| Literature DB >> 34675120 |
Takuya Osada1, Erika J Crosby1, Kensuke Kaneko1, Joshua C Snyder1, Joshua D Ginzel1, Chaitanya R Acharya1, Xiao-Yi Yang1, Thomas J Polascik1, Ivan Spasojevic2,3, Rendon C Nelson4, Amy Hobeika1, Zachary C Hartman1, Leonard M Neckers5, Andre Rogatko6, Philip F Hughes7, Jiaoti Huang8, Michael A Morse1,2, Timothy Haystead7, H Kim Lyerly9.
Abstract
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. ©2021 The Authors; Published by the American Association for Cancer Research.Entities:
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Year: 2021 PMID: 34675120 PMCID: PMC8742774 DOI: 10.1158/1535-7163.MCT-21-0334
Source DB: PubMed Journal: Mol Cancer Ther ISSN: 1535-7163 Impact factor: 6.261