WAWarren M. Allen

Warren M. Allen

*This is an algorithmically generated author record based on publicly available information.

Current Organizations / Institutes

The organizations/institutes from the scholar's latest article


Warren M. Allen has a total of 11 co-authors. Here are the top co-authors by number of shared publications:

  • Dave S.B. Hoon

    Department of Translational Molecular Medicine and Sequencing Center Saint John's Cancer Institute at Providence Saint John's Health Center Santa Monica California USA

    1 shared publication
  • David L. Krasne

    Department of Pathology, Providence St. John’s Cancer Institute, Santa Monica, CA 90404, USA

    1 shared publication
  • Jamie S. Moon

    Department of Translational Molecular Medicine and Sequencing Center, Saint John’s Cancer Institute, Providence Health Services, Santa Monica, California, USA

    1 shared publication
  • Jane Choe

    Department of Urologic Oncology, Providence St. John’s Cancer Institute, Santa Monica, CA 90404, USA

    1 shared publication
  • Matias A. Bustos

    Department of Translational Molecular Medicine, Saint John’s Cancer Institute (SJCI), Providence Saint John’s Health Center (SJHC), Santa Monica, USA

    1 shared publication
  • Rebecca Gross

    Department of Translational Molecular Medicine, Saint John’s Cancer Institute (SJCI), Providence Saint John’s Health Center (SJHC), Santa Monica, CA 90404, USA

    1 shared publication

Latest Publications

  • Open Access

    Urine Cell-Free MicroRNAs in Localized Prostate Cancer Patients

    by Yoko Koh, Matias A. Bustos, Jamie Moon, Rebecca Gross, Romela Irene Ramos, Suyeon Ryu, Jane Choe, Selena Y. Lin, Warren M. Allen, David L. Krasne, et al.

    Prostate cancer (PCa) is the most common cancer in men. Prostate-specific antigen screening is recommended for the detection of PCa. However, its specificity is limited. Thus, there is a need to find more reliable biomarkers that allow non-invasive screening for early-stage PCa. This study aims to explore urine microRNAs (miRs) as diagnostic biomarkers for PCa. We assessed cell-free miR (cfmiR) profiles of urine and plasma samples from pre- and post-operative PCa patients (n = 11) and normal healthy donors (16 urine and 24 plasma) using HTG EdgeSeq miRNA Whole Transcriptome Assay based on next-generation sequencing. Furthermore, tumor-related miRs were detected in formalin-fixed paraffin-embedded tumor tissues obtained from patients with localized PCa. Specific cfmiRs signatures were found in urine samples of localized PCa patients using differential expression analysis. Forty-two cfmiRs that were detected were common to urine, plasma, and tumor samples. These urine cfmiRs may have potential utility in diagnosing early-stage PCa and complementing or improving currently available PCa screening assays. Future studies may validate the findings.