Pascoal Carlota, Carrascal Mylène A, Barreira Daniela F, Lourenço Rita A, Granjo Pedro, Grosso Ana R, Borralho Paula, Braga Sofia, Videira Paula A
UCIBIO, Applied Molecular Biosciences Unit, Department of Life Sciences, NOVA School of Science and Technology, Universidade NOVA de Lisboa, 2819-516 Caparica, Portugal.
Associate Laboratory i4HB-Institute for Health and Bioeconomy, NOVA School of Science and Technology, Universidade NOVA de Lisboa, 2819-516 Caparica, Portugal.
Cancers (Basel). 2023 Jan 25;15(3):731. doi: 10.3390/cancers15030731.
Triple-negative breast cancer (TNBC) encompasses multiple entities and is generally highly aggressive and metastatic. We aimed to determine the clinical and biological relevance of Sialyl-Lewis X and A (sLe)-a fucosylated glycan involved in metastasis-in TNBC. Here, we studied tissues from 50 TNBC patients, transcripts from a TNBC dataset from The Cancer Genome Atlas (TCGA) database, and a primary breast cancer cell line. All 50 TNBC tissue samples analysed expressed sLe. Patients with high expression of sLe had 3 years less disease-free survival than patients with lower expression. In tissue, sLe negatively correlated with cytokeratins 5/6 (CK5/6, which was corroborated by the inverse correlation between fucosyltransferases and CK5/6 genes. Our observations were confirmed in vitro when inhibition of sLe remarkably increased expression of CK5/6, followed by a decreased proliferation and invasion capacity. Among the reported glycoproteins bearing sLe and based on the STRING tool, α6 integrin showed the highest interaction score with CK5/6. This is the first report on the sLe expression in TNBC, highlighting its association with lower disease-free survival and its inverse crosstalk with CK5/6 with α6 integrin as a mediator. All in all, sLe is critical for TNBC malignancy and a potential prognosis biomarker and therapeutic target.
三阴性乳腺癌(TNBC)包含多种类型,通常具有高度侵袭性和转移性。我们旨在确定参与TNBC转移的唾液酸化路易斯X和A(sLe)-a岩藻糖基化聚糖的临床和生物学相关性。在此,我们研究了50例TNBC患者的组织、来自癌症基因组图谱(TCGA)数据库的TNBC数据集的转录本以及一种原发性乳腺癌细胞系。分析的所有50个TNBC组织样本均表达sLe。sLe高表达的患者无病生存期比低表达的患者短3年。在组织中,sLe与细胞角蛋白5/6(CK5/6)呈负相关(岩藻糖基转移酶与CK5/6基因之间的负相关证实了这一点)。当sLe受到抑制时,CK5/6的表达显著增加,随后增殖和侵袭能力下降,这在体外实验中得到了证实。在已报道的带有sLe的糖蛋白中,基于STRING工具,α6整合素与CK5/6的相互作用得分最高。这是关于TNBC中sLe表达的首次报道,突出了其与较低无病生存期的关联以及以α6整合素为介导与CK5/6的反向相互作用。总而言之,sLe对TNBC的恶性程度至关重要,是一种潜在的预后生物标志物和治疗靶点。