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Induction of apoptosis by Hax-1 siRNA in melanoma cells

  • Wen Bin Li
  • , Jie Feng
  • , Song Mei Geng
  • , Peng Yu Zhang
  • , Xiao Ning Yan
  • , Gang Hu
  • , Cai Qing Zhang
  • , Bing Jun Shi
  • Xi'an Jiaotong University

Research output: Contribution to journal › Article › peer-review

24 Scopus citations

Abstract

HS1-associated protein X-1 (Hax-1) is a novel intracellular protein and recent studies suggested that it is an anti-apoptotic factor in different tumors. Hax-1 expression was upregulated in various metastatic tumors and cancer cell lines, including melanoma. To understand the role of Hax-1 in melanoma development and progression, we constructed Hax-1 short interfering RNA (siRNA) expression vectors to downregulate Hax-1 expression in a human melanoma A375 cell line. One of the two Hax-1 RNA interference (RNAi) constructs significantly reduced melanoma cell viability, which was due to induction of apoptosis in A375 cells. Molecularly, the induced apoptosis through downregulation of Hax-1 expression was mediated by activation of caspase-3 and poly-ADP-ribose polymerase (PARP) enzymatic activity in A375 cells. The data indicate that Hax-1 plays a role in suppression of apoptosis and promotion of melanoma cell growth, suggesting that this Hax-1 siRNA has a therapeutic indication in control of melanoma.

Original languageEnglish
Pages (from-to)548-554
Number of pages7
JournalCell Biology International
Volume33
Issue number4
DOIs
StatePublished - Apr 2009

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Apoptosis
  • Hax-1
  • Melanoma
  • RNAi

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