Opioids: Modulators of angiogenesis in wound healing and cancer
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Martina Ondrovics1, Andrea Hoelbl-Kovacic1 and Daniela Alexandra Fux1
1 Department for Biomedical Sciences, Institute of Pharmacology and Toxicology, University of Veterinary Medicine Vienna, Veterinaerplatz, Vienna, Austria
Daniela Alexandra Fux, email:
Keywords: opioids, angiogenesis, signaling mechanisms, tumor vascularization, wound healing
Received: December 01, 2016 Accepted: February 07, 2017 Published: February 16, 2017
Opioids are potent drugs that are widely used to control wound or cancer pain. Increasing evidence suggest that opioids mediate clinically relevant effects that go beyond their classical role as analgesics. Of note, opioids appear to modulate angiogenesis - a process that is critical in wound healing and cancer progression. In this review, we focus on pro- and anti-angiogenic facets of opioids that arise from the activation of individual opioid receptors and the usage of individual concentrations or application routes. We overview the still incompletely elucidated mechanisms of these angiogenic opioid actions. Moreover, we describe plausible opioids effects, which - although not primarily studied in the context of vessel formation - may be related to the opioid-driven processes of angiogenesis. Finally we discuss the use of opioids as an innovative therapeutic avenue for the treatment of chronic wounds and cancer.
Angiogenesis is the formation of new blood vessel out of pre-existing ones and includes endothelial cell activation, proliferation and chemotactic-driven migration. Angiogenesis has a pivotal role in embryonic development and growth , whereas desired and undesired effects are seen in adults. Beneficial effects of angiogenesis include efficient wound healing and the rescue of ischemic myocardium at early stages after myocardial infarction [2, 3]. Detrimental effects of angiogenesis appear in pathological processes such as macular degeneration, retinopathy, tumor growth, and metastasis [4-6].
Over recent years, the evidence has grown that opioids exceed their primarily known function as analgesic drugs and modulate wound healing and tumor progression [7, 8]. Opioids significantly influence wound closure or tumor growth by acting on endothelial cells and controlling angiogenesis. The review outlines the current knowledge of opioids’ action on angiogenic processes and discusses the potential exploitation of these effects for clinical use.
The opioid system and its role in angiogenesis
The endogenous opioid system represents a pivotal part of the innate central pain-relieving systems, which is operated by different opioid ligands and opioid receptors. Opioids are divided into “endogenous” and “exogenous” opiates, all having a potent analgesic effect. Endogenous opiates (Endorphins), such as beta-endorphin, Met-enkephalin, the endomorphins and the dynorphins are peptide hormones, which are generated in neurons of the nociceptive system and are released in pain and stress situations; exogenous opiates are non-peptidergic opioid receptor agonists. Prominent members of exogenous opiates are morphine, an alkaloid isolated from the poppy plant Papaver somniferum, and its semi-synthetic derivatives such as fentanyl, buprenorphine and oxycodone - classical analgesic drugs in clinical use [9, 10].
Opioid receptors belong to the family of G-protein coupled receptors (GPCRs) and are highly expressed in pain-modulating neurons of the central nervous system. Based on individual protein sequences and ligand selectivity, different opioid receptors can be distinguished. Besides the classical mu (µ-), delta (δ-) and kappa (κ-) opioid receptor types (further termed MOR, DOR and KOR), the opioid receptor family further includes the zeta (ζ-) receptor, also known as the Met-enkephalin receptor/opioid growth factor (OGF) receptor (further termed OGFR), and the nociception/orphanin stimulated FQ opioid-receptor like 1 (NOPr/ORL1) [11, 12]. Activation of opioid receptors initiates various intracellular signaling cascades which leads to the inhibition of adenylyl cyclase activity, modulation of ion conductance, transactivation of receptor tyrosine kinases, stimulation of phospholipase C, PI3K/AKT and the ras/raf/ERK1/2 signaling module [13-18]. Moreover, ligand binding also induces receptor phosphorylation, beta-arrestin recruitment and receptor internalization, which is believed to be a critical step in desensitization or termination of opioid receptor signaling . The physiological function of neuronal opioid receptors became obvious by selective knockout of individual opioid receptor types in mice, which uncovered their special roles in nociception and mood disorders [19-22].
In recent years, opioid receptors - together with Met-enkephalin and dynorphin - were also found in endothelial cells during pre- and post-natal blood vessel development in mice and rats [23-25]. However, individual opioid receptors appear to elicit individual angiogenic effects as exemplified by the stimulation of OGFR, DOR and MOR in endothelial cells of the chorioallantoic membrane: whereas activation of OGFR by Met-enkephalin inhibits the formation of blood vessels by the opioid-exposed endothelial cells , stimulation of DOR (by Deltorphin I) or MOR (by Endomorphin-1 and -2) enhances blood vessel formation in the experimental setting . In addition, inhibition of MOR by the antagonist naltrexone unexpectedly increased vessel formation by chorioallantoic membrane endothelial cells . This finding suggests that MORs possess divergent roles in angiogenesis: whereas receptor stimulation by an opioid agonist leads to pro-angiogenic effect, the naltrexone-sensitive, constitutive (basal) receptor activity transmits anti-angiogenic effects [26, 28]. These differences may be explained by specific receptor conformations which are responsible for constitutive and agonist-induced activity of GPCRs [29, 30]. It has been shown that specific receptor conformations lead to the activation of individual G-proteins, which in turn are coupled to different intracellular signaling cascades . It is therefore attractive to speculate that the constitutive active MOR conformation is coupled to inhibitory (anti-angiogenic), whereas agonist-occupied MORs are connected to stimulatory (pro-angiogenic) signaling pathways. Although further analysis of the divergent effects is missing, these findings yet indicate that opioid receptors may transmit both pro- and anti-angiogenic effects.
Opioid effects on isolated endothelial cells
Formation of new blood vessels during angiogenesis bases on endothelial cell proliferation, migration and tube formation. These processes are tightly coordinated by pro- and anti-angiogenic factors via stimulating respective cell surface receptors and signaling pathways in endothelial cells. A variety of pro-angiogenic factors have been identified during the last decades - the Vascular Endothelial Growth Factor (VEGF-A) and its splice variants VEGF121, VEGF165, VEGF189 being most potent [32, 33]. VEGF binds to and activates the receptor tyrosine kinases VEGF receptor-1 (VEGFR-1/Flt1) and VEGFR-2 (KDR/Flk-1) , which leads to the stimulation of JNK, ERK1/2, PI3K/AKT, and focal adhesion kinases. All of these VEGF/VEGFR-driven effector molecules are well-described regulators of endothelial cell survival, proliferation, cell migration, and thus vessel neo-formation .
Stimulatory opioid effects on endothelial cells
A close interaction of the opioid system and VEGF-mediated angiogenesis is suggested by two major observations. (i) VEGF enhances the expression of MOR in endothelial cells. (ii) Morphine activates endothelial VEGF receptors including their associated signaling molecules AKT and ERK1/2 . Gupta et al.  observed that treatment of endothelial cells (HDMEC; isolated from neonatal human foreskin) with VEGF165 as well as clinically relevant concentration of morphine cause cell proliferation and tube formation. Studies on endothelial cells derived from different tissues further confirmed a causal relationship of opioids and angiogenesis: proliferation and migration of dermal microvascular and retinal endothelial cells were enhanced upon morphine treatment [36, 38]. The mode by which morphine triggers these endothelial cell reactions is currently under debate. The classical signaling via binding to opioid receptors is rather unlikely as morphine-induced proliferation and tube formation cannot be blocked by the opioid-receptor antagonist naloxone . In contrast, the endothelial morphine effects could be blocked by a VEGF receptor inhibitor . This finding leads to the suggestion that morphine activates VEGF receptors and exploits their angiogenic signaling on endothelial cells. Detailed understanding of how morphine masters VEGF receptor activation is currently lacking. Activation of VEGF receptors may arise from two different mechanisms: one is VEGF-dependent, the other one is VEGF-independent. The growth factor-dependent mechanism bases on an activation of matrix metalloproteinases, which initiate VEGF receptor transactivation by the release of extracellular matrix-bound VEGF (“outside-in mechanism”). In contrast, the VEGF-independent mechanism triggers VEGF receptor activation through phosphorylation of the receptor protein by the intracellularly localized non-receptor tyrosine kinase c-Src . The “outside-in mechanism” seems to play a minor role in morphine-induced VEGF receptor activation, as morphine was shown to prevent VEGF121 and VEGF165 release from stimulated endothelial cells . Increasing evidence in turn supports the ligand-independent activation as c-Src was shown to be activated in endothelial cells upon morphine treatment . Moreover, c-Src knock-down by siRNA prevented morphine-induced VEGF receptor activation, endothelial cell proliferation and tube formation. These findings indicate that the pro-angiogenic morphine effects result from c-Src-dependent VEGF receptor transactivation .
This finding, however, raises the next question: how does morphine stimulate c-Src? A potential candidate stimulus is the platelet-derived growth factor (PDGF-BB). PDGF-BB was found to be released from morphine-stimulated endothelial cells . Moreover, PDGF-BB is known to induce c-Src activation upon binding to PDGF receptors (PDGFR; [42, 43]. As PDGFRs were additionally found to be co-activated with VEGF receptors in morphine-treated endothelial cells , these facts suggest that morphine may induce VEGF receptor activation by stimulating the PDGF/PDGFR/c-Src signaling cascade (Figure 1). Considering the release of PDGF as the critical starting point of this scenario, it is still unclear how morphine induces this process in an opioid-receptor independent manner. It might be speculated that morphine triggers PDGF secretion by direct activation of G-proteins, which was identified to account for histamine release from morphine-stimulated mast cells . However, the regulating processes of PDGF secretion as well as the identity of 454 non-redundant putative morphine off-targets are still obscure [45, 46]. Thus, the opioid-receptor independent signaling machinery behind morphine-induced PDGF release remains an unsolved question.
Figure 1: Proposed mechanism of morphine-mediated PDGFR/VEGFR co-activation in endothelial cells. Morphine stimulates the release of PDGF-BB by an opioid-receptor-independent, yet unknown mechanism. Released PDGF-BB leads to an autocrine activation of endothelial PDGF-β receptors, which subsequently recruit and activate c-Src kinase. Stimulated c-Src kinase triggers phosphorylation and thus VEGF-independent activation of VEGF receptors (VEGFR).
Inhibitory opioid effects on endothelial cells
Opioids were also shown to inhibit the angiogenic activity of endothelial cells [47-49]. In contrast to the aforementioned opioid receptor-independent morphine effects, stimulation of two specific opioid receptors types were identified to transmit anti-angiogenic effects on isolated endothelial cells. One is the vascular-selective µ3-opioid receptor, which was found to elicit the production of lethal amounts of nitrogen oxide (NO) after stimulation by a high dose of morphine [48, 50]. NO was further proven to have a causal role in morphine-induced death of endothelial cells, as inhibition of NO synthase by L-NAME rescued cells from apoptosis. Also, naloxone prevented cells from morphine-induced apoptosis  which underlines opioid receptor-dependent stimulation of NO synthase activity may counteract the angiogenic activity of endothelial cells.
The second opioid receptor type with anti-angiogenic properties is the KOR, which was shown to impair VEGF-induced endothelial cell responses. Stimulation of KORs by U50,488H or Nalfurafine reduced VEGR expression levels in endothelial cells and significantly hampered VEGF-induced migration and tube formation . These effects were reversed by the KOR antagonist nor-BNI or siRNA-mediated KOR knock-down, indicating that the regulation of VEGF receptor expression is indeed KOR-dependent. In line, Kor knockout mice show enforced expression of VEGF receptors in endothelial cells . The causative mechanisms of these findings have not been investigated so far, but it might be envisioned that KORs affect transcription factors, promoter activity or mRNA stability controlling VEGF receptor protein expression.
Opioid effects on plug vascularization
In analogy to the conflicting results obtained from isolated endothelial cells, morphine also exerts different effects on in-vivo vessel formation, which was revealed by Matrigel plug assays. In this approach, Matrigel plugs are implanted subcutaneously into mice and monitored for vascularization that is indicative for chemotactic endothelial cell migration, proliferation and vessel formation. When morphine was incorporated into the plug matrix, plugs were significantly stronger vascularized than morphine-free controls  - suggesting morphine a chemoattractant for invading endothelial cells as it has been reported for monocytes and neutrophils . Vascularization of morphine plugs was not affected by naloxone, which suggests morphine-triggered chemotaxis does not depend on opioid receptor stimulation . The processes of chemotaxis are highly complex and involve various signaling mechanisms and pathways, which might represent potential morphine off-target. In monocytes, for instance, chemotaxis is facilitated by activated potassium channels . Interestingly, morphine was found to stimulate ATP-dependent potassium currents by an opioid-receptor independent mechanism in hepatocytes  As ATP-dependent potassium channels are also expressed in endothelial cells , morphine might be assumed to stimulate chemotaxis via direct activation of potassium currents. Nevertheless, the precise factors accounting for morphine-stimulated chemotaxis are still elusive.
In a setting where morphine was applied systemically via intraperitoneal or subcutaneous injections for a long time (chronic application), plug vascularization was impaired. In these studies, implanted plugs contained lipopolysaccharide (LPS) or the angiogenic factors VEGF and FGF. Although all of these “plug ingredients” are potent inducers of angiogenesis, plug vascularization was significantly reduced upon long-term, systemic morphine application [47, 57, 58]. Thus, systemically applied morphine seems to prevent LPS- and VEGF/FGF-mediated endothelial cell invasion and subsequent vessel formation. A first mechanistic insight was given by the finding that vascularization of VEGF plugs was restored in MOR deficient mice, which revealed the inhibitory morphine effect depends on opioid receptor stimulation . Although further insights are lacking, alternative morphine effects may be considered to enlighten the processes of impaired plug vascularization. Vascularization of Matrigel implants is facilitated by endothelial cells which are attracted and finally stimulated by a gradient of angiogenic factors. In the case of VEGF plugs, endothelial cells are directly triggered by plug-released VEGF. The activity of endothelial cells to detect and follow the VEGF gradient is enhanced by the Endothelial Cell-Specific Chemoattractant Receptor (ECSCR), also known as the Endothelial Cell-Specific Molecule 2 (ECSM2), which improves the sensitivity and responsiveness of VEGF receptors towards VEGF stimulation [59, 60]. Expression of ECSCR is increased by inflammatory processes , so that local inflammation, which arises from plug injection - as indicated by the enrichment of inflammatory immune cells in the plug transplants  - strongly supports VEGF-mediated chemotactic activity of endothelial cells. Long-term, systemically applied morphine, however, has immune suppressive and anti-inflammatory effects . It could be said that morphine affects endothelial cell chemotaxis and therefore VEGF plug vascularization through its anti-inflammatory effect, which probably hinders ECSCR expression and angiogenic signaling in endothelial cells.
Plug-released LPS triggers vessel formation by direct stimulation of the angiogenic Toll-like receptor/TRAF6 signaling pathway in endothelial cells  and by attracting and stimulating VEGF-producing macrophages . Both processes may represent hypothetical morphine targets. A recent study reported that morphine-stimulated MORs on macrophages counteract LPS-induced miR-146a expression . As miR-146a triggers VEGF synthesis , morphine-exposed macrophages may fail to provide a sufficient VEGF gradient which is required for endothelial cell chemotaxis and activation. Moreover, chronic morphine was revealed to inhibit LPS-induced activation of TRAF6 signaling in macrophages by inducing miR-124 expression . If this effect would also occur in endothelial cells, morphine could hamper LPS-stimulated vessel formation by blocking the angiogenic TRAF6 signaling in endothelial cells.
The lack of FGF-plug vascularization may be also explained by a morphine effect on an angiogenic FGF signaling partner. FGF-induced vessel formation requires the presence of integrins, which serve as direct FGF-binding receptors as well as signaling partner and enhancer of the FGF/FGF receptor signal complex . A recent study has shown that long-term treatment of mice with morphine induces a reduction of integrin expression in neurons of the spinal cord . If this morphine effect also occurs outside the central nervous system, it may be possible that impaired vascularization of FGF-plugs arises from a morphine-induced loss of integrins in angiogenic active endothelial cells.
Opioid effects on wound vascularization
Wound healing is a highly dynamic process, which requires vasodilatation, fibrin clot formation, infiltration of neutrophils, macrophages and lymphocytes, proliferation of fibroblasts, re-epithelization by stimulated keratinocytes, and tissue maturation. Each of these healing phases is supported by wound vascularization, which guarantees restoration of tissue oxygenation, nutrition supply and stimulation of wound-associated cells to fill-up and re-organize the wound space . As opioid receptors have been discovered in wound-associated endothelial cells as well as in VEGF-expressing fibroblasts and keratinocytes, a prominent role of the opioid system in wound vascularization is suggested [72, 73].
Positive effects on wound angiogenesis
In an ischemic wound model, topically applied morphine, hydromorphone and fentanyl enhanced wound vascularization by inducing endothelial cell proliferation [74, 75]. As endothelial cells in opioid-exposed wounds showed an increased activation of PDGFR-β  and higher abundance of VEGFR-1 , the in-vitro observed endothelial PDGFR/VEGFR co-signaling  may also account for opioid-stimulated proliferation of endothelial cells in-vivo. As an additional, supportive effect, opioids could trigger endothelial cell proliferation via paracrine activation of PDGFR signaling that is facilitated by keratinocytes. Keratinocytes were identified to possess responsive opioid receptors [73, 76]. Moreover, keratinocytes represent the major source of cutaneous PDGF . It may be speculated that in analogy to C6 neuronal cells , keratinocyte stimulation by opioids results in paracrine release of PDGF, which in turn acts on endothelial PDGFRs and promotes angiogenesis (Figure 2).
The contribution of opioid-induced NO synthesis in wound angiogenesis is currently under debate. As described above, increased NO concentrations in-vitro leads to endothelial cell death. In contrast, increase of NO levels in-vivo - as observed in fentanyl-exposed skin defects - is associated with an enhanced endothelial cell proliferation and accelerated wound healing . The differences observed in in-vitro and in-vivo studies on NO effects may be explained by wound-specific mechanisms that counteract NO and lethal reactive nitrogen species (RNS). These mechanisms may include anti-oxidative tissue enzymes such as heme oxygenase, superoxide dismutase or glutathione peroxidase, which act as key players in wound healing and bring balance to NO-generated RNS . In addition, NO prompts other, non-endothelial wound infiltrating cells, especially keratinocytes and fibroblast for VEGF synthesis - thereby protecting endothelial cells from apoptosis and increasing their proliferation [80, 81]. Considering this multifactorial in-vivo scenario, opioid-induced NO synthesis in wounds is conceivable to support vascularization and healing process after topical opioid application.
Rather unexpected, was the observation that an opioid receptor antagonist may have beneficial effects on wound vascularization. Topically applied naltrexone was found to enhance VEGF-expressing endothelial cells in wounds . This observation raises the question by which mechanisms an opioid receptor antagonist may provide stimulatory effects. A possible route could be via the endothelial OGFR. Naltrexone is known to bind to OGFR and prevents its activation by endothelial Met-enkephalin. As OGFR signaling is reported to suppress proliferation of endothelial cells , binding of naltrexone to the OGFR is likely to promote vessel formation by counteracting the anti-angiogenic Met-enkephalin/OGFR signaling axis [24, 26]. As a concomitant effect, unbound Met-enkephalin - no longer able to bind OGFR - may stimulate a pro-angiogenic, naltrexone-insensitive opioid receptor. Such a scenario may be performed by DORs as the opioid receptor type is activated by Met-enkephalin and binds naltrexone only with low affinity [28, 83]. A pro-angiogenic signaling of stimulated DORs was already demonstrated for chorioallantoic vessels (see above) . Thus, a Met-enkephalin stimulated DOR signaling can be envisioned for wound-associated endothelial cells and may explain naltrexone-enhanced angiogenesis.
Negative effects on wound angiogenesis
In contrast to topical application, long-term application of morphine or morphine-sulfate via subcutaneous and intraperitoneal injections delayed vascularization and closure of an excisional skin injury in mice [47, 84]. Thus, a systemic morphine effect prevents the angiogenic activity of wound-associated endothelial cells. Wound vascularization is organized by vasculogenic cytokines and growth factors that stimulate adjacent endothelial cells (angiogenesis) and attract circulating endothelial progenitor cells for de-novo vessel formation (vasculogenesis) . The lack of wound angiogenesis is in line with previous observations, in which systemic, long-term application of morphine hampered endothelial cell chemotaxis towards growth-factor containing Matrigel plugs (see above). Moreover, long-term systemic application of morphine led to a significant reduction of circulating endothelial progenitor cells , which also points out a failure in vasculogenesis. Martin et al.  showed in an independent study that systemically applied morphine reduces the migration activity of macrophages and wound infiltration (Figure 2). It was further observed that morphine-exposed macrophages reduce the synthesis and release of monocyte chemotactic protein 1 (MCP-1) and VEGF  - both are important mobilizers and attractants for circulating endothelial progenitor cells [86, 87]. Hence, it is attractive to speculate that systemically applied morphine impairs wound vasculogenesis by inhibiting macrophage function. Whether morphine impairs macrophage functions by direct interaction with the immune cells or indirectly by enhancing cortisol concentration via activation of the hypothalamic pituitary adrenal axis  remains to be evaluated.
Figure 2: Wound angiogenesis under the influence of opioids. Topically applied opioids (left panel) increase VEGF receptor expression and stimulate PDGF receptors in wound-associated endothelial cells. Activation of PDGF receptors might result from PDGF, which is released from opioid-stimulated keratinocytes. Fentanyl augments NO concentration in wounds, which triggers VEGF synthesis in keratinocytes. Released VEGF may activate angiogenic signaling of up-regulated VEGF receptors in wound-associated endothelial cells. In contrast, systemic morphine prevents wound vascularization by hindering macrophages from wound infiltration and recruitment of endothelial progenitor cells (right panel).
Opioid effects on tumor angiogenesis
Angiogenesis is a prominent hallmark of cancer as it promotes tumor progression at two critical steps: first, it allows and supports tumor growth by providing nutrients and oxygen via de-novo formed capillary network [89-91]; and second, it enables metastasis by allocating a route for cancer cells leaving the primary tumor site towards the vascular system . Tumor angiogenesis requires a complex communication between tumor and endothelial cells, cancer-associated fibroblasts and immune cells, which is tightly orchestrated by diverse angiogenic factors including VEGF . The finding that plasma from morphine- and fentanyl-treated breast cancer patients is enriched with VEGF  leads to the assumption that opioids could influence tumor angiogenesis. However, in-vivo studies that were designed to further clarify the role of opioids in tumor vascularization yielded contradictory observations as both pro-and anti-angiogenic effects were reported.
Opioids - promoters of tumor angiogenesis
Pro-angiogenic opioid effects became evident in a breast cancer xenograft model (using human MCF-7 and MDA-MB-231 cells) where long-term subcutaneous application of therapeutically dosed morphine-sulfate enhanced tumor vascularization [37, 94]. Comparable effects were also observed in allograft tumor models using mammary carcinoma (SCK) cells or Ehrlich mammary adenocarcinoma cells [95, 96]. There, systemic morphine-sulfate treatment increased the density of dilated and branching vessels within the tumor. In line, morphine-sulfate enhanced vascularization in spontaneously grown mammary tumors in transgenic C3TAG mice [41, 97]. Nguyen et al.  found that morphine-mediated tumor vascularization in the spontaneous breast cancer model correlated with enhanced degranulation of cancer-associated mast cells and elevated levels of mast cell-specific tryptase within the tumor tissue (Figure 3). As tryptase is a pro-angiogenic protease, which promotes endothelial cell proliferation and tube formation , it seems obvious that morphine-triggered release of tryptase from mast cells promotes tumor angiogenesis.
The question remains whether the morphine-triggered tryptase effect is sufficient to initiate tumor vascularization. It seems likely that morphine supports tumor angiogenesis by a further process, such as “mast cell potentiation”. It has been shown that the angiogenic potential of mast cells is boosted by Prostaglandine E2 (PGE2), which induces VEGF synthesis and release . Farooqui et al.  demonstrated that morphine treatment leads to an up-regulation of cyclooxygenase-2 (COX-2) and release of PGE2 from mammary tumors (Figure 3). Thus, morphine-triggered tumor vascularization may result from mast cells, which are stimulated for VEGF synthesis and secretion by PGE2 released from COX-2 expressing tumor cells. Indeed, the inhibition of COX-2 by celecoxib strongly reduces tumor angiogenesis supporting the hypothesis that COX-2-mediated PGE2 synthesis is central to morphine´s angiogenic effect. As an additive effect, PGE2 may assist in the induction of proliferation, migration, and tube formation via stimulation of PGE2 receptor EP3 and FGF receptor transactivation in endothelial cells .
Figure 3: Opiodergic mechanisms of tumor angiogenesis. Pro-angiogenic opioid effect (left panel): Clinically relevant morphine concentrations induce degranulation of tumor-associated mast cells and release of pro-angiogenic tryptase. Moreover, morphine enhances COX-2 expression and PGE2 synthesis in breast cancer cells. PGE2 may further promote vessel formation by inducing VEGF expression in tumor-associated mast cells (“mast cell potentiation”) and by stimulating pro-angiogenic PGE receptor signaling in endothelial cells. Anti-angiogenic opioid effects (right panel): High dose morphine impairs VEGF expression in Lewis lung cancer cells, and prevents tumor infiltration by VEGF-producing immune cells in a MOR dependent manner (neutrophils and macrophages/monocytes [pink]). Nalfurafine impairs angiogenic signaling by inducing down-regulation of endothelial VEGF receptors via KOR stimulation.
Opioids - inhibitors of tumor angiogenesis
Other in-vivo studies report anti-angiogenic opioid effects on tumors. In a Lewis lung carcinoma (LLC) mouse model, tumor vascularization was prevented upon chronic subcutaneous application of morphine-sulfate via a MOR-dependent signaling mechanism [53, 57]. Two mechanisms may account for this observation. (i) Morphine is known to inhibit VEGF synthesis and release by interfering with the p38 MAP kinase/HIF-1α signaling axis in LLC cells . Consequently, tumor vascularization may be impaired because of insufficient cancer cell-derived VEGF. (ii) The anti-angiogenic effect of morphine may be also mediated by MOR-expressing host/non-tumor cells. This notion is supported by the fact that the amounts of tumor infiltrating neutrophils and monocyte/macrophage are drastically reduced in morphine-treated mice . As these immune cells are pivotal VEGF donors [101, 102], morphine might impair tumor angiogenesis by interfering with leukocyte transmigration. Indeed, previous in-vitro studies demonstrated that the transmigration activity of leukocytes is regulated by MORs and may be blocked by chronic morphine exposure . Transmigration activity involves chemotaxis and cell migration, both of which may be modulated by opioids. Chemotaxis of leukocytes was found to be suppressed by “trans-desensitization” of chemokine receptors in consequence of prolonged MOR and DOR stimulation . The phenomenon goes back to the formation of chemokine receptor heterodimers with MORs and DORs, which are internalized after opioid receptor activation by “sequestrating opioids” such as DAMGO . In contrast to other opioids, morphine is well known to fail MOR and DOR internalization, so that also chemokine receptors would rather remain at the plasma membrane than undergo desensitization and sequestration after morphine exposure [105-107]. Moreover, chronic morphine was shown to prevent internalization of heterologous GPCRs by affecting beta-arrestin function . Thus, dysfunctional chemotaxis rather plays a minor role in impaired leukocyte infiltration after chronic morphine exposure. As an alternative, inhibition of leukocyte migration activity may account for impaired tumor infiltration. Stimulation of leukocyte MORs and DORs has been reported to modulate cell migration in a concentration-dependent manner; whereas high doses prevent, low morphine concentrations promote cell migration . As LLC bearing mice were treated with supratherapeutic morphine concentrations, lack of tumor infiltration is likely to result from high dose inhibition of leukocytes migration activity.
An alternative anti-angiogenic in-vivo mechanism was postulated for Nalfurafine, a KOR agonist (Figure 3). Nalfurafine inhibits vascularization of B16 melanomas in mice by inducing VEGF receptor down-regulation in endothelial cells . As Nalfurafine had no effect on tumor angiogenesis in KOR knockout mice, the process requires KOR activity. The mechanism of VEGF receptor down-regulation has not been analyzed in detail yet. One possible explanation could be that VEGF receptors are co-internalized and degraded together with Nalfurafine-stimulated KORs [51, 109]. Alternatively, Nalfurafine may induce VEGF receptor down-regulation by activating PKC-ζ, as it initiates VEGF receptor internalization and degradation by C-tail phosphorylation  and represents a KOR-specific down-stream effector . This KOR specific signaling mechanism might also account for the anti-angiogenic morphine effect seen in the LLC tumor model as high morphine concentrations may also bind and stimulate KORs .
Opioid effects in wound healing and tumor angiogenesis - therapeutic relevance
As angiogenesis plays a central role in the pathogenesis of chronic wounds and cancer, the angiogenic opioid effects may be used as novel therapeutic avenues for these disorders. Impaired angiogenesis, together with the inability of fibroblasts and keratinocytes to proliferate and migrate, are hallmarks of chronic wounds . Topical application of opioids could combat chronic wounds from two different angles. First, opioids may restore wound vascularization. Second, opioids could act beneficially on fibroblast and keratinocyte abnormalities, because they may induce proliferation and migration as well as cytokine production required for wound healing [72, 73, 114]. Indeed, direct application of morphine on painful skin lesions exerted healing effects in two separately treated individuals, but failed to show significant effects in a small group of patients [115-117]. To further test opioids as potential “wound-healing agents”, clinical trials with larger patient groups and special focus on the healing benefit have been designed for topically applied morphine-sulfate and hydromorphine (https://clinicaltrials.gov/; NCT00306020, NCT00177060). Another ongoing trial is testing the topical application of morphine hydrochloride for healing of painful oral lesions (https://eudract.ema.europa.eu; EudraCT Number: 2007-007011-85 8). Moreover, two Phase III studies are currently running with the aspect of wound pain relief by topically applied morphine including wound assessment as a secondary outcome measure (NCT00755989; NCT02028923). In parallel to these clinical studies, there are investigations of new pharmaceutical formulations which should guarantee clinically relevant concentrations of topically applied opioids in wounds. One recently designed innovative drug vehicle are morphine-coated solid nanoparticles, which have been tested in an artificial 3D epidermis skin model . Whereas the in-vitro studies revealed a promising wound reepithelization, the nanoparticles still need to be tested in patients.
Systemic application of opioids can support or reduce tumor angiogenesis, depending on the opioid (morphine vs. Nalfurafine), the opioid receptor type (MOR vs. KOR), the concentration (clinically relevant vs. supratherapeutic) and possibly the tumor types (breast vs. lung cancer). Angiogenesis leads to tumor growth and metastasis, so that the use of pro-angiogenic drugs is highly critical for tumor patients. Morphine is the opioid of first choice for moderate and severe cancer pain . Thus, the pro-angiogenic morphine effect (seen with clinically relevant concentrations) may be associated with tumor-promoting side effects. This conclusion is supported by epidemiologic studies, which suggested the rate of cancer relapse and metastasis correlates with systemic morphine application in patients with rectal, lung, ovarial adenocarcinoma, prostate or breast cancer [119-123]. As treatment of cancer patients is inconceivable without morphine, two different strategies are currently discussed to circumvent the tumor-promoting side-effect: i) local (epidural, intrathecal, paravertebral) application of morphine, which reduced the incidence of cancer recurrence compared to systemic opioid application , ii) co-application with a solely peripheral acting opioid antagonists such as methylnaltrexone, which is already used to prevent peripheral opioid side effects such as obstipation without affecting analgesia . Before these treatment strategies are fully established, the tumor/angiogenesis-promoting opioid effects should be considered a critical side effect.
The central role of angiogenesis for tumor growth and metastasis also leads to the development of anti-angiogenic therapeutics to overcome tumor progression. Some promising therapeutics are the monoclonal antibodies Bevacicumab and Aflibercept, which bind and neutralize VEGF , and the small molecular VEGF receptor inhibitors Sunitinib, Sorafenib, Axitinib, and Pazopanib . By inducing down-regulation of VEGF receptors, the KOR agonist Nalfurafine may enhance therapeutic efficiency of the VEGF/VEGF receptor-targeting drugs. In addition, Nalfurafine may be useful to overcome the therapeutic problem of Bevacizumab resistance, which results from enhanced autocrine VEGF/VEGF receptor signaling in response to prolonged Bevacizumab exposure . Despite these promising therapeutic approaches, the safety of Nalfurafine in cancer patients needs to be further tested.
A variety of data, provided by in-vitro, animal and clinical studies indicate that opioids modulate angiogenesis. Depending on the opioid receptor type, concentration and application route, opioids act as pro- or anti-angiogenic factors during wound healing and tumor growth. The underlying processes include direct stimulation of endothelial cells, but also of fibroblasts, keratinocytes, immune cells, and tumor cells - triggering the release of angiogenic factors such as NO, PGE2, and VEGF. Detailed understanding of further participating factors that form up the opioid-controlled network are needed and indispensable to evaluate the clinical significances of opioids angiogenic effects. It also needs to be mentioned that most of the studies were carried out with morphine. Several opioid effects - including endothelial VEGF receptor activation and vessel formation - were found to be opioid receptor-independent, which points to causal morphine targets beyond the classical opioid receptor signaling cascades. Whether the summarized angiogenic potential and signaling mechanisms are common opioid effects, which could apply to other clinical relevant opioids, has yet to be evaluated.
DAMGO [D-Ala2, N-Me-Phe4, Gly5-ol]-Enkephalin
DOR δ-Opioid Receptor
ECSCR Endothelial Cell-Specific Chemotaxis Receptor
ERK Extracellular signal regulated kinase
FGF Fibroblast growth factor
GPCR G protein-coupled receptor
HDMEC Human Dermal Microvascular Endothelial Cells
JNK c-Jun-N-terminal kinase
KOR k-Opioid Receptor
LLC Lewis-Lung cell carcinoma
L-NAME Nω-Nitro-L-arginine methyl ester
MOR µ-Opioid Receptor
NO nitric oxide
OGFR Opioid Growth Factor Receptor
PDGF Platelet Derived Growth Factor
PGE Prostaglandine E
RNS Reactive Nitrogen Species
siRNA small interfering RNA
VEGF Vascular Endothelial Growth Factor
The authors like to thank Veronika Sexl for critical discussion. The authors are also grateful to Peter Alexander Martinek for graphical assistance and Paul Wright for critical reading of the manuscript.
Conflicts of interest
There is no conflict of interest.
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