HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

A novel SERPINE1-FOSB fusion gene in pseudomyogenic hemangioendothelioma results in activation of intact FOSB and the PI3K-AKT-mTOR signaling pathway and responsiveness to sirolimus.

Abstract
Pseudomyogenic hemangioendothelioma (PHE) is an extremely rare disease that affects mainly the young and more men than women. PHE are multicentric, locally aggressive, have low metastatic potential, and affect multiple tissue planes. Genetic aberrations are frequently detected in PHE and may play important roles in the occurrence, development, and treatment of this disease. In this study, we report a case of PHE with a novel SERPINE1-FOSB fusion gene. The fusion introduced a strong promoter near the coding region of FOSB, resulting in overexpression of intact FOSB. Immunohistochemical analysis showed overexpression of pAKT and mTOR in tumor cells, suggesting activation of the PI3K-AKT-mTOR signaling pathway. The patient responded well to targeted therapy with sirolimus, an mTOR inhibitor. Our study correlated dysregulation of a specific signaling pathway and the effectiveness of a targeted therapy to a specific genetic aberration. This information may be useful for future investigations of targeted therapeutics and provide a potential predictive biomarker for therapeutic effectiveness in PHE cases.
AuthorsJun Ren, Xiaohui Wang, Yulin Zhou, Xin Yue, Shouhui Chen, Xin Ding, Shengqiang Zeng, Xiaoyong Jiang, Xiaokun Liu, Qiwei Guo
JournalThe Journal of dermatology (J Dermatol) Vol. 48 Issue 12 Pg. 1900-1906 (Dec 2021) ISSN: 1346-8138 [Electronic] England
PMID34580903 (Publication Type: Case Reports, Journal Article)
Copyright© 2021 Japanese Dermatological Association.
Chemical References
  • FOSB protein, human
  • Plasminogen Activator Inhibitor 1
  • Proto-Oncogene Proteins c-fos
  • SERPINE1 protein, human
  • MTOR protein, human
  • Proto-Oncogene Proteins c-akt
  • TOR Serine-Threonine Kinases
  • Sirolimus
Topics
  • Female
  • Hemangioendothelioma (drug therapy, genetics)
  • Humans
  • Male
  • Phosphatidylinositol 3-Kinases (genetics)
  • Plasminogen Activator Inhibitor 1
  • Proto-Oncogene Proteins c-akt (genetics)
  • Proto-Oncogene Proteins c-fos (genetics, metabolism)
  • Signal Transduction (genetics)
  • Sirolimus (therapeutic use)
  • TOR Serine-Threonine Kinases (genetics)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: