We sought to independently replicate the effectiveness of cimetidine treatment as a possible therapeutic agent for lung adenocarcinoma, but not renal cell carcinoma, by performing an experiment in mice implanted with the A549 or ACHN cell lines, respectively. This experiment is similar to what was reported in Figure 4C–D and Supplemental Figure 1 of Sirota et al., 2011. Tumor volume was determined by caliper daily for the duration of the study (Figure 1, Figure 1—figure supplement 1). While the original study included three doses of cimetidine in the experimental design, this replication attempt was restricted to only the highest dose (100 mg/kg). Tumors from A549 cells treated with cimetidine grew to an average of 2.37 times their original volume by day 11 [n=13, SD=0.723], similar to the ~2.3 times reported in the original study. This is in comparison to tumors from A549 cells treated with vehicle, which grew to an average of 3.29 times their original volume by day 11 [n=14, SD=1.17], similar to the ~3.3 times reported in the original study. Tumors from ACHN cells treated with vehicle or cimetidine grew to an average of 2.96 [n=15, SD=0.952] or 3.37 [n=15, SD=1.50] times their original volume by day 11, respectively. ACHN derived tumors were similar in volume compared to tumors from A549 cells treated with vehicle in this study. This differed from the tumor volumes reported in Sirota et al., 2011, which were ~2.1 and ~2.0 times the original volume in tumors from ACHN cells treated with vehicle or cimetidine, respectively, compared to ~3.3 times the original volume in tumors from A549 cells treated with vehicle. Additionally, the relative standard deviation (RSD) associated with this replication attempt (A549 – vehicle treated = 35.6%; A549 – cimetidine treated = 30.5%; ACHN – vehicle treated = 32.1%; ACHN – cimetidine treated = 44.5%) was generally larger than the RSD observed in the original study (A549 – vehicle treated = 17.0%; A549 – cimetidine treated = 35.5%; ACHN – vehicle treated = 10.3%; ACHN – cimetidine treated = 12.0%), however, the range of RSD among the conditions was more consistent in this replication attempt compared to the original study.

There are multiple approaches that could be taken to explore these data (e.g. MANOVA, regression with RE/AR errors, area under the curve), however to provide a direct comparison to the original analysis, which used volume measurements at day 11, and the available original data, we are reporting the analysis specified a priori in the Registered Report (Kandela et al., 2015). To test if cimetidine is effective in the A549 derived xenograft model, but not in the ACHN derived xenograft model, we performed an analysis of variance (ANOVA) having two levels of tumors (A549 derived or ACHN derived) and two levels of drug treatment (vehicle or cimetidine). The ANOVA result on tumor volumes at day 11 (natural log-transformed) was not statistically significant for all effects at the 0.05 significance level. The interaction effect, with a sample size powered a priori to detect the effect based on the originally reported data, was not statistically significant, F(1,53) = 3.88, p=0.054. Thus, the null hypothesis that the effect of the drug treatment (difference between vehicle and cimetidine) on inhibiting tumor volume growth is similar for A549 and ACHN derived tumors can not be rejected. The main effect for cell line, F(1,53) = 1.21, p=0.277, and drug treatment F(1,53) = 1.13, p=0.292 were also not statistically significant.

As outlined in the Registered Report (Kandela et al., 2015), we planned to conduct three comparisons using the Bonferroni correction to adjust for multiple comparisons. Although the Bonferroni method is conservative, it was accounted for in the power calculations to ensure sample size was sufficient. The planned pairwise comparison of the tumor volumes from A549 derived tumors treated with vehicle compared to cimetidine was not statistically significant (t(53) = 2.16, uncorrected p=0.035, a priori Bonferroni adjusted significance threshold = 0.0167; (Bonferroni corrected p=0.105)). Additionally, the planned pairwise comparison of ACHN derived tumors treated with vehicle compared to cimetidine was not statistically significant (t(53) = −0.58, uncorrected p=0.562, a prior Bonferroni adjusted significance threshold = 0.0167; (Bonferroni corrected p>0.99)). While not statistically significant, the treatment of A549 derived tumors with cimetidine resulted in decreased tumor volume compared to vehicle control at day 11, which is in the same direction as the original study. The treatment of ACHN derived tumors with cimetidine did not result in an observational difference in tumor volume after treatment when compared to vehicle control treated tumors, similar to the original study.

As an additional control for tumor growth inhibition, tumors from A549 cells were treated with 2 mg/kg doxorubicin, similar to the original experimental design (Figure 1A). While tumors from A549 cells treated with vehicle grew to an average of 3.29 times their original volume by day 11, tumors in mice treated with doxorubicin grew to an average of 1.87 times the original volume by day 11 [n=4, SD=0.845], similar to the ~2.0 times, reported in Sirota et al., 2011 in the doxorubicin condition. Analysis of vehicle treated compared to doxorubicin treated tumor volumes at day 11, which was planned a priori, was not statistically significant (Welch’s t-test; t(6.73) = 2.68, uncorrected p=0.0325, a priori Bonferroni adjusted significance threshold = 0.0167; (Bonferroni corrected p=0.0976)). While not statistically significant, the treatment of tumors from A549 cells with doxorubicin resulted in a smaller volume when compared to vehicle control at day 11, which is in the same direction as the original study. Additionally, mice treated with doxorubicin started to lose weight and had a rough coat starting on approximately day 7 of the treatment schedule. A small reduction in tumor volume compared to vehicle control has also been reported in other studies that utilized low dose doxorubicin experimental designs (Hossain et al., 2012; Lopez et al., 2009; Wang et al., 2013, 2010).

At the completion of the treatment schedule, tumors were excised and imaged (available at https://osf.io/xcuh6/), similar to the representative A549 derived tumors treated with vehicle or 100 mg/kg cimetidine shown in Figure 4D of the original study (Sirota et al., 2011). The excised tumors were also weighed (Figure 2), as described in the Registered Report (Kandela et al., 2015). This was an additional measured parameter not included in the original study. The tumor weights were subjected to a two-way ANOVA having two levels of cell lines (A549 derived or ACHN derived), two levels of treatment (vehicle or cimetidine), and their interaction. The main effect of cell lines yielded an F ratio of F(1,53) = 7.560, p=0.00814, indicating that the mean tumor weight was significantly larger for A549 derived tumors [n=27, M=0.138, SD=0.0423] than for ACHN derived tumors [n=30, M=0.108, SD=0.0402]. The main effect of treatment was not significant (F(1,53) = 0.586, p=0.447) nor was the interaction effect (F(1,53) = 0.00005, p=0.994). Exploratory analysis of vehicle treated [n=14, M=0.134, SD=0.0444] compared to doxorubicin treated [n=4, M=0.110, SD=0.0576] A549 derived tumor weights was not statistically significant (Welch’s t-test; t(4.078) = 0.771, p=0.483). While not statistically significant, the treatment of tumors derived from A549 cells with doxorubicin resulted in a small effect (Cohen’s d = 0.51 [−0.62, 1.63]), which is in the expected direction. A small reduction in tumor weight compared to vehicle control has also been reported in other studies that utilized a similar low dose doxorubicin experimental design (Biswas et al., 2013; Hossain et al., 2012; Lopez et al., 2009; Wang et al., 2010).

Figure 2

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We performed a meta-analysis using a random-effects model to combine each of the effects described above on day 11 tumor volume comparisons as pre-specified in the confirmatory analysis plan (Kandela et al., 2015). To provide a standardized measure of the effect Cohen’s d was calculated for the original and replication studies. Cohen’s d is the standardized difference between two means using the pooled sample standard deviation.

The comparison of A549 derived tumor volumes treated with vehicle compared to cimetidine resulted in d = 1.36, 95% CI [0.06, 2.60] for the data estimated a priori from Figure 4C of the original study (Sirota et al., 2011). This compares to d = 0.93, 95% CI [0.12, 1.72] reported in this study. A meta-analysis (Figure 3) of these two effects resulted in d = 1.04, 95% CI [0.33, 1.75], p=0.0043. Both results are consistent when considering the direction of cimetidine’s effect. The point estimate of the replication effect size was within the confidence interval of the original result and vice versa. Further, the random effects meta-analysis resulted in a statistically significant effect of cimetidine on inhibiting A549 derived tumors.

Figure 3

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The comparison of ACHN derived tumor volumes treated with vehicle compared to cimetidine resulted in d = 0.61, 95% CI [−0.57, 1.76] for the data estimated a priori from Supplemental Figure 1 of the original study (Sirota et al., 2011). This compares to d = −0.18, 95% CI [−0.90, 0.54] reported in this study. A meta-analysis (Figure 3) of these two effects resulted in d = 0.04, 95% CI [−0.65, 0.73], p=0.917. The original and replication results were both not statistically significant. While both studies were in opposite directions, the point estimate of the replication effect size was within the confidence interval of the original result, but the original effect size was not within the confidence interval of the replication. The random effects meta-analysis did not result in a statistically significant effect suggesting there is no evidence that cimetidine is effective on ACHN derived tumors.

The comparison of A549 derived tumors treated with vehicle compared to doxorubicin resulted in d = 3.00, 95% CI [1.25, 4.70] for the data estimated a priori from Figure 4C of the original study (Sirota et al., 2011). This compares to d = 1.26, 95% CI [0.05, 2.44] reported in this study. A meta-analysis (Figure 3) of these two effects resulted in d = 1.98, 95% CI [0.30, 3.66], p=0.021. Both results are consistent when considering the direction of doxorubicin’s effect. The point estimate of the replication effect size was within the confidence interval of the original result, while the point estimate of the original effect size was not within the confidence interval of the replication result. Further, the random effects meta-analysis resulted in a statistically significant effect of doxorubicin on inhibiting A549 derived tumors.

This direct replication provides an opportunity to understand the present evidence of these effects. Any known differences, including reagents and protocol differences, were identified prior to conducting the experimental work and described in the Registered Report (Kandela et al., 2015). However, this is limited to what was obtainable from the original paper, which means there might be particular features of the original experimental protocol that could be critical, but unidentified. So while some aspects, such as site of injection, number of cells injected, strain of mice, and manufacturer of the drugs were maintained, others were unknown or not easily controlled for. These include variables such as circadian biological responses to therapy (Fu and Kettner, 2013), mouse sex and strain stocks (Clayton and Collins, 2014), the microbiome of recipient mice (Macpherson and McCoy, 2015), housing temperature in mouse facilities (Kokolus et al., 2013), cell line drift (Hughes et al., 2007), and differing compound potency resulting from different stock solutions (Kannt and Wieland, 2016). Whether these or other factors influence the outcomes of this study is open to hypothesizing and further investigation, which is facilitated by direct replications and transparent reporting.

A549 cells (ATCC, CCL-185) were maintained in F-12 Ham’s medium supplemented with 10% Fetal Bovine Serum (FBS) (Sigma-Aldrich, cat # F2442) and 2 mM sodium pyruvate. ACHN cells (ATCC, CRL-1611) were maintained in EMEM supplemented with 10% FBS, 2 mM glutamine, and 1 mM sodium pyruvate. All cells were grown at 37°C and at 5% CO₂. Quality control data for the A549 and ACHN cell lines are available on the OSF (https://osf.io/yt9fv/). This includes results confirming the cell lines were free of mycoplasma contamination and common mouse pathogens. Additionally, STR DNA profiling of the cell lines was performed and all cells were confirmed to be the indicated cell lines when queried against STR profile databases.

All animal procedures were approved by the Northwestern University IACUC# IS00000424 and were in accordance with the Northwestern University’s policies on the care, welfare, and treatment of laboratory animals. No blinding occurred during the experiments.

Six-week old female SCID mice (Charles River, strain code 236) were inoculated subcutaneously (s.c.) with A549 or ACHN cells at a density of 5 × 10⁶ cells in 100 µl of Dulbecco’s Phosphate Buffered Saline (DPBS) (Sigma-Aldrich, cat # D8537) in the right upper flank. Tumor (caliper measurements) and body weight (scale: Scout Pro O’Haus, model # SP202 (S/N: B443188875)) were measured three times a week before enrollment to reduce stress in the mice and were measured daily during the course of the experiment. Once the tumor reached 100 mm³, the mice were randomized into the treatment groups (vehicle (DPBS), 100 mg/kg cimetidine (dissolved in DPBS and pH adjusted and filtered through 0.22 µm syringe), or 2 mg/kg doxorubicin (dissolved in DPBS and filtered through 0.22 µm syringe)), taking into account the pre-specified group sizes. Two mice were not enrolled in the study due to unanticipated death and a small tumor size. Injections were administered via the intraperitoneal (IP) route using a 1 ml syringe (BD, cat # Z192090) with 27 gauge needles (BD, cat # 305109) as a repeat dose each day for cimetidine and twice a week for doxorubicin for 11 days with a dosing volume of 100 µl per 20 gram mouse. The volume of injection was calculated based on the total body weight obtained on the same day prior to injection. After repeat dosing for 11 days, all surviving animals were sacrificed 24 hr post last dose. Tumors were harvested and weighed (scale: Metler Toledo, Model # XL300), with pictures of the tumors taken with a ruler for scale similar to the representative examples shown in Figure 4D of the original study (available at: https://osf.io/xcuh6/).

Each cage contained up to five mice and offered Certified Rodent Diet (Harlan Teklad, cat # 7912) ad libitum. The animal room was set to maintain between 68–75°F, a relative humidity of 30–70%, a minimum of 15 room air changes per hour, and a 12 hr light/dark cycle, which was interrupted for study-related activities.

Statistical analysis was performed with R software (RRID: SCR_001905), version 3.2.3 (R Core Team, 2016). All data, csv files, and analysis scripts are available on the OSF (https://osf.io/hxrmm/). Confirmatory statistical analysis was pre-registered (https://osf.io/yc8k2/) before the experimental work began as outlined in the Registered Report (Kandela et al., 2015). Additional exploratory analysis was performed using the excised tumor weights. Data were checked to ensure assumptions of statistical tests were met. A meta-analysis of a common original and replication effect size was performed with a random effects model and the metafor package (Viechtbauer, 2010) (available at: https://osf.io/jcghv/). The original study data was extracted a priori from the published figures by determining the mean and upper/lower error values for each data point. The extracted data was published in the Registered Report (Kandela et al., 2015) and was used in the power calculations to determine the sample size for this study.

The source of FBS and DPBS were different than what is listed in the Registered Report, with the used source and catalog number listed above. (note: the original source was not specified). Additional materials and instrumentation not listed in the Registered Report, but needed during experimentation are also listed.

The funder had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

The Reproducibility Project: Cancer Biology would like to thank the following companies for generously donating reagents to the Reproducibility Project: Cancer Biology; American Type and Tissue Collection (ATCC), Applied Biological Materials, BioLegend, Charles River Laboratories, Corning Incorporated, DDC Medical, EMD Millipore, Harlan Laboratories, LI-COR Biosciences, Mirus Bio, Novus Biologicals, Sigma-Aldrich, and System Biosciences (SBI).

Animal experimentation: All animal procedures were approved by the Northwestern University IACUC# IS00000424 and were in accordance with the Northwestern University's policies on the care, welfare, and treatment of laboratory animals.

1. Received: April 18, 2016
2. Accepted: July 28, 2016
3. Version of Record published: January 19, 2017 (version 1)

© 2017, Kandela et al.

This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.