Expression des "activated leukocyte cell adhesion molecule" im Mammakarzinom. Prädiktivität für das Ansprechen auf eine taxanfreie Chemotherapie
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Expression des "activated leukocyte cell adhesion molecule" im Mammakarzinom. Prädiktivität für das Ansprechen auf eine taxanfreie Chemotherapie. / Kilic, E; Milde-Langosch, K; Müller, V; Wirtz, R; Ihnen, M.
In: PATHOLOGE, Vol. 29 Suppl 2, 11.2008, p. 347-52.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
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TY - JOUR
T1 - Expression des "activated leukocyte cell adhesion molecule" im Mammakarzinom. Prädiktivität für das Ansprechen auf eine taxanfreie Chemotherapie
AU - Kilic, E
AU - Milde-Langosch, K
AU - Müller, V
AU - Wirtz, R
AU - Ihnen, M
PY - 2008/11
Y1 - 2008/11
N2 - AIMS: Activated leukocyte cell adhesion molecule (ALCAM) is a cell surface immunoglobulin expressed in breast cancer (BC) and is assumed to be implicated in tumourigenesis and tumour progression. The importance of the adhesion molecule ALCAM for the response to taxane-free adjuvant chemotherapy was investigated.MATERIALS AND METHODS: Tissue specimens from 162 primary breast cancer patients were analyzed. Immunohistochemical staining (IHC) and Western blots (WB) were performed using monoclonal antibody against ALCAM. Relative protein amounts in WB bands were determined densitometrically. ALCAM mRNA expression was evaluated by microarray analysis (Affymetrix).RESULTS: In the normal breast ALCAM is expressed in luminal and basal epithelial cells. In BC samples, WB analysis showed a significant positive correlation of ALCAM levels with estrogen receptor status (p=0.04). For patients who received a taxane-free chemotherapy, a high ALCAM expression was predictive for a good response to chemotherapy. Median mRNA expression of ALCAM was 4.5-fold higher in patients alive at the time of follow-up compared to those who died of breast cancer.CONCLUSIONS: Higher ALCAM expression showed a positive correlation with estrogen receptor status and is a useful predictive marker for the response to taxane-free chemotherapy.
AB - AIMS: Activated leukocyte cell adhesion molecule (ALCAM) is a cell surface immunoglobulin expressed in breast cancer (BC) and is assumed to be implicated in tumourigenesis and tumour progression. The importance of the adhesion molecule ALCAM for the response to taxane-free adjuvant chemotherapy was investigated.MATERIALS AND METHODS: Tissue specimens from 162 primary breast cancer patients were analyzed. Immunohistochemical staining (IHC) and Western blots (WB) were performed using monoclonal antibody against ALCAM. Relative protein amounts in WB bands were determined densitometrically. ALCAM mRNA expression was evaluated by microarray analysis (Affymetrix).RESULTS: In the normal breast ALCAM is expressed in luminal and basal epithelial cells. In BC samples, WB analysis showed a significant positive correlation of ALCAM levels with estrogen receptor status (p=0.04). For patients who received a taxane-free chemotherapy, a high ALCAM expression was predictive for a good response to chemotherapy. Median mRNA expression of ALCAM was 4.5-fold higher in patients alive at the time of follow-up compared to those who died of breast cancer.CONCLUSIONS: Higher ALCAM expression showed a positive correlation with estrogen receptor status and is a useful predictive marker for the response to taxane-free chemotherapy.
KW - Antigens, CD
KW - Antineoplastic Combined Chemotherapy Protocols
KW - Blotting, Western
KW - Breast
KW - Breast Neoplasms
KW - Carcinoma, Ductal
KW - Carcinoma, Lobular
KW - Cell Adhesion Molecules, Neuronal
KW - Chemotherapy, Adjuvant
KW - Female
KW - Fetal Proteins
KW - Gene Expression Regulation, Neoplastic
KW - Humans
KW - Kaplan-Meier Estimate
KW - Neoplasm Staging
KW - Neoplasms, Hormone-Dependent
KW - Oligonucleotide Array Sequence Analysis
KW - Predictive Value of Tests
KW - Prognosis
KW - RNA, Messenger
KW - Receptors, Estrogen
KW - Taxoids
U2 - 10.1007/s00292-008-1080-5
DO - 10.1007/s00292-008-1080-5
M3 - SCORING: Zeitschriftenaufsatz
C2 - 18810438
VL - 29 Suppl 2
SP - 347
EP - 352
JO - PATHOLOGE
JF - PATHOLOGE
SN - 0172-8113
ER -