Projects per year
Project Details
Description (abstract)
Chemotherapy is one of the primary treatments for cancer, yet the efficacy is often limited by drug resistance. Emerging evidence suggests that non-genetic transient states in cancer cells contribute to drug resistance. This project aims to develop computational tools to understand the transient cellular states in chemoresistance and rationalize drug combination strategies for personalized medicine.
To achieve this goal, we are developing a single-cell based lineage tracing method (ResisTrace) to capture the primed resistant cells (i.e. pre-resistant cells) in treatment-naïve samples. I will build a probabilistic model to facilitate the experiment design and a data analysis pipeline to characterize the gene expression profiles for pre-resistant cells. We have performed successful pilot studies on an ovarian cancer cell line and identified the cells that are resistant to olaparib, carboplatin, or natural killer cells. Potential transcriptomics biomarkers for pre-resistant cells have been identified for further validation.
Furthermore, I will develop machine learning and network modelling approaches to predict synergistic drug combinations to treat multiple cell lineages effectively. To facilitate the model development, I have updated the DrugComb database by integrating publicly available drug screening and molecular profiling data for cancer cells. Furthermore, I have developed SynergyFinderPlus, a computational tool for drug combination data analysis. These tools shall help the rationalization of drug combinations from drug screening and ResisTrace data.
The computational tools will be tested initially on cancer cell lines and then applied on patient-derived samples from high-grade serous ovarian cancer (HGSOC) and pancreatic ductal adenocarcinoma (PDAC). In the end, all the tools will be integrated and published as web applications to facilitate the development of new combinatorial therapies for cancer patients who have become resistant to standard treatments.
To achieve this goal, we are developing a single-cell based lineage tracing method (ResisTrace) to capture the primed resistant cells (i.e. pre-resistant cells) in treatment-naïve samples. I will build a probabilistic model to facilitate the experiment design and a data analysis pipeline to characterize the gene expression profiles for pre-resistant cells. We have performed successful pilot studies on an ovarian cancer cell line and identified the cells that are resistant to olaparib, carboplatin, or natural killer cells. Potential transcriptomics biomarkers for pre-resistant cells have been identified for further validation.
Furthermore, I will develop machine learning and network modelling approaches to predict synergistic drug combinations to treat multiple cell lineages effectively. To facilitate the model development, I have updated the DrugComb database by integrating publicly available drug screening and molecular profiling data for cancer cells. Furthermore, I have developed SynergyFinderPlus, a computational tool for drug combination data analysis. These tools shall help the rationalization of drug combinations from drug screening and ResisTrace data.
The computational tools will be tested initially on cancer cell lines and then applied on patient-derived samples from high-grade serous ovarian cancer (HGSOC) and pancreatic ductal adenocarcinoma (PDAC). In the end, all the tools will be integrated and published as web applications to facilitate the development of new combinatorial therapies for cancer patients who have become resistant to standard treatments.
Status | Finished |
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Effective start/end date | 01/05/2020 → 31/12/2024 |
Fields of Science
- 3122 Cancers
- drug resistance
- drug combination
- 3111 Biomedicine
- bioinformatics
Projects
- 1 Finished
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DrugComb: ERC Starting Grant: Informatics approaches for the rational selection of personalized cancer drug combinations
Tang, J. (Project manager)
01/06/2017 → 31/05/2022
Project: Research project
Research output
- 2 Article
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Anticancer drug synergy prediction in understudied tissues using transfer learning
Kim, Y., Zheng, S., Tang, J., Jim Zheng, W., Li, Z. & Jiang, X., 15 Jan 2021, In: Journal of the American Medical Informatics Association. 28, 1, p. 42-51 10 p.Research output: Contribution to journal › Article › Scientific › peer-review
Open AccessFile -
DrugComb update: a more comprehensive drug sensitivity data repository and analysis portal
Zheng, S., Aldahdooh, J., Shadbahr, T., Wang, Y., Aldahdooh, D., Bao, J., Wang, W. & Tang, J., 2 Jul 2021, In: Nucleic Acids Research. 49, W1, p. W174-W184 11 p.Research output: Contribution to journal › Article › Scientific › peer-review
Open AccessFile
Datasets
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DrugComb
Tang, J. (Creator), University of Helsinki, 2019
DOI: 10.1093/nar/gkz337, http://drugcomb.org
Dataset