Loss of PTEN/MMAC1/TEP in EGF receptor-expressing tumor cells counteracts the antitumor action of EGFR tyrosine kinase inhibitors

Roberto Bianco, Incheol Shin, Christoph A. Ritter, F. Michael Yakes, Andrea Basso, Neal Rosen, Junji Tsurutani, Phillip A. Dennis, Gordon Mills, Carlos L. Arteaga

Research output: Contribution to journalArticle

402 Citations (Scopus)

Abstract

We have examined the possible mechanisms of resistance to the epidermal growth factor receptor (EGFR) inhibitors in tumor cells with variable levels of EGFR. ZD1839 (Iressa) is a small-molecular-weight, ATP-mimetic that specifically inhibits the EGFR tyrosine kinase. A431 cell growth was markedly inhibited by ZD1839 (IC50 ≤ 0.1 μM) whereas the MDA-468 cells were relatively resistant (IC50 < 2 μM). Low doses of ZD1839 delayed cell cycle progression and induced apoptosis in A431 cells but not in MDA-468 cells. In both cell lines, 0.1 μM ZD1839 eliminated EGFR phosphorylation. However, the basal activity of the phosphatidylinositol-3 kinase (PI3 K) target Akt was eliminated in A431 but not in MDA-468 cells, implying that their Akt activity is independent of EGFR signals. A431 cells express PTEN/MMAC1/TEP, a phosphatase that can dephosphorylate position D3 of phosphatidylinositol-3,4,5 trisphosphate, the site that recruits the plecstrin-homology domain of Akt to the cell membrane. On the contrary, MDA-468 cells lack the phosphatase and tensin homolog (PTEN), potentially setting Akt activity at a high threshold that is unresponsive to EGFR inhibition alone. Therefore, we reintroduced (PTEN) by retroviral infection in MDA-468 cells. In MDA-468/PTEN but not in vector controls, treatment with ZD1839 inhibited P-Akt levels, induced relocalization of the Forkhead factor FKHRL1 to the cell nucleus, and increased FKHRL1-dependent transcriptional activity. ZD1839 induced a greater degree of apoptosis and cell cycle delay in PTEN-reconstituted than in control cells. These data suggest that loss of PTEN, by permitting a high level of Akt activity independent of receptor tyrosine kinase inputs, can temporally dissociate the inhibition of the EGFR with that of Akt induced by EGFR inhibitors. Thus, in EGFR-expressing tumor cells with concomitant amplification(s) of PI3K-Akt signaling, combined blockade of the EGFR tyrosine kinase and Akt should be considered as a therapeutic approach.

Original languageEnglish (US)
Pages (from-to)2812-2822
Number of pages11
JournalOncogene
Volume22
Issue number18
DOIs
StatePublished - May 8 2003
Externally publishedYes

Fingerprint

Phosphoric Monoester Hydrolases
Epidermal Growth Factor Receptor
Protein-Tyrosine Kinases
Neoplasms
Inhibitory Concentration 50
Cell Cycle
Tensins
tetraethylpyrazine
Phosphatidylinositol 3-Kinase
Apoptosis
Receptor Protein-Tyrosine Kinases
gefitinib
Cell Nucleus
Phosphatidylinositol 3-Kinases
Adenosine Triphosphate
Molecular Weight
Phosphorylation
Cell Membrane
Cell Line

Keywords

  • Akt
  • Epidermal growth factor receptor
  • PTEN
  • Tyrosine kinase inhibitors
  • ZD1839

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Cancer Research

Cite this

Bianco, R., Shin, I., Ritter, C. A., Yakes, F. M., Basso, A., Rosen, N., ... Arteaga, C. L. (2003). Loss of PTEN/MMAC1/TEP in EGF receptor-expressing tumor cells counteracts the antitumor action of EGFR tyrosine kinase inhibitors. Oncogene, 22(18), 2812-2822. https://doi.org/10.1038/sj.onc.1206388

Loss of PTEN/MMAC1/TEP in EGF receptor-expressing tumor cells counteracts the antitumor action of EGFR tyrosine kinase inhibitors. / Bianco, Roberto; Shin, Incheol; Ritter, Christoph A.; Yakes, F. Michael; Basso, Andrea; Rosen, Neal; Tsurutani, Junji; Dennis, Phillip A.; Mills, Gordon; Arteaga, Carlos L.

In: Oncogene, Vol. 22, No. 18, 08.05.2003, p. 2812-2822.

Research output: Contribution to journalArticle

Bianco, R, Shin, I, Ritter, CA, Yakes, FM, Basso, A, Rosen, N, Tsurutani, J, Dennis, PA, Mills, G & Arteaga, CL 2003, 'Loss of PTEN/MMAC1/TEP in EGF receptor-expressing tumor cells counteracts the antitumor action of EGFR tyrosine kinase inhibitors', Oncogene, vol. 22, no. 18, pp. 2812-2822. https://doi.org/10.1038/sj.onc.1206388
Bianco, Roberto ; Shin, Incheol ; Ritter, Christoph A. ; Yakes, F. Michael ; Basso, Andrea ; Rosen, Neal ; Tsurutani, Junji ; Dennis, Phillip A. ; Mills, Gordon ; Arteaga, Carlos L. / Loss of PTEN/MMAC1/TEP in EGF receptor-expressing tumor cells counteracts the antitumor action of EGFR tyrosine kinase inhibitors. In: Oncogene. 2003 ; Vol. 22, No. 18. pp. 2812-2822.
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AU - Yakes, F. Michael

AU - Basso, Andrea

AU - Rosen, Neal

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