4.4 Review

ErbB-2 signaling in advanced prostate cancer progression and potential therapy

期刊

ENDOCRINE-RELATED CANCER
卷 26, 期 4, 页码 R195-R209

出版社

BIOSCIENTIFICA LTD
DOI: 10.1530/ERC-19-0009

关键词

ErbB-2; castration-resistant prostate cancer; ErbB-2-targeting therapies; ErbB-2 regulation

资金

  1. National Institutes of Health [CA88184]
  2. US Department of Defense PCRP Grant [PC121645, PC141559]
  3. University of Nebraska Food for Health Grant
  4. University of Nebraska Medical Center Bridge Fund
  5. Buffet Cancer Center Pilot Project Grant
  6. University of Nebraska Medical Center Cancer Biology Training Grant [T32CA009476]
  7. University of Nebraska Medical Center Graduate Fellowship
  8. Purdue Pharma Scholars Award

向作者/读者索取更多资源

Currently, prostate cancer (PCa) remains the most commonly diagnosed solid tumor and the second leading cause of cancer-related deaths in US men. Most of these deaths are attributed to the development of castration-resistant (CR) PCa. ErbB-2 and ErbB family members have been demonstrated to contribute to the progression of this lethal disease. In this review, we focus on updating the role of ErbB-2 in advanced PCa progression and its regulation, including its regulation via ligand activation, miRNAs and protein phosphorylation. We also discuss its downstream signaling pathways, including AKT, ERK1/2 and STATs, involved in advanced PCa progression. Additionally, we evaluate the potential of ErbB-2, focusing on its protein hyper-phosphorylation status, as a biomarker for aggressive PCa as well as the effectiveness of ErbB-2 as a target for the treatment of CR PCa via a multitude of approaches, including orally available inhibitors, intratumoral expression of cPAcP, vaccination and immunotherapy.

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