Development of Antimetastatic Drugs by Targeting Tumor Sialic Acids
AbstractOne-third of all cancer categories in clinics have a high incidence of neoplasm metastasis. Neoplasm metastasis is one of the leading causes of cancer deaths. However, the prevailing therapeutic approach to this pathogenic process is presently unsatisfactory. Paradoxically to our efforts and expectations, except for some antibodies, no obvious improvements and therapeutic benefits in currently used drugs have been achieved until now. Therapeutic benefits in late-stage or elderly cancer patients are especially poor and useless. One of the reasons for this, we would guess, is the lack of therapeutic targets specifically related to neoplasm metastasis. In order to enhance the therapeutic efficacy, the development of antimetastatic drugs transcending from current drug-screening pathways is urgently needed. Antimetastatic drugs targeting aberrantly sialylated in tumors have evolved for about a quarter of a century and might be a future therapeutic option other than the currently utilized antimetastatic drugs, such as antivascular and MMP inhibitors. Since neoplasm tissues often manifest high levels of sialic acids and sialyl antigens or glycoligands, some types of sialic acid analogue, such as N-glycolylneuraminic acid (Nau5Gc), occurred in most tumor tissues which is normally absent in most humans. Consequently, more attention is needed to work with new therapeutic approaches to target these changes. This review addresses and discusses the latest six types of therapeutic approaches targeting sialic acids in metastatic tissues.
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LU, D.-Y.; LU, T.-R.; WU, H.-Y. Development of Antimetastatic Drugs by Targeting Tumor Sialic Acids. Sci. Pharm. 2012, 80, 497-508.
LU D-Y, LU T-R, WU H-Y. Development of Antimetastatic Drugs by Targeting Tumor Sialic Acids. Scientia Pharmaceutica. 2012; 80(3):497-508.Chicago/Turabian Style
LU, Da-Yong; LU, Ting-Ren; WU, Hong-Ying. 2012. "Development of Antimetastatic Drugs by Targeting Tumor Sialic Acids." Sci. Pharm. 80, no. 3: 497-508.