Deregulation of sialidases in human normal and tumor tissues.

IF 1.9
Matilde Forcella, Alessandra Mozzi, Federico M Stefanini, Alice Riva, Samantha Epistolio, Francesca Molinari, Elisabetta Merlo, Eugenio Monti, Paola Fusi, Milo Frattini
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引用次数: 14

Abstract

Background: Aberrant sialylation is a characteristic feature associated with cancer. The four types of mammalian sialidases identified to date have been shown to behave in different manners during carcinogenesis. While NEU1, NEU2 and NEU4 have been observed to oppose malignant phenotypes, the membrane-bound sialidase NEU3 was revealed to promote cancer progression.

Objectives: With the aim of improving the knowledge about sialidases deregulation in various cancer types, we investigated the amount of NEU1, NEU3 and NEU4 transcripts in paired normal and tumor tissues from 170 patients with 11 cancer types.

Methods: mRNA was extracted from patients' tissue specimens and retrotranscribed into cDNA, which was quantified by Real-Time PCR.

Results: We found NEU1 and NEU3 to be up regulated, while NEU4 was down regulated in most cancer types. In particular, colorectal cancer tissues showed the highest increase in NEU3 expression. Both NEU1 and NEU3 showed a strong up-regulation in ovarian cancer.

Conclusions: Our data show that human sialidases are expressed at different levels in healthy tissues and are strongly deregulated in tumors. Moreover, sialidases expression in our European cohort showed significant differences from Asian populations. Some of these peculiar features open potential applications of sialidases in cancer diagnosis and therapy.

人正常和肿瘤组织唾液酸酶的解除。
背景:异常唾液酰化是与癌症相关的特征。迄今发现的四种哺乳动物唾液酸酶在癌变过程中表现出不同的行为方式。虽然NEU1, NEU2和NEU4被观察到对抗恶性表型,但膜结合唾液酸酶NEU3被发现促进癌症进展。目的:为了提高对不同癌症类型唾液酸酯酶失调的认识,我们研究了170例11种癌症类型的配对正常和肿瘤组织中NEU1、NEU3和NEU4转录本的数量。方法:从患者组织标本中提取mRNA,反转录成cDNA, Real-Time PCR定量。结果:我们发现NEU1和NEU3在大多数癌症类型中上调,而NEU4则下调。其中,结直肠癌组织中NEU3的表达升高幅度最大。NEU1和NEU3在卵巢癌中均表现出较强的上调。结论:我们的数据表明,人唾液酸酶在健康组织中以不同水平表达,在肿瘤中被强烈地解除调控。此外,唾液酸酶在我们的欧洲队列中的表达与亚洲人群有显著差异。这些特殊的特性打开了唾液酸酶在癌症诊断和治疗中的潜在应用。
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