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Construction of cancer pathways for personalized medicine 
| 
Presented By 
Date 
Construction of cancer pathways for personalized medicine 
Predictive, Preventive and Personalized Medicine & Molecular Diagnostics 
Dr. Anton Yuryev 
Nov 4, 2014
Construction of cancer pathways for personalized medicine 
| 
Curse of Dimensionality of OMICs data: We will never have enough patient samples to calculate robust signatures from large scale molecular profiling data 
2 
signature size 
# patients 
error rate 
Hua et al. Optimal number of features as a function of sample size for various classification rules. Bioinformatics. 2005 
Fig.3 Optimal feature size versus sample size for Polynomial SVM classifier. 
nonlinear model, correlated feature, G=1, r= 0.25. s2 is set to let Bayers error be 0.05
Construction of cancer pathways for personalized medicine 
| 
Mathematical requirements for short signature size vs. Biological reality 
Mathematical requirement 
Biological reality 
Signature size must be 20-30 genes 
Typical cancer transcriptomics profile has 500-2000 differentially expressed genes with p-value < 0.005 
Increasing number of samples above 200 does not change optimal signature size 
Typical cancer dataset has not more than 100 patients. 
Increasing number of patients results in finding different cancer sub-types each having small number of samples 
Error rate and robustness of signatures from uncorrelated feature is better than from correlated features 
Most DE genes are correlated due to transcriptional linkage and different TFs regulated by only few biological pathways 
We can use prior knowledge about transcriptional regulation to select most uncorrelated features, e.g. genes controlled by different TFs in different pathways 
3
Construction of cancer pathways for personalized medicine 
| 
4 
Our solution: Pathway Activity signature SNEA (sub-network enrichment analysis) -> pathway analysis 
Hanahan & Weinberg. Hallmarks of cancer: the next generation. Cell. 2011;144(5):646-74
Construction of cancer pathways for personalized medicine 
| 
Common misconception 
5 
Differential Expression of its components 
Pathway activity 
Pathway activity 
Differential Expression of its expression targets
Construction of cancer pathways for personalized medicine 
| 
STEP1: SNEA calculating activity transcriptional activity of upstream regulators 
6 
Input: DE fold changes + prior knowledgebase of known expression regulation events 
Molecular networks in microarray analysis. 
Sivachenko A, Yuryev A, Daraselia N, Mazo I. J Bioinform Comp. Biol. 2007 
SNEA 
Reverse Causal Reasoning 
Mann-Whitney enrichment test 
Fisher’s overlap test
Construction of cancer pathways for personalized medicine 
| 
Pathway Studio Knowledgebase for SNEA powered by Elsevier NLP 
7 
> 
Internal Documents 
Subscribed Titles 
613 Elsevier journals 
23,641,270 Pubmed abstracts from >9,500 journals 
884 non-Elsevier 
journals 
Custom data can be imported into dedicated PS instance 
Public databases 
>3,500,000 full-text articles 
27,243 
477,365 
Expression: Protein->Protein 
Promoter Binding: Protein TF->Protein
Construction of cancer pathways for personalized medicine 
| 
Example of expression regulators and Cell processes identified by SNEA 
in lung cancer patient
Construction of cancer pathways for personalized medicine 
| 
9 
STEP2: Mapping expression regulators on pathways 
Hypoxia->EMT 
Hypoxia->Angiogenesis 
Blue highlight – expression regulators in 
Lung cancer patient identified by SNEA
Construction of cancer pathways for personalized medicine 
| 
•Gallbladder/Liver cancer 
•Lung cancer #1 
•Lung cancer #2 
•Breast cancer metastasis in lung 
•Colon cancer metastasis in liver 
10 
Personalized Hematology-Oncology of Wake Forest 
5 cancer patients 
analyzed with SNEA to build cancer pathways
Construction of cancer pathways for personalized medicine 
| 
Upper estimate: 10 hallmarks X 250 tissues = 2,500 
In practice some pathways may be common for all tissues. Example: Cell cycle pathways 
11 
How many cancer pathways must be built? 
Red highlight – Activated SNEA regulators
Construction of cancer pathways for personalized medicine 
| 
12 
Cancer pathways: Insights to cancer biology 
EGFR activation by apoptotic clearance (wound healing pathway) 
Red highlight – 
Activated SNEA regulators 
Apoptotic debris
Construction of cancer pathways for personalized medicine 
| 
13 
TGF-b autocrine loop sustains EMT
Construction of cancer pathways for personalized medicine 
| 
14 
Avoiding immune response: N1->N2 polarization 
Highlights – SNEA regulators from different patients
Construction of cancer pathways for personalized medicine 
| 
15 
How to select anti-cancer drugs in Pathway Studio
Construction of cancer pathways for personalized medicine 
| 
Conclusions: 
16 
•48 pathways containing 2,796 proteins provide mechanism for advanced cancer in 5 patients 
•Pathways explain about 50% (378) of all top 100 SNEA regulators indentified in five patients 
•Pathways are validated by: 
•Scientific literature 
•Patient microarray data 
•Efficacy of personalized therapy

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Construction of cancer pathways for personalized medicine

  • 1. Construction of cancer pathways for personalized medicine | Presented By Date Construction of cancer pathways for personalized medicine Predictive, Preventive and Personalized Medicine & Molecular Diagnostics Dr. Anton Yuryev Nov 4, 2014
  • 2. Construction of cancer pathways for personalized medicine | Curse of Dimensionality of OMICs data: We will never have enough patient samples to calculate robust signatures from large scale molecular profiling data 2 signature size # patients error rate Hua et al. Optimal number of features as a function of sample size for various classification rules. Bioinformatics. 2005 Fig.3 Optimal feature size versus sample size for Polynomial SVM classifier. nonlinear model, correlated feature, G=1, r= 0.25. s2 is set to let Bayers error be 0.05
  • 3. Construction of cancer pathways for personalized medicine | Mathematical requirements for short signature size vs. Biological reality Mathematical requirement Biological reality Signature size must be 20-30 genes Typical cancer transcriptomics profile has 500-2000 differentially expressed genes with p-value < 0.005 Increasing number of samples above 200 does not change optimal signature size Typical cancer dataset has not more than 100 patients. Increasing number of patients results in finding different cancer sub-types each having small number of samples Error rate and robustness of signatures from uncorrelated feature is better than from correlated features Most DE genes are correlated due to transcriptional linkage and different TFs regulated by only few biological pathways We can use prior knowledge about transcriptional regulation to select most uncorrelated features, e.g. genes controlled by different TFs in different pathways 3
  • 4. Construction of cancer pathways for personalized medicine | 4 Our solution: Pathway Activity signature SNEA (sub-network enrichment analysis) -> pathway analysis Hanahan & Weinberg. Hallmarks of cancer: the next generation. Cell. 2011;144(5):646-74
  • 5. Construction of cancer pathways for personalized medicine | Common misconception 5 Differential Expression of its components Pathway activity Pathway activity Differential Expression of its expression targets
  • 6. Construction of cancer pathways for personalized medicine | STEP1: SNEA calculating activity transcriptional activity of upstream regulators 6 Input: DE fold changes + prior knowledgebase of known expression regulation events Molecular networks in microarray analysis. Sivachenko A, Yuryev A, Daraselia N, Mazo I. J Bioinform Comp. Biol. 2007 SNEA Reverse Causal Reasoning Mann-Whitney enrichment test Fisher’s overlap test
  • 7. Construction of cancer pathways for personalized medicine | Pathway Studio Knowledgebase for SNEA powered by Elsevier NLP 7 > Internal Documents Subscribed Titles 613 Elsevier journals 23,641,270 Pubmed abstracts from >9,500 journals 884 non-Elsevier journals Custom data can be imported into dedicated PS instance Public databases >3,500,000 full-text articles 27,243 477,365 Expression: Protein->Protein Promoter Binding: Protein TF->Protein
  • 8. Construction of cancer pathways for personalized medicine | Example of expression regulators and Cell processes identified by SNEA in lung cancer patient
  • 9. Construction of cancer pathways for personalized medicine | 9 STEP2: Mapping expression regulators on pathways Hypoxia->EMT Hypoxia->Angiogenesis Blue highlight – expression regulators in Lung cancer patient identified by SNEA
  • 10. Construction of cancer pathways for personalized medicine | •Gallbladder/Liver cancer •Lung cancer #1 •Lung cancer #2 •Breast cancer metastasis in lung •Colon cancer metastasis in liver 10 Personalized Hematology-Oncology of Wake Forest 5 cancer patients analyzed with SNEA to build cancer pathways
  • 11. Construction of cancer pathways for personalized medicine | Upper estimate: 10 hallmarks X 250 tissues = 2,500 In practice some pathways may be common for all tissues. Example: Cell cycle pathways 11 How many cancer pathways must be built? Red highlight – Activated SNEA regulators
  • 12. Construction of cancer pathways for personalized medicine | 12 Cancer pathways: Insights to cancer biology EGFR activation by apoptotic clearance (wound healing pathway) Red highlight – Activated SNEA regulators Apoptotic debris
  • 13. Construction of cancer pathways for personalized medicine | 13 TGF-b autocrine loop sustains EMT
  • 14. Construction of cancer pathways for personalized medicine | 14 Avoiding immune response: N1->N2 polarization Highlights – SNEA regulators from different patients
  • 15. Construction of cancer pathways for personalized medicine | 15 How to select anti-cancer drugs in Pathway Studio
  • 16. Construction of cancer pathways for personalized medicine | Conclusions: 16 •48 pathways containing 2,796 proteins provide mechanism for advanced cancer in 5 patients •Pathways explain about 50% (378) of all top 100 SNEA regulators indentified in five patients •Pathways are validated by: •Scientific literature •Patient microarray data •Efficacy of personalized therapy