Research

Department of Translational Medical Oncology

The Department for Translational Medical Oncology investigates the molecular and cellular mechanisms for cancer development, proliferation and evolution. The department engages in clinical as well as experimental activities to ensure a rapid turnaround of scientific results into clinical application and clinical outcome into new hypotheses. Experimentally, high-throughput, multi-parametric molecular profiling is used to discover differences in the genome of tumor and normal cells to identify novel targets for cancer therapy on the genomic or cellular level.

The group develops suitable model systems to functionally and mechanistically characterize their impact and assess the potential for clinical application. Clinically, a dedicated personalized oncology outpatient clinic provides consulting appointments to initiate innovative diagnostic approaches, and organizes a tumor board to discuss results of genetic tumor profiling and molecularly guided treatment strategies.

Understanding and targeting alterations in cancer

In the working group Experimental Translational Oncology within the TMO department, Dr. Ball's team investigates the biological foundations of tumor progression. To this end, patient-derived tumor models are generated, which capture the diverse functional and genetic heterogeneity of patient tumors. Innovative new approaches developed in the lab enable the systematic creation of patient-derived 3D models even from rare tumor entities with high efficiency. These developed 3D models are used in the lab to explore mechanisms of tumor progression and resistance development, as well as to identify new therapeutic targets and personalized treatment strategies.

To support molecularly informed precision medicine, the team has developed a method that systematically tests the response of patient-specific tumor models to a broad range of clinically relevant drugs. This integrative approach directly links comprehensive molecular datasets with functional in vitro test results, thereby further supporting the recommendation of tailored therapies for patients based on molecular analyses.

Additional projects in the laboratory investigate the significance of intra-tumoral heterogeneity for tumor progression and the development of resistance, as well as the development of novel therapeutic approaches to overcome such resistance.

Dr. Claudia Ball
Senior Scientist, Head of Laboratory
E-Mail: claudia.ball(at)nct-dresden.de

NCT MASTER Registry trial for patients

In an interdisciplinary approach, new discoveries are directly transferred into treatment recommendations using the NCT/DKTK MASTER registry trial. The NCT MASTER (Molecularly Aided Stratification for Tumor Eradication) protocol consents young patients or patients with rare tumor diseases for molecular diagnostics approaches with the explicit purpose of evaluating and stratifying for the best molecular treatment strategy and enrolment in diagnostic and therapeutic clinical trials. The NCT MASTER is a joint NCT program between NCT Heidelberg and NCT/UCC Dresden. You can find more information about registering for the program here or download the brochure here.

Center for Personalized Oncology

The NCT/UCC Dresden Center for Personalized Oncology aims at translating latest research as well as innovative technologies and cancer therapies into clinical practice. A dedicated personalized oncology outpatient clinic provides consulting appointments to discuss innovative diagnostic approaches, results of genetic tumor profiling and molecularly guided treatment strategies. Clinical data and results of molecular analyses as well as potential therapeutic implications are discussed within a molecular tumor board participated by an interdisciplinary team of specialists in molecular diagnostics, targeted cancer therapy as well as involved clinical departments.

Dr. med. Christoph Heining
Senior Attending Physician
E-Mail: christoph.heining(at)nct-dresden.de

Non-coding RNAs (ncRNAs) are functional RNA molecules that are transcribed from DNA but not translated into proteins. Considering that only around 2% of the human transcriptome is translated, ncRNAs represent a huge proportion of the DNA encoded genetic information. Many ncRNA subspecies have been described, for instance microRNAs, small nucleolar RNAs or long non-coding RNAs (lncRNAs). They play pivotal roles in a plethora of cellular processes in development and diseases, including cancer, and can interact with nearly all cellular components.
By exploring various cancer entities and state-of-the art techniques, we want to demonstrate that non-coding RNAs can drive tumorigenesis and influence anti-cancer treatment response. In addition, we will explore their suitability to function as biomarkers for precision oncology based approaches.

RESEARCH AIMS

  • Identification and characterization of cancer-driving ncRNAs
  • Characterization of ncRNA-epigenome landscapes in various cancers
  • Defining prognostic ncRNA scores for different targeted cancer therapies
  • Exploring therapy resistance associated ncRNAs

Dr. Alexander Wurm
Group Leader
E-Mail: alexander.wurm(at)nct-dresden.de

Dr. Marius Bill
Attending Physician
E-Mail: marius.bill(at)nct-dresden.de

MSNZ fellowship: Non-coding RNAs in cancer

The department closely collaborates with the Mildred-Scheel-Group “Biomedical Genomics”, headed by Dr. Anna Poetsch, exploring the possibilities of novel functional genomics and machine learning approaches to investigate DNA-damage response mechanisms in cancer.

Dr. Anna Poetsch
Group Leader
E-Mail: anna.poetsch(at)tu-dresden.de

MSNZ fellowship: Biomedical Genomics

2024

Ball, C. R., & Fröhling, S. (2024). Let’s get functional: Drug sensitivity profiling to enable precision sarcoma medicine. Cell Stem Cell, 31(10), 1389–1390. https://doi.org/10.1016/j.stem.2024.09.006

Dinter, L., Karitzky, P. C., Schulz, A., Wurm, A. A., Mehnert, M.-C., Sergon, M., Tunger, A., Lesche, M., Wehner, R., Müller, A., Käubler, T., Niessner, H., Dahl, A., Beissert, S., Schmitz, M., Meier, F., Seliger, B., & Westphal, D. (2024). BRAF and MEK inhibitor combinations induce potent molecular and immunological effects in NRAS-mutant melanoma cells: Insights into mode of action and resistance mechanisms. International Journal of Cancer, 154(6), 1057–1072. https://doi.org/10.1002/ijc.34807

Hamacher, R., Pabst, K. M., Cheung, P. F., Heilig, C. E., Hüllein, J., Liffers, S.-T., Borchert, S., Costa, P. F., Schaarschmidt, B. M., Kessler, L., Miera, M. A., Droste, M., Akbulut, M., Falkenhorst, J., Zarrad, F., Kostbade, K., Mavroeidi, I. A., Glimm, H., Umutlu, L., … Fendler, W. P. (2024). Fibroblast Activation Protein α-Directed Imaging and Therapy of Solitary Fibrous Tumor. Journal of Nuclear Medicine: Official Publication, Society of Nuclear Medicine, jnumed.123.266411. https://doi.org/10.2967/jnumed.123.266411

Kerle, I. A., Scheuble, A.-M., Kobitzsch, B., Stocker, G., Hiller, G. G. R., Badendick, M., William, D., Krueger, A., Gross, T., Koegler, A., Hartig, A., Richter, D., Aust, D. E., Schroeck, E., Heining, C., Glimm, H., & Hacker, U. T. (2024). Exceptional Response of BRAFV600E-Mutated Acinar Cell CUP to BRAF/MEK Inhibition. JCO Precision Oncology, 8, e2400030. https://doi.org/10.1200/PO.24.00030

Martins, L. R., Sieverling, L., Michelhans, M., Schiller, C., Erkut, C., Grünewald, T. G. P., Triana, S., Fröhling, S., Velten, L., Glimm, H., & Scholl, C. (2024). Single-cell division tracing and transcriptomics reveal cell types and differentiation paths in the regenerating lung. Nature Communications, 15(1), 2246. https://doi.org/10.1038/s41467-024-46469-4

Ruhnke, L., Bill, M., Zukunft, S., Eckardt, J.-N., Schäfer, S., Stasik, S., Hanoun, M., Schroeder, T., Fransecky, L., Steffen, B., Krause, S. W., Scholl, S., Hochhaus, A., Sauer, T., Kraus, S., Schäfer-Eckart, K., Kaufmann, M., Jost, E., Brümmendorf, T. H., … Röllig, C. (2024). Validation of the Revised 2022 European LeukemiaNet Risk Stratification in Adult Patients with Acute Myeloid Leukemia. Blood Advances, bloodadvances.2024013304. https://doi.org/10.1182/bloodadvances.2024013304

Schäfer, T. E., Knol, L. I., Haas, F. V., Hartley, A., Pernickel, S. C. S., Jády, A., Finkbeiner, M. S. C., Achberger, J., Arelaki, S., Modic, Ž., Schröer, K., Zhang, W., Schmidt, B., Schuster, P., Haferkamp, S., Doerner, J., Gebauer, F., Ackermann, M., Kvasnicka, H.-M., … Engeland, C. E. (2024). Biomarker screen for efficacy of oncolytic virotherapy in patient-derived pancreatic cancer cultures. EBioMedicine, 105, 105219. https://doi.org/10.1016/j.ebiom.2024.105219

Schmäche, T., Fohgrub, J., Klimova, A., Laaber, K., Drukewitz, S., Merboth, F., Hennig, A., Seidlitz, T., Herbst, F., Baenke, F., Ada, A.-M., Groß, T., Wenzel, C., Ball, C. R., Praetorius, C., Schmidt, T., Ringelband-Schilling, B., Koschny, R., Stenzinger, A., … Stange, D. E. (2024). Stratifying esophago-gastric cancer treatment using a patient-derived organoid-based threshold. Molecular Cancer, 23(1), 10. https://doi.org/10.1186/s12943-023-01919-3

Schöpf, J., Uhrig, S., Heilig, C. E., Lee, K.-S., Walther, T., Carazzato, A., Dobberkau, A. M., Weichenhan, D., Plass, C., Hartmann, M., Diwan, G. D., Carrero, Z. I., Ball, C. R., Hohl, T., Kindler, T., Rudolph-Hähnel, P., Helm, D., Schneider, M., Nilsson, A., … Scholl, C. (2024). Multi-omic and functional analysis for classification and treatment of sarcomas with FUS-TFCP2 or EWSR1-TFCP2 fusions. Nature Communications, 15(1), 51. https://doi.org/10.1038/s41467-023-44360-2

 

2023

Datzmann, T., Schoffer, O., Schmitt, J., Böhme, H., Fritzmann, J., Distler, M., Ubbelohde, U., Giehl-Brown, E., Henke, T., Krause, M., Glimm, H., Bornhäuser, M., & Weitz, J. (2023). Long-Term Observation of Patients With Cancer - an Entity-Independent Registry for Healthcare and Translational Research at the University Medicine Dresden (Cancer-Reg-VT). Gesundheitswesen (Bundesverband Der Arzte Des Offentlichen Gesundheitsdienstes (Germany)), 85(S 03), S226–S234. https://doi.org/10.1055/a-2129-7651

Floerchinger, A., Klein, J. E., Finkbeiner, M. S. C., Schäfer, T. E., Fuchs, G., Doerner, J., Zirngibl, H., Ackermann, M., Kvasnicka, H. M., Chester, K. A., Jäger, D., Ball, C. R., Ungerechts, G., & Engeland, C. E. (2023). A vector-encoded bispecific killer engager to harness virus-activated NK cells as anti-tumor effectors. Cell Death & Disease, 14(2), 104. https://doi.org/10.1038/s41419-023-05624-3

Illert, A. L., Stenzinger, A., Bitzer, M., Horak, P., Gaidzik, V. I., Möller, Y., Beha, J., Öner, Ö., Schmitt, F., Laßmann, S., Ossowski, S., Schaaf, C. P., Hallek, M., Brümmendorf, T. H., Albers, P., Fehm, T., Brossart, P., Glimm, H., Schadendorf, D., … Malek, N. P. (2023). The German Network for Personalized Medicine to enhance patient care and translational research. Nature Medicine, 29(6), 1298–1301. https://doi.org/10.1038/s41591-023-02354-z

Kerle, I., & Heining, C. (2023). [Histology-agnostic tumor treatment - a farewell to tumor entities?]. Deutsche Medizinische Wochenschrift (1946), 148(18), 1174–1181. https://doi.org/10.1055/a-1933-8141

Lauinger, M., Christen, D., Klar, R. F. U., Roubaty, C., Heilig, C. E., Stumpe, M., Knox, J. J., Radulovich, N., Tamblyn, L., Xie, I. Y., Horak, P., Forschner, A., Bitzer, M., Wittel, U. A., Boerries, M., Ball, C. R., Heining, C., Glimm, H., Fröhlich, M., … Brummer, T. (2023). BRAFΔβ3-αC in-frame deletion mutants differ in their dimerization propensity, HSP90 dependence, and druggability. Science Advances, 9(35), eade7486. https://doi.org/10.1126/sciadv.ade7486

Martins, L. R., Glimm, H., & Scholl, C. (2023). Single-cell RNA sequencing of mouse lower respiratory tract epithelial cells: A meta-analysis. Cells & Development, 174, 203847. https://doi.org/10.1016/j.cdev.2023.203847

Mock, A., Teleanu, M.-V., Kreutzfeldt, S., Heilig, C. E., Hüllein, J., Möhrmann, L., Jahn, A., Hanf, D., Kerle, I. A., Singh, H. M., Hutter, B., Uhrig, S., Fröhlich, M., Neumann, O., Hartig, A., Brückmann, S., Hirsch, S., Grund, K., Dikow, N., … Fröhling, S. (2023). NCT/DKFZ MASTER handbook of interpreting whole-genome, transcriptome, and methylome data for precision oncology. NPJ Precision Oncology, 7(1), 109. https://doi.org/10.1038/s41698-023-00458-w

Möhrmann, L., Cuberi, A., Brückmann, S., Stasik, S., Heukamp, L. C., Bornhäuser, M., Glimm, H., & Folprecht, G. (2023). Response to (K)RASG12C and EGFR Inhibition in a Patient With NRASG12C-Mutated Rectal Cancer. JCO Precision Oncology, 7, e2200666. https://doi.org/10.1200/PO.22.00666

Remde, H., Schmidt-Pennington, L., Reuter, M., Landwehr, L.-S., Jensen, M., Lahner, H., Kimpel, O., Altieri, B., Laubner, K., Schreiner, J., Bojunga, J., Kircher, S., Kunze, C. A., Pohrt, A., Teleanu, M.-V., Hübschmann, D., Stenzinger, A., Glimm, H., Fröhling, S., … Kroiss, M. (2023). Outcome of immunotherapy in adrenocortical carcinoma: a retrospective cohort study. European Journal of Endocrinology, 188(6), 485–493. https://doi.org/10.1093/ejendo/lvad054

Teleanu, M.-V., Fuss, C. T., Paramasivam, N., Pirmann, S., Mock, A., Terkamp, C., Kircher, S., Landwehr, L.-S., Lenschow, C., Schlegel, N., Stenzinger, A., Jahn, A., Fassnacht, M., Glimm, H., Hübschmann, D., Fröhling, S., & Kroiss, M. (2023). Targeted therapy of advanced parathyroid carcinoma guided by genomic and transcriptomic profiling. Molecular Oncology. https://doi.org/10.1002/1878-0261.13398

Wurm, A. A., Brilloff, S., Kolovich, S., Schäfer, S., Rahimian, E., Kufrin, V., Bill, M., Carrero, Z. I., Drukewitz, S., Krüger, A., Hüther, M., Uhrig, S., Oster, S., Westphal, D., Meier, F., Pfütze, K., Hübschmann, D., Horak, P., Kreutzfeldt, S., … Glimm, H. (2023). Signaling-induced systematic repression of miRNAs uncovers cancer vulnerabilities and targeted therapy sensitivity. Cell Reports. Medicine, 101200. https://doi.org/10.1016/j.xcrm.2023.101200

2022

Hoffmeister-Wittmann P, Mock A, Nichetti F, et al. Bcl-xL as prognostic marker and potential therapeutic target in cholangiocarcinoma. Liver Int. 2022;42(12):2855-2870. doi:10.1111/liv.15392

Jahn A, Rump A, Widmann TJ, et al. Comprehensive cancer predisposition testing within the prospective MASTER trial identifies hereditary cancer patients and supports treatment decisions for rare cancers. Ann Oncol. 2022;33(11):1186-1199. doi:10.1016/j.annonc.2022.07.008

Rieke DT, de Bortoli T, Horak P, et al. Feasibility and outcome of reproducible clinical interpretation of high-dimensional molecular data: a comparison of two molecular tumor boards. BMC Med. 2022;20(1):367. doi:10.1186/s12916-022-02560-5

Heilig CE, Laßmann A, Mughal SS, et al. Gene expression-based prediction of pazopanib efficacy in sarcoma. Eur J Cancer. 2022;172:107-118. doi:10.1016/j.ejca.2022.05.025

Möhrmann L, Werner M, Oleś M, et al. Comprehensive genomic and epigenomic analysis in cancer of unknown primary guides molecularly-informed therapies despite heterogeneity. Nat Commun. 2022;13(1):4485. doi:10.1038/s41467-022-31866-4

Dieter SM, Lovecchio D, Pataskar A, et al. Suppression of heparan sulfation re-sensitizes YAP1-driven melanoma to MAPK pathway inhibitors. Oncogene. 2022;41(32):3953-3968. doi:10.1038/s41388-022-02400-z

Heilig CE, Laßmann A, Mughal SS, et al. Gene expression-based prediction of pazopanib efficacy in sarcoma. Eur J Cancer. 2022;172:107-118. doi:10.1016/j.ejca.2022.05.025

Niger M, Nichetti F, Casadei-Gardini A, et al. MGMT inactivation as a new biomarker in patients with advanced biliary tract cancers. Mol Oncol. Published online May 27, 2022. doi:10.1002/1878-0261.13256

Schedel A, Friedrich UA, Morcos MNF, et al. Recurrent Germline Variant in RAD21 Predisposes Children to Lymphoblastic Leukemia or Lymphoma. Int J Mol Sci. 2022;23(9):5174. doi:10.3390/ijms23095174

Maurus K, Kosnopfel C, Kneitz H, et al. Cutaneous epithelioid haemangiomas show somatic mutations in the mitogen-activated protein kinase pathway. Br J Dermatol. 2022;186(3):553-563. doi:10.1111/bjd.20869

Veinalde R, Pidelaserra-Martí G, Moulin C, et al. Virotherapy combined with anti-PD-1 transiently reshapes the tumor immune environment and induces anti-tumor immunity in a preclinical PDAC model. Front Immunol. 2022;13:1096162. doi:10.3389/fimmu.2022.1096162

2021

Thomann S, Weiler SME, Wei T, et al. YAP-induced Ccl2 expression is associated with a switch in hepatic macrophage identity and vascular remodelling in liver cancer. Liver Int. 2021;41(12):3011-3023. doi:10.1111/liv.15048

Heilig CE, Horak P, Kreutzfeldt S, et al. Rationale and design of the CRAFT (Continuous ReAssessment with Flexible ExTension in Rare Malignancies) multicenter phase II trial. ESMO Open. 2021;6(6):100310. doi:10.1016/j.esmoop.2021.100310

Horak P, Heining C, Kreutzfeldt S, et al. Comprehensive Genomic and Transcriptomic Analysis for Guiding Therapeutic Decisions in Patients with Rare Cancers. Cancer Discov. 2021;11(11):2780-2795. doi:10.1158/2159-8290.CD-21-0126

Herbst F, Lang TJL, Eckert ESP, et al. The balance between the intronic miR-342 and its host gene Evl determines hematopoietic cell fate decision. Leukemia. 2021;35(10):2948-2963. doi:10.1038/s41375-021-01267-5

Dieter SM, Siegl C, Codó PL, et al. Degradation of CCNK/CDK12 is a druggable vulnerability of colorectal cancer. Cell Rep. 2021;36(3):109394. doi:10.1016/j.celrep.2021.109394

Vangala D, Ladigan S, Liffers ST, et al. Secondary resistance to anti-EGFR therapy by transcriptional reprogramming in patient-derived colorectal cancer models. Genome Med. 2021;13(1):116. doi:10.1186/s13073-021-00926-7

Koralli P, Tsikalakis S, Goulielmaki M, et al. Rational design of aqueous conjugated polymer nanoparticles as potential theranostic agents of breast cancer. Mater Chem Front. 2021;5(13):4950-4962. doi:10.1039/D1QM00479D

Simon M, Mughal SS, Horak P, et al. Deconvolution of sarcoma methylomes reveals varying degrees of immune cell infiltrates with association to genomic aberrations. J Transl Med. 2021;19(1):204. doi:10.1186/s12967-021-02858-7

Hanf D, Heining C, Laaber K, et al. Response to Cabozantinib Following Acquired Entrectinib Resistance in a Patient With ETV6-NTRK3 Fusion-Positive Carcinoma Harboring the NTRK3 G623R Solvent-Front Mutation. JCO Precision Oncology. 2021;(5):687-694. doi:10.1200/PO.20.00278

Wahjudi LW, Bernhardt S, Abnaof K, et al. Integrating proteomics into precision oncology. Int J Cancer. 2021;148(6):1438-1451. doi:10.1002/ijc.33301

Zowada MK, Tirier SM, Dieter SM, et al. Functional States in Tumor-Initiating Cell Differentiation in Human Colorectal Cancer. Cancers (Basel). 2021;13(5). doi:10.3390/cancers13051097

Koelsche C, Schrimpf D, Stichel D, et al. Sarcoma classification by DNA methylation profiling. Nat Commun. 2021;12(1):498. doi:10.1038/s41467-020-20603-4

Hlevnjak M, Schulze M, Elgaafary S, et al. CATCH: A Prospective Precision Oncology Trial in Metastatic Breast Cancer. JCO Precis Oncol. 2021;5:PO.20.00248. doi:10.1200/PO.20.00248

2020

Loosen SH, Gaisa NT, Schmeding M, et al. Prolonged Survival of a Patient with Advanced-Stage Combined Hepatocellular-Cholangiocarcinoma. Case Rep Gastroenterol. 2020;14(3):658-667. doi:10.1159/000511034

Thomann S, Weiler SME, Marquard S, et al. YAP orchestrates heterotypic endothelial cell communication via HGF/c-MET signaling in liver tumorigenesis. Cancer Res. Published online October 21, 2020. doi:10.1158/0008-5472.CAN-20-0242

Scherr AL, Mock A, Gdynia G, et al. Identification of BCL-XL as highly active survival factor and promising therapeutic target in colorectal cancer. Cell Death Dis. 2020;11(10):875. doi:10.1038/s41419-020-03092-7

Heilig CE, Horak P, Lipka DB, et al. Germline SDHB-inactivating mutation in gastric spindle cell sarcoma. Genes Chromosomes Cancer. 2020;59(10):601-608. doi:10.1002/gcc.22876

Laskin J, Liu SV, Tolba K, et al. NRG1 fusion-driven tumors: biology, detection, and the therapeutic role of afatinib and other ErbB-targeting agents. Annals of Oncology. Published online September 9, 2020. doi:10.1016/j.annonc.2020.08.2335

Cadranel J, Liu SV, Duruisseaux M, et al. Therapeutic Potential of Afatinib in NRG1 Fusion-Driven Solid Tumors: A Case Series. Oncologist. Published online August 27, 2020. doi:10.1634/theoncologist.2020-0379

Westphalen BC, Bokemeyer C, Büttner R, et al. Conceptual framework for precision cancer medicine in Germany: Consensus statement of the Deutsche Krebshilfe working group “Molecular Diagnostics and Therapy.” Eur J Cancer. 2020;135:1-7. doi:10.1016/j.ejca.2020.04.019

Möhrmann L, Zowada MK, Strakerjahn H, et al. A Perivascular Niche in the Bone Marrow Hosts Quiescent and Proliferating Tumorigenic Colorectal Cancer Cells. Int J Cancer. Published online July 15, 2020. doi:10.1002/ijc.32933

Rippinger N, Fischer C, Haun MW, et al. Cancer surveillance and distress among adult pathogenic TP53 germline variant carriers in Germany: A multicenter feasibility and acceptance survey. Cancer. Published online June 18, 2020. doi:10.1002/cncr.33004

Messerschmidt C, Obermayer B, Klinghammer K, et al. Distinct immune evasion in APOBEC-enriched, HPV-negative HNSCC. Int J Cancer. Published online May 29, 2020. doi:10.1002/ijc.33123

Voronina N, Wong JKL, Hübschmann D, et al. The landscape of chromothripsis across adult cancer types. Nat Commun. 2020;11(1):2320. doi:10.1038/s41467-020-16134-7

Berger AK, Mughal SS, Allgäuer M, et al. Metastatic adult pancreatoblastoma: Multimodal treatment and molecular characterization of a very rare disease. Pancreatology. 2020;20(3):425-432. doi:10.1016/j.pan.2020.02.017

Horak P, Uhrig S, Witzel M, et al. Comprehensive genomic characterization of gene therapy-induced T-cell acute lymphoblastic leukemia. Leukemia. Published online March 3, 2020. doi:10.1038/s41375-020-0779-z

Stenzinger A, Endris V, Budczies J, et al. Harmonization and Standardization of Panel-Based Tumor Mutational Burden (TMB) Measurement: Real-World Results and Recommendations of the QuIP Study. J Thorac Oncol. Published online February 28, 2020. doi:10.1016/j.jtho.2020.01.023

Ronellenfitsch MW, Harter PN, Kirchner M, et al. Targetable ERBB2 mutations identified in neurofibroma/schwannoma hybrid nerve sheath tumors. J Clin Invest. Published online February 4, 2020. doi:10.1172/JCI130787

2019

Weber S, Koschade SE, Hoffmann CM, et al. The notch target gene HEYL modulates metastasis forming capacity of colorectal cancer patient-derived spheroid cells in vivo. BMC Cancer. 2019;19(1):1181. doi:10.1186/s12885-019-6396-4

Weinberg F, Griffin R, Fröhlich M, et al. Identification and characterization of a BRAF fusion oncoprotein with retained autoinhibitory domains. Oncogene. Published online September 26, 2019. doi:10.1038/s41388-019-1021-1

Tirier SM, Park J, Preußer F, et al. Pheno-seq - linking visual features and gene expression in 3D cell culture systems. Sci Rep. 2019;9(1):12367. doi:10.1038/s41598-019-48771-4

Glocker K, Ahlbrandt J, Knurr A, Horak P, Heining C, Ückert F. Finding Options Beyond Standard of Care in Oncology: A Proposal for Workflows Utilizing Knowledge Databases. Stud Health Technol Inform. 2019;264:950-953. doi:10.3233/SHTI190364

Mühlenberg T, Ketzer J, Heinrich MC, et al. KIT-dependent and -independent genomic heterogeneity of resistance in gastrointestinal stromal tumors - TORC1/2 inhibition as salvage strategy. Mol Cancer Ther. Published online July 15, 2019. doi:10.1158/1535-7163.MCT-18-1224

Haffa M, Lin T, Holowatyj AN, et al. Transcriptome profiling of adipose tissue reveals depot-specific metabolic alterations among colorectal cancer patients. J Clin Endocrinol Metab. Published online June 21, 2019. doi:10.1210/jc.2019-00461

Feuerbach L, Sieverling L, Deeg KI, et al. TelomereHunter - in silico estimation of telomere content and composition from cancer genomes. BMC Bioinformatics. 2019;20(1):272. doi:10.1186/s12859-019-2851-0

Leichsenring J, Horak P, Kreutzfeldt S, et al. Variant classification in precision oncology. Int J Cancer. Published online April 22, 2019. doi:10.1002/ijc.32358

Horak P, Weischenfeldt J, von Amsberg G, et al. Response to olaparib in a PALB2 germline mutated prostate cancer and genetic events associated with resistance. Cold Spring Harb Mol Case Stud. 2019;5(2). doi:10.1101/mcs.a003657

Endris V, Buchhalter I, Allgäuer M, et al. Measurement of tumor mutational burden (TMB) in routine molecular diagnostics: in silico and real-life analysis of three larger gene panels. Int J Cancer. 2019;144(9):2303-2312. doi:10.1002/ijc.32002

Gröschel S, Hübschmann D, Raimondi F, et al. Defective homologous recombination DNA repair as therapeutic target in advanced chordoma. Nat Commun. 2019;10(1):1635. doi:10.1038/s41467-019-09633-9

Ehrenberg KR, Gao J, Oppel F, et al. Systematic Generation of Patient-Derived Tumor Models in Pancreatic Cancer. Cells. 2019;8(2). doi:10.3390/cells8020142

Wurm AA, Pina C. Long Non-coding RNAs as Functional and Structural Chromatin Modulators in Acute Myeloid Leukemia. Front Oncol. 2019;9:899. doi:10.3389/fonc.2019.00899

Mock A, Heilig CE, Kreutzfeldt S, et al. Community-driven development of a modified progression-free survival ratio for precision oncology. ESMO Open. 2019;4(6):e000583. doi:10.1136/esmoopen-2019-000583

Klose J, Trefz S, Wagner T, et al. Salinomycin: Anti-tumor activity in a pre-clinical colorectal cancer model. PLoS ONE. 2019;14(2):e0211916. doi:10.1371/journal.pone.0211916

2018

Lier A, Penzel R, Heining C, et al. Validating Comprehensive Next-Generation Sequencing Results for Precision Oncology: The NCT/DKTK Molecularly Aided Stratification for Tumor Eradication Research Experience. JCO Precis Oncol. 2018;2. doi:10.1200/PO.18.00171

Wünsche P, Eckert ESP, Holland-Letz T, et al. Mapping Active Gene-Regulatory Regions in Human Repopulating Long-Term HSCs. Cell Stem Cell. 2018;23(1):132-146.e9. doi:10.1016/j.stem.2018.06.003

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Open Positions


We currently offer the following bachelor/master thesis and lab rotations positions for life sciences students. Interested students are welcome to submit an application including motivation letter and certificates to julia.dorok(at)nct-dresden.de

  • Master thesis (dry lab) for students of biology/medicine/life sciences/(bio)informatics >> more Information


Contact
 

Prof. Dr. med. Hanno Glimm
Head of Department
Translational Medical Oncology
E-Mail: hanno.glimm(at)nct-dresden.de
Phone: +49 (0)351 458 5531

 

Julia Pönisch
Secretary
E-Mail: julia.poenisch(at)nct-dresden.de
Phone: +49 (0)351 458 5531

Dr. Daniela Richter
Scientific and Administrative Coordinator
E-Mail: daniela.richter(at)nct-dresden.de
Phone: +49 (0)351 458 5539