Asymmetric cell division is essential for stem cells to simultaneously generate new progeny and self- renew. An intricate regulatory network controls asymmetric division in both time and space. Impairments in this network can cause unrestrained replication, leading to dysplasia and tumorigenesis. An integrative systems biology approach is adopted to understand the mechanistic details of asymmetric cell division. Computational models and robustness analysis are combined to generate hypotheses that can be verified by experiments, and the addition of the verified hypotheses into the model will generate more insights into the system. This approach will first help study a bacterial model system, Caulobacter, using a multiscale hybrid model, where reactions are classified into categories based on their rates and regulatory functions and simulated by different numerical techniques, which is essential for modeling a system as complex as asymmetric cell division. The critical factors responsible for switching cell fate during asymmetric division will then be identified by checking the robustness of the model on different levels using a multi-tiered robustness analysis framework. To further characterize and understand the function of asymmetric localization of cell fate determinants, which are essential for causing the bifurcation of cell fates between the daughter cells, modular protein interaction domains and protein scaffolds are developed to perturb them spatially. This is the first demonstration that parts and devices designed from synthetic biology can be used to study systems biology. Colon cancer-initiating cells (CCIC) will then be studied using the same computational approach. CCIC are cancer stem cells that can self-renew and form tumors. An innovative technology enables in vitro CCIC cell lines to maintain their self-renewal and tumor formation capability. It is demonstrated for the first time that the level of the Notch signaling pathway is elevated in CCIC, the inhibition of which causes loss of asymmetry and eventually leads to apoptosis. The cell fate determinant NUMB, a notch inhibitor, is shown to asymmetrically localize during mitosis, indicating that asymmetric division plays a crucial role in cancer morphology. Using computational systems biology, signaling pathways like NOTCH and WNT, and cell fate determinants will be systematically perturbed. Based on the computational analysis of hight-throughput transcriptome changes in their downstream targets, which involves statistical analysis, clustering, utilizing bioinformatics databases and network visualization tools, a multiscale systems model will be built to help understand the CCIC asymmetric division and find novel regulatory functions. The proposed research will lead to a better understanding of cancer initiating cells in order to identify novel targets for cancer therapy. The computational and experimental techniques for the integrative systems biology approach will be readily available to the biomedical community to study other systems.

Public Health Relevance

In this proposal, an integrative approach combining multiscale modeling, robustness analysis, computational analysis of high-throughput transcriptome, and perturbation experiments will be developed to investigate the roles of polar localized cell fate determinants in asymmetric cell division. Starting from a well-established bacterial model system, the computational tools will then help study colon cancer-initiating cells, where asymmetrically localized cell fate determinants have been linked to self-renewal and tumor formation through the Notch pathway. This study can identify potential targets for future cancer therapies.

National Institute of Health (NIH)
National Institute of General Medical Sciences (NIGMS)
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Modeling and Analysis of Biological Systems Study Section (MABS)
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Lyster, Peter
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Cornell University
Engineering (All Types)
Schools of Engineering
United States
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Shen, Xiaomeng; Shen, Shichen; Li, Jun et al. (2017) An IonStar Experimental Strategy for MS1 Ion Current-Based Quantification Using Ultrahigh-Field Orbitrap: Reproducible, In-Depth, and Accurate Protein Measurement in Large Cohorts. J Proteome Res 16:2445-2456
Barth, Bradley B; Henriquez, Craig S; Grill, Warren M et al. (2017) Electrical stimulation of gut motility guided by an in silico model. J Neural Eng 14:066010
Wang, Yiwei; Huang, Dan; Chen, Kai-Yuan et al. (2017) Fucosylation Deficiency in Mice Leads to Colitis and Adenocarcinoma. Gastroenterology 152:193-205.e10
Wang, Lihua; Bu, Pengcheng; Ai, Yiwei et al. (2016) A long non-coding RNA targets microRNA miR-34a to regulate colon cancer stem cell asymmetric division. Elife 5:
Rothschild, Daniel E; Srinivasan, Tara; Aponte-Santiago, Linette A et al. (2016) The Ex Vivo Culture and Pattern Recognition Receptor Stimulation of Mouse Intestinal Organoids. J Vis Exp :
Chen, Huanhuan Joyce; Wei, Zhubo; Sun, Jian et al. (2016) A recellularized human colon model identifies cancer driver genes. Nat Biotechnol 34:845-51
Bu, Pengcheng; Wang, Lihua; Chen, Kai-Yuan et al. (2016) A miR-34a-Numb Feedforward Loop Triggered by Inflammation Regulates Asymmetric Stem Cell Division in Intestine and Colon Cancer. Cell Stem Cell 18:189-202
Srinivasan, Tara; Than, Elaine Bich; Bu, Pengcheng et al. (2016) Notch signalling regulates asymmetric division and inter-conversion between lgr5 and bmi1 expressing intestinal stem cells. Sci Rep 6:26069
Joe, Daniel J; Hwang, Jeonghyun; Johnson, Christelle et al. (2016) Surface Functionalized Graphene Biosensor on Sapphire for Cancer Cell Detection. J Nanosci Nanotechnol 16:144-51
Srinivasan, Tara; Walters, Jewell; Bu, Pengcheng et al. (2016) NOTCH Signaling Regulates Asymmetric Cell Fate of Fast- and Slow-Cycling Colon Cancer-Initiating Cells. Cancer Res 76:3411-21

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