|Confirmation screening of compounds that potentiate TRAIL-induced apoptosis in TRAIL-resistant cancer cells, MCF7 - BioAssay Summary
Cytotoxic chemotherapy induces apoptosis via a pathway involving mitochondria, sometimes referred to as the "intrinsic pathway." An acquired resistance to anticancer drugs commonly results from the accumulation of defects in components of the mitochondrial pathway for apoptosis. Discovering and identifying alternative pathways for triggering tumor cells apoptosis offer hope for more effective more ..
BioActive Compound: 1
Depositor Specified Assays
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG)
Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, CA)
Network: NIH Molecular Libraries Production Centers Network (MLPCN)
Grant Number: X01 MH083230-01
Assay Provider: Dr. Dmitri Rozanov, Sanford-Burnham Medical Research Institute, San Diego CA
Cytotoxic chemotherapy induces apoptosis via a pathway involving mitochondria, sometimes referred to as the "intrinsic pathway." An acquired resistance to anticancer drugs commonly results from the accumulation of defects in components of the mitochondrial pathway for apoptosis. Discovering and identifying alternative pathways for triggering tumor cells apoptosis offer hope for more effective outcomes. Members of the Tumor Necrosis Factor (TNF) family of "death receptors" induce apoptosis via a direct mechanism that proceeds without involving mitochondria - referred to as the "extrinsic pathway." These cytokine receptors are frequently employed by immune cells to attack tumors. The PI believes that a successful strategy can be implemented by identifying specific chemicals that will selectively potentiate the therapeutic effects of the Tumor necrosis factor-Related Apoptosis-Inducing Ligand (TRAIL). Unlike other TNF-family members, TRAIL is a powerful and safe cancer therapeutic because it can induce broad spectrum apoptosis of different cancer cells but not normal cells. Unfortunately many cancer cells have proven to be resistant to TRAIL alone.
The goal of this project is confirm the results of the primary screen for chemical compounds that selectively sensitize TRAIL-resistant tumor cells to the extrinsic apoptosis pathway activated by TRAIL, without affecting other cell death pathways and normal cells. These compounds would provide useful research tools for interrogating mechanisms of TRAIL-resistance, and they also might serve as the basis for future drug development programs to create a new generation of non-toxic anticancer drugs that restore sensitivity to endogenous pathways used by the immune system for eradicating tumors.
This assay was developed and performed to confirm hits originally identified in "uHTS for the identification of compounds that potentiate TRAIL-induced apoptosis of cancer cells" (AID 1443) and to study the structure-activity relationship on analogs of the confirmed hits in TRAIL-resistant MCF7 cells. Compounds are either acquired from commercial sources or synthesized internally.
The TRAIL-resistant cell line, MCF7 is used, because we would like to determine if compounds can potentiate TRAIL-mediated cytotoxicity not only in TRAIL-sensitive PPC-1 carcinoma cells(AIDs 1443 and 1624) but also in TRAIL-resistant cells.
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1) MCF7 cells and TRAIL were provided by the assay provider
2) ATPLite (Perkin Elmer)
Cytotoxicity assay protocol:
1) TRAIL-resistant MCF7 cells are grown in DMEM, 10% FBS, 4.5 g/l glucose, 2mM L-glutamine, 1mM Na-pyruvate, 15ug/ml gentamycin (DMEM/10%FBS). Cells are harvested at 80-90% confluency.
2) Cells are then seeded into a 96 well plate (Corning #3595) at a concentration of 2-3 x 10^3 cells/well in 80ul and incubated for 24 hours at 37 oC in a CO2 incubator to obtain 30-40% of confluence.
1) Add 10 ul of compound or DMSO to wells to obtain 1.25-5 uM (final concentration which refers to 100 ul of solution per well).
2) Incubate cells 4 hours at 37 oC in a CO2 incubator.
3) Add 10 ul of TRAIL in PBS without Mg2+ and Ca2+ (total volume of solution per well is 100 ul) or 1% NaN3 (100% cytotoxicity). The measured value of 100% cytotoxicity is the background for measurement and is subtracted from all values.
4) Incubate cells for an additional 24 hours at 37 oC in a CO2 incubator.
1) Add 12 ul of ATPlite reagent to each well and shake plate for 30 min at room temperature.
2) Read luminescence using a SpectraFluor Plus (Tecan) (integration time= maximum, gain=150).
Compounds in this assay were considered to be active if the cytotoxicity of TRAIL in the presence of the compound is greater than the sum of the cytotoxicity of the compound and the cytotoxicity of TRAIL separately at all three concentrations of compound(1.25, 2.5 and 5.0 uM).
Activity scoring rules were devised to take into consideration compound efficacy, its potential interference with the assay and the screening stage that the data was obtained. Details of the Scoring System will be published elsewhere. Briefly, the outline of the scoring system utilized for the PMI assay is as follows:
1) First tier (0-40 range) is reserved for primary screening data and is not relevant in this assay.
2)Second tier (41-80 range) is reserved for dose-response confirmation data and is not applicable to this assay
3) Third tier (81-100 range) is reserved for resynthesized true positives and their analogues
Compounds that are inactive in this assay are assigned a score of 81
Compounds that are active in this assay are assigned a score of 90
** Test Concentration.
Data Table (Concise)