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三阴性乳腺癌中唾液酸 Lewis 与细胞角蛋白的相互作用

Sialyl Lewis and Cytokeratin Crosstalk in Triple Negative Breast Cancer.

作者信息

Pascoal Carlota, Carrascal Mylène A, Barreira Daniela F, Lourenço Rita A, Granjo Pedro, Grosso Ana R, Borralho Paula, Braga Sofia, Videira Paula A

机构信息

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.

出版信息

Cancers (Basel). 2023 Jan 25;15(3):731. doi: 10.3390/cancers15030731.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa72/9913872/6e1fa2877663/cancers-15-00731-g001.jpg

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