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Gb3Cer 受体的生化、病理和肿瘤学相关性。

Biochemical, pathological and oncological relevance of Gb3Cer receptor.

机构信息

University of Split School of Medicine, Šoltanska 2, 21000 Split, Croatia.

出版信息

Med Oncol. 2011 Dec;28 Suppl 1:S675-84. doi: 10.1007/s12032-010-9732-8. Epub 2010 Nov 11.

Abstract

Glycosphingolipids are amphipathic molecules composed of hydrophilic oligosaccharide chain and a hydrophobic ceramide part, located primarily in the membrane microdomains of animal cells. Their oligosaccharide chains make them excellent candidates for the cell surface recognition molecules. Natural glycosphingolipid, globotriaosylceramide (Gal α1-4, Gal β1-4, Glc β1-1, ceramide), is also called CD77 and its expression was previously associated with proliferating centroblasts undergoing somatic hypermutation, but it has been demonstrate that globotriaosylceramide is not a reliable marker to discriminate human centroblasts from centrocytes. Globotriaosylceramide constitutes rare P k blood group antigen on erythrocytes, and it is also known as Burkitt's lymphoma antigen. On endothelial cells, globotriaosylceramide plays as the receptor for bacterial toxins of the Shiga family, also called verotoxins. Precise biological function and significance of globotriaosylceramide expression on endothelial cells remains to be the subject of many studies and it is believed globotriaosylceramide represents an example of a glycolipid antigen able to transduce a signal leading to apoptosis. In past decade, cancer researches put a great afford in determining new therapeutic agents such as bacterial toxins against tumor malignancies. Reports have demonstrated that verotoxin-1 induces apoptosis in solid tumor cell lines expressing globotriaosylceramide such as astrocytoma, renal cell carcinoma, colon cancer and breast cancer due to verotoxin-1 high specificity and apoptosis-inducing properties, and therefore, it is suggested to be an anticancer agent. Verotoxins have been investigated weather they could reduce treatment side-effects and toxicity to normal tissues and become a new oncological tool in cancer labeling.

摘要

糖鞘脂是由亲水性寡糖链和疏水性神经酰胺部分组成的两亲分子,主要位于动物细胞的膜微区。它们的寡糖链使它们成为细胞表面识别分子的优秀候选者。天然糖鞘脂,即神经节苷脂(Gal α1-4,Gal β1-4,Glc β1-1,神经酰胺),也称为 CD77,其表达以前与经历体细胞超突变的增殖中心母细胞有关,但已经证明神经节苷脂不是区分人类中心母细胞和中心细胞的可靠标记物。神经节苷脂在红细胞上构成罕见的 P k 血型抗原,也称为伯基特淋巴瘤抗原。在血管内皮细胞上,神经节苷脂作为细菌毒素 Shiga 家族的受体,也称为志贺毒素。神经节苷脂在血管内皮细胞上的表达的确切生物学功能和意义仍然是许多研究的主题,并且人们认为神经节苷脂代表了能够传递导致细胞凋亡信号的糖脂抗原的一个例子。在过去的十年中,癌症研究致力于确定新的治疗剂,如针对肿瘤恶性肿瘤的细菌毒素。有报道表明,由于志贺毒素-1 具有高度特异性和诱导凋亡的特性,因此在表达神经节苷脂的实体瘤细胞系(如星形细胞瘤、肾细胞癌、结肠癌和乳腺癌)中诱导凋亡。因此,它被认为是一种抗癌药物。已经研究了志贺毒素是否可以减少对正常组织的治疗副作用和毒性,并成为癌症标记的新肿瘤学工具。

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