http://orcid.org/0000-0001-7076-0476
Correction
1 Sep 2021: Jank P, Gehlhaar C, Lederer B, Fontanella C, Schneeweiss A, et al. (2021) Correction: MGMT promoter methylation in triple negative breast cancer of the GeparSixto trial. PLOS ONE 16(9): e0257142. https://doi.org/10.1371/journal.pone.0257142 View correction
Figures
Abstract
Triple-negative breast cancer (TNBC) is typically treated with chemotherapeutic agents, including carboplatin (Cb), an DNA platinating agent. The O6-methylguanine-DNA-methyltransferase gene (MGMT) encodes for the protein O6-alkylguanine-DNA-alkyltransferase (MGMT protein). MGMT protein is involved in DNA repair mechanisms to remove mutagenic and cytotoxic adducts from O6-guanine in DNA. In glioblastoma multiforme, MGMT methylation status is a predictive biomarker for increased response to temozolomide therapy. It has been suggested, that MGMT protein may have relevance for cellular adaptation and could have an influence on resistance to carboplatin therapy. We investigated the influence of MGMT promoter methylation on pathologic complete response and survival of patients with TNBC treated in the neoadjuvant GeparSixto trial. In 174 of 210 available TNBC tumors a valid MGMT promoter methylation status was determined by pyrosequencing of 5 CpG islands. In 21.8%, we detected a mean MGMT promoter methylation >10%. Overall, MGMT promoter methylation was not significantly associated with pathological complete response (pCR) rate. After stratification for the two therapy arms with and without Cb no statistically significant differences in therapy response rates between the two MGMT promoter methylation groups could be observed. Our results show that different MGMT promoter methylation status is not related to different chemotherapy response rates in the TNBC setting in GeparSixto.
Citation: Jank P, Gehlhaar C, Bianca L, Caterina F, Andreas S, Karn T, et al. (2020) MGMT promoter methylation in triple negative breast cancer of the GeparSixto trial. PLoS ONE 15(8): e0238021. https://doi.org/10.1371/journal.pone.0238021
Editor: Sushanta K. Banerjee, University of Kansas Medical Center and VA Medical Center, UNITED STATES
Received: May 13, 2020; Accepted: August 6, 2020; Published: August 25, 2020
Copyright: © 2020 Jank et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the paper and its Supporting Information files. The data underlying the results presented in the study are available from German Breast Group, some restriction apply due to confidentiality of patient data. Since these data are derived from a prospective clinical trial with ongoing follow up there are legal and ethical restrictions to share sensitive patient related data publicly. Interested groups may use the “Cooperation Proposal Form” on https://www.gbg.de/en/research/trafo.php. Data can be requested in context of a translational research project by sending the form to trafo@gbg.de. Translational research proposals are approved by the GBG scientific board.
Funding: YES: This project was partly funded by Monica Boscolo Research Grant 2013 to Caterina Fontanella and the Transcan BMBF project TH4Respons (JTC 2014-121).
Competing interests: I have read the journal's policy and the authors of this manuscript have the following competing interests: Dr. Schneeweiss reports grants from Celgene, grants from Roche, grants from AbbVie, grants from Molecular Partner, personal fees from Roche, personal fees from AstraZeneca, personal fees from Celgene, personal fees from Roche, personal fees from Roche, personal fees from Celgene, personal fees from Pfizer, personal fees from AstraZeneca, personal fees from Novartis, personal fees from MSD, personal fees from Tesaro, personal fees from Lilly, personal fees from Pfizer, other from Roche, outside the submitted work. Dr. v. Mackelenbergh reports travel grants and honoria from AstraZeneca, Amgen, Gebomic Health, Novartis, Lilly. Dr. Denkert reports personal fees from Novartis, personal fees from Roche, personal fees from MSD Oncology, from Daiichi Sankyo, grants from Myriad Genetics, other from Sividon Diagnostics / Myriad, outside the submitted work; In addition, Dr. Denkert has a patent EP18209672 pending, a patent EP20150702464 pending, and a patent Software (VMscope digital pathology) pending. All other authors declare no conflict of interest. We confirm that the patents do not alter our adherence to PLOS ONE policies on sharing data and materials. We would like to point out, that the patents had been added as general COI information but are not related to MGMT methylation.
Introduction
Triple-negative breast cancer (TNBC) shows an aggressive clinical behavior, poor clinical outcome and has limited option for targeted therapies. Due to the absence of targets, like estrogen receptor (ER), progesterone receptor (PR) and growth factor receptors (HER2), TNBC does not benefit from hormonal or anti-HER2-based therapies and therapy strategies are focused on the use of chemotherapeutic agents, for example carboplatin [1].
Alterations in epigenetics, for example methylation status of CpG islands of DNA promoter regions, were considered as early and common events in cancer and play a major role in tumor progression [2–5]. Methylation is a special form of alkylation and the most common alkylating reaction in biology. Most DNA methylations in mammals take place at carbon-5 of the cytosine residues of cytosine-phosphatidyl-guanosine (CpG) dinucleotides and lead to a hypermethylation of DNA [5, 6]. Hypermethylation of CpG islands in gene promoter regions results in loss of the target protein, lack of mRNA expression or reduced enzyme activity [7–9].
The O6-methylguanine-DNA-methyltransferase gene (MGMT) encodes for the protein O6-alkylguanine-DNA-alkyltransferase (MGMT protein) and is located on chromosome 10q26. MGMT DNA repair activity of tumor cells is believed to contribute to resistance of tumor cells from cytotoxic effects of alkylating agents. MGMT protein is involved in DNA repair mechanisms to remove mutagenic and cytotoxic adducts from O6-guanine in DNA by transferring the alkyl group from the O6 position of guanine to a cysteine residue of its active side [10–16] and inactivating itself followed by ubiquitination [17]. Thereby, DNA-lesions caused by alkylating substances are repaired. Mutagenic adducts are caused by ionizing radiation, UV light, tobacco smoke or alkylating agents for example used in chemotherapy, such as carboplatin [10, 12]. Altogether, MGMT protein provides protection of normal cells from exogenous carcinogens and tumor cells from chemotherapeutic agents [18].
For glioblastoma multiforme, it has been shown that tumors with no or low levels of MGMT activity are more responsive to therapy with the alkylating drug temozolomide [19, 20]. MGMT inactivation by epigenetic silencing through methylation of CpG islands in the promoter region correlates with the sensitivity of tumor cells to alkylating agents. Therefore, at least in glioblastoma multiforme, MGMT methylation status is a predictive biomarker for increased response to temozolomide therapy [19].
In previous studies, Fumagalli et al. showed that different levels of MGMT methylation were present in TNBC, suggesting a biological function. In a cohort of 84 patients receiving different types of neoadjuvant chemotherapy no statistical significance regarding MGMT methylation and pathological complete response (pCR) or any other clinical pathological characteristics were observed [21, 22]. We extended this approach in a clinical trial setting investigating a neoadjuvant clinical trial cohort randomized to receive carboplatin therapy vs no carboplatin in addition to the anthracycline-taxane combination.
In this project, we investigated the hypothesis that MGMT promoter hypermethylation in TNBC is associated with an increased chemosensitivity and therefore an increased pCR rate. Furthermore, we hypothesized that MGMT methylated TNBC should benefit from adding DNA-damaging chemotherapeutics such as Carboplatin since the ability of DNA-repair is compromised.
We therefore evaluated the MGMT promoter methylation status by methylation-specific polymerase-chain reaction (PCR) and subsequent pyrosequencing of 5 CpG islands in TNBC core biopsies, from patients enrolled in a clinical phase II trial.
Materials and methods
Study population and histopathological examination
We retrospectively evaluated a cohort of TNBC tumors of patients enrolled in the GeparSixto (NCT01426880) trial [23] between August 2011 to December 2012. Patients gave written informed consent for trial participation and use of tissue for translational research. Ethics committee of Charité University Hospital Berlin approved use of human tissue for translational research project (EA1/139/05). GeparSixto is a phase II trial for investigation of adding carboplatin to a neoadjuvant chemotherapy (NACT) for patients with triple negative or HER2-positive primary breast cancer. Patients with stage II or III TNBC were randomized to receive 18 weeks of NACT treatment with paclitaxel (80mg/m2 q1w) and non-pegylated liposomal doxorubicin (Myocet, 20 mg/m2 q1w) + bevacizumab (15 mg/kg, q3w) with or without addition of carboplatin (AUC 2.0 q1w later reduced to AUC1.5 q1w per amendment after 330 patients). The relevant authorities and ethic committees approved this study including a translational program for which pretherapeutical formalin-fixed paraffin-embedded (FFPE) core biopsies were prospectively collected in the German Breast Group (GBG) tumor biobank. Hormone-receptor (HR) status (positive if >1% of ER/PR stained cells), HER2 status via immune-histochemically staining (IHC) (positive if IHC 3+ or IHC 2+ and silver in-situ hybridization [SISH]-positive), and Ki67 expression were centrally assessed prior to randomization.
DNA preparation
FFPE core biopsy tissue with a tumor content ≥30% were cut as 3 x 5 μm into a reaction tube. For DNA preparation the slices were processed with QIAamp DNA-Mini-Kit from Qiagen GmbH (Hilden, Germany) according to manufacturer specifications. Genomic DNA was eluted in 20 μL PCR-water and concentration was determined using NanoDrop ND-1000 Spectrophotometer from Labtech International Ltd. (Ringmer, UK).
Bilsulfite conversion
500 ng of each isolated genomic DNA (gDNA) were converted by using EZ DNA Methylation Kit™ from Zymo Research (Irvine, CA, USA). Except for the following step, the manufacturer instruction was used: 200 μL instead of 100 μL M-Wash Buffer were used before M-desulphonation.
Pyrosequencing
The converted DNA was then amplified in a MGMT promoter specific PCR using the PyroMark Q24 System from Qiagen GmbH (Hilden, Germany). By adding 3 μL of converted DNA we followed the manufacturer instruction, but adapted the PCR cycling protocol (S1 Table).
After amplification, we followed the manufracturer instructions by using the PyroMark Vacuum Workstation and PyroMark Q24 System from Qiagen GmbH (Hilden, Germany) to detect methylated CpG islands in MGMT promoter DNA.
Results were determined by PyroMark Q24 software Qiagen GmbH (Hilden, Germany). Five CpG islands were measured and results reported as percentages. Out of five percent values we calculated a binary (MGMTbi) and a continuous (MGMTco) variable. For each CpG island the percentage of methylation was measured. In addition, the mean percentage of methylation across all CpG islands was calculated for each tumor. MGMT methylation was defined as positive if this mean value was >10%.
The continuous variable MGMTco (0–5) considered every single CpG island. The MGMTco value describes the number of CpG islands with a methylation of >10%.
Statistical evaluation
For statistical analyses pathohistological data, BRCA mutation status and therapy response were used.
Pathological complete response (pCR) was defined as ypT0, ypN0. Disease-free survival (DFS) was defined as the time from random assignment until relapse (local, distant, or contralateral invasive breast cancer or secondary malignancies) or death irrespective of cause. Overall survival (OS) was defined as time from random assignment until death irrespective of the underlying cause. DFS and OS were analysed by the Kaplan–Meier method and log-rank tests.
Associations between binary variables were investigated with Fisher’s exact and between other categorical variables χ2 test.
Results
Tumor and patient characteristics
As shown in Fig 1, 210 pretherapeutic core biopsies, from a total of 315 triple-negative tumors, had sufficient remaining FFPE material with a tumor content ≥30% and were available for the methylation assay. In 174 (82.9%) tumors the MGMT methylation assay was performed successfully.
A MGMT promoter hypermethylation (MGMTbi) was observed in 38 (21.8%) tumors and a methylation mean ≤10% in 136 (78.2%) tumors, which were determined as not methylated (Table 1). Most BC were invasive-ductal (NST) breast carcinomas.
Baseline characteristics, like Tumor staging, Nodal status, Grading and others factors were well balanced between the MGMT methylated and unmethylated subsets and shown in Table 1.
With respect to baseline characteristics, there were no differences between the GeparSixto trial cohort with and without known MGMT status, except for tumor grading and Ki-67 expression, as shown in S2 Table.
MGMT promoter methylation in study cohort
According to both therapy arms, the MGMT promoter methylation status was distributed nearly identically. In the carboplatin arm, 24.3% of patients had a hypermethylated MGMT promoter, while in the arm without carboplatin 19.4% of patients had a hypermethylated MGMT promoter region.
Regarding the number of methylated CpG islands in the MGMT promoter, we observed mostly none or two methylated CpG islands. Patients in the non-carboplatin therapy arm had more often 2 of 5 methylated CpG island compared to the cohort with carboplatin (Fig 2).
A. percent of patients with MGMT methylation status as binary variable (MGMTbi) B. percent of patients with MGMT methylation status as continuous variable (MGMTco).
Treatment benefit according to MGMT promoter methylation
Overall, MGMT promoter methylation was not significantly associated with pCR rate. The overall pCR rate was 44.8%, with no significant difference between the unmethylated subgroup (45.6%) and the methylated group (42.1%, P = 0.717; Fig 3).
Therapy regime: no Cb = non-Carboplatin arm, Cb = Carboplatin arm. BRCA: wt = BRCA wildtype, mut = BRCA mutated. P values shown are calculated by Fisher‘s exact test.
Similar results were obtained for the different therapy arms. In the carboplatin arm, pCR rates were 84.6% for unmethylated MGMT and 80.0% for methylated MGMT for BRCA mutated tumors (N = 18, P = 1.000), 57.5% for unmethylated MGMT and 50.0% for methylated MGMT for BRCA wildtype patients (N = 52, P = 0.746).
In the non-carbo arm lower pCR rates were observed: pCR rates were 40.0% for unmethylated MGMT and 50.0% for methylated MGMT for BRCA mutated patients (N = 12, P = 1.000), 27.1% for unmethylated MGMT and 25.0% for methylated MGMT for BRCA wildtype patients (N = 60, P = 1.000).
Survival analysis according to MGMT promoter methylation
In this cohort the median DFS and OS was not reached. We used the three years follow up (3Y-DFS, 3Y-OS) to determine possible differences: The 3Y-DFS in the MGMT promoter hypermethylated cohort is 81.1% and 3Y-OS = 88.6%, compared to the cohort with MGMT promoter unmethylated BC: 3Y-DFS = 78.4% and 3Y-OS is 88.6% (Fig 4). In addition, in S1 Fig we show the survival plots according to patients treated with and without the addition of Carboplatin.
DFS and OS time in months with binary MGMT promoter methylation status; p-values: log rank test.
Discussion
We investigated the influence of MGMT promoter methylation on therapy response and survival of patients with TNBC, treated with chemotherapy with and without adding of carboplatin.
The role of MGMT promoter methylation for therapy response has been reported previously, especially for glioblastoma. In glioblastoma, an increased MGMT promoter methylation has a predictive impact for increased pCR and therapy response to temozolomide [19, 20].
For TNBC, the impact of MGMT promoter methylation status for therapy response has not been studied to a great extent in standardized clinical trial cohorts. To our knowledge, this is the first time MGMT promoter methylation was investigated in TNBC including a stratification by BRCA status and therapy regime.
We showed that MGMT promoter is hypermethylated in around 22% of TNBC, in this trial cohort. We did not observe any significant differences in age, tumor staging, nodal status, cell proliferation, therapy arm or histology type regarding MGMT promoter methylation status. Our study demonstrates that MGMT promoter methylation status has no predictive impact on pCR or outcome of patients with TNBC, neither overall nor stratified by carboplatin vs. control chemotherapy.
Fumagalli et al. have investigated MGMT methylation in an institutional cohort of 84 TNBC patients [22] and its role for response to neoadjuvant chemotherapy in patients treated with different agents [21]. Fumagalli reported higher MGMT promoter methylation prevalence, from 32.5% to 70%, with significant dependence on age. With respect to the age structure, both cohorts are different which might lead to different MGMT distributions. In both approaches, no correlation between clinicopathological data with MGMT methylation status were found. The results from Fumagalli et al. are the same as in our investigation.
Asiaf et al. investigated MGMT methylation and MGMT protein expression in a cohort of 123 invasive ductal BC (NST) and described a MGMT promoter methylation prevalence of 39.8% (51 of 128). Interestingly, they reached significant results for correlations of MGMT promoter methylation with clinicopathological markers such as tumor staging and grading and estrogen and progesterone receptor expression. Tumors with methylated MGMT promoter were more often stage II–IV with higher grading. Regarding hormone receptor expression, MGMT methylated tumors were more often HR (PgR or ER) negative [24]. Regarding tumor staging, our results show an opposite trend. Our cohort and the cohort from Asiaf et al. show differences in baseline parameters, which can explain this different results. In our cohort we only used TNBC and can not compare HR expression with MGMT methylation.
Isono et al. described a MGMT protein expression profile in different breast cancer subtypes: In luminal breast cancer 67% were MGMT high expressing (high), 46% in the TNBC cohort and 30% in the HER2 positive cohort, with a p-value of < 0.001 [25]. Regarding cell culture experiments, Bobustuc et al. observed the same: ER positive breast cancer cell lines expressed higher MGMT on protein level compared to ER negative cell lines [26]. The meta-analysis from An et al. shows a significant association of MGMT methylation with ER negative and grade 3 breast tumors [27]. Increased MGMT protein activity is associated with HR-positive breast cancer subtypes, while lower expression reduces MGMT protein activity. Increased methylation is associated with higher histological grade in basal-like tumors.
The strength of our investigation is that we used a prospectively collected clinical trial cohort with standardized treatment and available outcome data. As a limitation, due to the small size of pretherapeutic neoadjuvant core biopsies, it was not possible to perform a successful analysis in all patients that participated in the trial.
Results for glioblastoma were determined via MethyQESD method, described by Bettstetter et al. [28], using MGMT promoter methylation specific quantitative real-time PCR [20]. Bettstetter et al. performed a proof-of-principle, using survival data for cutoff-fitting. If more than 11.7% of MGMT gene promoter were methylated, the tumor was determined as MGMT promoter hypermethylated [28]. In our methylation assay, we used the common cutoff of 10 percent, determined via different methylation assays as previously described [20].
There are numerous other studies dealing with MGMT promoter methylation, MGMT mRNA expression and MGMT protein expression or MGMT protein activity in breast tumors and other diseases. Preuss et al. described a lack of MGMT protein activity in breast tumors of 5 percent [29]. An et al. described a strong association between MGMT promoter methylation and lower (or negative) MGMT protein expression (OR = 4.65, p<0.001) in breast cancer [27]. This association has been shown for other tumor types as well as on mRNA level [30]. Regarding glioblastoma MGMT promoter methylation seems to be the gold standard in clinical routine [31].
It should be noted that for prediction of pCR and outcome analysis other factors in addition to methylation of MGMT promoter or MGMT protein expression might be relevant. For a comprehensive analysis, additional relevant genes for DNA repair mechanism should be included [32]. Domagala et al. investigated pCR after neoadjuvant cisplatin therapy in a cohort of 43 tumors and the association with downregulation of DNA repair enzymes, such as MGMT, in BRCA1-associated TNBC. They showed, that DNA repair enzymes in patients with residual tumor are downregulated and may profit from PARP inhibitor therapy [32].
Interestingly, there are several studies investigating the use of temozolomide for breast cancer patients with brain metastases (NCT00617539, NCT00875355) as well as advanced or metastatic breast cancer without a history of brain metastases (NCT00194766, NCT00614978). Results are awaited soon.
Taken together, our results show that in the GeparSixto clinical trial cohort MGMT promoter methylation has no direct impact on therapy response to NACT with or without the addition of carboplatin in TNBC.
Supporting information
S2 Table. Baseline characteristics in MGMT cohort compared to samples without MGMT status in GeparSixto trial.
https://doi.org/10.1371/journal.pone.0238021.s002
(TIF)
S1 Fig. Kaplan-Meier analysis for comparison of prognosis of patients treated with and without Carboplatin.
DFS and OS time in months with binary Carboplatin therapy regime; p-values: log rank test.
https://doi.org/10.1371/journal.pone.0238021.s003
(TIF)
References
- 1. Chacon RD, Costanzo MV. Triple-negative breast cancer. Breast Cancer Res. 2010;12 Suppl 2:S3.
- 2. Gao Y, Feng B, Han S, Lu L, Chen Y, Chu X, et al. MicroRNA-129 in Human Cancers: from Tumorigenesis to Clinical Treatment. Cell Physiol Biochem. 2016;39(6):2186–202. pmid:27802440
- 3. Jones PA, Baylin SB. The epigenomics of cancer. Cell. 2007;128(4):683–92. pmid:17320506
- 4. Simo-Riudalbas L, Esteller M. Cancer genomics identifies disrupted epigenetic genes. Hum Genet. 2014;133(6):713–25. pmid:24104525
- 5. Spitzwieser M, Holzweber E, Pfeiler G, Hacker S, Cichna-Markl M. Applicability of HIN-1, MGMT and RASSF1A promoter methylation as biomarkers for detecting field cancerization in breast cancer. Breast Cancer Res. 2015;17:125. pmid:26370119
- 6. Esteller M. Epigenetics in cancer. The New England journal of medicine. 2008;358(11):1148–59. pmid:18337604
- 7. Jacinto FV, Esteller M. MGMT hypermethylation: a prognostic foe, a predictive friend. DNA Repair (Amst). 2007;6(8):1155–60.
- 8. Herfarth KK, Brent TP, Danam RP, Remack JS, Kodner IJ, Wells SA Jr., et al. A specific CpG methylation pattern of the MGMT promoter region associated with reduced MGMT expression in primary colorectal cancers. Mol Carcinog. 1999;24(2):90–8. pmid:10078936
- 9. Lee S, Kim WH, Jung HY, Yang MH, Kang GH. Aberrant CpG island methylation of multiple genes in intrahepatic cholangiocarcinoma. Am J Pathol. 2002;161(3):1015–22. pmid:12213730
- 10. Brell M, Ibanez J, Tortosa A. O6-Methylguanine-DNA methyltransferase protein expression by immunohistochemistry in brain and non-brain systemic tumours: systematic review and meta-analysis of correlation with methylation-specific polymerase chain reaction. BMC cancer. 2011;11:35. pmid:21269507
- 11. Sabharwal A, Middleton MR. Exploiting the role of O6-methylguanine-DNA-methyltransferase (MGMT) in cancer therapy. Curr Opin Pharmacol. 2006;6(4):355–63. pmid:16777483
- 12. Gerson SL. MGMT: its role in cancer aetiology and cancer therapeutics. Nature reviews Cancer. 2004;4(4):296–307. pmid:15057289
- 13. Olsson M, Lindahl T. Repair of alkylated DNA in Escherichia coli. Methyl group transfer from O6-methylguanine to a protein cysteine residue. J Biol Chem. 1980;255(22):10569–71. pmid:7000780
- 14. Tubbs JL, Pegg AE, Tainer JA. DNA binding, nucleotide flipping, and the helix-turn-helix motif in base repair by O6-alkylguanine-DNA alkyltransferase and its implications for cancer chemotherapy. DNA Repair (Amst). 2007;6(8):1100–15.
- 15. Ishiguro K, Shyam K, Penketh PG, Sartorelli AC. Development of an O(6)-alkylguanine-DNA alkyltransferase assay based on covalent transfer of the benzyl moiety from [benzene-3H]O(6)-benzylguanine to the protein. Analytical biochemistry. 2008;383(1):44–51. pmid:18783719
- 16. Srivenugopal KS, Yuan XH, Friedman HS, Ali-Osman F. Ubiquitination-dependent proteolysis of O6-methylguanine-DNA methyltransferase in human and murine tumor cells following inactivation with O6-benzylguanine or 1,3-bis(2-chloroethyl)-1-nitrosourea. Biochemistry. 1996;35(4):1328–34. pmid:8573590
- 17. Tserga A, Michalopoulos NV, Levidou G, Korkolopoulou P, Zografos G, Patsouris E, et al. Association of aberrant DNA methylation with clinicopathological features in breast cancer. Oncol Rep. 2012;27(5):1630–8. pmid:22159596
- 18. Li A, Schuermann D, Gallego F, Kovalchuk I, Tinland B. Repair of damaged DNA by Arabidopsis cell extract. Plant Cell. 2002;14(1):263–73. pmid:11826311
- 19. Weller J, Tzaridis T, Mack F, Steinbach JP, Schlegel U, Hau P, et al. Health-related quality of life and neurocognitive functioning with lomustine-temozolomide versus temozolomide in patients with newly diagnosed, MGMT-methylated glioblastoma (CeTeG/NOA-09): a randomised, multicentre, open-label, phase 3 trial. Lancet Oncol. 2019.
- 20. von Rosenstiel C, Wiestler B, Haller B, Schmidt-Graf F, Gempt J, Bettstetter M, et al. Correlation of the quantitative level of MGMT promoter methylation and overall survival in primary diagnosed glioblastomas using the quantitative MethyQESD method. Journal of clinical pathology. 2019.
- 21. Fumagalli C, Della Pasqua S, Bagnardi V, Cardillo A, Sporchia A, Colleoni M, et al. Prevalence and clinicopathologic correlates of O(6)-methylguanine-DNA methyltransferase methylation status in patients with triple-negative breast cancer treated preoperatively by alkylating drugs. Clin Breast Cancer. 2014;14(4):285–90. pmid:24709436
- 22. Fumagalli C, Pruneri G, Possanzini P, Manzotti M, Barile M, Feroce I, et al. Methylation of O6-methylguanine-DNA methyltransferase (MGMT) promoter gene in triple-negative breast cancer patients. Breast Cancer Res Treat. 2012;134(1):131–7. pmid:22228432
- 23. Castrellon AB, Pidhorecky I, Valero V, Raez LE. The Role of Carboplatin in the Neoadjuvant Chemotherapy Treatment of Triple Negative Breast Cancer. Oncol Rev. 2017;11(1):324. pmid:28382189
- 24. Asiaf A, Ahmad ST, Malik AA, Aziz SA, Rasool Z, Masood A, et al. Protein expression and methylation of MGMT, a DNA repair gene and their correlation with clinicopathological parameters in invasive ductal carcinoma of the breast. Tumour Biol. 2015;36(8):6485–96. pmid:25820821
- 25. Isono S, Fujishima M, Azumi T, Hashimoto Y, Komoike Y, Yukawa M, et al. O(6)-methylguanine-DNA methyltransferase as a prognostic and predictive marker for basal-like breast cancer treated with cyclophosphamide-based chemotherapy. Oncol Lett. 2014;7(6):1778–84. pmid:24932232
- 26. Bobustuc GC, Kassam AB, Rovin RA, Jeudy S, Smith JS, Isley B, et al. MGMT inhibition in ER positive breast cancer leads to CDC2, TOP2A, AURKB, CDC20, KIF20A, Cyclin A2, Cyclin B2, Cyclin D1, ERalpha and Survivin inhibition and enhances response to temozolomide. Oncotarget. 2018;9(51):29727–42. pmid:30038716
- 27. An N, Shi Y, Ye P, Pan Z, Long X. Association Between MGMT Promoter Methylation and Breast Cancer: a Meta-Analysis. Cell Physiol Biochem. 2017;42(6):2430–40. pmid:28848211
- 28. Bettstetter M, Dechant S, Ruemmele P, Vogel C, Kurz K, Morak M, et al. MethyQESD, a robust and fast method for quantitative methylation analyses in HNPCC diagnostics using formalin-fixed and paraffin-embedded tissue samples. Lab Invest. 2008;88(12):1367–75. pmid:18936738
- 29. Preuss I, Eberhagen I, Haas S, Eibl RH, Kaufmann M, von Minckwitz G, et al. O6-methylguanine-DNA methyltransferase activity in breast and brain tumors. International journal of cancer Journal international du cancer. 1995;61(3):321–6. pmid:7729942
- 30. Shalaby SM, El-Shal AS, Abdelaziz LA, Abd-Elbary E, Khairy MM. Promoter methylation and expression of DNA repair genes MGMT and ERCC1 in tissue and blood of rectal cancer patients. Gene. 2018;644:66–73. pmid:29080834
- 31. Radke J, Koch A, Pritsch F, Schumann E, Misch M, Hempt C, et al. Predictive MGMT status in a homogeneous cohort of IDH wildtype glioblastoma patients. Acta Neuropathologica Communications. 2019;7(1):89. pmid:31167648
- 32. Domagala P, Hybiak J, Rys J, Byrski T, Cybulski C, Lubinski J. Pathological complete response after cisplatin neoadjuvant therapy is associated with the downregulation of DNA repair genes in BRCA1-associated triple-negative breast cancers. Oncotarget. 2016;7(42):68662–73. pmid:27626685