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Updated: May 24, 2026

Sequence-specific and Selective Recognition of Double-stranded RNAs over Single-stranded RNAs by Chemically Modified Peptide Nucleic Acids
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Antisense technologies targeting fatty acid synthetic enzymes.

Jinshun Lin1, Feng Liu, Yuyang Jiang

  • 1Guangdong Provincial Key Laboratory of Chemical Biology, Tsinghua University Graduate School at Shenzhen, Shenzhen, 518055, PR China.

Recent Patents on Anti-Cancer Drug Discovery
|February 21, 2012
PubMed
Summary

Antisense agents specifically inhibit gene expression, offering potential cancer therapies by targeting fatty acid synthesis enzymes. This review covers their applications and related patents, including those targeting miR-122.

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Area of Science:

  • Biochemistry
  • Molecular Biology
  • Oncology

Background:

  • Fatty acid synthesis involves multiple enzymes crucial for tumor growth.
  • Overexpression of these enzymes makes them targets for cancer therapy.
  • Antisense agents offer specific gene expression inhibition for research and therapy.

Purpose of the Study:

  • To review antisense agents for modulating fatty acid synthesis.
  • To discuss patents related to antisense agents targeting fatty acid synthetic enzymes.
  • To explore antisense agents targeting miR-122 for cancer therapy.

Main Methods:

  • Review of scientific literature on antisense agents and fatty acid synthesis.
  • Analysis of patents concerning antisense agents and fatty acid synthetic enzymes.
  • Examination of studies on miR-122's role in fatty acid synthesis regulation.

Main Results:

  • Antisense agents are effective tools for studying gene function and potential cancer therapeutics.
  • Various antisense agents can modulate fatty acid synthesis pathways.
  • Patents exist for antisense agents targeting key fatty acid synthetic enzymes and miR-122.

Conclusions:

  • Antisense technology holds promise for cancer treatment by targeting fatty acid synthesis.
  • Further research and development of antisense agents are warranted.
  • Inhibition of miR-122 represents a novel therapeutic strategy in this area.