We have synthesized a novel analogue of pancratistatin with comparable anti-cancer activity as native pancratistatin; interestingly, combinatory treatment with tamoxifen yielded a drastic enhancement in apoptotic and autophagic induction by mitochondrial targeting with minimal effect on noncancerous fibroblasts. Thus, JCTH-4 in combination with tamoxifen could provide a safe anti-cancer therapy.
Breast cancer is one of the most common cancers amongst women in North America. Many current anti-cancer treatments, including ionizing radiation, induce apoptosis via DNA damage. Unfortunately, such treatments are non-selective to cancer cells and produce similar toxicity in normal cells. We have reported selective induction of apoptosis in cancer cells by the natural compound pancratistatin (PST). Recently, a novel PST analogue, a C-1 acetoxymethyl derivative of 7-deoxypancratistatin (JCTH-4), was produced by de novo synthesis and it exhibits comparable selective apoptosis inducing activity in several cancer cell lines. Recently, autophagy has been implicated in malignancies as both pro-survival and pro-death mechanisms in response to chemotherapy. Tamoxifen (TAM) has invariably demonstrated induction of pro-survival autophagy in numerous cancers. In this study, the efficacy of JCTH-4 alone and in combination with TAM to induce cell death in human breast cancer (MCF7) and neuroblastoma (SH-SY5Y) cells was evaluated. TAM alone induced autophagy, but insignificant cell death whereas JCTH-4 alone caused significant induction of apoptosis with some induction of autophagy. Interestingly, the combinatory treatment yielded a drastic increase in apoptotic and autophagic induction. We monitored time-dependent morphological changes in MCF7 cells undergoing TAM-induced autophagy, JCTH-4-induced apoptosis and autophagy, and accelerated cell death with combinatorial treatment using time-lapse microscopy. We have demonstrated these compounds to induce apoptosis/autophagy by mitochondrial targeting in these cancer cells. Importantly, these treatments did not affect the survival of noncancerous human fibroblasts. Thus, these results indicate that JCTH-4 in combination with TAM could be used as a safe and very potent anti-cancer therapy against breast cancer and neuroblastoma cells.
Introduction
Apoptosis, or type I programmed cell death, is a physiological process that can operate extrinsically, via binding of a death ligand to a death receptor, or intrinsically. The intrinsic pathway of apoptosis is initiated by intracellular stress such as DNA damage and mitochondrial dysfunction; this ultimately leads to the permeabilization of the mitochondria, dissipation of mitochondrial membrane potential (MMP), release of apoptogenic factors from the mitochondrial intermembrane space, and subsequent execution of apoptosis1.
Autophagy is a process in which a cell breaks, degrades, and recycles its own intracellular components while maintaining plasma membrane integrity; it is triggered by different types of cellular stresses including oxidative stress, hypoxia, protein aggregates, nutrient deprivation, growth factor deprivation, and damaged organelles2. In the initial stages of this process, cytosolic material is engulfed by autophagosomes, double-membraned vesicles, which fuse to lysosomes to form autolysosomes. Post lysosomal fusion, cytosolic materials previously taken up by autophagosomes are degraded by lysosomal enzymes2. Extensive activation of this pathway yields extensive degradation of intracellular components which may lead to autophagic cell death or type II programmed cell death3.
Evasion of cell death has been considered one of the hallmarks of cancer4. Cancer is a disease characterized by uncontrolled cell growth and proliferation5. In particular, neuroblastoma arises from developing nerve cells of the sympathetic nervous system from the neural crest6. It is the most common solid tumor occurring in young children, accounting for approximately 9% of all childhood cancers7. Although much progress has been made to date, this disease remains problematic to both basic scientists and clinicians. On the other hand, breast cancer is the most common cancer amongst females8. Tamoxifen (TAM) has been frequently used for therapy in hormone-responsive breast cancers as an estrogen receptor (ER) antagonist9. Nonetheless, other reports provide evidence of additional independent mechanisms of apoptosis induction by TAM. In particular, TAM interacts with Complex I of the mitochondrial respiratory chain (MRC) at its flavin mononucleotide (FMN) site10.
PST is a natural compound isolated from the Hymenocallis littoralis plant. Contrasting from many chemotherapeutics currently in use, it has been shown to induce apoptosis, in a non-genotoxic manner, selectively in various cancer cell types via mitochondrial targeting11-15. However, preclinical and clinical work has been hindered by its availability; it is present at very low amounts in its natural source and many complications burden its chemical synthesis. We have synthesized and screened synthetic analogues of 7-deoxypancratistatin and observed similar anti-cancer activity in a C-1 acetoxymethyl derivative, JC-TH-acetate-4 (JCTH-4)16. We now have in hand a synthetic PST analogue with potent anti-cancer activity. Its synthesis has been standardized and can be scaled up to produce sufficient quantities for preclinical and clinical work. Since natural PST and TAM both target the mitochondria, it would be interesting to investigate the combined effect of a synthetic analogue of PST on human breast cancer and neuroblastoma cells in combination with TAM.
Herein, we report selective cytotoxicity of JCTH-4 in human neuroblastoma (SH-SY5Y) and breast adenocarcinoma (MCF7) cells. JCTH-4 was able to induce apoptosis in both cell lines by mitochondrial targeting; JCTH-4 caused dissipation of MMP and an increase in reactive oxygen species (ROS) production in isolated mitochondria from these cancer cells. Furthermore, autophagy was induced by JCTH-4 in MCF7 cells. Interestingly, the addition of TAM to JCTH-4 insult enhanced the aforementioned effects of JCTH-4 in SH-SY5Y and MCF7 cells. Morphological changes induced by JCTH-4 and TAM alone and in combination in MCF7 cells were monitored via time-lapse microscopy of phase contrast or bright field pictures. Normal human fetal fibroblasts (NFF) exhibited a marked decrease in sensitivity to JCTH-4 both alone and in combination with TAM. Therefore, these observations suggest JCTH-4, alone and in with TAM, to be a safe and effective chemotherapeutic agent against breast cancer and neuroblastoma.
Materials and Methods
1. Cell Culture
2. Drug Preparation
3. Time-Lapse Microscopy
4. Nuclear Staining
5. Annexin V Binding Assay
6. Water Soluble Tetrazolium Salt (WST-1) Assay for Cell Viability
7. Tetramethylrhodamine Methyl Ester (TMRM) Staining
8. Mitochondrial Isolation
9. Amplex Red Assay
10. Cellular Lysate Preparation
11. Western Blot Analyses
12. Monodansylcadaverine (MDC) Staining
13. Representative Results
Selective Induction of Apoptosis in Human Breast Adenocarcinoma and Neuroblastoma Cells by JCTH-4: Enhancement of Activity by TAM
Selective induction of apoptosis was shown in various cancer cells by natural PST (Fig. 1a)11-13. Because of the low availability of PST, we have synthesized analogues of 7-deoxypancratistatin (JCTH-4, Fig. 1b) and screened them for similar anti-cancer activity in human breast adenocarcinoma (MCF7) and neuroblastoma cells (SH-SY5Y). In the first phase of experiments, we wanted to monitor morphological changes over time following treatment with JCTH-4 and TAM alone and in combination in MCF7 cells. MCF7 cells were monitored for 18 hours, as seen in Video 1 produced by time-lapse microscopy with phase contrast pictures, with solvent treatment (control) for 48 hours; these cells exhibited no major changes in morphology. In contrast, after 48 hours of 1 μM JCTH-4 treatment, these cells exhibited morphological changes associated with apoptosis such as shrinkage, blebbing, apoptotic body formation as seen in Video 2. On the other hand, TAM treatment alone in MCF7 cells produced a very distinct morphology including punctate inclusions indicative of autophagosomes associated with autophagy (Video 3). Very minimal apoptotic morphology was observed and cells generally exhibited healthy morphology comparable to the solvent control treated MCF7 cells. Interestingly, in the presence of TAM, the apoptotic induction by JCTH-4 was drastically enhanced as indicated by increased apoptotic morphology in MCF7 cells after 48 hours as illustrated in Video 4.
In the second phase of experiments we utilized fluorescent dyes to evaluate the induction of apoptosis. After 72 hours and 48 hours of 1 μM JCTH-4 treatment in MCF7 and SH-SY5Y cells respectively, Hoechst dye was used and to monitor nuclear morphology. Results indicated condensed, brightly stained nuclei accompanied by apoptotic bodies in MCF7 and SH-SY5Y cells, indicative of apoptotic induction (Fig. 2a, b). TAM treatment alone yielded minimal apoptotic nuclear morphology in MCF7 and SH-SY5Y cells; nuclei were large, round, and dimly stained with Hoechst comparable to solvent control group (Fig. 2a, b). In agreement with Video 4, nuclei of MCF7 and SH-SY5Y cells displayed a marked increase in apoptotic morphology with the combination treatment after 72 hours (Fig. 2a, b).
To verify apoptotic induction, cells were evaluated for phosphatidylserine externalization, a marker for apoptosis, via an Annexin V binding assay17. MCF7 and SH-SY5Y cells treated for 72 and 48 hours respectively with 1 μM JCTH-4 alone and in combination with 10 μM TAM were positive for Annexin V binding, indicated by the green fluorescence, confirming the induction of apoptosis (Fig 3a, b). No evident externalization of phosphatidylserine was observed in MCF7 and SH-SY5Y cells treated with TAM alone, as well as in NFF cells treated with all the aforementioned treatments groups after 72 hours (Fig. 3c). Therefore, JCTH-4 alone and in combination with TAM selectively induces apoptosis in MCF7 and SH-SY5Y cells.
To quantify the effect of JCTH-4 alone and in combination with TAM, a WST-1 based colorimetric assay for cell viability, an indicator of active cell metabolism, was performed on MCF7 and NFF cells treated for 72 hours and SH-SY5Y cells treated for 48 hours. Compared to the solvent control groups, 1 μM JCTH-4 decreased active cell metabolism by over 50%, while 10 μM TAM alone exhibited no significant difference in both MCF7 and SH-SY5Y cells (Fig. 4a, b). Interestingly in MCF7 and SH-SY5Y cells, the addition of TAM to JCTH-4 insult resulted in a synergistic decrease in cell metabolism. NFF cells were drastically less sensitive to both JCTH-4 alone and JCTH-4 with TAM (Fig. 4c). Hence, JCTH-4 demonstrates selective synergistic activity with TAM in MCF7 and SH-SY5Y cells.
Mitochondrial Targeting of JCTH-4
To see if JCTH-4 is targeting the mitochondria to induce apoptosis mitochondrial membrane potential in whole cells and ROS generation in isolated mitochondria was monitored. MCF7 cells were treated for 72 hours and stained with TMRM. 1 μM JCTH-4 decreased MMP, indicated by the loss of red fluorescence (Fig. 5a). However, with the addition of 10 μM TAM, a greater dissipation of MMP was observed, while 10 μM TAM alone had no evident effect on MMP.
As increases ROS generation have been associated to mitochondrial membrane permeabilization and apoptosis induction, the production of ROS was assessed with Amplex Red dye in isolated mitochondria from SH-SY5Y cells treated with 1 μM JCTH-4 and 10 μM TAM, alone and in combination18-20. Fluorescence readings were expressed as relative fluorescence units (RFU). Increases in ROS generation were observed with JCTH-4 and TAM alone (Fig. 5b). Interestingly, combination treatment yielded a greater increase in ROS production. A well-known inducer of ROS production in mitochondria, PQ, was utilized as a positive control.
Induction of Autophagy by JCTH-4 and TAM
Autophagic induction has been associated to chemotherapeutic insult by many different compounds3. To evaluate the induction of autophagy, MDC staining was performed on MCF7 cells treated with 1 μM JCTH-4 and 10 μM TAM alone and in combination for 72 hours. Blue punctate fluorescence, indicative of autophagosomes, was present in MCF7 cells treated with JCTH-4 and TAM alone and in combination (Fig. 6a). Notably, the intensity of MDC staining was greatest with the combination treatment, followed by TAM alone, and JCTH-4 alone.
During autophagy, microtubule-associated protein 1 light chain 3 (LC3) normally situated in the cytosol (LC3-I), is lipidated with phosphatidylethanolamine and subsequently localized to the autophagosomal membranes (LC3-II)2. To verify the induction of autophagy, levels of LC3-II were assessed in MCF7 cells treated for 72 hours via western blot analyses. 1 μM JCTH-4 slightly induced the conversion of LC3-I to LC3-II while 10 μM TAM produced a greater autophagic response (Fig. 6b). Interestingly, combination treatment resulted in the greatest induction of autophagy, yielding a LC3-II to LC3-I ratio greater than 3. Therefore, these results demonstrate autophagic induction in MCF7 cells by JCTH-4 and TAM alone and in combination, with the greatest response in cells with the combination treatment.
Supplemental Video 1. Cellular morphology of MCF7 cells treated with solvent control. MCF7 cells were monitored between 48 and 66 hours post solvent control treatment (DMSO) using time-lapse microscopy with phase contrast pictures. Cells were maintained at 37 °C and 5% CO2. Images were captured at 400x magnification. Click here to watch video.
Supplemental Video 2. Induction of apoptotic cellular morphology in MCF7 cells treated with JCTH-4. MCF7 cells were monitored between 48 and 66 hours post treatment with 1 μM JCTH-4 using time-lapse microscopy with phase contrast pictures. Cells were maintained at 37 °C and 5% CO2. Images were captured at 400x magnification. Click here to watch video.
Supplemental Video 3. Induction of autophagic cellular morphology in MCF7 cells treated with TAM. MCF7 cells were monitored between 48 and 66 hours post treatment with 10 μM TAM using time-lapse microscopy with phase contrast pictures. Cells were maintained at 37 °C and 5% CO2. Images were captured at 400x magnification. Click here to watch video.
Supplemental Video 4. Enhanced apoptotic morphology by JCTH-4 with TAM in MCF7 cells. MCF7 cells were monitored between 48 and 66 hours post treatment with both 1 μM JCTH-4 and 10 μM TAM using time-lapse microscopy with phase contrast pictures. Cells were maintained at 37 °C and 5% CO2. Images were captured at 400x magnification. Click here to watch video.
Figure 1. Structural comparison of PST to a synthetic 7-deoxy analogue. (a) Chemical structure of pancratistatin (PST). (b) Chemical structure of JC-TH-acetate-4 (JCTH-4).
Figure 2. JCTH-4 induces nuclear apoptotic morphology with enhanced activity with TAM. Nuclear morphology of (a) MCF7 and (b) SH-SY5Y cells treated for 72 and 48 hours respectively with the indicated concentrations of TAM and JCTH-4 stained with Hoechst dye. Control groups were treated with solvent (DMSO). Images were taken at 400x magnification on a fluorescent microscope. Scale bar = 15 μm.
Figure 3. JCTH-4 causes phosphatidylserine externalization alone and in combination with TAM selectively in cancer cells. Annexin V binding to externalized phosphatidylserine was evaluated to verify induction of apoptosis induction in (a) MCF7 (72 hours), (b) SH-SY5Y (48 hours), and (c) NFF (72 hours) cells treated with JCTH-4 and TAM at the indicated concentrations. Control groups were treated with solvent (DMSO). Images were taken at 400x magnification on a fluorescent microscope. Scale bar = 15 μm.
Figure 4. TAM enhances viability decrease by JCTH-4 selectively in cancer cells. 96-well plates were seeded with (a) MCF7, (b) SH-SY5Y, and (c) NFF cells and treated with JCTH-4 and TAM at the indicated concentrations. MCF7 and NFF cells were treated for 72 hours and SH-SY5Y were treated for 48 hours. Post drug treatment and incubation, WST-1 reagent was added to each well, and absorbance readings were taken at 450 nm and expressed as a percentage of the control (DMSO). Statistics were performed using GraphPad Prism version 5.0. Values are expressed as mean ± SD from quadruplicates of 3 independent experiments. MCF7: *p<0.001, **p<0.0001 versus control; #p<0.05 versus 1 μM JCTH-4; †p<0.0001 versus 10 μM TAM. SH-SY5Y: *p<0.0005 versus control; #p<0.005 versus 1 μM JCTH-4; †p<0.005 versus 10 μM TAM. NFF: *p<0.005 versus 10 μM TAM + 1 μM JCTH-4 in MCF7 cells; #p<0.01 versus 10 μM TAM + 1 μM JCTH-4 in SH-SY5Y cells.
Figure 5. JCTH-4 and TAM act on the mitochondria. (a) MCF7 cells were grown on coverslips and treated with the indicated concentrations of drugs for 72 hours and stained with TMRM to evaluate MMP. Cells of the control group were treated with solvent (DMSO). Images were captured at 400x magnification on a fluorescence microscope. Scale bar= 15 μm. (b) Isolated mitochondria from SH-SY5Y cells were treated with JCTH-4 and TAM at the indicated concentrations and ROS production was assessed with Amplex Red substrate in presence of horseradish peroxidase (HRP). The control group cells were treated with solvent (DMSO). Paraquat (PQ) was used at a concentration of 250 μM as a positive control. Fluorescence readings were obtained after 2 hours of treatment at Ex. 560 nm and Em. 590 nm and expressed as relative fluorescence units (RFU). Statistics were obtained using GraphPad Prism version 5.0. Data is representative of 3 independent experiments with similar trends. Values are expressed as mean ± SD of quadruplicates of 1 independent experiment. *p<0.05, **p<0.005, ***p<0.001 versus control; #p<0.05 versus 1 μM JCTH-4; †p<0.05 versus 10 μM TAM; @p<0.05 versus 250 μM PQ.
Figure 6. TAM enhances autophagic induction of JCTH-4. (a) MCF7 cells were grown on coverslips and subjected to JCTH-4 and TAM insult at the indicated concentrations for 72 hours. Control group cells were treated with solvent (DMSO). Post treatment, MCF7 cells were stained with MDC to detect autophagic vacuoles. Images were captured at 400x magnification on a fluorescence microscope. Scale bar= 15 μm. (b) Western blot analyses were carried out for LC3 and β-Actin on cell lysates of MCF7 cells treated with the indicated concentrations of drugs for 72 hours. Densitometric analyses were executed using ImageJ software. Statistics were performed using GraphPad Prism version 5.0. Values are expressed as mean ± SD. *p<0.05, **p<0.005, ***p<0.0005 versus control; #p<0.001 versus 1 μM JCTH-4; †p<0.001 versus 10 μM TAM.
List of Abbreviations.
ER | estrogen receptor |
FMN | flavin mononucleotide |
JCTH-4 | JC-TH-acetate-4 |
LC3 | microtubule-associated protein 1 light chain 3 |
MDC | monodansylcadaverine |
MMP | mitochondrial membrane potential |
MRC | mitochondrial respiratory chain |
NFF | normal human fetal fibroblast |
PQ | paraquat |
PST | pancratistatin |
RFU | relative fluorescence units |
ROS | reactive oxygen species |
TAM | tamoxifen |
TMRM | tetramethylrhodamine methyl ester |
PST and similar compounds have been shown to have anti-cancer properties11-15,21. We have previously reported natural PST to destabilize the mitochondria selectively in cancer cells, which thereby induces apoptosis by the release of apoptogenic factors12,14. It is most likely that JCTH-4 acts through the same mechanism; JCTH-4 caused MMP collapse in MCF7 cells as seen with TMRM staining (Fig. 5a), and increased generation of ROS in isolated mitochondria from SH-SY5Y cells (Fig. 5b), indicative of mitochondrial dysfunction. Thus, induction of apoptosis by JCTH-4 is most probably through mitochondrial targeting in cancer cells.
Numerous differences exist between noncancerous and cancer cells which could serve as the basis for cancer selectivity by JCTH-4. Cancer cells are highly dependent on glycolysis and less on mitochondria for energy production; this phenomenon is referred to as the Warburg effect22. Such metabolic activity in the cancer cells leads to high acidity in the cytosol. Consequently, the acidic cytosolic environment contributes cancer cell mitochondria hyperpolarization which has been linked to an enhanced ability to invade and evade apoptosis23. Hyperpolariztion of cancer cell mitochondria however, may render cancer cells vulnerable to JCTH-4; once taken into the cell, JCTH-4 may acquire a positive charge through enzymatic processing and may selectively be taken up into cancer cell mitochondria due to their hyperpolarized nature. Moreover, an array of mitochondria associated antiapoptotic proteins have been shown to be highly expressed in cancer cells that prohibit mitochondrial membrane permeabilization and subsequent execution of apoptosis such as antiapoptotic proteins of the Bcl-2 family of proteins24-26.
In the presence of various forms of cellular stress, autophagy is triggered as a pro-survival response, allowing cells to survive under unfavourable conditions2. Over stimulation of this pathway however, can lead to extensive breakdown of vital intracellular components giving rise to autophagic cell death3. Both the pro-survival and pro-death autophagic responses have been associated to chemotherapeutic insult3. Mitochondrial dysfunction by JCTH-4 leading to oxidative stress could trigger an automatic default autophagic response. Indeed we did observe some autophagic induction along with apoptosis with JCTH-4 treatment (Fig. 2a, b 3a, b 6a, b). Although TAM has been well established as an ER antagonist in ER positive breast cancer cells, it has been recently shown to interact with the mitochondria, binding to the FMN site of Complex I10. Furthermore, TAM is a well-known inducer of autophagy across many cancer cell types3. Indeed, TAM did cause an increase in ROS generation in isolated mitochondria (Fig. 5b). However, such interaction proved to be insufficient to cause MMP collapse (Fig. 5a), but sufficient to induce a typical pro-survival autophagic response. Extensive autophagic induction was observed when JCTH-4 and TAM were used in combination (Fig. 6a, b), which was accompanied by an enhanced cytotoxic response (Fig. 4a, b), suggestive of a pro-death autophagic response; nonetheless, the cancer cells eventually die from apoptosis as a result of mitochondrial permeabilization and apoptogenic factor release. Such sensitization by TAM to JCTH-4 insult may be attributed to the increase in ROS generation by TAM. Because both TAM and JCTH-4 are able to generate oxidative stress, the combinatorial production of such stress with both compounds may lead to extensive autophagic induction giving rise to a detrimental autophagic response and/or extensive mitochondrial permeabilization and subsequent apoptosis. This combined treatment does not affect viability of noncancerous fibroblasts (Fig. 4c). These findings indicate that JCTH-4 alone and in combination with TAM can be used efficiently to treat breast cancer and neuroblastoma without causing adverse effects on noncancerous cells.
The authors have nothing to disclose.
This work has been supported by the Knights of Columbus Chapter 9671 (Windsor, Ontario), and a CIHR Frederick Banting and Charles Best Canada Graduate Scholarship awarded to Dennis Ma. Thank you to Robert Hodge and Elizabeth Fidalgo da Silva for their assistance with the time-lapse microscopy. Thank you to Katie Facecchia for editing the time-lapse microscopy videos. We would also like to thank Sudipa June Chatterjee and Phillip Tremblay for the critical review of this manuscript. This work is dedicated in memory of Kevin Couvillon who lost his battle against cancer in 2010.
Material Name | Company | Catalogue number |
SH-SY5Y cell line | ATCC | CRL-2266 |
Dulbecco’s Modified Eagles Medium F-12 HAM | Sigma-Aldrich | 51448C |
Fetal bovine serum | Gibco BRL | 16000-044 |
MCF7 cell line | ATCC | HTB-22 |
RPMI-1640 medium | Sigma-Aldrich | R 0883 |
Apparently normal human fetal fibroblast cell line (NFF) | Coriell Institute for Medical Research | AG04431B |
Dulbecco’s Modified Eagle’s Medium, High Glucose medium | Thermo Scientific | SH30022.01 |
Tamoxifen citrate salt | Sigma-Aldrich | T9262 |
35 mm glass bottom culture dishes | MatTek | P35G-014-C |
Leica DMI6000 B inverted microscope | Leica Microsystems | N/A |
Hoechst 33342 dye | Molecular Probes | H3570 |
Leica DM IRB inverted fluorescence microscope | Leica Microsystems | N/A |
Annexin V AlexaFluor-488 | Invitrogen | A13201 |
Trypan Blue solution | Sigma-Aldrich | T8154-20ML |
Haemocytometer | Fisher Scientific | 267110 |
WST-1 reagent | Roche Applied Science | 11644807001 |
Wallac Victor3 1420 Multilabel Counter | PerkinElmer | 1420-011 |
Tetramethylrhodamine methyl ester (TMRM) | Gibco BRL | T-668 |
Glass tissue grinder | Fisher Scientific | K8885300-0002 |
BioRad protein assay | Bio-Rad Laboratories | 500-0001Bottom of Form |
Amplex Red | Invitrogen | A12222 |
Horseradish peroxidase (HRP) | Sigma-Aldrich | P8125 |
SpectraMax Gemini XPS | Molecular Devices | 3126666 |
Anti-LC3 antibody raised in rabbit | Novus Biologicals | NB100-2220 |
Anti-mouse HRP-conjugated secondary antibody | Abcam | ab6728 |
Anti-rabbit HRP-conjugated secondary antibody | Abcam | ab6802 |
Chemiluminescence peroxidase substrate | Sigma-Aldrich | CPS160 |
Monodansylcadaverine | Sigma-Aldrich | 30432 |