1 Gabriella Aviello,1 Stefania Petrosino,2,3 Pierangelo Orlando,4Giovanni Marsicano,5,6,9 Beat Lutz,5,6 Francesca Borrelli,1 Raffaele Capasso,1 Santosh Nigam,7,8 Francesco Capasso,1 Vincenzo Di Marzo,2 and Endocannabinoid Research GroupAbstract
Colorectal cancer is an increasingly important cause of death in Western countries. Endocannabinoids inhibit colorectal carcinoma cell proliferation in vitro. In this paper, we investigated the involvement of endocannabinoids on the formation of aberrant crypt foci (ACF, earliest preneoplastic lesions) in the colon mouse in vivo. ACF were induced by azoxymethane (AOM); fatty acid amide hydrolase (FAAH) and cannabinoid receptor messenger ribonucleic acid (mRNA) levels were analyzed by the quantitative reverse transcription polymerase chain reaction (RT-PCR); endocannabinoid levels were measured by liquid chromatography–mass spectrometry; caspase-3 and caspase-9 expressions were measured by Western blot analysis. Colonic ACF formation after AOM administration was associated with increased levels of 2-arachidonoylglycerol (with no changes in FAAH and cannabinoid receptor mRNA levels) and reduction in cleaved caspase-3 and caspase-9 expression. The FAAH inhibitor N-arachidonoylserotonin increased colon endocannabinoid levels, reduced ACF formation, and partially normalized cleaved caspase-3 (but not caspase-9) expression. Notably, N-arachidonoylserotonin completely prevented the formation of ACF with four or more crypts, which have been show to be best correlated with final tumor incidence. The effect of N-arachidonoylserotonin on ACF formation was mimicked by the cannabinoid receptor agonist HU-210. No differences in ACF formation were observed between CB1 receptor-deficient and wild-type mice. It is concluded that pharmacological enhancement of endocannabinoid levels (through inhibition of endocannabinoid hydrolysis) reduces the development of precancerous lesions in the mouse colon. The protective effect appears to involve caspase-3 (but not caspase-9) activation.
Introduction
Colon cancer remains a leading cause of death because of cancer in the Western countries; the cumulative lifetime risk of developing colorectal cancer is approximately 5–6% [1]. Development of colon cancer is a multistep process involving a series of pathological alterations ranging from discrete microscopic mucosal lesions, like aberrant crypt foci (ACF), to malignant tumors [2]. ACF are early focal lesions of the colonic mucosa composed of one to several enlarged crypts, which are specifically induced by colon carcinogens [3]. Easily identified in methylene blue-stained whole-mount preparations under a dissecting microscope, ACF are used as early indicators of colon carcinogenesis [1–3].
Cannabinoids have been licensed for clinical use as palliative treatment of chemotherapy, but increasing evidence shows antitumor actions of cannabinoid agonists on several tumor cells in vitro and in animal models [4, 5]. The main psychotropic cannabinoid is Δ9-tetrahydrocannabinol, which exerts its biological effects mainly by activating two G protein-coupled cannabinoid receptors, named CB1 and CB2 receptors [5]. Endogenous ligands for the cannabinoid receptors have been identified; the best known are arachidonylethanolamide (anandamide) and 2-arachidonoylglycerol (2-AG) [4–6]. When released, anandamide and 2-AG are removed from extracellular compartments by a carrier-mediated reuptake process, and once within the cell, both endocannabinoids are hydrolyzed by intracellular hydrolytic enzymes of which the enzyme fatty acid amide hydrolase (FAAH) is capable of recognizing both compounds as substrates [5, 6].
The proposed mechanisms of the antitumoral effect of cannabinoids are complex and may involve induction of apoptosis in tumor cells, antiproliferative actions, and an antimetastatic effects through inhibition of angiogenesis and tumor cell migration [6]. Concerning the gastrointestinal tract, it has been shown that cannabinoid receptor agonists, mostly via CB1activation, potently inhibit the cell proliferation of colorectal carcinoma cell lines [7]. Furthermore, compounds capable of inhibiting endocannabinoid degradation and hence of prolonging the lifespan of endocannabinoids only when and where these compounds are produced to exert physiological or pathophysiological functions also inhibit colorectal carcinoma growth in vitro [7]. Finally, in a study performed on SW480 colon carcinoma cells, Joseph et al. [8] reported that CB1 activation by anandamide inhibited tumor cell migration, which is of paramount importance in metastasis development. However, the potential antitumoral effect of cannabinoids, endocannabinoids, and drugs that pharmacologically manipulate endocannabinoid levels and action in the gastrointestinal tract has never been explored in vivo.
Because CB1 receptor activation results in inhibition of colorectal cell proliferation in vitro [7], we investigated here the role of these receptors in the formation of ACF in vivo by using CB1 receptor-deficient mice. In addition, in pharmacological experiments, we also evaluated the effect of drugs that are known to increase endocannabinoid levels in the gastrointestinal tract (i.e., the FAAH inhibitor N-arachidonoylserotonin [AA-5-HT] and the endocannabinoid reuptake inhibitor VDM11 [(all Z) N-(2-methyl-3-hydroxy-phenyl)-5,8,11,14-eicosa-tetraenamide]), as well as the effect of the ultrapotent cannabinoid CB1/CB2 receptor agonist, HU-210, on the formation of ACF in the mouse colon in vivo. We also evaluated, by quantitative reverse transcription polymerase chain reaction (RT-PCR), the degree of expression of the messenger ribonucleic acids (mRNAs) encoding for the components of the endogenous cannabinoid system (i.e., CB1 receptor, CB2 receptor, transient receptor potential vanilloid type 1 [TRPV1], FAAH), which have been implicated in cell proliferation and/or apoptosis [4–6]. Finally, because cannabinoids might exert antitumor actions by counteracting caspase activation in tumor cells [4–6], we evaluated the expression of caspase-3 and caspase-9 by Western blot analysis. ACF were induced by the genotoxic chemical azoxymethane (AOM) [9].
Materials and methods
Animals
Experiments were performed on female 5-week-old C57BL/6N mice (Harlan Italy, Corezzana, MI; 20–22 g). In some experiments, female mice lacking the CB1 receptor gene, generated and genotyped as previously described [10], were used. Mutant mice were in a mixed genetic background with a predominance of C57BL/6N contribution (five backcrosses for both mutant lines). Mice were fed ad libitum with standard mouse food, except for the 12-h period immediately preceding the killing of the animals. All experiments complied with the Italian D.L. no. 116 of 27 January 1992 and associated guidelines in the European Communities Council Directive of 24 November 1986 (86/609/ECC).
Treatments
Mice were randomly divided into six groups as follows. Group 1 was treated with vehicles; group 2 was treated with AOM plus the vehicle used to dissolve cannabinoid drugs; group 3 was treated with AOM plus the FAAH inhibitor AA-5-HT (5 mg/kg); group 4 was treated with AOM plus the anandamide transporter inhibitor VDM11 (5 mg/kg); group 5 was treated with AOM plus the cannabinoid receptor agonist HU210 ((6aR)-trans-3-(1,1-dimethylheptyl)-6a,7,10,10a-tetrahydro-1-hydroxy-6,6-dimethyl-6H-dibenzo[b,d]pyran-9-methanol; 0.1 mg/kg). In another series of experiments, AOM was given both to wild-type and to CB1 deficient mice. AOM (16 mg/kg in total, IP) was administered during the first (3 m/kg at days 1 and 5), third (3 mg/kg at days 1 and 5), and at the 17th week (2 mg/kg at days 1 and 5) of treatment.
Cannabinoid drugs were given intraperitoneally every other day for the whole duration of the experiment (starting from a week before the first injection of AOM). The doses of cannabinoids were selected on the basis of previous published work dealing with the effects of these drugs in subchronic or chronic experiments [11–13].
All animals were euthanized by asphyxiation with CO2 6 months after the first injection of AOM. Based on our laboratory experience, this time (at the dose of AOM used) was associated with the occurrence of a significant number of ACF.
Aberrant crypt foci technique
For ACF determination, the colons were rapidly removed after killing, washed with saline, opened longitudinally, laid flat on a polystyrene board, and fixed with 10% buffered formaldehyde solution before being stained with 0.2% methylene blue in saline. The colons were examined using a light microscope at 40× magnification. Aberrant crypts were identified as previously described [9]. Briefly, in comparison to normal crypts, aberrant crypts have greater size, larger and often elongated openings, thicker lining of epithelial cells, compression of adjacent crypts, and are more darkly stained with methylene blue. According to the number of constituent crypt, ACF were divided into two groups: small ACF containing one to three crypts per focus and large ACF containing four or more crypts per focus. To determine crypt multiplicity, the number of aberrant crypts in each focus was recorded.
Identification and quantification of endocannabinoids and palmitoylethanolamide
Full-thickness colons from control and AOM-treated mice (in the presence or absence of AA-5-HT 5 mg/kg) were removed (6 months after the first injection of AOM), and tissue specimens were immediately weighed, immersed into liquid nitrogen, and stored at −70°C until extraction of endocannabinoids. Tissues were extracted with chloroform/methanol (2:1, by volume) containing each 200 pmol of d8-anandamide, d4-palmitoylethanolamide, and d5-2-AG, synthesized as described previously (for the former two compounds) [14], or provided by Cayman Chemicals (for d5-2-AG, AnnArbor, MI). The lipid extracts were purified by silica column chromatography and carried out as described previously [14], and the fractions containing anandamide, palmitoylethanolamide, and 2-AG were analyzed by isotope dilution liquid chromatography–atmospheric pressure–chemical ionization mass spectrometry carried out in the selected monitoring mode as described in detail elsewhere [10, 14]. Results were expressed as picomoles or nanomoles per milligram of extracted lipids.
Western blot analysis
Full-thickness colons from control and AOM-treated (6 months after the first injection of AOM) mice (in the presence or absence of AA-5-HT 5 mg/kg) were homogenized in lysis buffer (1:2 w/v) containing 0.5 M β-glycerophosphate, 20 mM MgCl2, 10 mM ethylene glycol tetraacetic acid, and supplemented with 100 mM dithiothreitol and protease/phosphatase inhibitors (100 mM dimethylsulfonyl fluoride, 2 mg/ml apronitin, 2 mM leupeptin, and 10 mM Na3VO4). Homogenates were centrifuged at 3,000 rpm for 5 min at 4°C; the supernatants were collected and recentrifuged at 12,000 rpm for 10 min at 4°C. Protein concentrations were determined using the method of Bradford [15]. For Western blot analysis, lysate aliquots containing 50 μg of proteins were denatured, separated on a 12% sodium dodecyl sulfate–polyacrylamide gel, and transferred to a nitrocellulose membrane (Amersham, Biosciences, UK) using a Bio-Rad Transblot (350 mA for 3 h). Proteins were visualized on the filters by reversible staining with Ponceau-S solution (Sigma, Milan, Italy) and destained in phosphate-buffered saline (PBS). Membranes were blocked at 4°C in milk buffer (5% nonfat dry milk in PBS 1×/Tween 0.1%) and then incubated overnight at 4°C with polyclonal antibodies for caspase-3 and caspase-9 (Calbiochem from VWR International, Italy). The rabbit polyclonal anti-caspase-3 and anti-caspase-9 were used at 1:1,000 dilution in milk buffer (5% nonfat dry milk in PBS 1×/Tween 0.1%). Subsequently, the membranes were incubated for 1 h at room temperature with 1:2,000 anti-rabbit IgG–horseradish peroxidase-conjugated secondary antibodies (Amersham Biosciences, UK). After washing with PBS 1×/Tween 0.1%, the membranes were analyzed by enhanced chemiluminescence (Amersham Biosciences). The optical density of the bands on autoradiographic films was determined by an image analysis system (GS 700 Imaging Densitometer, Bio-Rad) equipped with a software Molecular Analyst (IBM). After stripping, the membranes were probed with anti-α-tubulin antibody, to normalize the results.
Quantitative (real-time) RT PCR analysis
Full-thickness colons from control and AOM-treated (6 months after the first injection of AOM) mice were homogenized in 1 ml of Trizol® (Invitrogen). Total RNA was extracted according to manufacturer recommendations, dissolved in RNA storage solution (Ambion), UV quantified by a Bio-Photometer® (Eppendorf), and stored to −80°C. RNA aliquots (6 μg) were digested by RNAse-free DNAse I (Ambion deoxyribonucleic acid [DNA]-free™ kit) in a 20-μl final volume reaction mixture, to remove contaminating genomic DNA. After DNAse digestion, concentration and purity of RNA samples were evaluated by the RNA-6000-Nano® microchip assay, using a 2100 Bioanalyzer® equipped with a 2100-Expert-Software® (Agilent), following the manufacturer instructions. For all samples tested, the RNA integrity number was greater than 6 (relatively to a 0–10 scale). Three micrograms of total RNA, as evaluated by the 2100 Bioanalyzer, was reverse transcribed in a 25-μl reaction mixture containing: 50 mM Tris–HCl pH 8.3, 75 mM KCl, 3 mM MgCl2, 10 mM dithiothreitol, 1 mM deoxyribonucleotide triphosphates, 20 U of RNAse inhibitor (Invitrogen), 0.125 A260 units of hexanucleotide mixture (Invitrogen) for random priming and 200 U of MoMuLV Superscript® III reverse transcriptase (Invitrogen). The reaction mixture was incubated in a termocycler iCycler-iQ® for a 5 min at a 55°C step, followed by a rapid chilling for 2 min at 4°C. The protocol was stopped at this step and the MoMuLV reverse transcriptase was added to the samples, excepting the negative controls (−RT). The incubation was resumed by two thermal steps: 10 min at 20°C followed by 90 min at 50°C. Finally, the reaction was terminated by heating at 95°C for 10 min. Quantitative real-time PCR was performed by an iCycler-iQ® in a 25-μl reaction mixture containing: 1× iQ-SYBR®-Green-Supermix (Bio-Rad), 20 ng of complementary DNA (cDNA; calculated on the basis of the retro-transcribed RNA), and 330 nM for each primer. The amplification profile consisted of an initial denaturation of 2 min at 94°C and 40 cycles of 30 s at 94°C, annealing for 30 s at optimum annealing temperature (TaOpt, see below) and elongation for 45 s at 68°C. Fluorescence data were collected during the elongation step. A final extension of 7 min was carried out at 72°C, followed by melt-curve data analysis. Optimized primers for SYBR®-Green analysis (and relative TaOpt) were designed by the Beacon-Designer® software 6.0 version (Biosoft International, Palo Alto, CA) and were synthesized (high-performance liquid chromatography purification grade) by MWG-Biotech AG, Germany. Assays were performed in quadruplicate (maximum ΔCt of replicate samples less than 0.5), and a standard curve from consecutive fivefold dilutions (100 to 0.16 ng) of a cDNA pool representative of all samples was included, for PCR efficiency determination. Relative expression analysis, correct for PCR efficiency and normalized with respect to reference genes β-actin and glyceraldehyde-3-phosphate dehydrogenase (GADPH), was performed by GENEX software (Bio-Rad) for groupwise comparison and statistical analysis.
Drugs
AOM and HU210 were purchased from Sigma and Tocris Cookson (Bristol, UK), respectively. AA-5-HT and VDM11 were synthesized as described previously [16, 17]. All drugs (with the exception of AOM, which was dissolved in saline) were first dissolved in dimethylsulfoxide (DMSO) and then suspended in a lipophilic solution (Peceol/Gelucire 44/14, gift from Indena, Milan, Italy; 0.4% DMSO, 96.6% lipophilic solution). The drug vehicle (2.5 ml/kg) had no effect on the response under study.
Statistics
Data are expressed as the mean ± SEM. To determine statistical significance, analysis of varance followed by the Dunnett’s (or Bonferroni’s for endocannabinoid levels) test was used.
Results
Aberrant crypt foci formation
The total number of ACF/mouse and number of ACF/mouse with four or more crypts observed after 6 months of treatment with cannabinoid drugs in either the presence or absence of AOM treatment are shown in Table 1. AOM given alone induced the appearance of ACF in all the animals. The average number of ACF for each mouse was 12.8 ± 2.4 (0.57 ± 0.20 ACF with four or more crypts). The FAAH inhibitor AA-5-HT as well as the cannabinoid receptor agonist HU210 significantly reduced the total number of ACF/mouse and completely prevented the formation of ACF with four or more crypts in all animals. The anandamide reuptake inhibitor VDM11 showed a nonsignificant trend at reducing the total number of ACF/mouse and the number of ACF with four or more crypts.
Table 2 shows the result of experiments performed in wild-type and CB1-deficient mice. In this series of experiments, the total number of ACF/mouse and number of ACF/mouse with four or more crypts did not change significantly between the two groups of animals.
Endocannabinoid and palmitoylethanolamide content in the colon
Endocannabinoid and palmitoylethanolamide content in full-thickness colons of control and AOM-treated mice is shown in Table 3. AOM treatment significantly increased the levels of 2-AG and induced a nonsignificant trend to increase the levels of anandamide and palmitoylethanolamide. The FAAH inhibitor AA-5-HT further increased 2-AG content and significantly increased anandamide (but not palmitoylethanolamide) levels in AOM-treated mice. A nonsignificant trend to increase anandamide levels was observed also in AOM-treated mice treated with the anandamide cellular reuptake inhibitor VDM11.
Evaluation of CB1, CB2, FAAH, and TRPV1 mRNA levels by quantitative RT-PCR
The relative expression analysis, evaluated by quantitative RT-PCR, of CB1, CB2, FAAH, and TRPV1 mRNA in full-thickness colons from AOM-treated mice and controls, is depicted in Fig. 1. All targets were well detectable in the linearity range of analysis (CB1, mean cycle threshold = 26.5; CB2, mean cycle threshold = 26; FAAH, mean cycle threshold = 18; TRPV1, mean cycle threshold = 30; β-actin, mean cycle threshold = 16.5; GADPH, mean cycle threshold = 24.5). The amplification reaction efficiencies were comparable, ranging from 96 to 108%. Colon samples showed elevated expression (relatively to the other targets and to the housekeeping genes) of FAAH, thus confirming the relevant role of this enzyme in the digestive tract [18, 19], although no variation of expression levels in colon samples from AOM-treated mice and controls was observed. Likewise, no variation of CB1 and CB2expression levels was detected. On the contrary, a significant decrease (about fourfold) of TPRV1 expression was observed in colon samples of AOM-treated mice.
Expression of activated caspase-3 and caspase-9 on colon of AOM-treated mice
AOM significantly (p < 0.001) reduced the cleavage of the p34 precursor of caspases-3 into its p17 active fragment and the p46 precursor of caspases-9 into its p34 active fragment in full-thickness colons (Fig. 2a and b). Treatment with AA-5-HT significantly reduced the effect of AOM on the expression of the activated caspase-3 but not on the expression of the activated caspases-9 (Fig. 2a and b).
Discussion
ACF are believed to be the earliest identifiable neoplastic lesions in the colon carcinogenetic model [1–3, 20]. They exhibit a number of molecular mutations in regulatory genes consonant with the development of human colon cancer, most notably in the ras oncogene and antigen-presenting cell tumor suppressor gene [20]. In comparison to normal crypts, ACF have greater size, larger and often elongated openings, thicker lining of epithelial cells, compression of adjacent crypts, and are more darkly stained with methylene blue [1–3, 20]. Recent studies also suggest that ACF are precursors of colon cancer in humans, and this further stimulates the need to identify drugs that may prevent their progression [1–3, 20]. Our findings indicate that the blockade of endocannabinoid enzymatic degradation protects against ACF formation.
FAAH is a membrane-associated protein responsible of the degradation of endocannabinoids anandamide and 2-AG [21]. Mice lacking FAAH are severely impaired in their ability to degrade anandamide and, when treated with this endocannabinoid, exhibit an array of intense CB1-dependent behavioral responses, including hypomotility, analgesia, catalepsy, and hypothermia [22]. In the digestive tract, FAAH inhibition results in reduction in intestinal motility [23] and anti-inflammatory effects in vivo [12, 24]. Furthermore, FAAH knockout results in lower sensitivity to the proinflammatory agent dinitrobenzene sulfonic acid (DNBS) [12]. The anti-inflammatory role of FAAH is relevant in the light of the observation that inflammation plays an important role in colon carcinogenesis [25]. In this paper, we have shown that a 6-month treatment with AA-5-HT, a selective FAAH inhibitor, strongly reduces the formation of ACF in the mouse colon and completely prevented the number of ACF with crypt multiplicity of greater than or equal to 4. The significant reduction in the number of ACF with four or more crypts is relevant in the light of previous reports in which larger crypts were found to be best correlated with final tumor incidence [1–3, 20]. We believe that the effect of AA-5-HT is due to FAAH inhibition and not to nonspecific effects or interactions with cannabinoid receptors for the following reasons: (1) AA-5-HT administration increased the levels of anandamide and 2-AG in the colon of mice treated with AOM, similar to that previously observed in the small intestine of healthy mice after acute intraperitoneal administration [23] or in the colon or DNBS-treated mice after repeated intraperitoneal administration [24] with this compound; (2) AA-5-HT displays little or no affinity for cannabinoid receptors [16]; (3) AA-5-HT exerted protective effects in the present study at a dose (5 mg/kg) previously shown to be inactive in the “open field,” “hot plate,” and rectal hypothermia tests, which are predictive of CB1 activation in rodents [16]; (4) AA-5-HT was also previously found to be ineffective against anandamide cellular reuptake [16], a mechanism that, however, does not seem to be involved in the control of ACF formation, as VDM11, a selective inhibitor of anandamide cellular uptake, did not significantly affect ACF formation in the present study. The dose of VDM11 used in the present experiments was found to enhance rat hippocampal and mouse brain endocannabinoid levels and to exert neuroprotective effects when administered (intraperitoneally) subchronically every other day (as in our experimental conditions) [26]. Consistent with our results, it was previously shown that chronic administration of AA-5-HT (injected intratumor) inhibits the growth of K-ras-transformed rat thyroid cells in athymic mice in vivo [26]. More relevant to our present findings, AA-5-HT was also previously shown to inhibit the proliferation of human colorectal carcinoma cells in vitro in a way attenuated by CB1 receptor blockade, while increasing cell endocannabinoid levels [7]. However, in these two previous studies and unlike our present findings, VDM11 was also found to exert antitumor effects both in vivo (albeit injected intratumor) and in vitro.
The formation of ACF in mice after treatment with AOM was associated per se to an increase in intestinal 2-AG levels, with a trend toward the increase in anandamide levels too. It should be noted that we performed endocannabinoid assay on full-thickness segments, and thus the cell type responsible of 2-AG overproduction is presently unknown. However, it is likely that these variations reflects changes occurring in mucosal cells, as ACF are located on the mucosa of the intestine [2, 3]. No changes were observed, instead, in the expression of cannabinoid CB1 and CB2 receptors, as assessed by quantitative real-time PCR. This finding is consistent with human studies, which showed increased levels of endocannabinoids but not of cannabinoid receptors, in the mucosa of colorectal adenomatous polyps and carcinomas [7]. It is likely that the enhanced 2-AG levels in the gut exert protective effects on colon carcinogenesis for the following reasons: (1) Pharmacological blockade of endocannabinoid degradation and subsequent elevation of both 2-AG and anandamide levels results in a reduction in preneoplastic lesions (see above); (2) anandamide and 2-AG potently inhibit the proliferation of colorectal carcinoma cells [7]; (3) the protective effect of AA-5-HT on ACF formation observed here was mimicked by the synthetic cannabinoid receptor agonist HU210; we used HU210 rather than endocannabinoids because of its pharmacokinetic properties (i.e., longer half-life of HU210 as opposed to the high metabolic instability of both anandamide and 2-AG). On these bases, we speculate that the administration of AOM in animals increases 2-AG levels, which, in turn, exerts protective effects. A likely target of 2-AG is the cannabinoid CB2 receptor, whose stimulation is known to exert proapoptotic effects [27, 28] and to mediate antiproliferative effects on human colorectal carcinoma cell lines [7]. It is unlikely that 2-AG could act on cannabinoid CB1 receptors to mediate protective effects because in the present study we have observed no statistical differences in ACF formation between CB1-deficient and wild-type mice. Others have found that systemic or local treatment with cannabinoids inhibited the growth of various types of tumor or tumor cell xenografts in vivo, including lung carcinoma, glioma, thyroid epithelioma, lymphoma, breast carcinoma, and skin carcinoma in mice, via both CB1- and CB2-mediated pathways as well as through noncannabinoid receptor mechanisms [4–6, 29–30], including cyclooxygenase-2 in colorectal carcinoma cells [31]. It is interesting to note that a recent study showed that chronic oral administration to rats of the antiobesity drug orlistat, which is a very potent inhibitor of 2-AG biosynthesis [32], causes increased formation of ACF in rats [33]. This finding might be interpreted in the light of our present results, by hypothesizing that orlistat, by inhibiting 2-AG formation in the rat colon, might counteract the protection against ACF formation exerted by this endocannabinoid. We did not test the involvement of TRPV1 receptors, which have been proposed as an alternative target for anandamide in the gut under pathological conditions [34], because we found a significant increase only in the levels of 2-AG, which, in contrast to anandamide, does not activate TRPV1 receptors [5, 6].
Caspases, a group of cysteine proteases, play an essential role in programmed cell death [35, 36]. They convey the apoptotic signal in a proteolytic cascade, by cleaving and activating other enzymes that subsequently degrade cellular targets that lead to cell death. The initiator caspases include caspase-8 and caspase-9 [35, 36]. Caspase-8 is activated in response to receptors with a death domain that interacts with the fas-associated death domain (extrinsic pathway), whereas the activation of caspase-9 is a consequence of cytochrome c and apoptosis-activating factor 1 interaction with AP-1 (intrinsic pathway) [35, 36]. Both initiators lead to the activation of the final effector caspase-3, which cleaves and inactivates several vital cellular proteins (e.g., DNA repair enzymes) involved in cancer cell life [35, 36]. It has been experimentally demonstrated that during colorectal cancer formation, there is an increased cell proliferation correlated with a reduction in apoposis [37]. In agreement with a reduction in apoptosis in colon cancer [38], we have shown here that AOM treatment reduces the expression of the activated caspase-3 and caspase-9 in full-thickness colons. More importantly, treatment with the FAAH inhibitor AA-5-HT partially reversed the AOM effect on caspase-3, suggesting that the activation of this caspase isoform is involved in AA-5-HT-induced inhibition of ACF formation. Therefore, our data allow us to suggest that whatever their exact molecular target(s), pharmacologically elevated endocannabinoids reduce ACF formation via proapoptotic effects. It is very likely that the intrinsic pathway is not involved in these effects, as AA-5-HT did not affect the reduction in expression of activated caspase-9 observed in the colon of AOM-treated animals. In other experimental studies, it has been observed that cannabinoids induce apoptosis in other types of cancer with involvement of extrinsic or intrinsic pathways or both [4–6, 29].
In summary, the present study provides strong evidence that enhancement of colon endocannabinoid levels through pharmacological inhibition of their enzymatic hydrolysis may be protective against preneoplastic lesions in the mouse colon; a condition that, like humans adenomatous polyps and colorectal carcinoma [7], is accompanied by an elevated endocannabinoid tone. This protective effect could be due to indirect activation of one or more of the several targets proposed to date for the endocannabinoids and appears to involve caspase-3 activation and subsequent apoptosis of colon preneoplastic cells. Further studies will be required to investigate if cannabinoid CB2receptors are involved in the protective effects of AA-5-HT and HU210 and if these effects have any therapeutic relevance for the treatment of human colon carcinoma.
Acknowledgments
This work was supported by Prin, Enrico and Enrica Sovena Foundation, Regione Campania, Epitech, S.r.l. (to SP and VDM).
Competing interests The Authors declare no competing interests.
Abbreviations
| AA-5-HT | N-arachidonoylserotonin, |
| ACF | aberrant crypt foci, |
| anandamide | arachidonylethanolamide, |
| AOM | azoxymethane, |
| 2-AG | 2-arachidonylglycerol, |
| DMSO | dimethylsulfoxide; |
| FAAH | fatty acid amide hydrolase, |
| HU-210 | [(6aR)-trans-3-(1,1–dimethylheptyl)-6a,7,10,10a-tetrahydro-1-hydroxy-6,6-dimethyl-6H-dibenzo[b,d] pyran-9-methanol], |
| RT-PCR | reverse transcription polymerase chain reaction, |
| TRPV1 | transient receptor potential vanilloid type 1 |
Biographies
Footnotes
Angelo A. Izzo and Gabriella Aviello equally contributed to this work.
Angelo A. Izzo, Gabriella Aviello, Stefania Petrosino, Pierangelo Orlando, Francesca Borrelli, Raffaele Capasso, Francesco Capasso, and Vincenzo Di Marzo are part of the Endocannabinoid Research Group.
Contributor Information
Angelo A. Izzo, Fax: +39-081-678403, Email: ti.aninu@ozziaa.
Vincenzo Di Marzo, Fax: +39-081-8041770, Email: ti.rnc.an.bimci@ozramidv.
References
