HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Overexpression of long noncoding RNA HOXA-AS2 predicts an adverse prognosis and promotes tumorigenesis via SOX4/PI3K/AKT pathway in acute myeloid leukemia.

Abstract
Long noncoding RNAs (lncRNAs) play important roles in diverse cellular processes and carcinogenesis. Homeobox A cluster antisense RNA 2 (HOXA-AS2) is a 1,048-basepairs lncRNA located between human HOXA3 and HOXA4 genes, whose overactivation was previously found to promote the proliferation and invasion of solid tumors. However, its clinical and biological roles in acute myeloid leukemia (AML) remain unclear. This study showed that HOXA-AS2 was overexpressed in AML patients. In addition, the increased HOXA-AS2 expression was correlated with higher white blood cell and bone marrow blast counts, unfavorable karyotype classification, more measurable residual disease positivity, and earlier death. There was also a tendency toward inferior survival in patients with high HOXA-AS2 expression, and HOXA-AS2 was an independent prognostic factor among the normal-karyotype AMLs. Furthermore, the results of in vitro study showed that silencing HOXA-AS2 significantly inhibited the growth of leukemic cells by inducing G1/G0-phase arrest and apoptosis. Further analysis demonstrated that silencing HOXA-AS2 suppressed the phosphorylation level of PI3K and AKT, which thereafter promoted the expression of P21 and P27. Moreover, it was suggested that the sex-determining region Y-box 4 (SOX4), which is closely involved in the PI3K/AKT pathway, might be one of the major downstream targets of HOXA-AS2. Silencing HOXA-AS2 decreased the expression of SOX4, whereas the upregulation of SOX4 partially abrogated the inhibitory effect of silencing HOXA-AS2 on leukemic cells. In conclusion, these findings suggest that HOXA-AS2 probably functions as an oncogene via SOX4/PI3K/AKT pathway and might be a useful biomarker for the prognostic prediction in AML patients, providing a potential therapeutic target for AML.
AuthorsYi Qu, Yue Wang, Pingping Wang, Na Lin, Xiaojing Yan, Yan Li
JournalCell biology international (Cell Biol Int) Vol. 44 Issue 8 Pg. 1745-1759 (Aug 2020) ISSN: 1095-8355 [Electronic] England
PMID32369230 (Publication Type: Journal Article)
Copyright© 2020 International Federation for Cell Biology.
Chemical References
  • RNA, Long Noncoding
  • SOX4 protein, human
  • SOXC Transcription Factors
  • long noncoding RNA HOXA-AS2, human
  • Phosphatidylinositol 3-Kinase
  • Proto-Oncogene Proteins c-akt
Topics
  • Apoptosis
  • Carcinogenesis
  • Cell Cycle Checkpoints
  • Cell Line, Tumor
  • Cell Proliferation
  • Female
  • Humans
  • Leukemia, Myeloid, Acute (genetics, metabolism, mortality, pathology)
  • Male
  • Phosphatidylinositol 3-Kinase (metabolism)
  • Prognosis
  • Proto-Oncogene Proteins c-akt (metabolism)
  • RNA, Long Noncoding (antagonists & inhibitors, metabolism)
  • SOXC Transcription Factors (metabolism)
  • Signal Transduction

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: