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Molecular Basis of Cisplatin Resistance in Testicular Germ Cell Tumors

V. Bakardjieva-Mihaylova, K. Skvarova Kramarzova, M. Slamova, M. Svaton, K. Rejlova, M. Zaliova, A. Dobiasova, K. Fiser, J. Stuchly, M. Grega, B. Rosova, R. Zachoval, P. Klezl, V. Eis, E. Kindlova, T. Buchler, J. Trka, L. Boublikova,

. 2019 ; 11 (9) : . [pub] 20190906

Language English Country Switzerland

Document type Journal Article

Grant support
Thomayer hospital - TN, 00064190 MH CZ - DRO
CDRO00064203FNM and by the Ministry of Education UNCE 204012
LO1604 Youth and Sports NPU I nr.LO1604

The emergence of cisplatin (CDDP) resistance is the main cause of treatment failure and death in patients with testicular germ cell tumors (TGCT), but its biologic background is poorly understood. To study the molecular basis of CDDP resistance in TGCT we prepared and sequenced CDDP-exposed TGCT cell lines as well as 31 primary patients' samples. Long-term exposure to CDDP increased the CDDP resistance 10 times in the NCCIT cell line, while no major resistance was achieved in Tera-2. Development of CDDP resistance was accompanied by changes in the cell cycle (increase in G1 and decrease in S-fraction), increased number of acquired mutations, of which 3 were present within ATRX gene, as well as changes in gene expression pattern. Copy number variation analysis showed, apart from obligatory gain of 12p, several other large-scale gains (chr 1, 17, 20, 21) and losses (chr X), with additional more CNVs found in CDDP-resistant cells (e.g., further losses on chr 1, 4, 18, and gain on chr 8). In the patients' samples, those who developed CDDP resistance and died of TGCT (2/31) showed high numbers of acquired aberrations, both SNPs and CNVs, and harbored mutations in genes potentially relevant to TGCT development (e.g., TRERF1, TFAP2C in one patient, MAP2K1 and NSD1 in another one). Among all primary tumor samples, the most commonly mutated gene was NSD1, affected in 9/31 patients. This gene encoding histone methyl transferase was also downregulated and identified among the 50 most differentially expressed genes in CDDP-resistant NCCIT cell line. Interestingly, 2/31 TGCT patients harbored mutations in the ATRX gene encoding a chromatin modifier that has been shown to have a critical function in sexual differentiation. Our research newly highlights its probable involvement also in testicular tumors. Both findings support the emerging role of altered epigenetic gene regulation in TGCT and CDDP resistance development.

References provided by Crossref.org

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$a Bakardjieva-Mihaylova, Violeta $u Department of Pediatric Hematology and Oncology, CLIP, 2nd Faculty of Medicine, Charles University and University Hospital Motol, 150 00 Prague, Czech Republic. violeta.bakardjieva-mihaylova@lfmotol.cuni.cz.
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$a Molecular Basis of Cisplatin Resistance in Testicular Germ Cell Tumors / $c V. Bakardjieva-Mihaylova, K. Skvarova Kramarzova, M. Slamova, M. Svaton, K. Rejlova, M. Zaliova, A. Dobiasova, K. Fiser, J. Stuchly, M. Grega, B. Rosova, R. Zachoval, P. Klezl, V. Eis, E. Kindlova, T. Buchler, J. Trka, L. Boublikova,
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$a The emergence of cisplatin (CDDP) resistance is the main cause of treatment failure and death in patients with testicular germ cell tumors (TGCT), but its biologic background is poorly understood. To study the molecular basis of CDDP resistance in TGCT we prepared and sequenced CDDP-exposed TGCT cell lines as well as 31 primary patients' samples. Long-term exposure to CDDP increased the CDDP resistance 10 times in the NCCIT cell line, while no major resistance was achieved in Tera-2. Development of CDDP resistance was accompanied by changes in the cell cycle (increase in G1 and decrease in S-fraction), increased number of acquired mutations, of which 3 were present within ATRX gene, as well as changes in gene expression pattern. Copy number variation analysis showed, apart from obligatory gain of 12p, several other large-scale gains (chr 1, 17, 20, 21) and losses (chr X), with additional more CNVs found in CDDP-resistant cells (e.g., further losses on chr 1, 4, 18, and gain on chr 8). In the patients' samples, those who developed CDDP resistance and died of TGCT (2/31) showed high numbers of acquired aberrations, both SNPs and CNVs, and harbored mutations in genes potentially relevant to TGCT development (e.g., TRERF1, TFAP2C in one patient, MAP2K1 and NSD1 in another one). Among all primary tumor samples, the most commonly mutated gene was NSD1, affected in 9/31 patients. This gene encoding histone methyl transferase was also downregulated and identified among the 50 most differentially expressed genes in CDDP-resistant NCCIT cell line. Interestingly, 2/31 TGCT patients harbored mutations in the ATRX gene encoding a chromatin modifier that has been shown to have a critical function in sexual differentiation. Our research newly highlights its probable involvement also in testicular tumors. Both findings support the emerging role of altered epigenetic gene regulation in TGCT and CDDP resistance development.
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$a Skvarova Kramarzova, Karolina $u Department of Pediatric Hematology and Oncology, CLIP, 2nd Faculty of Medicine, Charles University and University Hospital Motol, 150 00 Prague, Czech Republic. karolina.skvarova@lfmotol.cuni.cz.
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$a Slamova, Martina $u Department of Pediatric Hematology and Oncology, CLIP, 2nd Faculty of Medicine, Charles University and University Hospital Motol, 150 00 Prague, Czech Republic. martina.slamova@lfmotol.cuni.cz.
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$a Svaton, Michael $u Department of Pediatric Hematology and Oncology, CLIP, 2nd Faculty of Medicine, Charles University and University Hospital Motol, 150 00 Prague, Czech Republic. michael.svaton@lfmotol.cuni.cz.
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$a Rejlova, Katerina $u Department of Pediatric Hematology and Oncology, CLIP, 2nd Faculty of Medicine, Charles University and University Hospital Motol, 150 00 Prague, Czech Republic. katerina.rejlova@lfmotol.cuni.cz.
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$a Zaliova, Marketa $u Department of Pediatric Hematology and Oncology, CLIP, 2nd Faculty of Medicine, Charles University and University Hospital Motol, 150 00 Prague, Czech Republic. marketa.zaliova@lfmotol.cuni.cz.
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$a Dobiasova, Alena $u Department of Pediatric Hematology and Oncology, CLIP, 2nd Faculty of Medicine, Charles University and University Hospital Motol, 150 00 Prague, Czech Republic. alena.dobiasova@lfmotol.cuni.cz.
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$a Fiser, Karel $u Department of Pediatric Hematology and Oncology, CLIP, 2nd Faculty of Medicine, Charles University and University Hospital Motol, 150 00 Prague, Czech Republic. karel.fiser@lfmotol.cuni.cz.
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$a Stuchly, Jan $u Department of Pediatric Hematology and Oncology, CLIP, 2nd Faculty of Medicine, Charles University and University Hospital Motol, 150 00 Prague, Czech Republic. jan.stuchly@lfmotol.cuni.cz.
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$a Grega, Marek $u Department of Pathology and Molecular Medicine, 2nd Faculty of Medicine, Charles University and University Hospital Motol, 150 00 Prague, Czech Republic. marek.grega@lfmotol.cuni.cz.
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$a Zachoval, Roman $u Department of Urology, 3rd Faculty of Medicine, Charles University and Thomayer Hospital, 140 00 Prague, Czech Republic. roman.zachoval@ftn.cz.
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$a Klezl, Petr $u Department of Urology, 3rd Faculty of Medicine, Charles University and University Hospital Kralovske Vinohrady, 100 00 Prague, Czech Republic. petr.klezl@fnkv.cz.
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$a Eis, Vaclav $u Department of Pathology, 3rd Faculty of Medicine, Charles University and University Hospital Kralovske Vinohrady, 100 00 Prague, Czech Republic. vaclav.eis@fnkv.cz.
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$a Kindlova, Eva $u Department of Radiotherapy and Oncology, 3rd Faculty of Medicine, Charles University and University Hospital Kralovske Vinohrady, 100 00 Prague, Czech Republic. eva.kindlova@fnkv.cz.
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$a Buchler, Tomas $u Department of Oncology, 1st Faculty of Medicine, Charles University and Thomayer Hospital, 140 00 Prague, Czech Republic. tomas.buchler@ftn.cz.
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$a Trka, Jan $u Department of Pediatric Hematology and Oncology, CLIP, 2nd Faculty of Medicine, Charles University and University Hospital Motol, 150 00 Prague, Czech Republic. jan.trka@lfmotol.cuni.cz.
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$a Boublikova, Ludmila $u Department of Pediatric Hematology and Oncology, CLIP, 2nd Faculty of Medicine, Charles University and University Hospital Motol, 150 00 Prague, Czech Republic. ludmila.boublikova@lfmotol.cuni.cz. Department of Oncology, 1st Faculty of Medicine, Charles University and Thomayer Hospital, 140 00 Prague, Czech Republic. ludmila.boublikova@lfmotol.cuni.cz.
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