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      Alterations in the Transcriptional Programs of Myeloma Cells and the Microenvironment during Extramedullary Progression Affect Proliferation and Immune Evasion.

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          Abstract

          In multiple myeloma, extramedullary progression is associated with treatment resistance and a high mortality rate. To understand the molecular mechanisms controlling the devastating progression of myeloma, we applied single-cell RNA-sequencing (RNA-seq) to myeloma in the bone marrow and myelomatous pleural effusions or ascites.

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          Author and article information

          Journal
          Clin Cancer Res
          Clinical cancer research : an official journal of the American Association for Cancer Research
          American Association for Cancer Research (AACR)
          1557-3265
          1078-0432
          February 15 2020
          : 26
          : 4
          Affiliations
          [1 ] Samsung Genome Institute, Samsung Medical Center, Seoul, Korea.
          [2 ] Department of Health Sciences and Technology, Samsung Advanced Institute for Health Sciences and Technology, Sunkyunkwan University School of Medicine, Seoul, Korea.
          [3 ] Department of Molecular Cell Biology, Sungkyunkwan University School of Medicine, Seoul, Korea.
          [4 ] Division of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
          [5 ] Department of Laboratory Medicine and Genetics, Sungkyunkwan University School of Medicine, Seoul, Korea.
          [6 ] Samsung Genome Institute, Samsung Medical Center, Seoul, Korea. woongyang@skku.edu haeock.lee@samsung.com kihyunk.kim@samsung.com.
          [7 ] Division of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea. woongyang@skku.edu haeock.lee@samsung.com kihyunk.kim@samsung.com.
          Article
          1078-0432.CCR-19-0694
          10.1158/1078-0432.CCR-19-0694
          31558476
          fc458d8e-f495-45f3-8431-ddd2f8743840
          History

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