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抗乙酰肝素酶适体作为口腔癌潜在的诊断和治疗剂。

Anti-heparanase aptamers as potential diagnostic and therapeutic agents for oral cancer.

作者信息

Simmons Suzanne C, Jämsä Hannaleena, Silva Dilson, Cortez Celia M, McKenzie Edward A, Bitu Carolina C, Salo Sirpa, Nurmenniemi Sini, Nyberg Pia, Risteli Juha, deAlmeida Carlos E B, Brenchley Paul E C, Salo Tuula, Missailidis Sotiris

机构信息

Department of Chemistry and Analytical Sciences, The Open University, Milton Keynes, United Kingdom.

Department of Diagnostics and Oral Medicine, Institute of Dentistry, University of Oulu, Oulu, Finland; Medical Research Center and Oulu University Hospital, Oulu, Finland.

出版信息

PLoS One. 2014 Oct 8;9(10):e96846. doi: 10.1371/journal.pone.0096846. eCollection 2014.

Abstract

Heparanase is an endoglycosidase enzyme present in activated leucocytes, mast cells, placental tissue, neutrophils and macrophages, and is involved in tumour metastasis and tissue invasion. It presents a potential target for cancer therapies and various molecules have been developed in an attempt to inhibit the enzymatic action of heparanase. In an attempt to develop a novel therapeutic with an associated diagnostic assay, we have previously described high affinity aptamers selected against heparanase. In this work, we demonstrated that these anti-heparanase aptamers are capable of inhibiting tissue invasion of tumour cells associated with oral cancer and verified that such inhibition is due to inhibition of the enzyme and not due to other potentially cytotoxic effects of the aptamers. Furthermore, we have identified a short 30 bases aptamer as a potential candidate for further studies, as this showed a higher ability to inhibit tissue invasion than its longer counterpart, as well as a reduced potential for complex formation with other non-specific serum proteins. Finally, the aptamer was found to be stable and therefore suitable for use in human models, as it showed no degradation in the presence of human serum, making it a potential candidate for both diagnostic and therapeutic use.

摘要

乙酰肝素酶是一种存在于活化白细胞、肥大细胞、胎盘组织、中性粒细胞和巨噬细胞中的内切糖苷酶,参与肿瘤转移和组织侵袭。它是癌症治疗的一个潜在靶点,人们已研发出各种分子来试图抑制乙酰肝素酶的酶促作用。为了开发一种与之相关的诊断检测方法的新型疗法,我们之前曾描述过针对乙酰肝素酶筛选出的高亲和力适体。在这项研究中,我们证明这些抗乙酰肝素酶适体能够抑制与口腔癌相关的肿瘤细胞的组织侵袭,并证实这种抑制是由于对该酶的抑制,而非适体的其他潜在细胞毒性作用。此外,我们已确定一个30个碱基的短适体作为进一步研究的潜在候选物,因为它比其更长的对应物表现出更高的抑制组织侵袭的能力,以及与其他非特异性血清蛋白形成复合物的可能性降低。最后,发现该适体是稳定的,因此适用于人体模型,因为它在人血清存在的情况下没有降解,使其成为诊断和治疗用途的潜在候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82dd/4189786/76d3e20b3dde/pone.0096846.g001.jpg

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