Human Breast Cancer Cell Lines Co-Express Neuronal, Epithelial, and Melanocytic Differentiation Markers In Vitro and In Vivo
Author(s) -
Qingbei Zhang,
Hanli Fan,
Jikun Shen,
Robert M. Hoffman,
H. Rosie Xing
Publication year - 2010
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0009712
Subject(s) - transdifferentiation , biology , skbr3 , cellular differentiation , lineage markers , cancer research , stem cell marker , breast cancer , cell culture , cancer , cancer stem cell , lineage (genetic) , pathology , stem cell , microbiology and biotechnology , genetics , progenitor cell , medicine , gene , human breast
Differentiation programs are aberrant in cancer cells allowing them to express differentiation markers in addition to their tissue of origin. In the present study, we demonstrate the multi-lineage differentiation potential of breast cancer cell lines to express multiple neuronal/glial lineage-specific markers as well as mammary epithelial and melanocytic-specific markers. Multilineage expression was detected in luminal (MCF-7 and SKBR3) and basal (MDA-MB-231) types of human breast cancer cell lines. We also observed comparable co-expression of these three cell lineage markers in MDA-MB-435 cells in vitro , in MDA-MB-435 primary tumors derived from parental and single cell clones and in lung metastases in vivo . Furthermore, ectoderm multi-lineage transdifferentiation was also found in human melanoma (Ul-MeL) and glioblastoma cell lines (U87 and D54). These observations indicate that aberrant multi-lineage transdifferentiation or lineage infidelity may be a wide spread phenomenon in cancer.
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