IDEAS home Printed from https://ideas.repec.org/a/adp/jgjpps/v5y2018i1p5-7.html
   My bibliography  Save this article

Celastrol Mediated Hsp90 Protein Inhibition in Cancer

Author

Listed:
  • Dharambir Kashyap
  • Hardeep Singh Tuli

    (Department of Histopathology, Postgraduate Institute of Medical Education and Research (PGIMER), India
    Department of Biotechnology, Maharishi Markandeshwar University, India)

Abstract

In 2012, according to the globocan data 14.2 million new cases of cancer and 8.2 million cancer associated deaths had been reported. Lack of knowledge in cancer biology has major role for such disaster which increasing the enthusiasm to come up with promising anti-cancer therapy [1]. Discovery of new drug targets in cancer cell urgently required to reduce the mortality and to increase survival rate. The aberrant expression of Heat shock protein (Hsp) 90 has been correlated in all the cancer processes such as cell cycle arrest, angiogenesis, and metastasis [2-8]. So, identification of Hsp90 function in tumor cell may really be helpful which could serve as prognosis biomarker. The Hsp90 is a major molecular chaperone abundantly expressed in all cell types and plays pivotal role in correct folding and functionality of client proteins [9,10].

Suggested Citation

  • Dharambir Kashyap & Hardeep Singh Tuli, 2018. "Celastrol Mediated Hsp90 Protein Inhibition in Cancer," Global Journal of Pharmacy & Pharmaceutical Sciences, Juniper Publishers Inc., vol. 5(1), pages 5-7, february.
  • Handle: RePEc:adp:jgjpps:v:5:y:2018:i:1:p:5-7
    DOI: 10.19080/GJPPS.2018.05.555652
    as

    Download full text from publisher

    File URL: https://juniperpublishers.com/gjpps/pdf/GJPPS.MS.ID.555652.pdf
    Download Restriction: no

    File URL: https://juniperpublishers.com/gjpps/GJPPS.MS.ID.555652.php
    Download Restriction: no

    File URL: https://libkey.io/10.19080/GJPPS.2018.05.555652?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
    ---><---

    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:adp:jgjpps:v:5:y:2018:i:1:p:5-7. 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: Robert Thomas (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.