THERAPEUTIC IMPLICATIONS OF A STEM-CELL MODEL FOR HUMAN-BREAST CANCER - A HYPOTHESIS
- 1 January 1983
- journal article
- research article
- Vol. 67 (7-8), 659-663
Abstract
A model for human breast cancer is proposed in which a subpopulation of relatively undifferentiated tumor stem cells gives rise to clones of cells by a process of exponential division. The progeny progressively become more differentiated but lose their proliferative potential. The model implies that breast cancers are heterogeneous with respect to differentiation features such as hormone receptors, both between different clones and within individual clones. Therefore, endocrine therapies are preferentially directed towards differentiated cells and are unlikely to be curative either in advanced disease or in the adjuvant setting. The reduction of differentiated cells by hormonal maneuvers may leave a population of more actively dividing tumor stem cells which are more sensitive to chemotherapy. Hormonal therapy followed by cytotoxic chemotherapy may be more likely to kill tumor stem cells than either form of therapy given alone.This publication has 17 references indexed in Scilit:
- The origin of metastatic heterogeneity in tumorsEuropean Journal of Cancer (1965), 1981
- Estradiol receptors in subpopulations of breast cancer cells isolated from human primary tumorsCancer, 1981
- Relationship between proliferative activity and estrogen receptors in breast cancerCancer, 1979
- OVARIAN IRRADIATION AND PREDNISONE THERAPY FOLLOWING SURGERY AND RADIOTHERAPY FOR CARCINOMA OF THE BREAST1979
- SELF-RENEWAL IN CULTURE OF PROLIFERATIVE BLAST PROGENITOR CELLS IN ACUTE MYELOBLASTIC-LEUKEMIA1979
- Growth of human tumour cell colonies from biopsies using two soft-agar techniquesBritish Journal of Cancer, 1978
- Low incidence of estrogen receptor in breast carcinomas with rapid rates of cellular replicationCancer, 1977
- Primary Bioassay of Human Tumor Stem CellsScience, 1977
- Chronic myelocytic leukemia: Clonal origin in a stem cell common to the granulocyte, erythrocyte, platelet and monocyte/macrophageAmerican Journal Of Medicine, 1977
- The Clonal Evolution of Tumor Cell PopulationsScience, 1976