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|Title:||Epithelial-to-mesenchymal transition and autophagy induction in breast carcinoma promote escape from t-cell-mediated lysis||Authors:||Akalay, I.
De Cremoux, P.
|Issue Date:||15-Apr-2013||Citation:||Akalay, I., Janji, B., Hasmim, M., Noman, M.Z., André, F., De Cremoux, P., Bertheau, P., Badoual, C., Vielh, P., Larsen, A.K., Sabbah, M., Tan, T.Z., Keira, J.H., Hung, N.T.Y., Thiery, J.P., Mami-Chouaib, F., Chouaib, S. (2013-04-15). Epithelial-to-mesenchymal transition and autophagy induction in breast carcinoma promote escape from t-cell-mediated lysis. Cancer Research 73 (8) : 2418-2427. ScholarBank@NUS Repository. https://doi.org/10.1158/0008-5472.CAN-12-2432||Abstract:||Epithelial-to-mesenchymal transition (EMT) mediates cancer cell invasion, metastasis, and drug resistance, but its impact on immune surveillance has not been explored. In this study, we investigated the functional consequences of this mode of epithelial cell plasticity on targeted cell lysis by cytotoxic T lymphocytes (CTL). Acquisition of the EMT phenotype in various derivatives of MCF-7 human breast cancer cells was associated with dramatic morphologic changes and actin cytoskeleton remodeling, with CD24-/CD44 +/ALDH+ stem cell populations present exhibiting a higher degree of EMT relative to parental cells. Strikingly, acquisition of this phenotype also associated with an inhibition of CTL-mediated tumor cell lysis. Resistant cells exhibited attenuation in the formation of an immunologic synapse with CTLs along with the induction of autophagy in the target cells. This response was critical for susceptibility to CTL-mediated lysis because siRNA-mediated silencing of beclin1 to inhibit autophagy in target cells restored their susceptibility to CTL-induced lysis. Our results argue that in addition to promoting invasion and metastasis EMT also profoundly alters the susceptibility of cancer cells to T-cell-mediated immune surveillance. Furthermore, they reveal EMT and autophagy as conceptual realms for immunotherapeutic strategies to block immune escape. Cancer Res; 73(8); 2418-27. © 2013 American Association for Cancer Research.||Source Title:||Cancer Research||URI:||http://scholarbank.nus.edu.sg/handle/10635/117008||ISSN:||00085472||DOI:||10.1158/0008-5472.CAN-12-2432|
|Appears in Collections:||Staff Publications|
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