Optical coding of fusion genes using multicolor quantum dots for prostate cancer diagnosis

Int J Nanomedicine. 2017 Jun 12:12:4397-4407. doi: 10.2147/IJN.S138081. eCollection 2017.

Abstract

Recent studies have found that prostate cancer expresses abnormal genetic markers including multiple types of TMPRSS2-ERG fusion genes. The expression level of different TMPRSS2-ERG fusion genes is correlated to pathologic variables of aggressive prostate cancer and disease progression. State-of-the-art methods for detection of TMPRSS2-ERG fusion genes include reverse transcription polymerase chain reaction (RT-PCR) with a detection limit of 1 fmol at urinary condition. RT-PCR is time consuming, costly, and inapplicable for multiplexing. Ability to identify multiple fusion genes in a single sample has become important for diagnostic and clinical purposes. There is a need for a sensitive diagnostic test to detect multiple TMPRSS2-ERG fusion genes for an early diagnosis and prognosis of prostate cancer. Here, we propose to develop an assay for prostate cancer diagnosis using oligonucleotide-functionalized quantum dot and magnetic microparticle for optical detection of rearranged TMPRSS2-ERG fusion genes at a low concentration in urine. We found that our assay was able to identify three different types of fusion gene with a wide detection range and detection limit of 1 fmol (almost the same level of the RT-PCR result reported). Here, we show detection of multiple TMPRSS2-ERG fusion genes using color-coded oligonucleotides in cell lysate and urine.

Keywords: fusion genes; multiplexed assay; optical detection; prostate cancer; quantum dots.

MeSH terms

  • Cell Line, Tumor
  • Humans
  • Magnetite Nanoparticles
  • Male
  • Oncogene Proteins, Fusion / analysis
  • Oncogene Proteins, Fusion / genetics
  • Oncogene Proteins, Fusion / urine*
  • Optics and Photonics / instrumentation
  • Optics and Photonics / methods*
  • Prognosis
  • Prostatic Neoplasms / genetics*
  • Prostatic Neoplasms / urine
  • Quantum Dots* / chemistry

Substances

  • Magnetite Nanoparticles
  • Oncogene Proteins, Fusion
  • TMPRSS2-ERG fusion protein, human