Poster Presenter
Link Betweeen Multidrug Resistence-Related
Proteins And Histo-Pathological Features In Breast Cancer.
S. Rybárová, I. Hodorová, Vecanová,
J. Slovak Republic.
Slovakia
The aim of this work was
to determine the expression of the multidrug resistance (MDR) proteins,
namely MDR1 (P-glycoprotein), MRP1 (multidrug resistance-related
protein) and LRP (lung resistance related protein) in breast carcinoma.
Detection of these proteins was provided in 87 samples of breast
cancer by using of indirect enzymatic immunohistochemistry. Our
findings were compared with other clinical and pathological parameters,
as are: expression of Her2/neu, estrogen (ER) and progesteron (PR)
receptor status, histological grade and regional lymph node status.
For statistical anlysis, non-parametric two sided Mann-Whitney -
U - test was used.
Majority of breast carcinoma specimens show the positivity for these
proteins. The MDR1 and MRP1 signal was found in the cytoplasm od
cancer cells. The expression of LRP was found in the cytoplasm close
to the nuclear membrane. The samples were positive for MDR1 protein
in 57%, for MRP1 in 84% and for LRP in 79%. In comparison of our
results with other clinical and pathological parameters, the negative
correlation between ER, PR and MDR1 expressions and histological
grading status was found. No associations were observed between
the two proteins and histological grading, as well as between the
expression of all three proteins and other clinicaly relevant parameters.
In conclusion, high frequency of expression of MDR proteins in breast
carcinoma cells suggests, that these proteins might be an important
factor of drug resistance in breast cancer. Nevertheles, the negative
correlation between the histological grade of malignancy of tumor
and the expression of ER, PR and MDR1 indicates the possible influence
of progressive tumor cell dediferentiation. However, this findings
has to be confirmed in additional evaluations.
We are grateful to League Against Cancer of Slovak Republic for
generous finantial support of our work. This study was also supported
by the VEGA grant 1/0388/08.
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