Patrick Cahan, PhD
Other appointments:: Institute of Cell Engineering
Office: Miller Research Building 653
Lab: Cahan Lab
PhD, Computational Biology, Washington University, 2009
Gene regulatory networks (GRNs) govern the cell’s transcriptional output both at steady state and in response to perturbations, and thus act as major molecular determinants of cell-type identity. The long-term aims of my research program are:
- to develop computational and experimental tools to map mammalian GRNs,
- to better understand how canonical signaling pathways modulate and are modulated by transiently established GRNs in the developing embryo, and
- to characterize how cell type specific GRNs are rewired during tumorigenesis and progression.
Towards these ends, we work across several disciplines including molecular and developmental biology, manipulation of pluripotent stem cells, population based and single-cell genomics, and computational and network biology. The outcomes of my research program will include improving the fidelity of directed differentiation to mesendodermal lineages (for purposes of disease modeling, drug screening, and regenerative medicine), the generation of fundamental insights into the interactions between GRNs, signaling pathways, and cell fate decisions, and improved models of human tumors.
Kumar P, Tan Y, Cahan P. Understanding development and stem cells using single cell-based analyses of gene expression. Development. 2017 Jan 1;144(1):17-32.
Bian Q, Cahan P. Computational Tools for Stem Cell Biology. Trends in Biotechnology. 2016 Jun. 10.1016/j.tibtech.2016.05.010.
Kumar RM*, Cahan P*, Shalek A, Satija R, DaleyKeyser A, Li H, Zhang J, Pardee K, Gennert D, Trombetta JJ, Ferrante TC, Regev A, Daley GQ, and Collins JJ. Deconstructing transcriptional heterogeneity in pluripotent stem cells. Nature. 2014 Dec 4;516(7529):56–61.
Cahan P*, Li H*, Morris SA*, Lummertz da Rocha E, Daley GQ, Collins JJ. CellNet: Network Biology Applied to Stem Cell Engineering. Cell. 2014 Aug 14;158(4):903–15.
Morris SA*, Cahan P*, Li H*, Zhao AM, San Roman AK, Shivdasani RA, Collins JJ, Daley GQ. Dissecting Engineered Cell Types and Enhancing Cell Fate Conversion via CellNet. Cell. 2014 Aug 14;158(4):889–902.
Cahan P, Daley GQ. Origins and implications of pluripotent stem cell variability and heterogeneity. (2013). Nature Reviews Molecular Cell Biology 14:357–68.
McKinney-Freeman S*, Cahan P*, Li H*, Lacadie SA, Huang HT, Curran M, Loewer S, Naveiras O, Kathrein KL, Konantz M, Langdon EM, Lengerke C, Zon LI, Collins JJ, Daley GQ. The transcriptional landscape of hematopoietic stem cell ontogeny. Cell Stem Cell. 2012 Nov 2;11(5):701–14.
Cahan P, Li Y, Izumi M, Graubert TA. The impact of copy number variation on local gene expression in mouse hematopoietic stem and progenitor cells. Nature Genetics. 2009 Apr;41(4):430–7.
*Denotes equal contribution