Education and Training
Michael Meister is Scientist at the Translational Research Unit (STF) at the Thoraxklinik Heidelberg. He graduated in Biology and conducted his PhD studies at the University of Heidelberg. His postdoctoral research was performed at the Brigham and Women’s Hospital in Boston, USA and the University of Ulm. Since 2004 he is employed at Thoraxklinik Heidelberg.
Expertise
The research of the STF aims to better understand the molecular causes of thoracic diseases. One of the department's main research area is the identification of molecular biomarkers in lung cancer. Michael Meister coordinates and supervises the research activities of the STF in collaboration with the team. He has coordinated both national (LungSys) and international (CANCERALIA, EU-7th) research projects. Currently there is a focus on the establishment of new model systems (organoids, 3D cell culture systems) to research the interaction of different cell types in the tumor context.
- Biomarkers in thoracic diseases
- Prognostic and predictive biomarkers in lung cancer
- Glycodelin in non-small cell lung cancer (NSCLC)
- Lung Cancer
- Platform Biobanking
- Richtmann S, Marwitz S, Muley T, Koistinen H, Christopoulos P, Thomas M, Kazdal D, Allgäuer M, Winter H, Goldmann T, Meister M, Klingmüller U, Schneider MA. The pregnancy-associated protein glycodelin as a potential sex-specific target for resistance to immunotherapy in non-small cell lung cancer. Transl Res. 2024 Oct;272:177-189.
- Muley T, Schneider MA, Meister M, Thomas M, Heußel CP, Kriegsmann M, Holdenrieder S, Wehnl B, Rolny V, Mang A, Gerber R, Herth F. CYFRA 21-1, CA 125 and CEA provide additional prognostic value in NSCLC patients with stable disease at first CT scan. Tumour Biol. 2024;46(s1):S163-S175.
- Faltus C, Lahnsteiner A, Barrdahl M, Assenov Y, Hüsing A, Bogatyrova O, Laplana M, Johnson T, Muley T, Meister M, Warth A, Thomas M, Plass C, Kaaks R, Risch A. Identification of <i>NHLRC1</i> as a Novel AKT Activator from a Lung Cancer Epigenome-Wide Association Study (EWAS). Int J Mol Sci. 2022 Sep 14;23(18):10699.
- Gründing AR, Schneider MA, Richtmann S, Kriegsmann M, Winter H, Martinez- Delgado B, Varona S, Liu B, DeLuca DS, Held J, Wrenger S, Muley T, Meister M, Welte T, Janciauskiene S. Lung Adenocarcinoma Cell Sensitivity to Chemotherapies: A Spotlight on Lipid Droplets and <i>SREBF1</i> Gene. Cancers (Basel). 2022 Sep 14;14(18):4454.
- Trefzer TB, Schneider MA, Jechow K, Chua RL, Muley T, Winter H, Kriegsmann M, Meister M, Eils R, Conrad C. Intratumoral Heterogeneity and Immune Modulation in Lung Adenocarcinoma in Female Smokers and Never Smokers. Cancer Res. 2022 Sep 2;82(17):3116-3129. PMC9437562.
- Schneider MA, Richtmann S, Gründing AR, Wrenger S, Welte T, Meister M, Kriegsmann M, Winter H, Muley T, Janciauskiene S. Transmembrane serine protease 2 is a prognostic factor for lung adenocarcinoma. Int J Oncol. 2022 Apr;60(4):39.
- Angeles AK, Christopoulos P, Yuan Z, Bauer S, Janke F, Ogrodnik SJ, Reck M, Schlesner M, Meister M, Schneider MA, Dietz S, Stenzinger A, Thomas M, Sültmann H. Early identification of disease progression in ALK-rearranged lung cancer using circulating tumor DNA analysis. NPJ Precis Oncol. 2021 Dec 7;5(1):100.
- Magios N, Bozorgmehr F, Volckmar AL, Kazdal D, Kirchner M, Herth FJ, Heussel CP, Eichhorn F, Meister M, Muley T, Elshafie RA, Fischer JR, Faehling M, Kriegsmann M, Schirmacher P, Bischoff H, Stenzinger A, Thomas M, Christopoulos P. Real-world implementation of sequential targeted therapies for EGFR-mutated lung cancer. Ther Adv Med Oncol. 2021 Mar 24;13:1758835921996509.
- Budczies J, Kirchner M, Kluck K, Kazdal D, Glade J, Allgäuer M, Kriegsmann M, Heußel CP, Herth FJ, Winter H, Meister M, Muley T, Goldmann T, Fröhling S, Wermke M, Waller CF, Tufman A, Reck M, Peters S, Schirmacher P, Thomas M, Christopoulos P, Stenzinger A. Deciphering the immunosuppressive tumor microenvironment in ALK- and EGFR-positive lung adenocarcinoma. Cancer Immunol Immunother. 2022 Feb;71(2):251-265.
- Goldmann T, Schmitt B, Müller J, Kröger M, Scheufele S, Marwitz S, Nitschkowski D, Schneider MA, Meister M, Muley T, Thomas M, Kugler C, Rabe KF, Siebert R, Reck M, Ammerpohl O. DNA methylation profiles of bronchoscopic biopsies for the diagnosis of lung cancer. Clin Epigenetics. 2021 Feb 17;13(1):38.
Karsten Senghas | Datamanagement | ||||||
Dr. rer. nat. Kadriya Yuskaeva | Datamanagement | ||||||
M. Sc. Lisa Strotmann | PhD Student | ||||||
Anja Anweiler | Study-Assistent | ||||||
Birgit Beelte | Study-Assistent | ||||||
Anna-Lisa Beier | Study-Assistent | ||||||
Natalie Enns | Study-Assistent | ||||||
Maja Gräbner | Study-Assistent | ||||||
Ingrid Heinzmann-Groth | Study-Assistent | ||||||
Andrea Kress | Study-Assistent | ||||||
Karin Schnorr-Teichert | Study-Assistent | ||||||
Christa Stolp | Study-Assistent | ||||||
Martin Fallenbüchel | Technical Assistent | ||||||
Carmen Hoppstock | Technical Assistent | ||||||
Liz Meister | Technical Assistent | ||||||
Alena Rühl | Technical Assistent | ||||||
Dr. sc. hum. Sabine Wessels | Scientific Coordinator | ||||||
Dr. rer. nat. Marc Schneider | Head of Department |
Lung Research - Projects
- Identification of molecular biomarkers in lung cancer
Genetic and biological factors can have a lasting impact on the biology of tumor cells and their response to therapy. Using different techniques, molecular components (nucleic acids, proteins, metabolites) are isolated from the biomaterial samples from the lung biobank of the Thoraxklinik. A large number of analyses are carried out with these starting materials. From all the data obtained, tumor-specific, biomarkers are to be identified, which serve to expand and refine the diagnosis and therapy of the patients, considering the established clinical parameters. These studies are carried out with national and international cooperation partners. - Development of primary tissue cultures, 3D-organoid-models, and co-cultures in lung cancer
NSCLC-tumors show a high heterogeneity regarding cell composition. In addition to malignant cells, one can find also fibroblasts, normal lung cells, and immune cells. To understand the complex interaction of these cells, we work with organoid-models and co-cultures of primary cells derived from patient material. Using these model systems, we want to develop new therapeutic substances for personalized cancer therapy. - Glycodelin in NSCLC
The immunosuppresive role of glycodelin (gene name PAEP) during pregnancy is well characterized since several years. We found glycodelin strongly upregulated in NSCLC. It was detectable in serum of NSCLC patients and correlated with clinical follow-up. We are currently working to elucidate the function of glycodelin in NSCLC and to establish glycodelin as a follow-up biomarker and potential therapeutic target.

H&E = hematoxylin and eosin, PC = phosphatidylcholine, SCC = squamous cell carcinoma (Reprduced from Marien, E. et al. Oncotarget. 2016;7(11):12582-12597. doi:10.18632/oncotarget.7179)




