Skip to content
2000
Volume 12, Issue 1
  • ISSN: 1574-8928
  • E-ISSN: 2212-3970

Abstract

Background: Heat shock proteins (Hsp) are major chaperone molecules that have recently emerged as cancer therapeutic targets owing to their involvement in tumor cell proliferation, differentiation, invasion and metastasis. High levels of extracellular Hsp90 and Hsp70 have been closely associated with a wide range of human cancers. Accumulating evidence suggests that the pharmacological inhibition of these molecules can play a pivotal role in non-surgical cancer treatment. Efforts have been taken to develop monoclonal antibodies (mAbs) and antibody fragments targeting extracellular Hsp90 and Hsp70, alone or conjugated with standard anticancer agents, to control several types of cancer, such as breast, colon, prostate or melanoma. Objective: To provide an overview on the development of monoclonal antibodies and antibody fragments with capacity to bind Hsp90 and Hsp70, aiming at being used for cancer treatment. Methods: A systematic review was performed using European Patent Office and Google patents databases. Results: Based on the available literature and patents, we report the potential anticancer strategies based on these biological molecules. Conclusions: Supported by the recent developments in this field, Hsp targeting antibodies therapy may emerge for clinical use in the future for cancer patients, namely as antibody-drug conjugates combining the specificity of these antibodies with the potency of cytotoxic drugs.

Loading

Article metrics loading...

/content/journals/pra/10.2174/1574892812666161123141516
2017-02-01
2025-09-30
Loading full text...

Full text loading...

/content/journals/pra/10.2174/1574892812666161123141516
Loading

  • Article Type:
    Research Article
Keyword(s): Antibody; cancer treatment; chaperones; heat-shock proteins; patent
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test