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A new cell line from human infiltrating ductal carcinoma of the breast: establishment and characterization
Authors:W Zoli  L Roncuzzi  A Flamigni  R Gruppioni  A Sensi  N Zini  D Amadori  A Gasperi-Campani
Institution:(1) Department of Medical Oncology, G. B. Morgagni-L. Pierantoni Hospital, Viale Forlanini, 47100 Forli, Italy;(2) Biotechnology Unit, National Institute for the Research on Cancer (Genova), Bologna, Italy;(3) Department of Experimental Pathology, University of Bologna, Italy;(4) Istituto Oncologico Romagnolo, Forli, Italy;(5) Institute of Medical Genetics, Arcispedale S. Anna, University of Ferrara, Italy;(6) CNR Institute of Normal and Pathologic Cytomorphology, c/o I.O.R., Bologna, Italy;(7) Interdepartmental Center for Research on Cancer, University of Bologna, Italy
Abstract:We established a novel cancer cell line (MAST) from the ascitic fluid of a metastatic infiltrating ductal carcinoma of the breast. The epithelial and neoplastic nature of the MAST cells was confirmed by ultrastructural analysis. The cell line was maintained as a monolayer with a doubling time of about 68 h, and it possessed an abnormal karyotype with a modal chromosome number of 60, a trisomy of chromosome 18 and other unidentified rearranged chromosomes. Among the markers consistently found in MAST metaphases, we noted a t(14; 14) and a very large subtelocentric, a large satellited acrocentric and a very large submetacentric chromosome with striking fluorescent bands. Immunoenzymatic assay demonstrated that the MAST cell line was positive for estrogen and progesterone receptors. The in vitro drug-sensitivity assay showed a marked resistance of the cell line to 5-fluorouracil and 4-hydroperoxycyclophosphamide and a moderate resistance to etoposide and 4prime-epidoxorubicin. The molecular analysis showed a four- to sixfold amplification of the c-myc gene and no amplification or rearrangement of theint-2, c-erbB-2, c-Ha-ras, c-mos andhst-1 genes.
Keywords:Human breast cancer  Permanent cell line  Cytogenetics  oncogenes
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