Quantitative Virus-Associated RNA Detection to Monitor Oncolytic Adenovirus Replication.
Tereza BrachtlovaJing LiIda H van der Meulen-MuilemanFemke SluiterWillem von MeijenfeldtIsabella WitteSanne MassaarRuben van den OeverJeroen de VrijVictor W van BeusechemPublished in: International journal of molecular sciences (2024)
Oncolytic adenoviruses are in development as immunotherapeutic agents for solid tumors. Their efficacy is in part dependent on their ability to replicate in tumors. It is, however, difficult to obtain evidence for intratumoral oncolytic adenovirus replication if direct access to the tumor is not possible. Detection of systemic adenovirus DNA, which is sometimes used as a proxy, has limited value because it does not distinguish between the product of intratumoral replication and injected virus that did not replicate. Therefore, we investigated if detection of virus-associated RNA (VA RNA) by RT-qPCR on liquid biopsies could be used as an alternative. We found that VA RNA is expressed in adenovirus-infected cells in a replication-dependent manner and is secreted by these cells in association with extracellular vesicles. This allowed VA RNA detection in the peripheral blood of a preclinical in vivo model carrying adenovirus-injected human tumors and on liquid biopsies from a human clinical trial. Our results confirm that VA RNA detection in liquid biopsies can be used for minimally invasive assessment of oncolytic adenovirus replication in solid tumors in vivo.
Keyphrases
- loop mediated isothermal amplification
- clinical trial
- label free
- real time pcr
- induced apoptosis
- nucleic acid
- endothelial cells
- minimally invasive
- peripheral blood
- gene therapy
- ionic liquid
- cell cycle arrest
- randomized controlled trial
- stem cells
- ultrasound guided
- cell death
- oxidative stress
- sensitive detection
- endoplasmic reticulum stress
- phase iii