Humanin Promotes Tumor Progression in Experimental Triple Negative Breast Cancer

Humanin (HN) is a mitochondrial-derived peptide with cytoprotective efect in many tissues. Administration of HN analogs has been proposed as therapeutic approach for degenerative diseases. Although HN has been shown to protect normal tissues from chemotherapy, its role in tumor pathogenesis is poorl...

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Detalles Bibliográficos
Autores: Moreno Ayala, Mariela A., Gottardo, María Florencia, Zuccato, Camila Florencia, Pidre, Matías Luis, Nicola Candia, Alejandro Javier, Asad, Antonela Sofia, Imsen, Mercedes, Romanowski, Víctor, Cretón, Aldo, Isla Larrain, Marina Teresita, Seilicovich, Adriana, Candolfi, Marianela
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2020
País:Argentina
Institución:Universidad Nacional de La Plata
Repositorio:SEDICI (UNLP)
Idioma:español
OAI Identifier:oai:sedici.unlp.edu.ar:10915/107851
Acceso en línea:http://sedici.unlp.edu.ar/handle/10915/107851
Access Level:acceso abierto
Palabra clave:Ciencias Médicas
Ciencias Exactas
Humanin
Tumor progression
Breast cancer
Immunohistochemistry
Descripción
Sumario:Humanin (HN) is a mitochondrial-derived peptide with cytoprotective efect in many tissues. Administration of HN analogs has been proposed as therapeutic approach for degenerative diseases. Although HN has been shown to protect normal tissues from chemotherapy, its role in tumor pathogenesis is poorly understood. Here, we evaluated the efect of HN on the progression of experimental triple negative breast cancer (TNBC). The meta-analysis of transcriptomic data from The Cancer Genome Atlas indicated that HN and its receptors are expressed in breast cancer specimens. By immunohistochemistry we observed up-regulation of HN in TNBC biopsies when compared to mammary gland sections from healthy donors. Addition of exogenous HN protected TNBC cells from apoptotic stimuli whereas shRNA-mediated HN silencing reduced their viability and enhanced their chemo-sensitivity. Systemic administration of HN in TNBC-bearing mice reduced tumor apoptotic rate, impaired the antitumor and anti-metastatic efect of chemotherapy and stimulated tumor progression, accelerating tumor growth and development of spontaneous lung metastases. These fndings suggest that HN may exert pro-tumoral efects and thus, caution should be taken when using exogenous HN to treat degenerative diseases. In addition, our study suggests that HN blockade could constitute a therapeutic strategy to improve the efcacy of chemotherapy in breast cancer.