|uHTS for the identification of compounds that potentiate TRAIL-induced apoptosis of cancer cells - 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 Compounds: 883
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 to screen for chemical compounds that selectively sensitize 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.
Bodmer JL, Meier P, Tschopp J, Schneider P. Cysteine 230 is essential for the structure and activity of the cytotoxic ligand TRAIL. J Biol Chem 2000, 275:20632-7.
Lawrence D, Shahrokh Z, Marsters S, Achilles K, Shih D, Mounho B, Hillan K, Totpal K, DeForge L, Schow P, Hooley J, Sherwood S, Pai R, Leung S, Khan L, Gliniak B, Bussiere J, Smith CA, Strom SS, Kelley S, Fox JA, Thomas D, Ashkenazi A. Differential hepatocyte toxicity of recombinant Apo2L/TRAIL versions. Nat Med 2001, 7:383-5.
Singh TR, Shankar S, Chen X, Asim M, Srivastava RK. Synergistic interactions of chemotherapeutic drugs and tumor necrosis factor-related apoptosis-inducing ligand/Apo-2 ligand on apoptosis and on regression of breast carcinoma in vivo. Cancer Res 2003, 63:5390-400
Greil R, Anether G, Johrer K, Tinhofer I. Tracking death dealing by Fas and TRAIL in lymphatic neoplastic disorders: pathways, targets, and therapeutic tools. J Leukoc Biol 2003, 74:311-30.
Smyth MJ, Takeda K, Hayakawa Y, Peschon JJ, van den Brink MR, Yagita H. Nature's TRAIL-on a path to cancer immunotherapy. Immunity 2003, 18:1-6.
1) PPC-1 cells and TRAIL were provided by the assay provider
2) ATPLite (Perkin Elmer)
1) PPC-1 cells are grown in DMEM without phenol red, 10% FBS, 2mM L-glutamine, 1mM Na-pyruvate, 15ug/ml gentamycin and are harvested at 100% confluency.
2) Using a Biomek FX cells are seeded into a 1536 well plate (Corning #3727) at a concentration of 250 cells/well in 5ul. Cells are seeded in columns 3 through 48. Media is added to wells in columns 1 and 2 (Positive control).
3) Plates are spun in an Eppendorf model 5810 centrifuge @ 500 RPM for 5min.
4) Plates are placed in stacks of 6 (with a dummy plate filed on the top and bottom of each stack) and wrapped in Saran Wrap. This helps to eliminate any edge effects.
5) Incubate overnight in 37 oC 5% CO2 incubator
1) Unwrap plates
2) Add 10nl of 2mM compound to wells (columns 5-48).
3) Add 10nl of 100% DMSO to wells in columns 1 through 4.
4) Add 10nl of 1ug/ml Trail in PBS w/ Mg2+ and Ca2+
5) Plates are spun in an Eppendorf model 5810 centrifuge @ 500 RPM for 5min
6) Plates are placed in stacks of 6 (with a dummy plate filed on the top and bottom of each stack) and re-wrapped in Saran Wrap.
7) Incubate overnight in 37 oC 5% CO2 incubator
1) Unwrap plates
2) Add 3ul of ATPlite to each well
3) Spin plate in a Velocity11 Vspin
4) Shake plate
5) After 20 min read luminescence using a Perkin Elmer Viewlux (read time= 10sec, filter=clear, gain=high, binning=2x)
Compounds with greater than 50% activity at the primary screening concentration of 4 uM were reordered from the MLSMR and retested at a 5uM final concentration in duplicate. Compounds that reconfirmed with an average of 50% activity are defined as actives in this assay.
To simplify the distinction between the inactives of the primary screen and of the confirmatory screening stage, the Tiered Activity Scoring System was developed and implemented. Its utilization for the assay is described below.
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 assay is as follows:
1) First tier (0-40 range) is reserved for primary screening data. The score is correlated with % activity in the assay demonstrated by a compound at 4 uM concentration:
a. If primary % inhibition is less than 0%, then the assigned score is 0
b. If primary % inhibition is greater than 100%, then the assigned score is 40
c. If primary % inhibition is between 0% and 100%, then the calculated score is (% Inhibition)*0.4
Active compounds will have activity scores between 20 and 40. While inactive compounds will have activity scores between 0 and 20.
2) Second tier (41-80 range) is reserved for liquid resupply single concentration confirmation and or dose-response confirmation data
3) Third tier (81-100 range) is reserved for resynthesized true positives and their analogues
** Test Concentration.
Data Table (Concise)