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EGFR role in cancer: A potential therapeutic target

  • Allyson E. Koyen
    ,
  • Geraldine Nabeta
    ,
  • Stevin Bienfait
    ,
  • Ashley J. Schlafstein
    ,
  • David S. Yu
    ,
  • Waaqo Daddacha(corresponding author)
*Corresponding author for this work
  • Emory University
Scholary Output:
Chapter in Book/Report/Conference proceeding
Chapter

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Protein kinases play a vital role in the regulation of pathways that control cell growth, proliferation, survival, and differentiation. Epidermal growth factor receptor (EGFR) is a key protein kinase that when dysregulated, disrupts these pathways and, accordingly, is associated with several cancers. Thus, EGFR has been a focus of investigation as a therapeutic target for cancer treatment for the past several decades, with fair success. Despite this success, EGFR-targeted therapies are not universally effective across cancers, and improving the specificity and efficiency of EGFR-targeted therapies is an area of continued investigation. This chapter discusses recent progress made in understanding the role of EGFR in cancer and how the knowledge have been used to develop more precise EGFR-based therapeutic regimens for cancer patients.

Publication Information

Output type

Scholary Output:
Chapter in Book/Report/Conference proceeding
Chapter

Original language

English (US)

Pages from-to (Number of pages)

Pages 225-234 (10 pages)

Publication milestones

  • Published - 01/01/2018

Publication status

Published - 01/01/2018

Publisher

Springer Singapore, Singapore
9789811314858

ISBN (Electronic)

9789811314865

Publication IDs

  • Scopus: 85063420894

Host publication title

Role of Tyrosine Kinases in Gastrointestinal Malignancies

Publication metrics

Metrics

Fractional count
1
Fractional count
0.17
Fractional count
5
Fractional count
0.83
Fractional count
1
Fractional count
1
SciVal
Author count
6
SciVal
Paper percentile
27
Scopus
citations

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7
Citation count
3