Development of antimetastatic drugs by targeting tumor sialic acids

Da-Yong Lu1, Ting-Ren Lu, Hong-Ying Wu

  • 1School of Life Sciences, Shanghai University, Shanghai 200444, China.

Scientia Pharmaceutica
|September 26, 2012
PubMed

Insights

Neoplasm metastasis, a major cause of cancer death, lacks effective treatments. Targeting aberrant sialylation in tumors offers a promising new therapeutic strategy for antimetastatic drugs.

Area of Science:

  • Oncology
  • Cancer Metastasis Research
  • Drug Discovery

Background:

  • Neoplasm metastasis occurs in one-third of cancer cases and is a primary cause of cancer-related mortality.
  • Current therapeutic strategies for metastasis are largely unsatisfactory, with limited benefits observed in late-stage or elderly patients.
  • A significant challenge is the lack of specific therapeutic targets for neoplasm metastasis.

Purpose of the Study:

  • To review and discuss novel therapeutic approaches targeting sialic acids in metastatic tissues.
  • To highlight the potential of antimetastatic drugs that target aberrant sialylation in tumors.
  • To address the urgent need for new drug-screening pathways beyond current antimetastatic agents.

Main Methods:

  • Review of existing literature on therapeutic strategies for neoplasm metastasis.
  • Analysis of the role of aberrant sialylation and sialic acid analogues (e.g., N-glycolylneuraminic acid) in tumor tissues.
  • Discussion of six distinct therapeutic approaches targeting sialic acids in metastatic cancers.

Main Results:

  • Neoplasm tissues frequently exhibit elevated levels of sialic acids and sialyl antigens.
  • Sialic acid analogues, like N-glycolylneuraminic acid (Nau5Gc), are present in tumor tissues but typically absent in normal human tissues.
  • Targeting aberrantly sialylated structures in tumors represents a developing therapeutic avenue.

Conclusions:

  • Antimetastatic drugs targeting aberrant sialylation are a potential future therapeutic option.
  • These approaches may offer advantages over current treatments like antivascular agents and MMP inhibitors.
  • Further research and development of therapies targeting sialic acid modifications in metastasis are crucial.

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