University Medical Center (UMC) Mainz
Maria Felicia Basilicata Christian Behl Benedikt Berninger Luciana Berod Tobias Bopp Andreas Daiber Sven Danckwardt Carsten Deppermann Stephan Grabbe Thomas Hofmann Thomas Kindler Daniela Kramer Daniela Krause Dilja Krueger-Burg Michael Kühn Beat Lutz Johannes Mayer Wolfram Ruf Susann Schweiger Natalia Soshnikova Tim Sparwasser Oliver Tüscher Sara Vieira-Silva Ari Waisman Philipp Wild Jennifer Winter Fatemeh Zare-ShahnehRole of oncogenic signalling in epigenetics and DNA repair
In our laboratory, we are interested in understanding signal transduction pathways in cancer cells, with a focus on hematopoietic malignancies. A detailed understanding of aberrant signaling should provide insights into the process of malignant transformation, mechanisms of drug resistance and vulnerability of cancer cells. In addition, the identification of functional differences between cancer stem cells and their normal counterparts will allow us to develop novel therapeutic strategies. In this context we use a variety of distinct experimental approaches and tumor models, including cell culture, defined mouse models (e.g. Flt3-ITD knock-in, conditional KrasG12D knock-in, bone marrow transplantation) and primary tumor samples.
Positions held
- Since 2009: Group Leader, University Medical Center (UMC), Mainz
- Since 2009: Assistant Professor, University Medical Center (UMC), Mainz
- Since 2008: Attending Physician, Department of Hematology and Oncology, University Medical Center (UMC), Mainz
- 2005 - 2008: Postdoc, Harvard Medical School, Boston, USA
Education
- 1994 - 1998: Medical Thesis, Institute of Immunology, Ludwig Maximilian University, Munich
- 1997: Medical License, Ludwig Maximilian University, Munich
Selected publications by Thomas Kindler
Fischer J, Paret C, El Malki K, Alt F, Wingerter A, Neu MA, Kron B, Russo A, Lehmann N, Roth L, Fehr EM, Attig S, Hohberger A, Kindler T and Faber J (2017) CD19 Isoforms Enabling Resistance to CART-19 Immunotherapy Are Expressed in B-ALL Patients at Initial Diagnosis. J Immunother, 40(5):187-195
Sasca D, Hähnel PS, Szybinski J, Khawaja K, Kriege O, Pante SV, Bullinger L, Strand S, Strand D, Theobald M and Kindler T (2014) SIRT1 prevents genotoxic stress-induced p53 activation in acute myeloid leukemia. Blood, 124:121-133
Hähnel PS, Enders B, Sasca D, Roos WP, Kaina B, Bullinger L, Theobald M and Kindler T (2014) Targeting components of the alternative NHEJ pathway sensitizes KRAS mutant leukemic cells to chemotherapy. Blood, 123:2355-2366
Hartwell KA, Miller PG, Mukherjee S, Kahn AR, Stewart AL, Logan DJ, Negri JM, Duvet M, Järås M, Puram R, Dancik V, Al-Shahrour F, Kindler T, Tothova Z, Chattopadhyay S, Hasaka T, Narayan R, Dai M, Huang C, Shterental S, Chu LP, Haydu JE, Shieh JH, Steensma DP, Munoz B, Bittker JA, Shamji AF, Clemons PA, Tolliday NJ, Carpenter AE, Gilliland DG, Stern AM, Moore MA, Scadden DT, Schreiber SL, Ebert BL and Golub TR (2013) Niche-based screening identifies small-molecule inhibitors of leukemia stem cells. Nat Chem Biol, 9:840-848
Mercher T, Cornejo MG, Sears C, Kindler T, Moore SA, Aster JC and Gilliland DG (2008) Notch signaling specifies megakaryocyte development. Cell Stem Cell, 3, 314-326