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PI3K isoform-selective inhibitors in cancer

  • Leslie Duncan
    ,
  • Chloe Shay
    ,
  • Yong Teng(corresponding author)
*Corresponding author for this work
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

PI3K inhibitors are a common area of research in finding a successful treatment of cancer. The PI3K pathway is important for cell growth, apoptosis, cell metabolism, cell survival, and a multitude of other functions. There are multiple isoforms of PI3K that can be broken down into three categories: class I, II, and III. Each isoform has at least one subunit that helps with the functionality of the isoform. Mutations found in the PI3K isoforms are commonly seen in many different types of cancer and the use of inhibitors is being tested to stop the cell survival of cancer cells. Individual PI3K inhibitors have shown some inhibition of the pathway; however, there is room for improvement. To better treat cancer, PI3K inhibitors are being combined with other pathway inhibitors. These combination therapies have shown better results with cancer treatments. Both the monotherapy and dual therapy treatments are still currently being studied and data collected to better understand cancer and other treatment options.

Publication Information

Output type

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

Original language

English (US)

Pages from-to (Number of pages)

Pages 165-173 (9 pages)

Publication milestones

  • Published - 2020

Publication status

Published - 2020

Publisher

Springer

Publication series

  • Publication series name: Advances in Experimental Medicine and Biology
    ISSN (Print): 0065-2598
    ISSN (Electronic): 2214-8019
    Volume: 1255

Publication IDs

  • Scopus: 85091324227
  • PubMed: 32949399
  • ORCID: /0000-0002-1856-7289/work/82035244

Host publication title

Advances in Experimental Medicine and Biology

Publication metrics

Metrics

Fractional count
1
Fractional count
0.33
Fractional count
2
Fractional count
0.67
Fractional count
1
Fractional count
1
SciVal
FWCI
1.28
SciVal
Author count
3
SciVal
citations
2
SciVal
Paper percentile
78
Scopus
citations

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Citation count
11
Captures
5

Funding Details

This work was supported in part by Augusta University CURS Summer Scholars. Competing interests: The authors declare that they have no competing interests.
FundersFunding number
NIDCR
R03DE028387
Augusta University-