Insights into Aptamer-Drug Delivery Systems against Prostate Cancer

Molecules. 2022 May 26;27(11):3446. doi: 10.3390/molecules27113446.

Abstract

Prostate cancer is a common cancer in elderly males. Significant progress has been made in the drug therapies for prostate cancer in recent years. However, side effects are still problems that have not been overcome by the currently used anti-prostate cancer drugs. Novel technologies can be applied to reduce or even eliminate the side effects of drugs. An aptamer may be a sequence of nucleic acids or peptides that can specifically recognize proteins or cells. Taking advantage of this feature, scientists have designed aptamer-drug delivery systems for the development of anti-prostate cancer agents. Theoretically, these aptamer-drug delivery systems can specifically recognize prostate cancer cells and then induce cell death without attacking normal cells. We collected the relevant literature in this field and found that at least nine compounds have been prepared as aptamer-drug delivery systems to evaluate their precise anti-prostate cancer effects. However, the currently studied aptamer-drug delivery systems have not yet entered the market due to defects. Here, we analyze the published data, summarize the characteristics of these delivery systems, and propose ways to promote their application, thus promoting the development of the aptamer-drug delivery systems against prostate cancer.

Keywords: aptamer; curcumin; docetaxel; doxorubicin; drug delivery systems; paclitaxel; prostate cancer; thymoquinone.

Publication types

  • Review

MeSH terms

  • Aged
  • Antineoplastic Agents* / chemistry
  • Antineoplastic Agents* / pharmacology
  • Antineoplastic Agents* / therapeutic use
  • Aptamers, Nucleotide* / chemistry
  • Cell Line, Tumor
  • Doxorubicin / pharmacology
  • Drug Delivery Systems
  • Humans
  • Male
  • Peptides / therapeutic use
  • Prostatic Neoplasms* / drug therapy

Substances

  • Antineoplastic Agents
  • Aptamers, Nucleotide
  • Peptides
  • Doxorubicin