Your browser doesn't support javascript.
loading
High expression of apoptosis protein (Api-5) in chemoresistant triple-negative breast cancers: an innovative target.
Bousquet, Guilhem; Feugeas, Jean-Paul; Gu, Yuchen; Leboeuf, Christophe; Bouchtaoui, Morad El; Lu, He; Espié, Marc; Janin, Anne; Benedetto, Melanie Di.
Afiliación
  • Bousquet G; Université Paris Diderot, Sorbonne Paris Cité, Laboratoire de Pathologie, UMR-S 1165, F-75010, Paris, France.
  • Feugeas JP; INSERM, U942, F-75010, Paris, France.
  • Gu Y; Université Paris 13, Sorbonne Paris Cite, F-93000, Villetaneuse, France.
  • Leboeuf C; AP-HP, Hôpital Avicenne, Medical Oncology, F-93000, Bobigny, France.
  • Bouchtaoui ME; INSERM, U1137-Paris, F-75018, France.
  • Lu H; Université Paris Diderot, Sorbonne Paris Cité, Laboratoire de Pathologie, UMR-S 1165, F-75010, Paris, France.
  • Espié M; Université Paris Diderot, Sorbonne Paris Cité, Laboratoire de Pathologie, UMR-S 1165, F-75010, Paris, France.
  • Janin A; INSERM, U942, F-75010, Paris, France.
  • Benedetto MD; INSERM, U942, F-75010, Paris, France.
Oncotarget ; 10(61): 6577-6588, 2019 Nov 12.
Article en En | MEDLINE | ID: mdl-31762939
Anti-apoptotic protein-5 (API-5) is a survival protein interacting with the protein acinus, preventing its cleavage by caspase-3 and thus inhibiting apoptosis. We studied the effect of targeting API-5 in chemoresistant triple negative breast cancers (TNBCs), to reverse chemoresistance. 78 TNBC biopsies from patients with different responses to chemotherapy were analysed for API-5 expression before any treatment. Further studies on API-5 expression and inhibition were performed on patient-derived TNBC xenografts, one highly sensitive to chemotherapies (XBC-S) and the other resistant to most tested drugs (XBC-R). In situ assessments of necrosis, cell proliferation, angiogenesis, and apoptosis in response to anti-API-5 peptide were performed on the TNBC xenografts. Clinical analyses of the 78 TNBC biopsies revealed that API-5 was more markedly expressed in endothelial cells before any treatment among patients with chemoresistant TNBC, and this was associated with greater micro-vessel density. A transcriptomic analysis of xenografted tumors showed an involvement of anti-apoptotic genes in the XBC-R model, and API-5 expression was higher in XBC-R endothelial cells. API-5 expression was also correlated with hypoxic stress conditions both in vitro and in vivo. 28 days of anti-API-5 peptide efficiently inhibited the XBC-R xenograft via caspase-3 apoptosis. This inhibition was associated with major inhibition of angiogenesis associated with necrosis and apoptosis. API-5 protein could be a valid therapeutic target in chemoresistant metastatic TNBC.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Oncotarget Año: 2019 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Oncotarget Año: 2019 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Estados Unidos