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HSP90-Specific nIR Probe Identifies Aggressive Prostate Cancers: Translation from Preclinical Models to a Human Phase I Study.
Osada, Takuya; Crosby, Erika J; Kaneko, Kensuke; Snyder, Joshua C; Ginzel, Joshua D; Acharya, Chaitanya R; Yang, Xiao-Yi; Polascik, Thomas J; Spasojevic, Ivan; Nelson, Rendon C; Hobeika, Amy; Hartman, Zachary C; Neckers, Leonard M; Rogatko, Andre; Hughes, Philip F; Huang, Jiaoti; Morse, Michael A; Haystead, Timothy; Lyerly, H Kim.
Afiliación
  • Osada T; Department of Surgery, Duke University Medical Center, Durham, North Carolina.
  • Crosby EJ; Department of Surgery, Duke University Medical Center, Durham, North Carolina.
  • Kaneko K; Department of Surgery, Duke University Medical Center, Durham, North Carolina.
  • Snyder JC; Department of Surgery, Duke University Medical Center, Durham, North Carolina.
  • Ginzel JD; Department of Surgery, Duke University Medical Center, Durham, North Carolina.
  • Acharya CR; Department of Surgery, Duke University Medical Center, Durham, North Carolina.
  • Yang XY; Department of Surgery, Duke University Medical Center, Durham, North Carolina.
  • Polascik TJ; Department of Surgery, Duke University Medical Center, Durham, North Carolina.
  • Spasojevic I; Department of Medicine, Duke University Medical Center, Durham, North Carolina.
  • Nelson RC; Pharmacokinetics/Pharmacodynamics Core Laboratory of Duke Cancer Institute, Durham, North Carolina.
  • Hobeika A; Department of Radiology, Duke University Medical Center, Durham, North Carolina.
  • Hartman ZC; Department of Surgery, Duke University Medical Center, Durham, North Carolina.
  • Neckers LM; Department of Surgery, Duke University Medical Center, Durham, North Carolina.
  • Rogatko A; Urologic Oncology Branch, NCI, Rockville, Maryland.
  • Hughes PF; Biostatistics and Bioinformatics Research Center, Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, California.
  • Huang J; Department of Pharmacology and Cancer Biology, Duke University, Durham, North Carolina.
  • Morse MA; Department of Pathology, Duke University Medical Center, Durham, North Carolina.
  • Haystead T; Department of Surgery, Duke University Medical Center, Durham, North Carolina.
  • Lyerly HK; Department of Medicine, Duke University Medical Center, Durham, North Carolina.
Mol Cancer Ther ; 21(1): 217-226, 2022 01.
Article en En | MEDLINE | ID: mdl-34675120
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.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Neoplasias de la Próstata / Proteínas HSP90 de Choque Térmico Idioma: En Revista: Mol Cancer Ther Asunto de la revista: ANTINEOPLASICOS Año: 2022 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Neoplasias de la Próstata / Proteínas HSP90 de Choque Térmico Idioma: En Revista: Mol Cancer Ther Asunto de la revista: ANTINEOPLASICOS Año: 2022 Tipo del documento: Article