Differential expression of the α2,3-sialic acid residues in breast cancer is associated with metastatic potential

Differential expression of the α2,3-sialic acid residues in breast cancer is associated with metastatic potential
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DOI:
10.3892/or.2011.1192
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发表时间:
2011-05-01
期刊:
影响因子:
4.2
通讯作者:
Liu, Jicheng
Liu, Jicheng
中科院分区:
医学3区
文献类型:
--
作者:
Cui, Hongxia;Lin, Yu;Liu, Jicheng

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Aberrant sialylation is closely associated with the malignant phenotype of cancer cells and metastatic potential. However, the precise nature of the molecules in breast cancers has not been unveiled. In this study, we investigated the expression levels of alpha 2,3-sialic acid residues of 50 primary tumor cases, 50 pair-matched lymph node metastasis tumor samples and in the MDA-MB-231, T-47D and MCF-7 breast cancer cell lines with different metastatic potential. The expression of alpha 2,3-sialic acid residues was analyzed by histochemistry, cytochemistry and flow cytometry with Maackia amurensis lectin (MAL). The invasion and migration abilities of cells were examined using cell adhesion and transwell in vitro assays. Pair-matched lymph node metastasis tumor samples exhibited higher levels of expression of alpha 2,3-sialic acid residues compared to that of primary tumors (P=0.0432). Furthermore, of 38 tumors cases in T1/T2 stages, 31(81.58%) had weak staining for MAL, which specifically binds to alpha 2,3-sialic acid residues, whereas of 12 tumor cases in T3/T4 stages, only 1 (8.33%) had weak reactions for MAL. The highly metastatic breast cancer cell line MDA-MB-231 exhibited the strongest binding to MAL and the highest expression levels of alpha 2,3-sialic acid residues among the selected cell lines, depending on mRNA expression levels of alpha 2,3-sialyltransferase gene. The adhesion, invasion and migration activities confirmed that MDA-MB-231 exhibited the greater cell adhesion to, migration toward and invasion to Matrigel. Taken together, the high expression of alpha 2,3-sialic acid residues in breast cancer was associated with metastatic potential. This property may be important for developing new therapeutic approaches for breast cancer.