Detection of MAGE-A3 in breast cancer patients' sentinel lymph nodes

被引:30
作者
Wascher, RA
Bostick, PJ
Huynh, KT
Turner, R
Qi, K
Giuliano, AE
Hoon, DSB [1 ]
机构
[1] St Johns Hlth Ctr, John Wayne Canc Inst, Dept Mol Oncol, Santa Monica, CA 90404 USA
[2] St Johns Hlth Ctr, John Wayne Canc Inst, Joyce Eisenberg Keefer Breast Ctr, Santa Monica, CA 90404 USA
[3] St Johns Hlth Ctr, John Wayne Canc Inst, Dept Pathol, Santa Monica, CA 90404 USA
[4] St Johns Hlth Ctr, John Wayne Canc Inst, Div Biostat, Santa Monica, CA 90404 USA
关键词
breast cancer; MAGE-A3; micrometastases; RT-PCR; sentinel lymph node;
D O I
10.1054/bjoc.2001.2079
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The detection of occult metastatic breast cancer cells by RT-PCR is limited by the poor specificity of most tumour mRNA markers. MAGE-A3 is a highly specific tumour mRNA marker that is not expressed in non-cancer cells. This study assesses MAGE-A3 mRNA as a molecular marker for the detection of turnout cells in the sentinel lymph nodes (SLN) of breast cancer patients. Serial frozen sections of SLN (n = 121) were obtained from 77 AJCC (American Joint Committee on Cancer) Stage I-IIIA breast cancer patients. MAGE-A3 mRNA analysis of SILN was performed by RT-PCR and Southern blot analysis. Tumour cells were detected in 48 of 121 (40%) SLN from 77 patients by H&E or IHC staining, and 35 of 77 (45%) patients, overall, had histopathologically (H&E and/or IIHC) positive SLN. Among histopathologically negative SLN, 28 of 73 (38%) SLN were MAGE-A3 mRNA positive by RT-PCR. Overall, 41 of 77 (53%) patients and 50 of 121 (41%) SLN were positive for MAGE-A3. MAGE-A3 mRNA expression in the SLN occurred more frequently with infiltrating lobular carcinoma (P < 0.001) than with infiltrating ductal carcinoma, adding further evidence of possible phenotypic differences between these 2 subtypes of breast cancer. Due to its high specificity, MAGE-A3 mRNA is a potentially useful marker for detecting breast cancer cells in the SLN. One half of breast tumours expressed MAGE-A3 mRNA, which has important potential implications for antigen-specific targeted immunotherapy. (C) 2001 Cancer Research Campaign.
引用
收藏
页码:1340 / 1346
页数:7
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