- Open Access
Clinical implications of novel activating EGFR mutations in malignant peritoneal mesothelioma
© Foster et al; licensee BioMed Central Ltd. 2010
- Received: 3 May 2010
- Accepted: 13 October 2010
- Published: 13 October 2010
There is a paucity of information about the molecular perturbations involved in MPM tumor formation. We previously reported that EGFR-TK mutations in MPM were predictive of achieving optimal surgical cytoreduction, but the status of EGFR pathway activation potential of these mutations was not known. Here we present the mutant EGFR activating potential and the matured survival data of the EGFR mutant(mut+) relative to wild type EGFR(mut-) mesothelioma.
Twenty-nine patients were evaluated and their tumors were probed for mutations in the catalytic TK-domain. Twenty-five patients were treated with cytoreductive surgery and complete clinical data was available for comparison of the mut+ and mut- groups. A COS-7 cell expression model was used to determine mutation activating profiles and response to erlotinib.
Functional mutations were found in 31%(9/29) of patients; 7 of these mutations were novel and another was the L858R mutation. All missense mutations were found to be activating mutations and responsive to erlotinib. Of the 25 patients managed surgically, there were 7 mut+ and 18 mut-. Two of 7 (29%) mut+ developed progressive disease and died with a median follow-up time of 22 months; while 13/18 (72%) mut- developed progressive disease and 10/18 (56%) died with median TTP of 12 months and median survival of 14 months.
The novel EGFR mutations identified are activating mutations responsive to erlotinib. The mut+ subset have a 'relative' improved outcome. Erlotinib may have a role in MPM and exploration for mutations in a larger patient cohort is warranted.
- Epidermal Growth Factor Receptor
- Epidermal Growth Factor Receptor Mutation
- Malignant Mesothelioma
- Epidermal Growth Factor Receptor Inhibitor
Discovering the molecular pathways and mutations active in cancer has resulted in the emergence of novel therapies, as well as, the development of objective predictors of clinical outcome and response to cancer therapies. Perturbations and mutations in the epidermal growth factor receptor gene family have been identified in many cancer subtypes with gain of function alterations occurring at all levels of gene and protein expression [1–4]. Recent studies in non small cell lung cancer (NSCLC) have revealed that mutations in epidermal growth factor receptor (EGFR) occur in 15% of Caucasians and 30% of Asians with NSCLC, and the presence of specific EGFR mutations is predictive of response to therapy and cancer outcome [5–8]. The reported mutations in NSCLC are deletion or missense mutations that occur between exons 18-24 in the tyrosine kinase domain of the receptor. Investigation of EGFR mutations in lung cancers has become a pivotal research paradigm that has begun to unlock the utility of mutations in predicting clinical outcomes, selection of patients for therapies (EGFR-TKIs), and predicting response/resistance to these therapies.
Recapitulation of EGFR mutations in lung cancer cells in vitro have demonstrated that it is an example of an 'oncogenic addiction' mutation which provides a biologic explanation for the improved outcome seen in this EGFR mutant NSCLC group relative to the wild type group. EGFR mutations are likely not limited to lung cancer and pervasive in other cancer. A potential cancer type similar to NSCLC that might harbor functional EGFR mutations is malignant mesothelioma. The first feature common to both malignancies is that EGFR expression is quite common in malignant mesothelioma[10–12]. Also malignant mesothelioma, like NSCLC, is a highly lethal cancer that can arise de novo in the pleural cavity; but unlike NSCLC, mesothelioma can also originate in the peritoneal cavity and soft tissue. Malignant peritoneal mesothelioma (MPM), like pleural mesothelioma, is quite aggressive, with most patients succumbing to this disease within 7-14 months after diagnosis . Treatment of MPM with systemic chemotherapy, radiation, and/or palliative surgery has largely been unsuccessful in improving outcome or extending survival. However, over the last two decades, many groups have shown that aggressive surgical cytoreduction consolidated with intraperitoneal hyperthermic chemotherapy (CRS/IPHC) can improve improved patient outcome in a subset of patients. CRS/IPHC has been the only treatment modality that has yielded long-term survival and cure in selected patients [10, 14–19]. At our institution, we perform a high volume of CRS/IPHC for all forms of peritoneal surface malignancies. Through this experience it is evident that many mesothelioma patients do not experience the long term benefits of this aggressive surgical intervention, but all must endure the associated morbidity and mortality. Therefore, identification of surrogate markers that can predict response to CRS/IPHC and lead to novel therapeutic targets in mesothelioma prompted the pursuit of EGFR mutations. We have previously reported that EGFR mutations occur in 31% of MPM, a rate similar to that reported in NSCLC . When mutations were present they correlated with optimal surgical resection in 100% of the patients. Since most patients who present with MPM are unresectable, achieving optimal resection is important because it represents the only reproducible (surrogate) factor that predicts long-term survival . Here we report the first identification of EGFR activating mutations in mesothelioma, as well as, the updated clinical outcome.
Twenty-nine consecutive cases of newly diagnosed malignant peritoneal mesothelioma evaluated at Creighton University Medical Center from January 1, 2003 to July 31, 2006 were reviewed. All cases had paraffin embedded tissue available to perform immunostaining and mutation analysis. Institutional review board approval was obtained for this investigation.
Mutation analysis of EGFR in malignant mesothelioma
Tumor tissues were procured from patients who had undergone surgical resection at the department of surgery, Creighton University Medical Center, Omaha, from January 2003 to July 2006. Twenty-nine formalin-fixed paraffin-embedded tissues were available for the analysis. All patients had pathologically proven MPM. The study was approved by the institutional review board of the Creighton University Medical Center. Medical records and hematoxylin and eosin-stained slides of the specimen were reviewed by two pathologists. Tumor tissue with a tumor cell content of greater than 30-40% was chosen for the analysis. In several cases, tissue sections were microdissected manually to obtain both tumor and histologically normal tissue.
Genomic DNA was isolated from tumors embedded in paraffin blocks using Puregene DNA Purification kits (Gentra systems® MN, USA) according to manufacturer's protocol. The EGFR gene (Epidermal growth factor receptor, EGFR; MIM 131550), (Ensembl Gene ID ENSG00000146648) has a total of 28 exons. Genomic DNA were PCR-amplified for 7 different genomic regions of EGFR (Exon 18-24) covering the entire coding sequence of the tyrosine kinase domain and all associated splice junctions. Amplified PCR products were first screened by DHPLC heteroduplex analysis using the Transgenomic WAVE® system (Transgenomic, Omaha, NE) as previously described. Samples with variant DHPLC profiles were purified with QIAquick spin columns and sequenced directly (BigDye® Terminators sequencing kit, Foster City, CA) in both directions using an automated ABI 3100 genetic analysis system and analyzed using the Sequencer 4.1 software program package (Gene Codes®, Ann Arbor, MI). Mutant alleles were also cloned by use of the original TA cloning kit (Invitrogen Carlsbad, CA) according to manufacturer's protocol, after PCR amplification, purified and subjected to nucleotide sequencing.
Functional Analyses of Mutant EGFRs
Full length wild-type EGFR cDNA (Gene bank accession No. NM_005228) were cloned into pIRES-hrGFP-2a expression vector (Stratagene® La Jolla, CA). Mutations (W731L, E734Q, T785A, C797Y, Y801H, L831H, L858R and E868G) were introduced into full-length EGFR coding sequence by using a QuikChange II XL Site-Directed Mutagenesis kit (Stratagene). All mutant clones were sequenced to ensure that no additional mutations were introduced. The COS-7 cell line was obtained from American Type Culture Collection (ATCC® Manassas, VA) and grown in DMEM with high glucose, 10% FCS, 2 mM L-glutamine (GIBCO® Carlsbad, CA), 10 units/ml penicillin, and 10 μg/ml streptomycin. Cells were transfected (Lipofectamine LXT, Invitrogen) using one tube protocol. Briefly, 12.5 μg of the expression constructs were mixed thoroughly with 2.5 ml of Opti-MEM I reduced serum medium (Invitrogen) and incubated for 30 minutes at room temperature. DNA-Lipofectamine complexes were then added to 8 ml of Opti-MEM I reduced serum medium then plated equal volume in five p60 tissue culture dishes (Falcon® San Jose, CA) and incubated at 37°C and 5% CO2. Six hours after the transfection, 2 ml of DMEM with high glucose, 20% FCS was added to each dish. The next day, cells were switched to reduced serum medium and incubated overnight with 10 ng of EGF per milliliter (Sigma® St. Louis, MO). To evaluate the in vitro responsiveness of mutant receptors to EGFR inhibitor, cells were treated with various concentrations of Erlotinib (Tarceva® LC laboratories, Woburn, MA) three hours before the addition of 10 ng of EGF per milliliter. The Stock solutions of Erlotinib were prepared in DMSO and prior to use, diluted in fresh DMEM media. Three independent experiments were performed for all analyses. Cells were exposed to EGF for 15 minutes. The protein preparation and Western blot analysis was performed following the methods described previously.
Equal amounts of protein were prepared in 50 μl of Laemmli loading buffer and resolved using 4-15% criterion precast Tris-HCL gel electrophoresis (Bio-Rad® Hercules, CA), transferred to nitrocellulose membranes. The efficiency of transfer and uniformity of loading were determined by Ponceau S (Sigma) staining. Western blot analysis was performed with the use of either super signal West femto maximum sensitivity substrate and/or West pico chemiluminescent substrate reagents (Thermo scientific® Rockford, IL). Nitrocellulose membranes were incubated overnight and probed with anti-phospho-EGFR (Cell Signaling Technology®, Danvers, MA), and EGFR antibody (Cell Signaling Technology). The densities of specific protein bands were analyzed by densitometry (Quantity One GS-800 Imaging Densitometer, Bio-Rad®).
Survival and time to progression analysis
The statistical analyses were performed in an exploratory manner on twenty-five patients who underwent surgical exploration for cytoreductive surgery and intraperitoneal hyperthermic chemotherapy. When IPHC was performed, patients received either 30-40 mg of Mitomycin C or 800 mg/M2 of Carboplatin at an inflow temperature of 40.5-42°C for 90-120 minutes. The level of cytoreduction was scored as R1 -- no visible disease, R2a -- residual tumor nodules ≤ 5 mm, R2b -- residual tumor nodules > 5 mm ≤ 2 cm, R2c > 2 cm, and R3-unresectable. Optimal resectability was defined as an R1 or R2a resection. To determine the impact of the presence of mutation on survival and time to progression, a log rank analysis was performed.
EGFR and ERBB2 copy number status was assessed using FISH and quantitative PCR, and no evidence of amplification of either gene was found in all specimens (data not shown). Expression of the EGFR alternative transcript variant, EGFRvIII, could not be detected by RT-PCR (data not shown).
Time-response studies of EGFR on MM mutations in COS 7 cells
Dose response studies of Erlotinib on COS-7 transfected cells
Impact of EGFR mutations on survival and time to progression (TTP)
We have identified seven novel and one known point mutations in the EGFR-TK domain in MPM patients. All mutations are clustered and reside near the ATP-binding cleft of the tyrosine kinase domain. Presence of each mutation in heterozygous condition indicates that these mutant proteins with intact domains may influence wild-type protein expressed from the non-affected allele and/or other EGFR factors in a dominant-negative manner by the occupation of their binding sites through mutant EGFR proteins. These mutation add to the list of previously identified mutations within the kinase domain of the EGFR gene, and also extends the spectrum of malignancies that harbor functional EGFR mutations. To our knowledge, this is the first report identifying functional EGFR mutations in malignant mesothelioma.
Functional analyses of these mutant EGFRs in the cultured cells demonstrated that all EGFR mutants have enhanced tyrosine kinase activity in response to epidermal growth factor and increased sensitivity to EGFR inhibitor Erlotinib. Like other mutants reported in the literature, all eight EGFR mutants were ligand dependent and in the absence of EGF stimulation there was little or no activation of any mutant EGFR. These results confirm previous observations showing activation of TKD mutant EGFR as being ligand dependent in similar transient expression systems (NIH3T3 and HeLa cells), while there was no evidence of significant ligand independent EGFR activation.
The impact of EGFR mutations in MPM strikingly parallels the observation reported in NSCLC. Specifically the finding that EGFR mutations are predictive of response to therapy [5–8, 21–25]. In lung cancer this has been demonstrated in the context of systemic chemotherapy and/or EGFR-TK therapy. In this study, treatment is cytoreductive surgery with intraperitoneal hyperthermic chemotherapy. The finding that EGFR mutations identify responders to therapy mechanistically is explained at the cellular/molecular by the 'oncogenic addition (shock)' model [9, 26–28]. In this model, cancers that are dependent on critical oncogenic pathways, like the EGFR pathway for tumor cellular maintenance, undergo an exaggerated/prolonged apoptosis relative to wild type tumor cells when exposed to the same cytotoxic agents . The improved outcome in EGFR MPM mutants is also supported by this model. First, all gross disease is removed surgically, leaving only microscopic to low volume residual disease. This residual disease subsequently is treated with high dose intra-peritoneal chemotherapy and hyperthermia given intra-operatively, and the intrinsic susceptibility of EGFR MPM mutant tumors makes these cells more likely to undergo more extensive apoptosis which manifests as a prolonged progression free survival (Figure 9B).
Although the mutant EGFR group experienced a prolonged survival, two patients in this group have succumbed to their disease, and likely with longer follow-up, more mutant EGFR patients will develop progressive disease. Therefore, the improved outcome observed in the mutant EGFR group is a 'relative' phenomenon. This 'relative' outcome improvement in mutant MPM patients also parallels the observations in metastatic lung cancer which report prolonged median survival but ultimately most patients, including EGFR mutants succumb to progressive diseases. Since NSCLC clinically are responsive to TKI therapy and given the in vitro response of the MPM mutations to Erlotinib, there may be a role for EGFR-TKI therapy in MPM EGFR mutant patients who develop disease recurrence or present with bulky unresectable tumor. Currently EGFR-TKI therapy has not been investigated in peritoneal mesothelioma but a recent trial in pleural mesothelioma did not show any benefit . Interestingly in this erlotinib trial, the high EGFR expressing tumor group experienced a 2-fold longer survival, but study did not interrogate tumors for EGFR mutations. Therefore it is unknown if EGFR mutations occur in pleural mesothelioma or if a subset of mesothelioma patients might benefit from EGFR-TKI therapy and further investigation for perturbations in the EGFR pathway in pleural mesothelioma is warranted.
In summary, we have identified novel activating EGFR mutations in MPM associated with optimal resectability and prolonged survival. Clinically these mutations may ultimately have utility in patient selection for surgery, systemic therapy, and selection for EGFR-TKI. The identification of EGFR mutations in peritoneal mesothelioma expands the spectrum of cancers with EGFR pathway perturbations and provides the first evidence of function EGFR mutations in mesothelioma. Not only does the 'in vitro' biological behavior of these mutations parallel those identified in NSCLC, but the clinical course of MPM patients with EGFR mutant tumors appear to share same 'relative' improved clinical outcome like mutant EGFR-NSCLC. Expanding the cohort of peritoneal mesothelioma and probing for mutations in pleural based disease is warranted.
We especially thank Cavenee Webster for the wild-type EGFR cDNA. We thank Boosani C, Akulapalli S from Boys Town Research Hospital, Omaha and Maiti A.K. from University of Texas, Galveston for advice and assistance. The work was supported by Paul and Michelle Zygielbaum Cancer Research Fund and also in part by anonymous donors.
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