Analysis of PI3K pathway components in human cancers

Jamila Daragmeh, Waseim Barriah, Bashar Saad, Hilal Zaid

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

Abstract

Recent advances in genomics, proteomics, cell biology and biochemistry of tumors have revealed new pathways that are aberrantly activated in numerous cancer types. However, the enormous amount of data available in this field may mislead scientists in focused research. As cancer cell growth and progression is often dependent upon the phosphoinositide 3-kinase (PI3K)/AKT pathway, there has been extensive research into the proteins implicated in the PI3K pathway. Using data available in the Human Protein Atlas database, the current study investigated the expression of 25 key proteins that are known to be involved with PI3K pathway activation in a distinct group of 20 cancer types. These proteins are AKTIP, ARP1, BAD, GSK3A, GSK3B, MERTK-1, PIK3CA, PRR5, PSTPIP2, PTEN, FOX1, RHEB, RPS6KB1, TSC1, TP53, BCL2, CCND1, WFIKKN2, CREBBP, caspase-9, PTK2, EGFR, FAS, CDKN1A and XIAP. The analysis revealed pronounced expression of specific proteins in distinct cancer tissues, which may have the potential to serve as targets for treatments and provide insights into the molecular basis of cancer.

Original languageEnglish
Pages (from-to)2913-2918
Number of pages6
JournalOncology Letters
Volume11
Issue number4
DOIs
StatePublished - 1 Apr 2016
Externally publishedYes

Keywords

  • AKT
  • Cancer
  • EGFR
  • Human protein atlas
  • PI3K
  • PTEN
  • TSC1
  • Tumorigenesis

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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