Hakomori S
Pacific Northwest Research Foundation, Department of Pathobiology, University of Washington, Seattle 98195, USA.
Cancer Res. 1996 Dec 1;56(23):5309-18.
Aberrant glycosylation expressed in glycosphingolipids and glycoproteins in tumor cells has been implicated as an essential mechanism in defining stage, direction, and fate of tumor progression. This general concept is supported by results from three lines of study: (a) Numerous clinicopathological studies have shown a clear correlation between aberrant glycosylation status of primary tumor and invasive/metastatic potential of human cancer as reflected by 5- or 10-year survival rates of patients. (b) Carbohydrates expressed in tumor cells are either adhesion molecules per se or modulate adhesion receptor function. Some are directly involved in cell adhesion. They are recognized by selectins or other carbohydrate-binding proteins or by complementary carbohydrates (through carbohydrate-carbohydrate interaction). N- or O-glycosylation of functionally important membrane components may alter tumor cell adhesion or motility in a direction that either promotes or inhibits invasion and metastasis. Examples of such receptors are E-cadherin, integrins, immunoglobulin family receptors (e.g., CD44), and lysosome-associated membrane protein. (c) Gangliosides and sphingolipids modulate transmembrane signaling essential for tumor cell growth, invasion, and metastasis. The transducer molecules susceptible to gangliosides and sphingolipids include integrin receptors, tyrosine kinase-linked growth factor receptors, protein kinase C, and G-protein-linked receptor affecting protein kinase A. Some glycosphingolipids (e.g., Gb3Cer, Le(y), ceramide, and sphingosine induce tumor cell differentiation and subsequent apoptosis. Shedded gangliosides may block immunogenicity of tumor cells, providing conditions favorable for "escape" from immunological suppression of tumor growth by the host. Various reagents that block carbohydrate-mediated tumor cell adhesion or block glycosylation processing have been shown to inhibit tumor cell metastasis. This provides the basis for further development of "anti-adhesion therapy." Ganglioside analogues and sphingolipid analogues that inhibit protein kinase C and receptor-associated tyrosine kinase have been applied for inhibition of metastasis. A crucial mechanism for inhibition of metastasis by these reagents may involve blocking of transmembrane signaling for expression of P- and E-selectin. This provides the basis for development of "ortho-signaling therapy."
肿瘤细胞中糖鞘脂和糖蛋白所表达的异常糖基化被认为是定义肿瘤进展阶段、方向和命运的关键机制。这一普遍概念得到了三个研究方向结果的支持:(a)众多临床病理研究表明,原发性肿瘤的异常糖基化状态与人类癌症的侵袭/转移潜能之间存在明显关联,这可通过患者的5年或10年生存率反映出来。(b)肿瘤细胞中表达的碳水化合物本身就是黏附分子,或者可调节黏附受体功能。有些直接参与细胞黏附。它们可被选择素或其他碳水化合物结合蛋白识别,或者被互补碳水化合物识别(通过碳水化合物 - 碳水化合物相互作用)。功能重要的膜成分的N - 或O - 糖基化可能会改变肿瘤细胞的黏附或运动性,其改变方向可能促进或抑制侵袭和转移。这类受体的例子有E - 钙黏蛋白、整合素、免疫球蛋白家族受体(如CD44)和溶酶体相关膜蛋白。(c)神经节苷脂和鞘脂调节肿瘤细胞生长、侵袭和转移所必需的跨膜信号传导。易受神经节苷脂和鞘脂影响的转导分子包括整合素受体、酪氨酸激酶连接的生长因子受体、蛋白激酶C以及影响蛋白激酶A的G蛋白连接受体。一些糖鞘脂(如Gb3Cer、Le(y)、神经酰胺和鞘氨醇)可诱导肿瘤细胞分化及随后的凋亡。脱落的神经节苷脂可能会阻断肿瘤细胞的免疫原性,为肿瘤细胞从宿主对肿瘤生长的免疫抑制中“逃逸”创造有利条件。已证明各种阻断碳水化合物介导的肿瘤细胞黏附或阻断糖基化加工的试剂可抑制肿瘤细胞转移。这为进一步开发“抗黏附疗法”提供了依据。抑制蛋白激酶C和受体相关酪氨酸激酶的神经节苷脂类似物和鞘脂类似物已被用于抑制转移。这些试剂抑制转移的关键机制可能涉及阻断P - 和E - 选择素表达的跨膜信号传导。这为开发“正交信号疗法”提供了依据。