2010 Jan 19
Preexistence and Clonal Selection of MET Amplification in EGFR Mutant NSCLC
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Preexistence and Clonal Selection of MET Amplification in EGFR Mutant NSCLC
MET amplification activates ERBB3/PI3K/AKT signaling in EGFR mutant lung cancers and causes resistance to EGFR kinase inhibitors. We demonstrate that MET activation by its ligand, HGF, also induces drug resistance, but through GAB1 signaling. Using high-throughput FISH analyses in both cell lines and in patients with lung cancer, we identify subpopulations of cells with MET amplification prior to drug exposure. Surprisingly, HGF accelerates the development of MET amplification both in vitro and in vivo. EGFR kinase inhibitor resistance, due to either MET amplification or autocrine HGF production, was cured in vivo by combined EGFR and MET inhibition. These findings highlight the potential to prospectively identify treatment naive, patients with EGFR-mutant lung cancer who will benefit from initial combination therapy.
Copyright (c) 2010 Elsevier Inc. All rights reserved.
Figure 1. HCC827 PFR cells are resistant to PF00299804, but combined MET and EGFR inhibition blocks PI3K/AKT and ERK signaling and restores sensitivity
in vitro and in vivo
(A) Parental and resistant HCC827 PFR5 cells treated with increasing concentrations of PF00299804. Cell viability relative to untreated controls measured after 72 hours. Each data point represents the mean ±SD of 6 wells. (B) HCC827 and HCC827 PFR5 and PFR6 cells were treated for 6 hours with 1 μM PF00299804 or gefitinib, PHA-665,752, or their combination. Cell lysates were immunoblotted to detect indicated proteins. (C) Upper, HCC827 PFR6 cells treated with increasing concentrations of PF00299804, PF2341066, or their combination. Lower, HCC827 PFR6 cells treated with increasing concentrations of gefitinib alone or in combination with PF2341066. Cell viability relative to untreated controls measured after 72 hours. Each data point represents the mean ±SD of 6 wells. (D) HCC827 PFR xenogafts in nu/nu mice were treated with PF2341066, PF00299804, or their combination. Tumors measured twice weekly. Only combination treatment led to tumor shrinkage and was the most effective treatment in vivo (p < 0.0001). Treatment was stopped after 56 days (arrow) and no tumor re-growth was observed in 35 weeks. Each data point represents the mean ±SD for 5 mice.
Figure 2. HCC827 PFR cells have a focal amplification in
MET that is similar to HCC827 GR cells
(A) MET copy number determined by quantitative PCR. Parental (Par) HCC827 and MET amplified HCC827 GR (GR5) cells were used as negative and positive controls, respectively. Each column represents the mean ±SD for 3 independent experiments. (B) Parental HCC827 cells and PFR clones were immunoblotted to detect indicated proteins. (C) Genome wide view of copy number changes generated using Human Mapping 250K Sty single nucleotide polymorphism (SNP) array and analyzed using the dChip program (see Experimental Procedures). HCC827 GR clones were compared with HCC827 PFR and HCC827 parental clones. Blue curve indicates degree of amplification of each SNP from 0 (left) to 8 (right). (D) Chromosome 7 view of copy number changes in HCC827 parental, GR and PFR cells. Arrow indicates MET oncogene.
Figure 3. HGF induces MET dependent resistance only in cell lines in which it activates PI3K/AKT, ERK and mTORC1 signaling
(A, B) HCC827 cells treated with (A) increasing concentrations of gefitinib alone or in combination with PHA-665,752, in the absence or presence of HGF (50ng/mL), or (B) increasing concentrations of gefitinib alone or in combination with the indicated concentrations of HGF. Cell viability relative to untreated controls measured after 72 hours. Each data point represents the mean ±SD of 6 wells. (C) HCC827 cells were treated for 6 hours with 1μM gefitinib alone or in combination with the indicated concentrations of HGF. Cell lysates were immunoblotted to detect indicated proteins. ( D) Cells were treated for 6 hours with gefitinib (HCC827, PC-9), PF00299804 (H1975), or lapatinib (BT-474, SKBR3), alone or in combination with HGF (50ng/mL). All drugs were used at 1μM. Cell lysates were immunoblotted to detect indicated proteins. *indicates cross-reaction by the p-EGFR antibody against p-HER2. Cell lines in which HGF rescued viability are labeled in blue, and cell lines in which HGF did not rescue viability are labeled in red. (E) HCC827-HGF xenografts in nu/nu mice treated with PF2341066, gefitinib, or their combination and tumors measured twice weekly. Some growth inhibiton was observed with gefitinib alone, however only combination treatment led to complete tumor shrinkage (p = 0.002). Each data point represents the mean ±SD for 5 mice. See also Figure S2.
Figure 4. IGF rescues PI3K/AKT and mTORC1 signaling in some cell lines, but fails to activate ERK
(A) IC 50 values for viability curves (Figure S1) in the presence or absence of HGF and IGF. Cells were treated with increasing concentrations of the appropriate TKI alone (red) or in combination with 50ng/mL HGF (blue) or 75ng/mL IGF (green). (B) Cells were treated for 6 hours with gefitinib (HCC827, PC-9, A431, HN11), PF00299804 (H1975) or lapatinib (BT-474, SKBR3) alone or in combination with HGF (50ng/mL) or IGF (75ng/mL). All drugs were used at 1μM. Cell lysates immunoblotted to detect indicated proteins. BT-474 and SKBR3 cell lysates were run on the same gel, and no MET or IGF-1Rβ was detected in SKBR3 cells relative to BT-474 cells. See also Table S1 for quantification.
Figure 5. HGF rescue of PI3K/AKT signaling is mediated though GAB1 instead of ERBB3
(A) Cells treated for 6 hours with gefitinib (HCC827, PC-9), PF00299804 (H1975), or lapatinib (BT-474, SKBR3), alone or in combination with HGF (50ng/mL). All drugs were used at 1μM. Cell extracts were immunoprecipitated with an anti-p85 antibody followed by Western blot with anti-p-Tyr, anti-ERBB3 and anti-p85 antibodies. (B) HCC827 cells were transfected with a negative control or GAB1 siRNA for 48 hours. Transfected cells were treated for 6 hours with gefitinib (1μM) alone or in combination with HGF (50ng/mL). Cell lysates were immunoblotted to detect indicated proteins. See also Figure S3. (C) HCC827 cells were transfected with GAB1 siRNA or a negative control siRNA for 48 hours, then treated with increasing concentrations of gefitinib, alone or in combination with 50ng/mL HGF. Left, cell viability relative to untreated controls measured after 72 hours. Each data point represents the mean ±SD of 6 wells. Right, plot of IC 50 values corresponding to cell viability curves.
Figure 6. Transient HGF exposure leads to
MET amplification and stable ligand-independent gefitinib resistance in HCC827 cells
(A) HCC827 cells treated with HGF (50ng/mL) and 1μM gefitinib are resistant to gefitinib (HCC827-50 cells). After the removal of HGF, stably resistant HGF-independent HCC827-50GR cells survive in 1μM gefitinib alone. In contrast, parental HCC827 cells do not survive when treated with 1μM gefitinib. (B) Parental HCC827 cells and HCC827-50 cells (pre-treated with gefitinib in combination with HGF (50ng/mL) for 14 days) were grown in media alone (No Rx) or media treated with 1μM gefitinib (+Gef) for 7 days. Viable cells were visualized and quantified using Syto60 staining. (C) Fluorescence in situ hybridization (FISH) of MET/EGFR/CEP7 probe set with HCC827 and HCC827-50GR cells. MET (orange) EGFR (green) CEP7 (aqua). Metaphase spread ( bottom) shows multiple copies of EGFR and MET (arrow) on individual chromosomes. Scale bars represent 10μm. (D) HCC827-50GR cells ( upper) and HCC827-50GR cells grown in media alone (without gefitinib) for 8 weeks, 50GR 8wks R5 ( lower), were treated with increasing concentrations of gefitinib or PHA-665,752 or their combination for 72 hours. Cell viability was measured relative to untreated controls. Each data point represents the mean ±SD of 6 wells. (E) HCC827 cells and stably resistant HCC827-50GR cells were treated for 6 hours with gefitinib, PHA-665,752, or their combination. All drugs were used at 1μM. Cell lysates were immunoblotted to detect indicated proteins. See also Figure S4 and Table S2 and S3.
Figure 7. HGF treatment selects out a small pre-existing population of
MET amplified HCC827 cells from the parental population in vitro and in vivo
(A) Fluorescence in situ hybridization (FISH) of MET/EGFR/CEP7 probe set. MET (red) EGFR (green) CEP7 (aqua). Left, tumor sections from control HCC827 xenograft models that do not express HGF showed normal MET copy number. Right, tumor sections from one of three HCC827-HGF xenografts treated with gefitinib (Figure 3E) showed significant MET amplification (arrow). (B) High-throughput FISH analysis of HCC827 cells identifies a subpopulation harboring MET amplification (arrow). MET (RP-11-95I120; red); 7qter (RP-11-6903; green). All scale bars represent 10μm. (C) Parental HCC827 cells and three independent clones harbor a small percentage of MET amplified cells. No pre-existing MET amplification was detected in H3255 or PC-9 cell populations. (D) Left, HCC827 cells were spiked with approximately 0.1% of GFP labeled HCC827 cells or GFP labeled MET amplified HCC827 GR6 cells. Each population was grown in either media alone or media treated with gefitinib (1μM) with HGF (50ng/mL). Cells were collected after 19 days and GFP levels were quantified using FACS. Each data point for cells treated with gefitinib+HGF represents the mean ±SD for 3 independent wells. Fold change is the ratio of Day 19 to Day 0 (%GFP). Right, diagrammatic depiction of results. See also Figure S5.
Figure 8. HGF expression and pre-existing
MET amplification can be detected in tumor specimens from NSCLC patients
(A) Summary of tumors from geftinib/erlotinib treated patients, including 16 paired, and 11 drug resistant samples only. Samples were evaluated for EGFR mutational status, MET amplification and HGF expression *Specimen contained less < 30% tumor cells. ** MET amplification defined by qPCR as previously described (Engelman et al., 2007b). Data on EGFR T790M and MET amplification in resistant specimens only from patients 1-4 and 17-19 has been previously published (Engelman et al., 2007b). N/A; not available. (B) FISH analysis of pre-treatment sample from patient 10 shows evidence of a subset of MET amplified cells (arrow) before exposure to an EGFR TKI. MET (RP-11-95I120; orange); CEP 7 (aqua). Scale bars represent 10μm. See also Figure S6.
All figures (8)
MET Amplification Leads to Gefitinib Resistance in Lung Cancer by Activating ERBB3 Signaling
JA Engelman et al.
Science 316 (5827), 1039-43.
The epidermal growth factor receptor (EGFR) kinase inhibitors gefitinib and erlotinib are effective treatments for lung cancers with EGFR activating mutations, but these …
Acquired Resistance of Non-Small Cell Lung Cancer Cells to MET Kinase Inhibition Is Mediated by a Switch to Epidermal Growth Factor Receptor Dependency
U McDermott et al.
Cancer Res 70 (4), 1625-34.
Cancer cells harboring MET amplification display striking sensitivity to selective small molecule inhibitors of MET kinase, prompting their clinical evaluation. Similar t …
Combined Therapy With Mutant-Selective EGFR Inhibitor and Met Kinase Inhibitor for Overcoming Erlotinib Resistance in EGFR-mutant Lung Cancer
T Nakagawa et al.
Mol Cancer Ther 11 (10), 2149-57.
Although the EGF receptor tyrosine kinase inhibitors (EGFR-TKI) erlotinib and gefitinib have shown dramatic effects against EGFR mutant lung cancer, patients become resis …
Current Mechanism of Acquired Resistance to Epidermal Growth Factor Receptor-Tyrosine Kinase Inhibitors and Updated Therapy Strategies in Human Nonsmall Cell Lung Cancer
K Zhang et al.
J Cancer Res Ther 12 (Supplement), C131-C137.
Lung cancer continues to be a major health problem and the most common cancer-related mortality worldwide with about 80%-85% patients suffering from nonsmall cell lung ca …
Targeting the MET Gene for the Treatment of Non-Small-Cell Lung Cancer
F Gelsomino et al.
Crit Rev Oncol Hematol 89 (2), 284-99.
Recently, a better understanding of the specific mechanisms of oncogene addiction has led to the development of antitumor strategies aimed at blocking these abnormalities …
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I Jeong et al.
J Cancer Prev 24 (4), 217-223.
Based on these findings, AXL was found to be a promising therapeutic target to overcome the intrinsic resistance to gefitinib in NSCLC. Furthermore, YD is able to effecti …
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Pemetrexed/carboplatin plus gefitinib is a promising treatment option for EGFR-mutant NSCLC patients in the first-line setting.
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Z Zhang et al.
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EGFR-tyrosine kinase inhibitors (EGFR-TKIs) have achieved remarkable outcomes in the treatment of patients with EGFR-mutant non-small-cell lung cancer, but acquired resis …
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The biggest hurdle to targeted cancer therapy is the inevitable emergence of drug resistance. Tumor cells employ different mechanisms to resist the targeting agent. Most …
Oligosaccharyltransferase: A Gatekeeper of Health and Tumor Progression
Y Harada et al.
Int J Mol Sci 20 (23).
Oligosaccharyltransferase (OST) is a multi-span membrane protein complex that catalyzes the addition of glycans to selected Asn residues within nascent polypeptides in th …
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