980068-9

10.1111%2Fj.1524-4741.1996.tb00076.x

10.1002%2Fijc.2910630612

10.1038%2Fnrm1175

10.1053%2Fplac.1999.0441

10.1080%2F00313020220131273

10.1242%2Fjcs.00936

10.1172%2FJCI200421358

10.1111%2Fj.1365-2559.1996.tb01396.x

10.1002%2Fpath.1797

10.1002%2Fijc.20763

10.1007%2Fs11064-004-6880-2

10.1083%2Fjcb.200601018

10.1016%2FS0945-053X%2899%2900036-0

10.1046%2Fj.1432-0436.2001.067001041.x

10.1083%2Fjcb.127.6.2021

10.1189%2Fjlb.0405190

10.1038%2Fsj.onc.1209265

10.1083%2Fjcb.147.3.631

10.1038%2F35021093

10.1186%2Fbcr298

10.1007%2Fs10549-005-1483-4

10.1016%2Fj.ejca.2006.08.015

10.1046%2Fj.1523-1755.2002.00430.x

10.1152%2Fajprenal.00064.2004

10.1016%2Fj.ejcb.2005.09.019

10.1002%2F%28SICI%291097-0215%2819960729%2967%3A3%3C353%3A%3AAID-IJC8%3E3.0.CO%3B2-Q

10.1016%2FS0092-8674%2800%2981009-0

10.1002%2Fjcp.20062

10.1038%2Fnrm1835

10.1002%2Fjcp.1041500314

10.1007%2FBF01753886

10.1158%2F0008-5472.CAN-05-0616

10.1186%2Fbcr578

10.1016%2Fj.placenta.2005.02.014

10.1038%2Fsj.onc.1207226

10.1158%2F1078-0432.CCR-05-0632

10.1016%2FS0002-9440%2810%2962351-6

10.1016%2FS0002-9440%2810%2962533-3