To address the complexity of heterogeneous cancers that are resistant to chemotherapy and frequently recur or metastasize, we propose to develop a set of tools based on multidisciplinary innovations combining Synthetic Biology, Cancer Organoid Technology, and Bioinformatics. These Synthetic Tools to Annotate Reporter Organoids for Cancer Heterogeneity and Recurrence Development (StarOrchard) include: Synthetic Promoter Activated Recombination of Kaleidoscopic Organoids (SPARKO), Combinatorial Genetics En Masse (CombiGEM), and single-cell RNA sequencing panorama (Scanorama). SPARKO can annotate heterogeneous cancer populations in living cells via fluorescent protein expression libraries to make multi- colored tumor organoids. CombiGEM can rapidly identify potential therapeutic targets via large-scale, massively parallel, and unbiased combinatorial genetic screens. Scanorama can integrate the analysis of large datasets of single-cell transcriptomics via sophisticated bioinformatics algorithms. These tools focus on barcoding strategies to enable accurate tracking and analysis of individual tumor cells that harbor distinct genetic aberrations, and substantially expand the utility of the Next Generation Cancer Models (NGCMs) for cancer mechanistic investigations or therapeutic discovery. The StarOrchard tools enable targeted genetic perturbations in annotated heterogeneous tumor phenotypes without destroying cells for sequencing. These tools will be applied to a large number and variety of NGCMs to optimize experimental protocol. To ensure success, we have convened an outstanding team: PI Timothy K. Lu, MD, PhD, has made strikingly original contributions to Synthetic Biology tools that enable high-throughput genetic interrogation of cancer cell drug dependency; PI mer Yilmaz, MD, PhD, has extensive expertise in cancers of the gastrointestinal tract and has developed novel technologies to maintain patient-derived colon cancer organoids for in vivo modeling; and PI Bonnie Berger, PhD, will use her expertise in bioinformatics and her Scanorama algorithm to integrate data across all tumor types based on dynamic single cell RNA sequencing (scRNAseq). We are also supported by leading experts in cancer biology and various cancer types at both the basic science and clinical oncology frontiers of cancer research. The collective commitment and multidisciplinary contributions of the entire team ensure the establishment of an openly distributed investigative tool set that accelerates advancements in cancer biology and therapeutic discovery

Public Health Relevance

We propose to develop a collection of Synthetic Tools to Annotate Reporter Organoids for Cancer Heterogeneity and Recurrence Development (StarOrchard) to enable wide adoption of the Next Generation Cancer Models in the cancer research community. These tools, SPARKO, CombiGEM, and Scanorama, are the result of multidisciplinary innovations combining synthetic biology, cancer organoid technologies, and bioinformatics.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project--Cooperative Agreements (U01)
Project #
1U01CA250554-01
Application #
10004966
Study Section
Special Emphasis Panel (ZCA1)
Program Officer
Gerhard, Daniela
Project Start
2020-07-08
Project End
2023-06-30
Budget Start
2020-07-08
Budget End
2021-06-30
Support Year
1
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Miscellaneous
Type
Organized Research Units
DUNS #
001425594
City
Cambridge
State
MA
Country
United States
Zip Code
02142