High-throughput drug and genetic assays for cellular transformation
A method for detecting oncogenic growth and viability, and/or degree of cellular transformation and/or identifying an agent that inhibits cellular transformation is disclosed. The method including: providing a cellular sample, such as a sample of cells obtained from a subject or a cell line; culturing the cellular sample in low attachment conditions; and detecting growth and7or cell viability of the sample, wherein increased growth relative and/or viability relative to a control or control level indicative of basal growth and/or viability indicates cellular transformation. In some embodiments, the method includes introducing a n expression vector into cells of the cellular sample, wherein the expression vector comprises a gene product expression sequence being tested for transformation ability. In some embodiments the cellular sample is contacted with a test agent and growth and/or cell viability of the sample is determined to determine if the agent inhibits transformation.
1. A method for identifying an agent that inhibits cellular growth and/or viability of tumorigenic or transformed cells in combination with a genetic perturbation, the method comprising:
providing a cellular sample of transformed cells and/or cells obtained from the tumor of a subject, wherein the transformed cells and/or cells obtained from the tumor are adherent cells;
infecting the cells with a barcoded library of lentiviruses encoding one or more CRISPR genetic perturbations, wherein the barcode identifies the one or more CRISPR genetic perturbations;
culturing the cellular sample for at least 5 days under low attachment conditions comprising agitating the cells, wherein the conditions inhibit cell attachment to the culture surface;
contacting or incubating the cellular sample with the agent; and
identifying the one or more genetic perturbations that are depleted in the sample contacted with the agent as compared to a control not contacted with the agent, whereby the agent inhibits cellular growth and/or viability of tumorigenic or transformed cells in combination with the one or more depleted genetic perturbations.
2. The method of claim 1 , wherein the tumor is a solid tumor.
3. The method of claim 1 , wherein the agent is a chemical compound, a small molecule, or an antibody.
4. The method of claim 1 , wherein the cells are aliquoted into one or more containers,
wherein the containers are the wells of a microtiter plate, or
wherein the containers comprise one or more mixing circuits of a microfluidic device.
5. The method of claim 4 , wherein the mixing circuit comprises a pneumatically actuated pump for circulating cells in the mixing circuit; and/or
wherein the mixing circuit comprises one or more valves configured to act in concert to circulate the cells around the mixing circuit,
thereby inhibiting attachment of the cells to internal surfaces of the microfluidic device.
6. The method of claim 4 , wherein the individual wells of the microtiter plate or individual mixing circuits of the microfluidic device are treated with different test agents, and/or concentrations of test agents.
7. The method of claim 4 , wherein the microfluidic device comprises an input port in fluid connection with the mixing circuit;
a holding chamber in fluid communication with the mixing circuit;
an output port; and/or
one or more additional valves.
8. The method of claim 7 , wherein at least one of the one or more valves is a sieve valve; and/or
wherein at least one or more of the valves is a conventional valve; and/or
wherein a valve is positioned between the input port and the mixing circuit; and/or
wherein one or more valves is positioned between the mixing circuit and the holding chamber; and/or
wherein one or more valves is positioned between the mixing circuit, the holding chamber and the output port; and/or
wherein one or more valves are positioned between the two or more mixing circuits.
9. The method of claim 4 , further comprising splitting the cellular sample between two or more microfluidic mixing circuits of the microfluidic device, wherein a different test agent is loaded into each microfluidic mixing circuit, before, after, or concurrent with the cellular sample.
10. The method of claim 1 , wherein culturing under low attachment conditions comprises culturing the cells on a surface treated with at least one compound that inhibits cell attachment.
11. The method of claim 1 , wherein culturing under low attachment conditions comprises culturing the cells on an ultra-low attachment surface.
12. The method of claim 1 , wherein the genetic perturbation is a gene knock-in, a gene knock-out, one or more nucleotide insertions, deletions, substitutions, or mutations, or a combination thereof.