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Impact of Circulating Tumor Cell-Expressed Prostate-Specific Membrane Antigen and Prostate-Specific Antigen Transcripts in Different Stages of Prostate Cancer.
Cho, Hyungseok; Byun, Seok-Soo; Son, Nak-Hoon; Chung, Jae Il; Seo, Won Ik; Lee, Chan Ho; Morgan, Todd M; Han, Ki-Ho; Chung, Jae-Seung.
Affiliation
  • Cho H; Department of Nanoscience and Engineering Center for Nano Manufacturing, Inje University, Gimhae, South Korea.
  • Byun SS; Department of Urology, Seoul National University Bundang Hospital, Seongnam, South Korea.
  • Son NH; Department of Statistics, Keimyung University, Daegu, South Korea.
  • Chung JI; Department of Urology, Busan Paik Hospital, Inje University, Busan, South Korea.
  • Seo WI; Department of Urology, Busan Paik Hospital, Inje University, Busan, South Korea.
  • Lee CH; Department of Urology, Busan Paik Hospital, Inje University, Busan, South Korea.
  • Morgan TM; Department of Urology, University of Michigan, Ann Arbor, Michigan.
  • Han KH; Department of Nanoscience and Engineering Center for Nano Manufacturing, Inje University, Gimhae, South Korea.
  • Chung JS; Department of Urology, Haeundae Paik Hospital, Inje University, Busan, South Korea.
Clin Cancer Res ; 30(9): 1788-1800, 2024 May 01.
Article in En | MEDLINE | ID: mdl-38587547
ABSTRACT

PURPOSE:

Prostate-specific membrane antigen (PSMA)-based images, which visually quantify PSMA expression, are used to determine prostate cancer micrometastases. This study evaluated whether a circulating tumor cell (CTC)-based transcript platform, including PSMA mRNA, could help identify potential prognostic markers in prostate cancer. EXPERIMENTAL

DESIGN:

We prospectively enrolled 21 healthy individuals and 247 patients with prostate cancer [localized prostate cancer (LPCa), n = 94; metastatic hormone-sensitive prostate cancer (mHSPC), n = 44; and metastatic castration-resistant prostate cancer (mCRPC), n = 109]. The mRNA expression of six transcripts [PSMA, prostate-specific antigen (PSA), AR, AR-V7, EpCAM, and KRT 19] from CTCs was measured, and their relationship with biochemical recurrence (BCR) in LPCa and mCRPC progression-free survival (PFS) rate in mHSPC was assessed. PSA-PFS and radiological-PFS were also calculated to identify potential biomarkers for predicting androgen receptor signaling inhibitor (ARSI) and taxane-based chemotherapy resistance in mCRPC.

RESULTS:

CTC detection rates were 75.5%, 95.3%, and 98.0% for LPCa, mHSPC, and mCRPC, respectively. In LPCa, PSMA [hazard ratio (HR), 3.35; P = 0.028) and PSA mRNA (HR, 1.42; P = 0.047] expressions were associated with BCR. Patients with mHSPC with high PSMA (HR, 4.26; P = 0.020) and PSA mRNA (HR, 3.52; P = 0.042) expressions showed significantly worse mCRPC-PFS rates than those with low expression. Increased PSA and PSMA mRNA expressions were significantly associated with shorter PSA-PFS and radiological PFS in mCPRC, indicating an association with drug resistance.

CONCLUSIONS:

PSMA and PSA mRNA expressions are associated with BCR in LPCa. In advanced prostate cancer, PSMA and PSA mRNA can also predict rapid progression from mHSPC to mCRPC and ARSI or taxane-based chemotherapy resistance.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biomarkers, Tumor / Prostate-Specific Antigen / Glutamate Carboxypeptidase II / Neoplastic Cells, Circulating / Neoplasm Staging / Antigens, Surface Limits: Aged / Aged80 / Humans / Male / Middle aged Language: En Journal: Clin Cancer Res Journal subject: NEOPLASIAS Year: 2024 Document type: Article Affiliation country: South Korea

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biomarkers, Tumor / Prostate-Specific Antigen / Glutamate Carboxypeptidase II / Neoplastic Cells, Circulating / Neoplasm Staging / Antigens, Surface Limits: Aged / Aged80 / Humans / Male / Middle aged Language: En Journal: Clin Cancer Res Journal subject: NEOPLASIAS Year: 2024 Document type: Article Affiliation country: South Korea