4.6 Article

The role of the histone H3 variant CENPA in prostate cancer

期刊

JOURNAL OF BIOLOGICAL CHEMISTRY
卷 295, 期 25, 页码 8537-8549

出版社

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.RA119.010080

关键词

Centromere; prostate cancer; epigenetics; histone; gene expression; centromere protein A (CENPA); gene regulation; transcription; chromatin; cell proliferation; centromere

资金

  1. National Institutes of Health [R01-DK109188, 5T32GM007863-34, F30-CA-210379, F30-CA-200328, R01-CA-158286-S1, RM-08-029, P30U54ES017885]
  2. University of Michigan Cancer Biology Fellowship
  3. Scleroderma Foundation
  4. Prostate Cancer Foundation [17YOUN13]
  5. Biomedical Research Core Facilities Epigenomics Core at the University of Michigan
  6. A. Alfred Taubman Medical Research Institute
  7. Howard Hughes Medical Institute Investigatorship
  8. A. Alfred Taubman Scholarship
  9. American Cancer Society Professorship

向作者/读者索取更多资源

Overexpression of centromeric proteins has been identified in a number of human malignancies, but the functional and mechanistic contributions of these proteins to disease progression have not been characterized. The centromeric histone H3 variant centromere protein A (CENPA) is an epigenetic mark that determines centromere identity. Here, using an array of approaches, including RNA-sequencing and ChIP-sequencing analyses, immunohistochemistry-based tissue microarrays, and various cell biology assays, we demonstrate that CENPA is highly overexpressed in prostate cancer in both tissue and cell lines and that the level of CENPA expression correlates with the disease stage in a large cohort of patients. Gain-of-function and loss-of-function experiments confirmed that CENPA promotes prostate cancer cell line growth. The results from the integrated sequencing experiments suggested a previously unidentified function of CENPA as a transcriptional regulator that modulates expression of critical proliferation, cell-cycle, and centromere/kinetochore genes. Taken together, our findings show that CENPA overexpression is crucial to prostate cancer growth.

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