Abstract
BACKGROUND:
Breast cancer cell lines are widely
used tools to investigate breast cancer biology and to develop new therapies.
Breast cancer tissue contains molecularly heterogeneous cell populations. Thus,
it is important to understand which cell lines best represent the primary tumor
and have similarly diverse phenotype. Here, we describe the development of five
breast cancer cell lines from a single patient's breast cancer tissue. We
characterize the molecular profiles, tumorigenicity and metastatic ability in
vivo of all five cell lines and compare their responsiveness to
4-hydroxytamoxifen (4-OHT) treatment.
METHODS:
Five breast cancer cell lines were derived
from a single patient's primary breast cancer tissue. Expression of different
antigens including HER2, estrogen receptor (ER), CK8/18, CD44 and CD24 was
determined by flow cytometry, western blotting and immunohistochemistry (IHC).
In addition, a Fuorescent In Situ Hybridization (FISH) assay for HER2 gene
amplification and p53 genotyping was performed on all cell lines. A xenograft
model in nude mice was utilized to assess the tumorigenic and metastatic
abilities of the breast cancer cells.
RESULTS:
We have isolated, cloned and
established five new breast cancer cell lines with different tumorigenicity and
metastatic abilities from a single primary breast cancer. Although all the cell
lines expressed low levels of ER, their growth was estrogen-independent and all
had high-levels of expression of mutated non-functional p53. The HER2 gene was
rearranged in all cell lines. Low doses of 4-OHT induced proliferation of these
breast cancer cell lines.
CONCLUSIONS:
All five breast cancer cell lines
have different antigenic expression profiles, tumorigenicity and organ specific
metastatic abilities although they derive from a single tumor. None of the
studied markers correlated with tumorigenic potential. These new cell lines
could serve as a model for detailed genomic and proteomic analyses to identify
mechanisms of organ-specific metastasis of breast cancer.
Source: Multiple breast cancer
cell-lines derived from a single tumor differ in their molecular
characteristics and tumorigenic potential. Mosoyan G, Nagi C, Marukian S,
Teixeira A, Simonian A, Resnick-Silverman L, Difeo A, Johnston D, Reynolds SR,
Roses DF, Mosoian A (arevik.mosoian@mssm.edu).
PLoS One. 2013;8(1):e55145.
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