Abstract
The principle of drug sensitivity testing is to expose cancer cells to a library of different drugs and measure its effects on cell viability. Recent technological advances, continuous approval of targeted therapies, and improved cell culture protocols have enhanced the precision and clinical relevance of such screens. Indeed, drug sensitivity testing has proven diagnostically valuable for patients with advanced hematologic cancers. However, different cell types behave differently in culture and therefore require optimized drug screening protocols to ensure that their ex vivo drug sensitivity accurately reflects in vivo drug responses. For example, primary chronic lymphocytic leukemia (CLL) and multiple myeloma (MM) cells require unique microenvironmental stimuli to survive in culture, while this is less the case for acute myeloid leukemia (AML) cells. Here, we present our optimized and validated protocols for culturing and drug screening of primary cells from AML, CLL, and MM patients, and a generic protocol for cell line models. We also discuss drug library designs, reproducibility, and quality controls. We envision that these protocols may serve as community guidelines for the use and interpretation of assays to monitor drug sensitivity in hematologic cancers and thus contribute to standardization. The read-outs may provide insight into tumor biology, identify or confirm treatment resistance and sensitivity in real time, and ultimately guide clinical decision-making.
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Introduction
Drug screens can identify sensitivity and resistance to anticancer drugs. The method was first introduced as the “human tumor stem-cell assay” more than four decades ago [1, 2], but was criticized as too premature for clinical implementation [3]. Since then, technological advances, development and approval of additional targeted therapies, and optimization of cell culture protocols have led to improvement, increased relevance, and validation of the method as a diagnostic tool [4,5,6,7,8,9,10,11]. In addition, the method has been used to increase our understanding of tumor biology and to stratify hematologic cancers [12,13,14].
Precision medicine has, in several contexts, become synonymous with genomic precision medicine. However, functional precision medicine, which guides treatment decisions based on functional tests such as drug sensitivity screens, has gained increased attention and acceptance in recent years [15]. This is showcased by a steadily increasing number of scientific publications in reputable journals, reviewed in [15,16,17]. A PubMed search for “functional precision medicine” retrieved 19 results in 2022, versus 5 results in 2020. To further encourage and promote research and development of functional precision medicine, the Society for Functional Precision Medicine (https://www.sfpm.io/) has been established. Their mission is to improve patient care and outcomes by facilitating the clinical implementation of functional precision medicine. Furthermore, the European Hematology Association (EHA) recently decided that the existing Specialized Working Group (SWG) “Precision Medicine” would incorporate functional precision hematology to become the new SWG “Precision Hematology”.
While neither genomic nor functional precision medicine alone has the power to identify effective treatments for all patients [16], it is likely that the integration of genomic and functional approaches can identify actionable and available drugs for a larger number of patients. It is therefore critical that the diagnostic tools are continuously assessed and validated for each application to ensure the best possible predictions and patient care. A key requirement is reproducibility between testing locations, and several clinical studies are under way to develop harmonized protocols, such as the LD-VenEx clinical trial (ClinicalTrials.gov Identifier NCT05431257), EXALT-2 (NCT04470947), and IMPRESS-Norway (NCT04817956) (Table 1). An important part of this process is the establishment of a set of community guidelines for performing drug screens.
Here, we present our optimized and validated protocols for drug screening of primary cells from AML, CLL, and MM patients, and of cell line models. These protocols may serve as guidelines for the use, interpretation, and further development of assays to monitor drug sensitivity in hematologic cancers.
Drug sensitivity screening protocols
Protocols to screen for drug sensitivity have been developed for both cell line models of hematologic cancers and primary cells derived from patients. We describe protocols that have been optimized in our laboratories for drug sensitivity assessment of models that represent each class of hematologic cancer—leukemia, lymphoma and myeloma (Fig. 1a). In these protocols, the cells are exposed to drugs for 72 h. Drug exposure times may be optimized further by the user for different cell types and drug classes as sensitivity and kinetics may vary. Furthermore, primary cells are sensitive to environmental changes, and it is therefore important to control for spontaneous cell death over time to exclude non-drug induced effects on cell viability. Positive (for example, 100 µM benzethonium chloride) and negative (the drug solvent, i.e., 0.1% DMSO) controls should be included on each drug plate, which allows for measurement of the Z-prime (see the “Reproducibility and quality controls of drug screens” section) [18]. Experiments that fail this quality control should be discarded. In general, we observe that the viability of fresh primary AML cells remains around 70–80% after 48–72 h of culture, while the viability of biobanked samples may be lower ([19] and our unpublished observations). To prevent spontaneous apoptosis of primary CLL cells, they are transiently cultured with feeder cells prior to the drug exposure [8]. Primary MM cells from bulk bone marrow (BM) samples are activated with autologous BM T helper cells in the presence of IL-2 and a T-cell expansion cocktail (anti-CD3/CD28 beads) prior to drug screening [20]. Stimulation with IL-6 has also been shown to support MM survival and proliferation [21, 22]. The stimulation approaches for both CLL and MM sustain cell viability beyond the experimental window of 72 h [8, 20].
While AML and CLL patient samples are dominated by tumor cells, this is less the case for MM BM samples. The protocol for MM therefore includes a cell isolation step to avoid contamination of the result, and the pre-stimulation induces cell proliferation which allows to reach enough viable CD138+ MM cells to perform a drug screen [20, 23].
The common principles of drug sensitivity assays on hematologic cancers are illustrated in Fig. 1b.
Cell lines
Any cell line, adherent or in suspension, can be analyzed with the protocol described below. Whether the assay can be performed on cells that have been in culture, or if the cells can be screened directly after thawing, needs to be determined prior to the start of the experiment. The latter may reduce variability between replicates [24, 25], but can be associated with substantial cell death resulting from the freeze-thaw cycle. Prior to the experiment it is recommended to carefully characterize the cells, establishing the optimal culturing medium, the doubling time of the cells, and the appropriate cell seeding density per well of the drug plate. This can be done by studying the cells’ growth curve over time, for example by using a live-cell imaging platform such as the Incucyte® S3 (Sartorius AG, Göttingen, Germany) which can monitor live cells in real time (Box 1). Select the cell confluency that results in optimal growth of the cells to avoid growth inhibition at the experimental end point (Box 1). The cell number needs to be optimized for the plate format to be used in the assay (i.e. 96-well, 384-well, or 1536-well plate; Box 1). Below, we describe assays performed in a 384-well plate format. Plate color (transparent, black, or white) needs to be adapted to the assay type (Box 2, 1a). Experiments should be carried out under sterile and clean conditions when indicated (see below and Box 2, 1b, c).
Preparation of cells (Day 1)
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1.
If the cells are adherent, bring them into suspension (i.e. by trypsinization). Collect the cells in a 50 mL tube and spin at 300 g for 5 min at room temperature (RT)
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2.
Discard the supernatant and resuspend the cells in fresh, pre-warmed medium.
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3.
Filter the cell suspension using a 40 µm cell strainer to assure a single-cell suspension (Box 2, 2a).
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4.
Count the cells using the preferred method, such as a hematocytometer or an automated cell counter.
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5.
Resuspend the cells in cell medium to the dilution determined based on the growth curve of the cell line (Box 1, Panel a).
Drug sensitivity and resistance testing (DSRT) (Day 1)
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1.
Transfer the cell suspension to preprinted drug plates at the appropriate volume (25 µl/well for 384-well plates) using a liquid dispenser such as the CERTUS Flex (Gwatt, Switzerland) (Fig. 1b, third panel). It is recommended to sonicate the valves of the dispenser before each use (Box 2, 1c).
-
2.
OPTIONAL: Cover the plates with membranes that allow CO2 and O2 flow, but limit H2O evaporation (Box 2, 2b).
-
3.
Leave the plates in an incubator at 5% CO2, 37 °C for the preferred length of time, e.g. 72 h (Box 2, 2c).
Measurement of cell viability with CellTiter-Glo (Day 4)
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1.
Equilibrate the CellTiter-Glo and the assay plates at RT for 15–30 min (Box 2, 2c). If the plates were covered with membranes (Box 2, 2b), these can be removed.
-
2.
Add 25 μL pre-filtered CellTiter-Glo (Table 2) to each well in the 384-well plates (see Box 3 for experimental details and an alternative method).
-
3.
Read the luminescence with a luminometer (Fig. 1b, fourth panel).
Primary AML cells
AML cells can be isolated from BM or peripheral blood (PB) and analyzed fresh or after storage in liquid nitrogen [26, 27]. A change in cell composition of the sample after cryopreservation has been reported, with a reduction of CD117+ cells, granulocytes, and CD45- cells (erythropoietic cells) [27]. Overall, drug responses are highly correlated between fresh and frozen samples, with some exceptions [26, 27]. It is important to note that significant changes in the cell composition after thawing, such as a large reduction of granulocytic cells, can impact the drug sensitivity measurement when assessing bulk sample sensitivity. It is therefore recommended to specify the state of the samples when reporting the results. Cell culturing conditions may also impact drug screening results. See Box 4 for considerations to be made regarding culturing media.
The below protocol for drug sensitivity screening of BM or PB mononuclear cells (MCs) from AML patient samples was adapted from a previous report [9].
Isolation of mononuclear cells (MCs) from AML patient samples
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1.
Dilute the blood 1:1 with phosphate-buffered saline (PBS).
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2.
Prepare a density gradient medium according to the manufacturer’s instructions. As an example, if using Lymphoprep (Table 2), prepare a set of 15 mL tubes adding 3 mL of RT Lymphoprep to each tube.
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3.
Carefully add up to 5 mL of diluted PB or BM on top of the density gradient.
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4.
Centrifuge the tubes at 500 g for 20 min without breaks. The MCs will now be visible as a white layer on top of the density gradient medium (Fig. 1b, left panel).
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5.
Use a Pasteur pipette to transfer the MCs into a new 50 mL tube. Wash the cells twice with PBS.
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6.
Centrifuge the cells at 500 g for 5 min with the breaks on.
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7.
NOTE: In certain AML samples, the presence of erythroid cell contamination may be observed following density gradient centrifugation. Therefore, red blood cell (RBC) lysis is recommended.
Discard the supernatant and resuspend the pellet in 2 mL 1 x RBC lysis buffer (Table 2) for 5 min at RT.
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8.
Stop the reaction by diluting the cell solution with 25 mL PBS.
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9.
Filter the cells with a 40 µm cell strainer (Box 2, 2a).
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10.
Count the cells using the preferred method.
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11.
Centrifuge at 300 g for 15 min.
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12.
Discard the supernatant and proceed to “Cryopreservation of MCs from AML patient samples” or “DSRT of AML patient samples (Day 1)”.
Cryopreservation of MCs from AML patient samples
Resuspend the cells in fetal bovine serum (FBS) supplemented with 10% DMSO, aliquot, and store in liquid nitrogen (Box 2, 4a)
DSRT of AML patient samples (Day 1)
MCs in AML drug screens are used at a standard count of 10,000 cells/well in a final volume of 25 μL for 384-well plates. The final volume of the cell suspension should be adapted to the total number of drug plates in the experiment. If the number of available cells is limited, the counts may be adapted. Preferably, the counts should be above 1000 cells/well, although reproducible results have been observed with as little as 300 cells/well (our unpublished observation).
Fresh cells
Resuspend the cells in mononuclear cell medium (MCM) to a final concentration of 4.0 × 105 cells/mL. This will allow for 10,000 cells/well in a 25 μL/well volume.
Cryopreserved cells
Cryopreserved AML cells may show up to 40–50% viability loss due to the procedure. Calculate the final number of cells needed for the experiment and thaw twice the amount if available (Box 2, 4b). Place the cells in fresh MCM and recover overnight in an incubator at 5% CO2, 37 °C. Resuspend the cells in MCM to a final concentration of 4.0 × 105 cells/mL. This will allow for 10,000 cells/well in a 25 μL/well volume.
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1.
Transfer the cell suspension to preprinted drug plates at the appropriate volume using a liquid dispenser such as the CERTUS Flex (Fig. 1b, third panel). It is recommended to sonicate the valves of the dispenser before each use (Box 2, 1c).
-
2.
OPTIONAL: Cover the plates with membranes that allow CO2 and O2 flow, but limit H2O evaporation (Box 2, 2b).
-
3.
Leave the plates in an incubator at 5% CO2, 37 °C for the preferred length of time, e.g., 72 h (Box 2, 2c).
Measurement of cell viability with CellTiter-Glo (Day 4)
-
1.
Equilibrate the CellTiter-Glo and the assay plates at RT for 15–30 min (Box 2, 2c). If the plates were covered with membranes (Box 2, 2b), these should be removed.
-
2.
Add 25 μL pre-filtered CellTiter-Glo (Table 2) to each well in the 384-well plates (see Box 3 for experimental details and an alternative method).
-
3.
Read the luminescence with a luminometer (Fig. 1b, fourth panel).
Primary CLL cells
CLL cells can be isolated from PB and analyzed fresh or after storage in liquid nitrogen. Cryopreservation of primary B cells from healthy blood donors and CLL patients has been shown to not affect cell signaling [28], supporting the use of biobanked samples for functional assays. This makes it possible to analyze historical samples, to perform several assays over time on samples collected from the same patient, and to store samples for later use.
The below protocols for isolation, cryopreservation, and drug sensitivity screening of peripheral blood mononuclear cells (PBMCs) from CLL patient samples were adapted from previous reports [8, 29, 30].
Isolation and cryopreservation of PBMCs from CLL patient samples
NOTE: Blood samples procured from CLL patients should be processed the same day.
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1.
Dilute the blood 1:1 with PBS and transfer the solution to 50 mL tubes (not more than 30 mL/tube).
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2.
Carefully layer 10 mL of a density gradient medium (e.g., Lymphoprep, Table 2) to the bottom of the tube using a 10 mL pipette.
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3.
Centrifuge the tube at 800 g for 20 min with the brakes off. The PBMCs will now be visible as a white layer on top of the density gradient medium (Fig. 1b, left panel).
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4.
Use a Pasteur pipette to transfer the PBMCs into two new 50 mL tubes. Wash the cells twice with PBS.
-
5.
Centrifuge the cells at 300 g for 15 min.
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6.
NOTE: Steps 6–8 are optional.
Discard the supernatant and resuspend the pellet in 5 mL 1 x RBC lysis buffer (Table 2). Leave the cell solution for 10 min at RT
-
7.
Stop the reaction by diluting the cells with 25 mL PBS.
-
8.
Count the cells using the preferred method.
-
9.
Centrifuge at 300 g for 15 min.
-
10.
Discard the supernatant and resuspend the cells in FBS supplemented with 10% DMSO, aliquot, and store in liquid nitrogen.
CLL cells undergo rapid, spontaneous apoptosis outside of their natural microenvironment. To ensure that the monitored cell death in drug sensitivity screens is induced by drug treatment only, it is necessary to prevent the spontaneous apoptosis. This can be done by mimicking the tumor microenvironment by including microenvironmental stimuli in the growth conditions of the CLL cells. Below is a protocol that uses transient stimulation of the CLL cells by co-culturing them with fibroblasts that express APRIL, BAFF, and CD40L. The CLL cells are separated from the fibroblasts before the drug sensitivity screening so that the cell viability measurements only come from the CLL cells. This protocol has been used to predict treatment vulnerabilities in CLL, and to guide precision medicine for patients with relapsed disease [6, 8, 11]. The development of the co-culture protocol was previously reported [8].
Co-culture of CLL cells with APRIL/BAFF/CD40L+ fibroblasts (Day 1)
NOTE: Three 3T3 fibroblast cell lines stably expressing GFP-APRIL, GFP-BAFF, or GFP-APRIL + CD40L (CD40LA) are used in this protocol. The cell lines are cultured in separate cell culture flasks with RPMI 1640 medium (Table 2) supplemented with 1× sodium pyruvate, 1× MEM non-essential amino acids, penicillin/streptomycin, and 10% FBS (complete medium; Fig. 1b, second panel).
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1.
Detach the fibroblast cell lines from their culturing flasks by trypsinization. Transfer each cell line to a separate 15 mL tube.
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2.
Centrifuge the fibroblasts at 300 g for 5 min. Discard the supernatant.
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3.
Resuspend the fibroblasts in 5 mL complete medium. Keep the cells on ice to prevent them from re-attaching to the plastic.
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4.
Irradiate the APRIL+ and BAFF+ fibroblast cell lines at 125 Gy, and the CD40LA cell line at 50 Gy.
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5.
Seed the irradiated APRIL/BAFF/CD40L+ fibroblasts (1:1:1) in a tissue culture flask to allow a final ratio of 1:10 fibroblasts:CLL cells. Leave the flask in an incubator at 5% CO2, 37 °C to let the cells attach to the plastic.
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6.
Quickly thaw a frozen aliquot of CLL cells in a 37 °C water bath.
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7.
Wash the cells once with 10 mL complete medium.
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8.
Centrifuge at 300 g for 5 min. Discard the supernatant.
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9.
Resuspend the CLL cells in complete medium and transfer them to the culture flask containing APRIL/BAFF/CD40L+ fibroblasts.
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10.
Leave the co-culture in an incubator at 5% CO2, 37 °C for 24 h.
Drug sensitivity screens can be performed in different formats. Here, we describe a protocol for drug sensitivity screening in a 384-well plate format.
Drug sensitivity testing in a 384-well plate format (Day 2)
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1.
Separate the soluble CLL cells from the adherent fibroblast layer by transferring the cell culture medium to a 50 mL tube. Carefully rinse the flask with a 10 mL pipette to collect most of the CLL cells while leaving the fibroblasts undisturbed.
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2.
Filter the cell suspension using a 40 µm cell strainer to assure a single-cell suspension (Box 2, 2a).
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3.
Count the cells using the preferred method.
-
4.
Centrifuge the cells at 300 g for 5 min. Discard the supernatant.
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5.
Resuspend the cells in complete medium to a final concentration of 2.0 × 105–4.0 × 105 cells/mL. This will allow for 5000–10,000 cells/well in a volume of 25 μL/well.
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6.
Transfer the cell suspension to preprinted 384-well drug plates at 25 μL/well using a liquid dispenser such as the CERTUS Flex (Fig. 1b, third panel). It is recommended to sonicate the valves of the dispenser before each use (Box 2, 1c).
-
7.
Leave the plates in an incubator at 5% CO2, 37 °C for 72 h.
Measurement of cell viability with CellTiter-Glo (Day 5)
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1.
Add 25 μL pre-filtered CellTiter-Glo (Table 2) to each well in the 384-well plates (see Box 3 for experimental details and an alternative method).
-
2.
Read the luminescence with a luminometer (Fig. 1b, fourth panel).
Primary MM cells
MM cells cannot be biobanked but need to be processed fresh. The below protocol for isolation, culturing and drug sensitivity screening of MM cells was previously reported [23].
Isolation of bone marrow mononuclear cells (BMMCs) from MM patient BM samples (Day 1)
NOTE: Sections “Introduction”, “Drug sensitivity screening protocols”, “Drug library design” and “Reproducibility and quality controls of drug screens” should be performed under sterile conditions in a tissue culture hood. BM samples procured from MM patients should be processed the same day.
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1.
Pipette the BM gently up and down with a 10 mL pipette to remove clumps and filter the sample through a sterile 70 μm nylon filter into a 50 mL tube. Wash the filter once with 5 mL PBS.
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2.
Dilute the BM 1:1 with PBS.
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3.
Split the cell suspension equally into two 50 mL tubes.
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4.
Carefully layer 10 mL density gradient medium (Lymphoprep; Table 2) to the bottom of the tubes using a 10 mL pipette.
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5.
Centrifuge for 25 min at 800 g at room temperature, without breaks. The BMMCs are now visible on top of the density gradient medium layer (Fig. 1b, left panel).
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6.
Transfer the cells into two new 50 mL tubes using a Pasteur pipette.
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7.
Wash the cells with PBS by filling up the tube to 40–45 mL.
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8.
Centrifuge at 300 g for 15 min.
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9.
Discard the supernatant and wash the cells with PBS by filling up the tube to 40–45 mL.
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10.
Centrifuge at 300 g for 10 min.
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11.
Discard the supernatant and resuspend the cell pellet in PBS.
Removal of CD8+ T cells (Day 1)
After BMMC isolation, CD8+ cells are removed by addition of CD8 magnetic beads coated with anti-CD8 antibody (Dynabeads #11147D, Thermo Fisher Scientific) following the manufacturer’s protocol.
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1.
Count the BMMCs using the preferred method.
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2.
Centrifuge the BMMCs at 300 g for 5 min.
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3.
Resuspend the pellet in MACS buffer (1 mL per 1 × 107 cells) and incubate with Dynabeads CD8 (25 μL per 1 × 107 cells) for 30 min at 2–8 °C in the dark with gentle rotation.
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4.
Place the tube in a magnetic rack for 1–2 min to remove bead-bound CD8+ cells.
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5.
Transfer the supernatant to a new tube.
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6.
Centrifuge the cells at 300 g for 5 min.
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7.
Resuspend the pellet to a final concentration of 0.5–1 × 106 cells/mL with RPMI 1640 medium (Table 2) supplemented with 2 mm L-glutamine, 10% fetal bovine serum, 1 µm sodium pyruvate, 1% penicillin and streptomycin (hereafter referred to as RPMI).
Stimulation of MM cells (Day 1)
Following isolation, the MM cells are stimulated with a T-cell expansion cocktail.
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1.
Culture the CD8-depleted BMMCs (0.5–1 × 106 cells/mL) for 48 h at 37 °C in RPMI supplemented with human rIL-2 (100 U/mL) and human T cell activator CD3/CD28 magnetic beads (25 μL per 1 × 106 T cells, Dynabeads #11132D) according to the manufacturer’s instructions (Fig. 1b, second panel).
CD138+ MM cell enrichment (Day 3)
After stimulation, MM cells are enriched using CD138-MACS magnetic beads (Miltenyi Biotec, #130-051-301) according to the manufacturer’s instructions.
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1.
Transfer the cells to a tube and place it in a magnetic rack for 1–2 min to remove bead-bound T cells.
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2.
Transfer the supernatant to a new tube.
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3.
Count the cells using the preferred method.
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4.
Centrifuge the cells at 300 g for 5 min.
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5.
Resuspend the cell pellet in MACS buffer (80 μL per 2 × 107 total cells) with CD138-MACS magnetic beads (20 μL per 2 × 107 total cells) and incubate for 15 min at 2–8 °C in the dark with gentle rotation.
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6.
Place an LS MACS column (Miltenyi Biotec #130-042-401) onto a magnetic rack and wash once by adding 3 mL MACS buffer according to protocol. Let the MACS buffer run through.
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7.
Place a tube below the empty LS column.
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8.
Transfer the cell suspension to the LS column. Collect the run-through in the tube.
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9.
Wash the LS column three times with 1 mL MACS buffer. Collect the run-through in the same tube (CD138− cells).
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10.
Replace the collection tube with a new tube.
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11.
Add 5 mL MACS buffer to the LS column. Flush out the bead-bound CD138+ MM cells by pushing a plunger into the column.
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12.
Centrifuge the collected cells at 300 g for 5 min.
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13.
Resuspend the cell pellet in 1 mL RPMI.
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14.
Count the cells using the preferred method.
Dispensing of cells into assay plates (Day 3)
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1.
Resuspend the cells in RPMI to a final concentration of 2 × 105 cells/mL. This will allow for 5000 cells/well in a volume of 25 µL/well.
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2.
Transfer the cell suspension to preprinted 384-well drug plates at 25 µL/well using a liquid dispenser such as the CERTUS Flex (Fig. 1b, third panel). It is recommended to sonicate the valves of the dispenser before each use (Box 2, 1c).
-
3.
Leave the plates in an incubator at 5% CO2, 37 °C for 72 h.
Measurement of cell viability with CellTiter-Glo (Day 6)
Drug library design
Single-drug dose-response curves
Drug sensitivity testing can be performed with pre-designed drug libraries that are commercially available from suppliers such as Selleck Chemicals (https://www.selleckchem.com/screening-libraries.html) or MedChemExpress (https://www.medchemexpress.com/), or with custom drug libraries designed by the user. The drug library is designed with high throughput in mind, accounting for the solubility of the compounds, favoring those that can be dissolved in DMSO or water. Each drug is typically tested at multiple concentrations, such as five 10-fold serial dilutions. The concentration range can be determined for each drug individually, or a more general approach can be applied where an equally broad concentration range is used for all drugs. The drug sensitivity curves provide information on drug efficacy and allow for calculation of parameters such as the EC50 (half maximal effective concentration), the bend points where the effect of the drug changes from exponential to asymptotic, and the dynamic range or the range located between the EC10 and EC90 (Fig. 1c). Fitting concentration-response curves to efficiently calculate EC50 values requires a minimum of 5 doses, with 6 being optimal: two doses before the low bend point, two doses after the high bend point and at least one dose, ideally two, in the slope (Fig. 1c) [31].
Drug combinations
Different approaches can be taken when screening for drug interactions. The most complete approach would be to test the two drugs at every possible concentration combination, the so-called full matrix (Fig. 1d, left panel). However, this approach is highly resource-demanding. To reduce the number of patient cells and amount of reagents required for testing drug responses in multiple concentration combinations, the user can choose to test only part of the concentration-combinations using one of the following designs (Fig. 1d): (i) Fixed-concentration, or anchored, design: various concentrations of one agent are tested with a pre-defined concentration of the second agent (Fig. 1d, second panel); (ii) Fixed-ratio diagonal design: the diagonal dose-combination elements of the full pairwise concentration response matrix are tested (Fig. 1d, third panel); (iii) Fixed-ratio x-design: both diagonal concentration-combination elements (the “x”) of the full pairwise concentration response matrix are tested (Fig. 1d, right panel). Data analysis tools are available that can predict the full matrix of drug responses based on these fixed designs [32].
The definition of a concentration range for the single drug sensitivity curves provides information on the drug concentrations that may be used for drug combination screening. Those concentrations are recommended to fall between the EC10 and the EC90, referred to here as the dynamic range (Fig. 1c). Going below the EC10 poses a risk of using a concentration with little effect at all, while going above the EC90 will leave little room to detect additional effects of the drug combination compared to either single agent alone.
Reproducibility and quality controls of drug screens
Drug sensitivity screens have been shown to be reproducible over time [24]. Here, we further show that drug screens are reproducible independently of operator and what platform that printed the drug plates (the drug plate source; Fig. 2). Four experiments performed on the lymphoma cell line KARPAS1718 [33] and with variation in performance were selected for illustration purposes. The cell line was confirmed mycoplasma negative with the MycoAlert Detection Kit (Lonza, Basel, Switzerland). Two operators (A and B, Fig. 2a) performed the experiments, and the drug plates were obtained from three different sources (I-III, Fig. 2a). The drug sensitivity scores (DSS), which are quantitative measurements derived from the area under the concentration response curves with further normalization [34], were highly correlated between experiments performed by the same operator with different plate sources, or by different operators with the same plate source (R squared 0.91 and 0.92, respectively; Fig. 2b). These findings support the performance of one drug screen per patient sample and that the experiments can be performed by different users with drug plates produced by different sources without introduction of significant variability.
The Z-prime is commonly used as a quality control for drug screens [18]. This factor describes how well the positive and negative controls in the experiment separate and indicates the likelihood of false positives or negatives. Z-prime values between 0.5–1 are excellent, values between 0–0.5 may be acceptable, while values below 0 indicate a poor assay. In the experiments performed on the KARPAS1718 cell line, the drugs were distributed on four 384-well plates (A-D). In two of the experiments, the Z-prime for the A-plate was < 0.5 (0.41 and −2.53), while it was > 0.5 in the other two experiments (Fig. 2a). For the remaining plates, 11/12 (92%) of the experiments had a Z-prime > 0.5 (Fig. 2a). When the DSS for the drugs on Plate A were plotted for the four experiments, it showed that the two experiments with low Z-prime (Experiments 3 and 4) had many outliers relative to the high-quality experiments (Experiments 1 and 2; Fig. 2c). This trend was clearly visible when looking at the viability curves (Fig. 2d). Interestingly, the two experiments with Z-prime < 0.5 resulted in highly diverging results for many of the treatments (Fig. 2c, d). These findings highlight the importance of including quality controls in each experiment. Of note, we found that although part of an experiment (i.e. one of the plates) showed a Z-prime < 0.5, the other parts of the experiment with a Z-prime > 0.5 could still be used. In Fig. 2e, Plate A from Experiment 3 (Z-prime < 0.5) was replaced with Plate A from Experiment 2 (Z-prime > 0.5), resulting in a shift from low to high correlation with the DSS from Experiment 1 (Z-prime > 0.5; R squared 0.37 and 0.89, respectively). This indicates that it is acceptable to repeat only that part of the experiment which shows a Z-prime < 0.5, when relevant.
Discussion
High heterogeneity in clinicobiological features such as genetic aberrations and clinical outcomes among patients with hematologic cancers has led to the realization that treatment strategies tailored to the individual patient are needed to improve disease management. Genomic strategies do to some extent guide treatment decisions [36, 37], but further precision is required to avoid ineffective therapies [38].
Functional precision medicine guides treatment decisions based on functional analyses, often a drug sensitivity screen, of the patient’s tumor cells [15, 16]. This approach allows for the monitoring of treatment sensitivities in real time. The protocol is fast; it provides test results in 3–5 days after collection of the patient sample, with limited computational skills required for the data analysis. This is in contrast to genomic analyses which can take several weeks to process and require high computational skills for data analysis [16].
Here, we report our optimized and validated protocols for drug sensitivity screening of hematologic cancers. We show that reproducible results can be acquired on the same material analyzed by different operators or screened with drug libraries printed at different platforms. We previously reported that the results also are reproducible over time [24]. These features are critical for successful implementation in clinical trials and routine clinical practice. Clinical trials have been initiated that use these drug sensitivity screening results as biomarkers to guide precision medicine in hematologic cancers (Table 1), with encouraging results [4, 5, 19].
While we present ex vivo screening protocols that use the CellTiter-Glo assay or flow cytometry as a read-out, alternative approaches to ex vivo drug sensitivity screening have been established and previously reported, including three-dimensional cell culture models [39,40,41,42,43] and protocols with image-based read-outs [19, 44,45,46]. Continuous development of the screening protocols, including the consideration of microenvironmental effects on drug sensitivity, is expected to expand their applicability, both when it comes to disease indications and to drug classes that can be assessed. Miniaturization of the set-up further enables screening of cancers with very limited tumor material [47]. While functional precision medicine is spearheaded by hematologic cancers, development in solid tumors follows suit [15, 16]. This is a clear indication that functional precision medicine will find its place in future cancer care.
Data availability
The data that support the findings of this study are available from the corresponding author (sigrid.skanland@ous-research.no) upon reasonable request.
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Acknowledgements
We thank the High-Throughput Chemical Biology Screening Platform at Centre for Molecular Medicine Norway (NCMM), University of Oslo; the High Throughput Biomedicine Unit at Institute for Molecular Medicine Finland (FIMM), University of Finland; and DK-OPENSCREEN, Lyngby, Denmark for assistance with drug sensitivity screens.
Funding
This work was supported by the Research Council of Norway (262652) under the frames of ERA PerMed (CLL-CLUE: 322898) and Digital Life Norway (PINpOINT: 294916), the European Union’s Horizon 2020 research and innovation programme (RESCUER: 847912), the South-Eastern Norway Regional Health Authority (2015031, 2018012 and 2019096), the Norwegian Cancer Society (182524 and 208012), Stiftelsen Kristian Gerhard Jebsen (Grant 19), the Norwegian Center for Clinical Research (MATRIX: Research Council of Norway and the Norwegian Cancer Society joint grant 328827), and the Danish Research Center for Precision Medicine in Blood Cancers (Danish Cancer Society grant no. R223-A13071).
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PA-D, JUH, MG, YY, RH, SG, HK, and SSS developed experimental protocols. PA-D, JUH, and SSS performed experiments. AMB, RH, and ANA developed computational procedures. PA-D and SSS wrote the manuscript. KT, KW, JME, and SSS supervised the study. All authors read, revised, and approved the manuscript.
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SSS has received honoraria from AbbVie and AstraZeneca, and research support from BeiGene and TG Therapeutics. The other authors declare no competing interests.
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The study was approved by the Regional Committee for Medical and Health Research Ethics of South-East Norway. All donors signed a written informed consent prior to sample collection. The research on human blood was carried out in accordance with the Declaration of Helsinki.
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Ayuda-Durán, P., Hermansen, J.U., Giliberto, M. et al. Standardized assays to monitor drug sensitivity in hematologic cancers. Cell Death Discov. 9, 435 (2023). https://doi.org/10.1038/s41420-023-01722-5
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DOI: https://doi.org/10.1038/s41420-023-01722-5
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