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Cited by 302

The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.

Epithelial-to-Mesenchymal Transition and Autophagy Induction in Breast Carcinoma Promote Escape from T-cell–Mediated Lysis

Akalay, Intissar, Janji, Bassam, Hasmim, Meriem, Noman, Muhammad Zaeem, André, Fabrice, De Cremoux, Patricia, Bertheau, Philippe, Badoual, Cécile, Vielh, Philippe, Larsen, Annette K., Sabbah, Michèle, Tan, Tuan Zea, Keira, Joan Herr, Ying Hung, Nicole Tsang, Thiery, Jean Paul, Mami-Chouaib, Fathia, Chouaib, Salem·2013·Cancer Research

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 AACR.

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Metadata

Authors
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., Ying Hung, N. T., Thiery, J. P., Mami-Chouaib, F., & Chouaib, S.
Venue
Cancer Research
Published
2013-04-15
Volume
73
Issue
8
Pages
2418-2427
ISSN
  • 0008-5472 (ISSN-L)
  • 1538-7445
OpenAlex
W2157005857
Cited by
302
References
3
FWCI
12.96
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Epithelial-to-Mesenchymal Transition and Autophagy Induction in Breast Carcinoma Promote Escape from T-cell–Mediated Lysis. https://app.cochat.ai/papers/10.1158/0008-5472.can-12-2432
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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., Ying Hung, N. T., Thiery, J. P., Mami-Chouaib, F., & Chouaib, S. (2013). Epithelial-to-Mesenchymal Transition and Autophagy Induction in Breast Carcinoma Promote Escape from T-cell–Mediated Lysis. Cancer Research. https://doi.org/10.1158/0008-5472.can-12-2432

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.