Skip to content
2000
Volume 19, Issue 23
  • ISSN: 1568-0266
  • E-ISSN: 1873-4294

Abstract

Kirsten rat sarcoma 2 viral oncogene homolog (KRAS) is the most commonly mutated oncogene in human cancer. The developments of many cancers depend on sustained expression and signaling of KRAS, which makes KRAS a high-priority therapeutic target. Scientists have not successfully developed drugs that target KRAS, although efforts have been made last three decades. In this review, we highlight the emerging experimental strategies of impairing KRAS membrane localization and the direct targeting of KRAS. We also conclude the combinatorial therapies and RNA interference technology for the treatment of KRAS mutant cancers. Moreover, the virtual screening approach to discover novel KRAS inhibitors and synthetic lethality interactors of KRAS are discussed in detail.

Loading

Article metrics loading...

/content/journals/ctmc/10.2174/1568026619666190905164144
2019-09-01
2025-09-13
Loading full text...

Full text loading...

/content/journals/ctmc/10.2174/1568026619666190905164144
Loading

  • Article Type:
    Review Article
Keyword(s): Cancer treatment; KRAS; Mutant cancers; Oncogene; Therapeutic target; Viral oncogene
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