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Molecular signatures mostly associated with NK cells are predictive of relapse free survival in breast cancer patients

BACKGROUND: Recent observations suggest that immune-mediated tissue destruction is dependent upon coordinate activation of immune genes expressed by cells of the innate and adaptive immune systems. METHODS: Here, we performed a retrospective pilot study to investigate whether the coordinate expressi...

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Detalles Bibliográficos
Autores principales: Ascierto, Maria Libera, Idowu, Michael O, Zhao, Yingdong, Khalak, Hanif, Payne, Kyle K, Wang, Xiang-Yang, Dumur, Catherine I, Bedognetti, Davide, Tomei, Sara, Ascierto, Paolo A, Shanker, Anil, Bear, Harry D, Wang, Ena, Marincola, Francesco M, De Maria, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3694475/
https://www.ncbi.nlm.nih.gov/pubmed/23758773
http://dx.doi.org/10.1186/1479-5876-11-145
Descripción
Sumario:BACKGROUND: Recent observations suggest that immune-mediated tissue destruction is dependent upon coordinate activation of immune genes expressed by cells of the innate and adaptive immune systems. METHODS: Here, we performed a retrospective pilot study to investigate whether the coordinate expression of molecular signature mostly associated with NK cells could be used to segregate breast cancer patients into relapse and relapse-free outcomes. RESULTS: By analyzing primary breast cancer specimens derived from patients who experienced either 58–116 months (~5-9 years) relapse-free survival or developed tumor relapse within 9–76 months (~1-6 years) we found that the expression of molecules involved in activating signaling of NK cells and in NK cells: target interaction is increased in patients with favorable prognosis. CONCLUSIONS: The parameters identified in this study, together with the prognostic signature previously reported by our group, highlight the cooperation between the innate and adaptive immune components within the tumor microenvironment.