Novel Monte Carlo Approaches to Identify Aberrant Pathways in Cancer
| dc.contributor.author | Gu, Jinghua | en |
| dc.contributor.committeechair | Xuan, Jianhua Jason | en |
| dc.contributor.committeemember | Abbott, A. Lynn | en |
| dc.contributor.committeemember | Wang, Yue J. | en |
| dc.contributor.committeemember | Lu, Chang-Tien | en |
| dc.contributor.committeemember | Silva, Luiz A. | en |
| dc.contributor.department | Electrical and Computer Engineering | en |
| dc.date.accessioned | 2015-04-30T06:00:59Z | en |
| dc.date.available | 2015-04-30T06:00:59Z | en |
| dc.date.issued | 2013-08-27 | en |
| dc.description.abstract | Recent breakthroughs in high-throughput biotechnology have promoted the integration of multi-platform data to investigate signal transduction pathways within a cell. In order to model complicated dynamics and heterogeneity of biological pathways, sophisticated computational models are needed to address unique properties of both the biological hypothesis and the data. In this dissertation work, we have proposed and developed methods using Markov Chain Monte Carlo (MCMC) techniques to solve complex modeling problems in human cancer research by integrating multi-platform data. We focus on two research topics: 1) identification of transcriptional regulatory networks and 2) uncovering of aberrant intracellular signal transduction pathways. We propose a robust method, called GibbsOS, to identify condition specific gene regulatory patterns between transcription factors and their target genes. A Gibbs sampler is employed to sample target genes from the marginal function of outlier sum of regression t statistic. Numerical simulation has demonstrated significant performance improvement of GibbsOS over existing methods against noise and false positive connections in binding data. We have applied GibbsOS to breast cancer cell line datasets and identified condition specific regulatory rewiring in human breast cancer. We also propose a novel method, namely Gibbs sampler to Infer Signal Transduction (GIST), to detect aberrant pathways that are highly associated with biological phenotypes or clinical information. By converting predefined potential functions into a Gibbs distribution, GIST estimates edge directions by learning the distribution of linear signaling pathway structures. Through the sampling process, the algorithm is able to infer signal transduction directions which are jointly determined by both gene expression and network topology. We demonstrate the advantage of the proposed algorithms on simulation data with respect to different settings of noise level in gene expression and false-positive connections in protein-protein interaction (PPI) network. Another major contribution of the dissertation work is that we have improved traditional perspective towards understanding aberrant signal transductions by further investigating structural linkage of signaling pathways. We develop a method called Structural Organization to Uncover pathway Landscape (SOUL), which emphasizes on modularized pathways structures from reconstructed pathway landscape. GIST and SOUL provide a very unique angle to computationally model alternative pathways and pathway crosstalk. The proposed new methods can bring insight to drug discovery research by targeting nodal proteins that oversee multiple signaling pathways, rather than treating individual pathways separately. A complete pathway identification protocol, namely Infer Modularization of PAthway CrossTalk (IMPACT), is developed to bridge downstream regulatory networks with upstream signaling cascades. We have applied IMPACT to breast cancer treated patient datasets to investigate how estrogen receptor (ER) signaling pathways are related to drug resistance. The identified pathway proteins from patient datasets are well supported by breast cancer cell line models. We hypothesize from computational results that HSP90AA1 protein is an important nodal protein that oversees multiple signaling pathways to drive drug resistance. Cell viability analysis has supported our hypothesis by showing a significant decrease in viability of endocrine resistant cells compared with non-resistant cells when 17-AAG (a drug that inhibits HSP90AA1) is applied. We believe that this dissertation work not only offers novel computational tools towards understanding complicated biological problems, but more importantly, it provides a valuable paradigm where systems biology connects data with hypotheses using computational modeling. Initial success of using microarray datasets to study endocrine resistance in breast cancer has shed light on translating results from high throughput datasets to biological discoveries in complicated human disease studies. As the next generation biotechnology becomes more cost-effective, the power of the proposed methods to untangle complicated aberrant signaling rewiring and pathway crosstalk will be finally unleashed. | en |
| dc.description.degree | Ph. D. | en |
| dc.format.medium | ETD | en |
| dc.identifier.other | vt_gsexam:1495 | en |
| dc.identifier.uri | http://hdl.handle.net/10919/51950 | en |
| dc.publisher | Virginia Tech | en |
| dc.rights | In Copyright | en |
| dc.rights.uri | http://rightsstatements.org/vocab/InC/1.0/ | en |
| dc.subject | Microarray Data Analysis | en |
| dc.subject | Transcriptional Regulatory Network Protein-Protein-Interaction Network | en |
| dc.subject | Aberrant Signaling Pathway Markers | en |
| dc.title | Novel Monte Carlo Approaches to Identify Aberrant Pathways in Cancer | en |
| dc.type | Dissertation | en |
| thesis.degree.discipline | Electrical Engineering | en |
| thesis.degree.grantor | Virginia Polytechnic Institute and State University | en |
| thesis.degree.level | doctoral | en |
| thesis.degree.name | Ph. D. | en |
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