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The biology of breast tumor progression. Acquisition of hormone independence and resistance to cytotoxic drugs.
Leonessa, F; Boulay, V; Wright, A; Thompson, E W; Brünner, N; Clarke, R.
Affiliation
  • Leonessa F; Vincent T. Lombardi Cancer Research Center, Georgetown University Medical School, Washington, DC 20007.
Acta Oncol ; 31(2): 115-23, 1992.
Article in En | MEDLINE | ID: mdl-1622625
ABSTRACT
Many breast tumors appear to follow a predictable clinical pattern, being initially responsive to endocrine therapy and to cytotoxic chemotherapy but ultimately exhibiting a phenotype resistant to both modalities. Using the MCF-7 human breast cancer cell line as an example of an 'early' phenotype (estrogen and progesterone receptor positive, steroid responsive, low metastatic potential), we have isolated and characterized a series of hormone-independent but hormone-responsive variants (MIII and MCF7/LCC1). However, these variants remain responsive to both antiestrogens and cytotoxic drugs (methotrexate and colchicine). MIII and MCF7/LCC1 cells appear to mimic some of the critical aspects of the early progression to a more aggressive phenotype. An examination of the phenotype of these cells suggests that some hormone-independent breast cancer cells are derived from hormone-dependent parental cells. The development of a hormone-independent phenotype can arise independently of acquisition of a cytotoxic drug resistant phenotype.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms / Drug Resistance Type of study: Etiology_studies / Prognostic_studies Limits: Animals / Female / Humans Language: En Journal: Acta Oncol Journal subject: NEOPLASIAS Year: 1992 Document type: Article
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Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms / Drug Resistance Type of study: Etiology_studies / Prognostic_studies Limits: Animals / Female / Humans Language: En Journal: Acta Oncol Journal subject: NEOPLASIAS Year: 1992 Document type: Article