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Quantifying Y chromosome loss in primary and metastatic prostate cancer by chromosome painting.
Rajanala, Sai Harisha; Ghale, Romina; Nandakumar, Subhiksha; Chadalavada, Kalyani; Lee, Gwo-Shu Mary; Stopsack, Konrad H; Chen, Yu; Nanjangud, Gouri J; Chakraborty, Goutam; Kantoff, Philip W.
Affiliation
  • Rajanala SH; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, United States of America.
  • Ghale R; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, United States of America.
  • Nandakumar S; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, United States of America.
  • Chadalavada K; Molecular Cytogenetics Core, Memorial Sloan Kettering Cancer Center, New York, New York, United States of America.
  • Lee GM; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Masacheussets, United States of America.
  • Stopsack KH; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, United States of America.
  • Chen Y; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, United States of America.
  • Nanjangud GJ; Molecular Cytogenetics Core, Memorial Sloan Kettering Cancer Center, New York, New York, United States of America.
  • Chakraborty G; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, United States of America.
  • Kantoff PW; Department of Urology, Icahn School of Medicine at Mount Sinai, New York, New York, United States of America.
PLoS One ; 19(4): e0301989, 2024.
Article in En | MEDLINE | ID: mdl-38683764
ABSTRACT
Somatic Y chromosome loss in hematopoietic cells is associated with higher mortality in men. However, the status of the Y chromosome in cancer tissue is not fully known due to technical limitations, such as difficulties in labelling and sequencing DNA from the Y chromosome. We have developed a system to quantify Y chromosome gain or loss in patient-derived prostate cancer organoids. Using our system, we observed Y chromosome loss in 4 of the 13 (31%) patient-derived metastatic castration-resistant prostate cancer (mCRPC) organoids; interestingly, loss of Yq (long arm of the Y chromosome) was seen in 38% of patient-derived organoids. Additionally, potential associations were observed between mCRPC and Y chromosome nullisomy. The prevalence of Y chromosome loss was similar in primary and metastatic tissue, suggesting that Y chromosome loss is an early event in prostate cancer evolution and may not a result of drug resistance or organoid derivation. This study reports quantification of Y chromosome loss and gain in primary and metastatic prostate cancer tissue and lays the groundwork for further studies investigating the clinical relevance of Y chromosome loss or gain in mCRPC.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Chromosome Painting / Chromosomes, Human, Y / Neoplasm Metastasis Limits: Humans / Male Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2024 Type: Article Affiliation country: United States

Full text: 1 Database: MEDLINE Main subject: Chromosome Painting / Chromosomes, Human, Y / Neoplasm Metastasis Limits: Humans / Male Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2024 Type: Article Affiliation country: United States