Patients diagnosed with triple-negative breast cancer (TNBC) have a high rate of tumor metastasis and a poor prognosis. The treatment option for these patients is currently chemotherapy, which results in very low response rates. Strategies that exploit the immune system for the treatment of cancer have now shown the ability to improve survival in several tumor types. Identifying potential targets for immune therapeutic interventions is an important step in developing novel treatments for TNBC. In this study, in silico analysis of publicly available datasets and immunohistochemical analysis of primary and metastatic tumor biopsies from TNBC patients were conducted to evaluate the expression of the transcription factor brachyury, which is a driver of tumor metastasis and resistance and a target for cancer vaccine approaches. Analysis of breast cancer datasets demonstrated a predominant expression of brachyury mRNA in TNBC and in basal vs luminal or HER2 molecular breast cancer subtypes. At the protein level, variable levels of brachyury expression were detected both in primary and metastatic TNBC lesions. A strong association was observed between nuclear brachyury protein expression and the stage of disease, with nuclear brachyury being more predominant in metastatic vs primary tumors. Survival analysis also demonstrated an association between high levels of brachyury in the primary tumor and poor prognosis. Two brachyury-targeting cancer vaccines are currently undergoing clinical evaluation; the data presented here provide rationale for using brachyury-targeting immunotherapy approaches for the treatment of TNBC.

Hamilton, D.h., Roselli, M., Ferroni, P., Costarelli, L., Cavaliere, F., Taffuri, M., et al. (2016). Brachyury, a vaccine target, is overexpressed in triple-negative breast cancer. ENDOCRINE-RELATED CANCER, 23(10), 783-796 [10.1530/ERC-16-0037].

Brachyury, a vaccine target, is overexpressed in triple-negative breast cancer

ROSELLI, MARIO;
2016-10

Abstract

Patients diagnosed with triple-negative breast cancer (TNBC) have a high rate of tumor metastasis and a poor prognosis. The treatment option for these patients is currently chemotherapy, which results in very low response rates. Strategies that exploit the immune system for the treatment of cancer have now shown the ability to improve survival in several tumor types. Identifying potential targets for immune therapeutic interventions is an important step in developing novel treatments for TNBC. In this study, in silico analysis of publicly available datasets and immunohistochemical analysis of primary and metastatic tumor biopsies from TNBC patients were conducted to evaluate the expression of the transcription factor brachyury, which is a driver of tumor metastasis and resistance and a target for cancer vaccine approaches. Analysis of breast cancer datasets demonstrated a predominant expression of brachyury mRNA in TNBC and in basal vs luminal or HER2 molecular breast cancer subtypes. At the protein level, variable levels of brachyury expression were detected both in primary and metastatic TNBC lesions. A strong association was observed between nuclear brachyury protein expression and the stage of disease, with nuclear brachyury being more predominant in metastatic vs primary tumors. Survival analysis also demonstrated an association between high levels of brachyury in the primary tumor and poor prognosis. Two brachyury-targeting cancer vaccines are currently undergoing clinical evaluation; the data presented here provide rationale for using brachyury-targeting immunotherapy approaches for the treatment of TNBC.
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MED/06 - Oncologia Medica
Settore MED/04 - Patologia Generale
English
Con Impact Factor ISI
TNBC; brachyury; tumor antigen; vaccine target
Hamilton, D.h., Roselli, M., Ferroni, P., Costarelli, L., Cavaliere, F., Taffuri, M., et al. (2016). Brachyury, a vaccine target, is overexpressed in triple-negative breast cancer. ENDOCRINE-RELATED CANCER, 23(10), 783-796 [10.1530/ERC-16-0037].
Hamilton, D; Roselli, M; Ferroni, P; Costarelli, L; Cavaliere, F; Taffuri, M; Palena, C; Guadagni, F
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/2108/170831
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