HSP90-Specific nIR Probe Identifies Aggressive Prostate Cancers: Translation from Preclinical Models to a Human Phase I Study.
Takuya OsadaErika J CrosbyKensuke KanekoJoshua C SnyderJoshua D GinzelChaitanya R AcharyaXiao-Yi YangThomas J PolascikIvan SpasojevicRendon C NelsonAmy HobeikaZachary Conrad HartmanLeonard M NeckersAndré RogatkoPhilip F HughesJiaoti HuangMichael A MorseTimothy HaysteadHerbert Kim LyerlyPublished in: Molecular cancer therapeutics (2021)
A noninvasive test to discriminate indolent prostate cancers from lethal ones would focus treatment where necessary while reducing overtreatment. We exploited the known activity of heat shock protein 90 (Hsp90) as a chaperone critical for the function of numerous oncogenic drivers, including the androgen receptor and its variants, to detect aggressive prostate cancer. We linked a near-infrared fluorescing molecule to an HSP90 binding drug and demonstrated that this probe (designated HS196) was highly sensitive and specific for detecting implanted prostate cancer cell lines with greater uptake by more aggressive subtypes. In a phase I human study, systemically administered HS196 could be detected in malignant nodules within prostatectomy specimens. Single-cell RNA sequencing identified uptake of HS196 by malignant prostate epithelium from the peripheral zone (AMACR+ERG+EPCAM+ cells), including SYP+ neuroendocrine cells that are associated with therapeutic resistance and metastatic progression. A theranostic version of this molecule is under clinical testing.
Keyphrases
- heat shock protein
- prostate cancer
- heat shock
- radical prostatectomy
- single cell
- induced apoptosis
- endothelial cells
- cell cycle arrest
- benign prostatic hyperplasia
- squamous cell carcinoma
- photodynamic therapy
- small cell lung cancer
- heat stress
- cell death
- stem cells
- emergency department
- signaling pathway
- quantum dots
- fluorescence imaging
- living cells
- cell therapy
- drug delivery
- endoplasmic reticulum stress
- transcription factor
- copy number
- cell proliferation
- drug release
- dna methylation
- combination therapy
- psychometric properties
- liquid chromatography
- pi k akt
- replacement therapy