Analysis of the circulating myeloid-derived suppressor cells during androgen deprivation therapy for prostate cancer.

androgen antagonists myeloid‐derived suppressor cells prognosis prostate‐specific antigen prostatic neoplasms

Journal

IJU case reports
ISSN: 2577-171X
Titre abrégé: IJU Case Rep
Pays: Australia
ID NLM: 101764958

Informations de publication

Date de publication:
Nov 2021
Historique:
received: 23 04 2021
revised: 20 06 2021
accepted: 08 07 2021
entrez: 10 11 2021
pubmed: 11 11 2021
medline: 11 11 2021
Statut: epublish

Résumé

The present study showed the involvement of immunosuppressive myeloid-derived suppressor cells during the disease progression in a 69-year-old man with a prostate cancer. The patient with metastatic PC (cT4N1M1ab) was initially treated with primary androgen deprivation therapy for 5 months and then chemotherapy with docetaxel, but he expired at the 8th month. In order to investigate whether myeloid-derived suppressor cells are implicated in the cancer exacerbation during androgen deprivation therapy, we assessed the long-term changes in peripheral blood myeloid-derived suppressor cell fractions by using flow cytometry. While prostate-specific antigen levels decreased after androgen deprivation therapy, the population of each myeloid-derived suppressor cell subsets increased during disease deterioration. Increase in myeloid-derived suppressor cells populations was correlated with prostate cancer progression.

Identifiants

pubmed: 34755058
doi: 10.1002/iju5.12351
pii: IJU512351
pmc: PMC8560438
doi:

Types de publication

Case Reports

Langues

eng

Pagination

367-370

Informations de copyright

© 2021 The Authors. IJU Case Reports published by John Wiley & Sons Australia, Ltd on behalf of the Japanese Urological Association.

Déclaration de conflit d'intérêts

The authors declare no conflict of interest.

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Auteurs

Yuki Kohada (Y)

Division of Urology Faculty of Medicine Tohoku Medical and Pharmaceutical University Sendai Japan.
Department of Urology Hiroshima University Graduate School of Biomedical Sciences Hiroshima Japan.

Yasuhiro Kaiho (Y)

Division of Urology Faculty of Medicine Tohoku Medical and Pharmaceutical University Sendai Japan.

Kazuya Takeda (K)

Divisions of Immunology Faculty of Medicine Tohoku Medical and Pharmaceutical University Sendai Japan.

Akito Kuromoto (A)

Division of Urology Faculty of Medicine Tohoku Medical and Pharmaceutical University Sendai Japan.

Jun Ito (J)

Division of Urology Faculty of Medicine Tohoku Medical and Pharmaceutical University Sendai Japan.

Jun Teishima (J)

Department of Urology Hiroshima University Graduate School of Biomedical Sciences Hiroshima Japan.

Yasuhiro Nakamura (Y)

Division of Pathology Faculty of Medicine Tohoku Medical and Pharmaceutical University Sendai Japan.

Tomonori Kaifu (T)

Divisions of Immunology Faculty of Medicine Tohoku Medical and Pharmaceutical University Sendai Japan.

Akira Nakamura (A)

Divisions of Immunology Faculty of Medicine Tohoku Medical and Pharmaceutical University Sendai Japan.

Makoto Sato (M)

Division of Urology Faculty of Medicine Tohoku Medical and Pharmaceutical University Sendai Japan.

Classifications MeSH