IDEAS home Printed from https://ideas.repec.org/a/adm/journl/v8y2019i4p27-32.html
   My bibliography  Save this article

Isatin Inhibits SH-SY5Y Neuroblastoma Cell Invasion and Metastasis through LSD1 Activity Inhibition

Author

Listed:
  • Shaobo Cong
  • Lin Hou
  • Haoyue Luo
  • Yanan Hua
  • Xue Li
  • Fangling Wang
  • Li Zhang
  • Zheng Zhang
  • Ning Li

Abstract

Isatin has received much attention in recent years due to its anti-cancer properties[1], which offer important medical benefits. Isatin is an endogenous oxidized indole with a wide spectrum of behavioral and metabolic effects[2] and is commonly found in mammalian tissues and fluids[3]. It has many possible uses on the biomedical field[4] [5]and has also been investigated as a potential anti-cancer drug. However, its effects on neuroblastoma (NB) cells is still a mystery. This research aimed to elucidate the effects of Isatin on neuroblastoma cells metastasis and invasion and the underlying mechanism. Neuroblastoma cells viability was tested by CCK8. NB cells invasion and migration ability were tested by transwell and wound healing experiment. The mRNA relative expression of related molecules are detected by Rt-PCR and q-PCR. The protein relative expression of related molecules are detected by Simple western blotting. Our results demonstrated that isatin could inhibit neuroblastoma cell proliferation, invasion, and migration in a dose-dependent manner. Moreover, isatin increases the expression level of H3K4m1, PTEN. All results support the potential anti-metastatic effect of isatin in neuroblastoma cells.

Suggested Citation

  • Shaobo Cong & Lin Hou & Haoyue Luo & Yanan Hua & Xue Li & Fangling Wang & Li Zhang & Zheng Zhang & Ning Li, 2019. "Isatin Inhibits SH-SY5Y Neuroblastoma Cell Invasion and Metastasis through LSD1 Activity Inhibition," International Journal of Sciences, Office ijSciences, vol. 8(04), pages 27-32, April.
  • Handle: RePEc:adm:journl:v:8:y:2019:i:4:p:27-32
    DOI: 10.18483/ijSci.1986
    as

    Download full text from publisher

    File URL: https://www.ijsciences.com/pub/article/1986
    Download Restriction: no

    File URL: https://www.ijsciences.com/pub/pdf/V82019041986.pdf
    Download Restriction: no

    File URL: https://libkey.io/10.18483/ijSci.1986?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    More about this item

    Keywords

    Isatin; Neuroblastoma; PTEN; LSD1; Invasion;
    All these keywords.

    JEL classification:

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:adm:journl:v:8:y:2019:i:4:p:27-32. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Staff ijSciences (email available below). General contact details of provider: .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.