Molecular aspects of breast cancer resistance to drugs (Review)

Thumbnail
Authors
Calaf, Gloria M.
Zepeda, Andrea B.
Castillo, Rodrigo L.
Figueroa, Carolina A.
Arias, Consuelo
Figueroa Villalobos, Elías
Farias, Jorge G.
Authors
Date
Datos de publicación:
INTERNATIONAL JOURNAL OF ONCOLOGY,Vol.47,437-445,2015
Keywords
Abstract
Despite continuous advances in the knowledge of breast cancer pathophysiology, this type of neoplasia remains a leading cause of cancer-related death in women worldwide. Carcinogenesis takes a progressive course from somatic mutations, alteration of the DNA repair mechanisms, inhibition of growth suppressors, followed by cell proliferation, tissue invasion and risk of metastasis. Less than 10% of all cancers are hereditary, and in the case of breast cancer only 8%, a phenomenon linked to genetic changes in BRCA1 or BRCA2. All the other cancers can be caused by an infection (15%) or in most cases (75%) the etiology is unknown. Patients with genetic mutations in BRCA1 or BRCA2 have 30-60% likelihood of developing a second primary breast cancer and between 11 and 45% risk of ovarian cancer, HER-2/neu is overexpressed in similar to 30% of human breast tumors and it has a predictive role in chemotherapy and endocrine therapy.
Description
Journal Volumes
Journals
Journal Issues
relationships.isJournalVolumeOf
relationships.isArticleOf
Journal Issue
Organizational Units
relationships.isArticleOf
Organizational Units
relationships.isPersonaOf
Organizational Units
relationships.isTesisOfOrg