REICHERT LAB

Principal Investigator

Prof. Maximilian Reichert

I studied Medicine in Heidelberg and at the Technical University of Munich. I graduated with my thesis focusing on PI3K signaling and cell cycle progression in pancreatic cancer (PDAC) with summa cum laude. During my postdoctoral fellowship at the University in Pennsylvania, Philadelphia, USA, I discovered novel mechanisms of transcriptional regulation of PDAC cell plasticity using 3D culture models. After my return to Germany, I transferred my knowledge of advanced 3D culture systems successfully to cancer patients generating a cancer patient-derived organoid repository at TUM.

We are Groot. – Groot, Guardians of the Galaxy, MCU

Postdoc & Lab manager

Dr. Laura Schmidleitner

After receiving my bachelor’s and master’s degree in biology from the University of Regensburg, I did my PhD at the Helmholtz Center Munich and the Technical University Munich. I investigated the role of the epithelial-mesenchymal transition to identify factors that play a role in the progression of breast cancer. Since 2021, I manage the lab located in Garching and support the other scientists of our group.

Be grateful.

PhD candidate

Aristeidis Papargyriou

I received my master’s degree from the University of Patras, Greece in Applied Biochemistry and Biotechnology. In my master thesis I studied the role of Src kinases and microRNAs in the pathogenesis of breast cancer. I joined the lab in October 2018 as joint PhD student between the Reichert lab and the Scheel lab (HMGU) to work on Targeting Epithelial Plasticity in PDAC. My current project focus is laid on cellular plasticity with emphasis in the generation of advanced 3D organoid models to decipher and target PDAC heterogeneity.

Science for the improvement of human lives – or in a funny way: branch strong!

PhD candidate

Aashreya Ravichandra

I completed my Bachelor’s in Biology and my Master’s in Biotechnology from CUNY Hunter College in 2018 before working as a research technician for 2 years at the Schwabe Lab at Columbia University. I started working in Max Reichert’s lab in April 2021 and my project focuses on understanding how cancer associated fibroblast (CAF) plasticity and heterogeneity alters tumor vascularization and endothelial cells in intrahepatic cholangiocarcinoma, a rare cancer of the liver.

Science never solves a problem without creating ten more.

MD candidate

Sophia Schirmer

I investigate the genetic and morphological heterogeneity in murine derived 3D PDAC organoids with the aim of contributing to the development of personalized, targeted chemotherapy. I analyse different phenotypes arising from murine lineages with different mutations, hereby also taking their interaction with desmoplasic stroma into account.

Nothing in life is to be feared, it is only to be understood. Now is the time to understand more, so we can fear less. – Marie Curie

PhD Candidate

Raphela Ranjan

I joined the group in 2019 May as a PhD candidate. I did my bachelor’s degree in Biomedical Sciences (2016) at the Sri Ramachandra University, Chennai (India) and my Master’s degree in Molecular Medicine (2018) at the Friedrich-Alexander University Erlangen-Nuremberg (Germany). During my Master’s, I developed chorioallantoic membrane (CAM) xenografts to model various entities of cancer for functional studies of cancer hallmarks. During my PhD I am focusing on establishing the CAM model to study the interaction of tumor cells and Cancer associated fibroblasts in the regulation of metastasis by in ovo CRISPR/Cas9 dropout screening.

Success is a decision.

Research Associate

Lisa Fricke

I did my Master in Nutrition and Biomedicine at TUM. Since February 2020 I am working for clinical studies at MRI. Within the SFB1321 I take care of the samples for pancreatic cancer patient-derived organoids and provide the link between the clinic and the research lab.

Never stop exploring.

PhD candidate

Akul Shastri

I completed my masters at the LMU Munich during which I had the opportunity to work on a research course in the Reichert lab, which was based on understanding the individualistic effect of specific growth factors and agonists on the morphology of PDAC organoids in vitro. I then stayed on as a master’s student with the lab. During my thesis, we were able to define a media composition which would enable branching morphogenesis in patient-derived organoid (PDOs) lines. This would allow us to understand the pathways that are involved in the phenomenon of branching morphogenesis in PDOs.

Valentina Leone

Aurora Albanese

MD candidate

Arlett Schäfer

I study human medicine at the TUM. My MD project in the Reichert lab is the analysis of treatment-imposed genotypic and phenotypic alterations using the translational model of organoids.

The proper function of man is to live, not to exist. – Jack London