TY - JOUR
T1 - Illuminating breast cancer invasion
T2 - Diverse roles for cell-cell interactions
AU - Cheung, Kevin J.
AU - Ewald, Andrew J.
N1 - Funding Information:
K.J.C. and A.J.E. thank Erik Sahai for crucial comments on the manuscript. K.J.C. is supported by a postdoctoral fellowship from the U.S. Department of Defense ( W81XWH-12-1-0018 to K.J.C.) and a Burroughs Wellcome Fund Career Award for Medical Scientists. A.J.E. is supported by a Research Scholar Grant ( RSG-12-141-01-CSM ) from the American Cancer Society , by funds from the NIH/NCI ( U01 CA155758 ), by a Jerome L. Greene Foundation Discovery Project, by a grant from the Mary Kay Ash Foundation (036-13), by funds from the Cindy Rosencrans Fund for Triple Negative Breast Cancer Research, and by a grant from the Breast Cancer Research Foundation .
PY - 2014/10
Y1 - 2014/10
N2 - Metastasis begins when tumors invade into surrounding tissues. In breast cancer, the study of cell interactions has provided fundamental insights into this complex process. Powerful intravital and 3D organoid culture systems have emerged that enable biologists to model the complexity of cell interactions during cancer invasion in real-time. Recent studies utilizing these techniques reveal distinct mechanisms through which multiple cancer cell and stromal cell subpopulations interact, including paracrine signaling, direct cell-cell adhesion, and remodeling of the extracellular matrix. Three cell interaction mechanisms have emerged to explain how breast tumors become invasive: epithelial-mesenchymal transition, collective invasion, and the macrophage-tumor cell feedback loop. Future work is needed to distinguish whether these mechanisms are mutually exclusive or whether they cooperate to drive metastasis.
AB - Metastasis begins when tumors invade into surrounding tissues. In breast cancer, the study of cell interactions has provided fundamental insights into this complex process. Powerful intravital and 3D organoid culture systems have emerged that enable biologists to model the complexity of cell interactions during cancer invasion in real-time. Recent studies utilizing these techniques reveal distinct mechanisms through which multiple cancer cell and stromal cell subpopulations interact, including paracrine signaling, direct cell-cell adhesion, and remodeling of the extracellular matrix. Three cell interaction mechanisms have emerged to explain how breast tumors become invasive: epithelial-mesenchymal transition, collective invasion, and the macrophage-tumor cell feedback loop. Future work is needed to distinguish whether these mechanisms are mutually exclusive or whether they cooperate to drive metastasis.
UR - http://www.scopus.com/inward/record.url?scp=84906051957&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84906051957&partnerID=8YFLogxK
U2 - 10.1016/j.ceb.2014.07.003
DO - 10.1016/j.ceb.2014.07.003
M3 - Review article
C2 - 25137487
AN - SCOPUS:84906051957
SN - 0955-0674
VL - 30
SP - 99
EP - 111
JO - Current Opinion in Cell Biology
JF - Current Opinion in Cell Biology
IS - 1
ER -