The 2-series Eicosanoids in Cancer: Future Targets for Glioma Therapy?

The 2-series eicosanoids are structurally related lipid-soluble hormones synthesized by cyclooxygenase enzymes from arachidonic acid. These compounds have well-established roles in the inflammatory response and the coagulation cascade. More recently, the eicosanoids have garnered attention for their potential roles in cancers of the lung, colon, breast, and brain. In this paper, we review the contributions of the different cyclooxygenase metabolites (i.e. prostaglandins, prostacyclins and thromboxanes) to cancer development, progression and recurrence, with special attention paid to their relevance to glioma biology. Our review suggests that 2-series eicosanoids merit further study as possible targets for therapy in patients with glioma.


Introduction
Despite advances in surgical technique, available chemotherapies, and radiation therapy, the prognosis for patients diagnosed with a glioma remains grim.Median survival for patients with glioblastoma treated with aggressive multi-modality therapy is fourteen months [1].While significant attention has been given to the genetic changes that underlie gliomagenesis, recent work has also focused on the importance of signalling within the tumor milieu and intratumoural communication in glioma development, progression and recurrence.In this review, we will focus on eicosanoid signalling and its possible role in glioma biology.
Eicosanoid signaling has long been a therapeutic target in inflammatory conditions.More recent research has delineated a role for eicosanoids in the development and progression of multiple cancers, including those of the breast [2], lung [3], colon [4], kidney [5], prostate [6] and brain [7].Eicosanoids have been proposed to activate oncogenes [8] and the epithelial-to-mesenchymal transition (EMT) [9], to inhibit tumor suppressor genes [10], to participate in tumor cell evasion of the immune response [3], and to initiate angiogenesis [4].In Table 1, we highlight the known roles of the 2-series eicosanoids in CNS and systemic cancers.
Eicosanoid synthesis begins with phospholipase A 2 , which releases arachidonic acid (AA) from membrane-bound phospholipids.AA is subsequently converted to prostaglandin H 2 (PGH 2 ) by the cyclooxygenase enzymes (COX-1, COX-2 and COX-3), which are also known as prostaglandin H synthase (PGHS) [11].PGH 2 subsequently serves for the substrate for the 2-series eicosanoids, a group of compounds that includes prostaglandins-D 2 (PGD 2 ), E 2 (PGE 2 ), F 2α (PGF 2α ), and J 2 (PGJ 2 )prostacyclin (PGI 2 ) and thromboxane (TxA 2 ) (Figure 1).Owing to their inherently unstable chemical structure, eicosanoids decay rapidly and are thus only able to mediate local (i.e.paracrine or autocrine) signaling.The 2-series eicosanoids signal in one of two ways: they either activate a G protein-coupled receptor (GPCR) [3]which in turn affects the levels of second messengers like cyclic adenosine monophosphate (cAMP) or calcium (Ca 2+ )-or bind to nuclear receptors that alter DNA transcription [12,13].Given the diverse roles of eicosanoids in human disease, there has been significant research in developing new drugs that can modulate eicosanoid signaling in a selective manner.
Gliomas represent a unique therapeutic challenge in part because they are chemically isolated from the rest of the body.In the context of cancer therapy, the bloodbrain barrier (BBB) is a significant obstacle as it can prevent chemotherapeutic agents that are active in the periphery from achieving therapeutic concentrations in the CNS.The drug tamoxifen, for example, is an agent that is profoundly effective in the treatment of metastatic breast cancer, but that has limited efficacy against brain  Production regulated by Wnt/β-catenin signaling [2]  PGE 2 mediates NR4A2-dependent 5-fluorouracil resistance [63]  FoxP3 + T reg induction [19]  VEGF-dependent angiogenesis [4]  hTERT induction [71]  EP4-Rap-dependent migration [5]  Antagonism of PTEN tumor-suppressor [10]  Suppression of host immune response in glioma and glioblastoma [73][74]  Anti-proliferative effects [55] on glioma cells and ROS-dependent induction of apoptosis [56] TxA 2  Potential role as therapeutic target in lung cancer [105]  Interaction with RhoA in prostate cancer progression [6]  Overproduction of IL-6 in astrocytoma cells via p38 MAPK and PKA pathways [107]  Cerebral edema dependent on RhoA activity [108]  TXAS expression correlates with resistance to chemotherapy [111] and radiotherapy [110] metastases because it is excluded from the CNS by the BBB [14].Due to their lipid-soluble structure, derivatives of 2-series eicosanoids have the potential to cross the BBB and overcome this problem.In the following sections, we discuss the signaling pathways associated with COX and each of the 2-series eicosanoids, and compare their roles in systemic cancers and glioma.In Table 2, we list pharmacologic agents that have been used to target different eicosanoid pathways.

Role of COX in Systemic Cancers
Early studies recognized that growth factors, tumor promoters, and oncogenes all induce prostaglandin synthesis [15].More recent studies have demonstrated that COX-2 has an important role in cancer generation and progression, but that the role of prostaglandins varies in a tumor-specific manner.Analysis of normal and neoplastic human breast tissue samples has shown that COX-2 expression correlates with expression of oncogenes such as HER-2/neu [16].COX-2 may also contribute to drug resistance in MCF-7 breast cancer cells via concomitant effects on the phosphoinositide-3-kinase (PI3K)/Akt, mitogen-activated protein kinase (MAPK), epidermal growth factor receptor (EGFR), and matrix metalloproteinase-2(MMP2) and -9(MMP9) pathways [8].For example, pharmacologic inhibition of COX-2 decreased invasiveness of MDA-MB-231 human breast cancer cells by preventing MMP2 release [17].Furthermore, transgenic loss of COX-2 delayed tumor progression in a mouse mammary epithelial cell model of breast cancer.These effects were driven by COX-2 genetic deletion, which resulted in an enhanced host immune response, and could be overcome by providing exogenous PGE 2 (a product of COX-2 activity) [18].Tumor-induced immune modulation is similarly relevant incolon cancer, where inhibition of the COX-2/ PGE 2 pathway decreases the levels of FoxP3 + regulatory T cells (T regs ) and results in an enhanced antitumor immune response [19].Long-term COX-2 inhibition also appears to have protective benefits against non-small cell lung [20] and colon [21] cancers, suggesting a more general role for COX-2 in immune surveillance against neoplastic cells.
The role of COX-2 in tumor biology appears to extend beyond the immune response.COX-2 inhibitors can induce the expression of tumor-suppressors such as MAGI1 [22] in colorectal cancer cells (SW480 and HCT116) and 15-hydroxyprostaglandin deh drogenase (15-PGDH) in y colon (HT29), lung (A549) and glioblastoma (T98G) cancer cells [23].In addition, COX-2 has a direct effect on cell proliferation and survival in SGC-7901 and AGS gastric cancer cells [24].In HepG2 human hepatocellular carcinoma cells, COX-2 inhibition also results in decreased expression of the drug efflux pumps P-glycoprotein and MRP1 [25].Thus, COX-2 inhibitors might render tumor cells more sensitive to chemotherapy.Further, in HepG2 cells, COX-2 inhibition with nonsteroidal anti-inflammatory drugs (NSAIDs) can induce apoptosis through oxidative stress and mitochondrial toxicity [26].
The pro-apoptotic effect of COX-2 inhibition on hepatocellular carcinoma cells does not, however, hold true for all cancers.Treatment with NSAIDs appeared to protect U937 human hematopoietic cancer cells from apop-tosis [27].Furthermore, it is not universally true that COX-2 expression correlates with cell proliferation.In a T24 bladder cancer cell model of interstitial cystitis, anti-proliferative factor (APF) inhibits cell proliferation by decreasing β-catenin expression, which results in increased COX-2 expression [28].The data from T24 cells provides the first example of a cancer cell line where increased COX-2 expression is associated with decreased proliferation.This observation stands in stark contrast to the cases of breast and colon cancers previously discussed where COX-2 activity drives cellular proliferation.
A phase II study of temozolomide, thalidomide and celecoxib combination therapy in glioblastoma patients unfortunately failed to demonstrate a statistically significant improvement in patient survival [30].One reason why this study may not have shown a survival benefit is that patients did not receive temozolomide during radiotherapy, which is now considered the standard of care.It remains to be determined whether the combination of temozolomide, concomitant radiation therapy and a prostaglandin signaling modulator would confer a survival benefit over the current standard-of-care.

PGD 2 Signaling
PGD 2 is derived from PGH 2 via the action of prostaglandin D synthases (PGDS), of which there are lipocalin (L-PGDS) and hematopoietic (H-PGDS) subtypes.L-PGDS shares a structural homology with other members of the lipocalin family, which are extracellular proteins that bind to a lipophilic substrate.Interestingly, H-PGDS is a sigma-class glutathione transferase [31], suggesting that PGD 2 synthesis could be regulated by environmental oxidative stress through depletion of glutathione (GSH).PGD 2 can either signal directly by binding to its cognate receptor or by being converted to PGJ 2 , the actions of which will be discussed later.PGD 2 signaling is mediated by two receptors: DP1 (or DP) and DP2 (also called CRTH2), which are both GPCRs.DP1 initiates a Gα s /cAMP/protein kinase A (PKA) cascade, while DP2 signals through Gα i proteins that mobilize Ca 2+ store and actives PI3K [32].

PGD 2 in Systemic Cancers
In mice implanted with Lewis lung cancer cells, administration of a synthetic DP1 agonist impairs angiogenesis [33].PGD 2 appears to inhibit prostate cancer cell proliferation in tumors expressing aldoketoreductase 1C3 (AKR1C3, also called 17β-hydroxysteroid dehydrogenase (17β-HSD) type 5) [34].Likewise, a study of tumor-prone Apc Min/+ mice showed that high levels of H-PGDS can suppress colon tumorigenesis [35].Together, these observations establish PGD 2 as a tumor-suppressing molecule that could be exploited as an anti-cancer and anti-angiogenesis therapeutic.

PGD 2 in Glioma
PGD 2 has long been known to inhibit cell proliferation in glioma cell lines (NCE-G 2,3,7,8,17) in vitro [7].More recently, loss of L-PGDS expression was found to be a defining event in the progression of Grade II to Grade III astrocytomas; further, PDGS expression was noted to vary inversely with survival across all glioma grades [36].
Treatment of A172 glioma cells in culture with PGD 2 inhibits cell proliferation and induces apoptosis; these effects were amplified by concomitant inhibition of COX-2 [36].Interestingly, PKC, which is driver of EMT [37], activates PGDS in TE671 medulloblastoma cells [38].Thus, the effect of PGD 2 appears to be tumor-specific even among tumors of the CNS.Regardless, these findings establish a potential role for exogenous PGD 2 analogues in the treatment of glioma.

PGJ 2 Signaling
15-deoxy-Δ12,14-prostaglandin J2 (15-d-PGJ 2 ) is produced in vivo by the metabolism of PGD 2 .15-d-PGJ 2 signals via the DP2 and PPARγ receptors, but also has direct effects on glycolytic enzymes, molecular chaperones and cytoskeletal proteins in neuronal membranes [39,40].An unusual aspect of 15-d-PGJ 2 signaling is its ability to signal by redox reactions.15-d-PGJ 2 induces Akt and Nrf2 signaling by forming a covalent adduct with GSH [41].This does not appear to be an isolated phenomenon, but a normal process in 15-d-PGJ 2 signaling.In addition, 15-d-PGJ 2 oxidizes p38 at cysteine residues near the protein surface resulting inp38 inactivation [42].Similarly, Δ 12 -PGJ 2 reacts with human serum albumin to form a covalent adduct with histidine-146, a reaction which chemically stabilizes the bound prostaglandin [43].

PGJ 2 in Systemic Cancers
Of all the prostaglandins, PGJ 2 exerts the broadest range of effects in cancer, echoing its biochemical diversity.15-d-PGJ 2 induces expression of the tumor suppressor, HtrA3, in 786-O and RCC4 renal cell carcinoma lines through a mechanism dependent on MEK/ERK signaling, but not PPARγ [12].15-d-PGJ 2 also augments the antitumor activity of the alkylating agent, camptothecin, against Caki-2 renal cell carcinoma cellsin a manner independent of topoisomerase-II and PPARγ signaling pathways [44].
Moreover, 15-d-PGJ 2 signaling appears to modulate cell survival and apoptosis pathways in multiple cancer types.15-d-PGJ 2 signaling induces expression of EGFR and COX-2 in MG-63 osteosarcoma cells via reactive oxygen species (ROS) and the p38 and p42/p44 MAPK pathways [48].On the one hand, PGJ 2 -dependent inflammation and induction of EGFR could promote cancer genesis and survival.Conversely, ROS formation by 15-d-PGJ 2 has been shown to induce apoptosis in A549 lung cancer cells [49] and synergistically enhance histone deacetylase inhibitor-driven apoptosis in DLD-1 colon cancer cells [50].In MCF-7 breast cancer cells, 15-d-PGJ 2 activates a Ca 2+ -ERK1/2 signal transduction cascade that increases levels of the transcription factor, EGR1, which acts as an inhibitor of breast cancer cell proliferation [51].EGR1 is also a positive regulator of the tumor suppressor gene, PTEN [52].In MCF-7 cancer cells, 15-d-PGJ 2 also reacts with GSH to form a 15-d-PGJ 2 -GSH conjugate, which subsequently activates Akt and Nrf2 and results in MRP1-dependent export of the 15-d-PGJ 2 -GSH molecules [41].Depletion of the intracellular GSH pool is in turn believed to trigger apoptosis, while relatively moderate depletion of GSH stores is thought to augment adaptation of cancer cells to external stresses.This mechanism suggests that one could exploit the anti-cancer effects of 15-d-PGJ 2 by concomitant administration of selective inhibitors of MRP1.
Studies examining the function of 15-d-PGJ 2 in normal cells have revealed other novel effects of this molecule on cellular physiology that could be relevant to human disease and cancer therapy.For example, 15-d-PGJ 2 signaling has been found to modulate CRM1 transporter-dependent nuclear protein export [53].Altering trafficking between the nucleus and cytosol using modulators of 15-d-PGJ 2 signaling could be used to perturb the actions of oncogenes by limiting their access to their nuclear targets.Also interesting, in murine cell lines 15-d-PGJ 2 signaling inhibits mitochondrial fission activities, which leads to subsequent remodeling of mitochondrial proteins [54] and results in increased ROS formation.Conceivably, 15-d-PGJ 2 signaling could be used to therapeutically trigger apoptosis in malignant cells.

PGJ 2 in Glioma
Like PGD 2 , Δ 12 -PGJ 2 alters the morphology of C6BU-1 rat glioma cells and substantially slows their proliferation [55].Furthermore, 15-d-PGJ 2 has been shown to induce caspase-independent apoptosis in human A172 glioma cells through ROS formation and mitochondrial damage [56].Curiously, 15-d-PGJ 2 was found to protect rat C6 glioma cells from methylmercury toxicity-precisely by preventing damage to the mitochondrial membrane [57].Further study is needed to determine under what circumstances PGJ 2 signaling is cytotoxic or cytoprotectivebefore modulators of PGJ 2 signaling can be considered for treatment of human gliomas.

PGE 2 Signaling
PGE 2 signals through four receptors-EP1, EP2, EP3 and EP4-which are all GPCRs.EP2 and EP4 are linked to Gα s and activate a cAMP/PKA pathway, EP1 is thought to be linked to Gα q, and EP3 to Gα i 3 .EP3 also appears to be linked to PLCγ signaling [58].Not surprisingly, PGE 2 has the most diverse physiologic effects of any of the prostaglandins.Its activities include effects on the inflammatory response, lipid metabolism, tumorigenesis, neurotransmission (via GABA and dopamine), and B cell survival [59].

PGE 2 in Systemic Cancers
Inhibitors of PGE 2 synthesis, such as curcumin, are being tested in clinical trials as agents for cancer prevention.Phase IIa studies have shown that curcumin can prevent the formation of aberrant crypt foci in the colon, which are thought to precede development of colon cancer [60].
Treatment of the human colon cancer cell line HT-29 with epinephrine stimulated cell proliferation and increased PGE 2 synthesis and release, which in turn increased vascular endothelial growth factor (VEGF) secretion (likely via EP4 signaling [61]) and MMP9 activity 4 .Protein kinase CK2 and the Wnt/β-catenin pathway also activate production of PGE 2 , with subsequent proliferation of human colon (HT29-US and DLD-1) and breast (ZR-75) cancer cells.In addition to its effects as a promoter of cell proliferation and angiogenesis in colon cancer, PGE 2 has also been shown to help colon cancer cells evade the immune response and advantageously alter their energy metabolism.In LS-174T and HCT-116 colon cancer cells, PGE 2 signaling activates the nuclear orphan receptor NR4A2, which increases fatty acid oxidation as an alternative fuel source to glucose [62].This activity could promote tumor survival under conditions of starvation.Inhibition of PGE 2 synthesis has also been associated with decreased incidence of colon cancer in murine studies and decreased levels of tumor-cell protective FoxP3 + T regs _ENREF_19 [19].
Interestingly, NR4A2, under the regulation of PGE 2 , is involved in the development of drug resistance in human oral squamous cell carcinoma.In HSC3, HSC4, Ho-1u-1 and Ca9-22 lines, PGE 2 was shown to promote 5fluorouracil resistance of EGFR-dependent tumors by induction of NR4A2 [63].
As in colon cancer, PGE 2 is a stimulator of angiogenesis in breast cancer.Apoptotic MCF-7 breast cancer cells were shown to signal via the sphingosine-1-phosphate (S1P) S1P1 and S1P3 receptors in order to induce PGE 2 production in macrophages.The activated macrophages then released PGE 2 , thereby triggering vascular endothelial cell migration and subsequent angiogenesis in breast tumors [64].As is the case in colon cancer, PGE 2 also appears to plays a role in immune evasion in breast cancer.PGE 2 produced ad secreted by breast cancer cells suppresses NK cell function through activation of the EP4 receptor.PGE 2 also induces expression of the oncogene aromatase in breast adipose fibroblasts in a pathway that involves JunD and JunB [65].Aromatase activity subsequently results in elevated levels of estradiol.This finding could explain why clinical studies have shown that COX-1 levels correlate with high levels of serum estradiol in patients with breast cancer [66].In fact, therapeutic agents targeting the PGE 2 signaling pathway have been studied as potential adjuncts for breast cancer treatment.The natural PGE 2 antagnoists frondoside A (which inhibits EP2 and EP4 receptors) [67] and saponin (which also acts via an AMP-activated protein kinase pathway to inhibit COX-2) [68] have been shown to slow breast cancer progression and induce apoptosis in Balb/ cfC 3 H mouse and MCF-7 human breast cancer cells, respectively.
Current understanding of the role of PGE 2 in other cancer types is more fragmented, but several recent findings are worth noting.PGE 2 expression by blood mononuclear cells induced by AsPC-1 and MiaPaCa-2 pancreatic cancer cell lines is critical to generate a supportive tumor microenvironment [69].PGE 2 has also been shown to induce the crucial oncogene telomerase (hTERT) in a signaling cascade dependent on EP4 and Sp1 in both lung (H1838 and H1792) [70] and cervical (HeLa, SiHa, Caski) [71] cancer cell lines.In renal cell carcinoma cell lines (RCC7 and Caki-1), PGE 2 stimulates tumor cell migration and invasion via the EP4-Rap pathway [5].
Microsomal prostaglandin E synthase-1 (mPGES-1) is known to inhibit the tumor suppressor protein phosphate and tensin homolog (PTEN), which supports biliary tract cancer progression [10].This effect could be an extension of the normal function of EP1, which signals via Gα q , leading to Ca 2+ mobilization [3] and PI3K activation, which directly antagonizes PTEN.A similar role for EP1 signaling through Ca 2+ mobilization has been postulated inthe development of melanoma [72].Importantly, the biological effects of PGE 2 signaling on cancer progression do not appear to be isolated from one another; rather, they appear to be related by a more fundamental process, the EMT.Vaid et al. demonstrated that natural products isolated from grape seeds can reverse EMT in melanoma cell lines (A375 and Hs294) and that this effect was duplicated by inhibiting PGE 2 with celecoxib [9].Thus, one can conclude that PGE 2 signaling affects all the essential processes of tumor generation and malignant progression-from antagonizing tumor suppressor genes and activating oncogenes, to stimulating immune system evasion, angiogenesis, cell migration and the EMT.

PGE 2 in Glioma
As in colon cancer, PGE 2 released by glioma cells has an inhibitory effect on host immunity.Release of PGE 2 by glioblastoma cells decreases induction and cytotoxicity of anti-tumor lymphocytes [73].PGE 2 secretion by MG-377 glioblastoma cells can also stimulate CD11c + dendritic cells to induce CD4 + T regs , which again results in suppression of the host immune response [74].It also appears that human U251 and T98G glioblastoma cells secrete soluble factors that drive macrophages to produce PGE 2 [75].In an induced glioma mouse model, blockade of systemic PGE 2 synthesis using COX-2 inhibitors or knock-out of COX-2 suppressed gliomagenesis, possibly due to an increase in host immune surveillance [76].Interestingly, macrophages that are capable of killing T9 rat glioma cells are resistant to the immunosuppressive effects of PGE 2 [77].
The role of PGE 2 inglioma biology extends beyond its effects as an immunomodulator.In U87-MG glioma xenografts, mPGES-1 drives tumor cell proliferation and tumor growth via activation of type II PKA [78], which in turn inhibits ERK and increases CREB transcriptional activity [79].This mechanism mirrors the inhibitory effect of mPGES-1on PTEN seen in biliary tract cancers [10].There also seems to be a role for PGE 2 in glioma cell invasion via its activation of PKC [80].
Thus far, it appears that PGE 2 signaling almost universally drives cancer proliferation and migration, but this may not uniformly be the case.In one study, PGE 2 was found to induce Bax-dependent apoptosis in primary glioblastoma cells, and patients expressing a high level of mPGES-1 were found longer survival times than those with low levels of mPGES-1 [81].In principle, this trend could be explained by pro-apoptotic PGE 2 signaling through the EP4 receptor [59].Whereas the EP4 receptor may mediate the clinically important effects of PGE 2 in gliomas, in medulloblastoma it appears that the EP1 and EP3 receptors are more crucial.Specifically, EP1 and EP3 drive proliferation of medulloblastoma cells [82].These differing roles of PGE 2 in different cancers and contexts speak to the intricacy of prostaglandin signaling, and how development of prostaglandin-based therapies will require an appreciation of this complexity.
Finally, these observations suggest that EP1 and EP3 modulators could provide a novel means of treating gliomas by augmenting the host anti-tumor immune response, similar to the use of ipilimumab in the treatment of metastatic melanoma [83].

PGF 2α Signaling
In humans, aldoketoreductase (AKR) 1B1 is the primary enzyme that produces PGF 2α from PGH 2 [84], while AKR1C3 plays a minor role in PGF 2α synthesis [34].The PGF 2α receptor FP is a GPCR linked to Gα q , which affects Ca 2+ homeostasis and regulates smooth muscle cell contraction, most notably in the intestines [85] and uterus [86].PGF 2α analogues (e.g.latanoprost) are also used clinically to lower intraocular pressure in the treatment of glaucoma [87].

PGF 2α in Systemic Cancers
The PGF 2α metabolite 8-isoPGF 2α has been found to be a reliable marker of cancer progression in a rat breast cancer model [88].Levels of 8-isoPGF 2α have also been monitored to track cellular damage associated with renal oxidative stress [89] and bladder obstruction [90] ,which are considered risk factors for the development of renal cell and uroepithelial cancers, respectively.

PGF 2α in Glioma
In NG108-15 hybrid neuroblastoma-glioma cells, PGF 2α (and also PGD 2 and PGE 2 ) raises intracellular Ca 2+ levels via a cGMP-dependent mechanism [91].Since these early studies, very little attention has been given to the role of PGF 2α in CNS cancers.The few described effects of PGF 2α in glioblastoma have focused on its roleon tumor-associated vasculature.Glioma cells appear to synthesize high levels of both PGF 2α and TxA 2 , but the disproportionate increase in TxA 2 synthesis over PGF 2α synthesis is believed to contribute to the changes seen in vascular permeability and the resulting cerebral edema [92].It appears that PGF 2α signaling is also involved in the remodeling of cerebral vascular architecture: in SV40-transfected microglial cells, PGF 2α acts via a Ras/Raf-and Tcf-pathway dependent to increase production of the CYR61 protein [93], which induces physiologic angiogenesis in the corpus luteum [94].Thus, building on the work of Kesari et al. [30], modulators of PGF 2α signaling might be good targets as angiogenesis inhibitors in the treatment of glioblastoma multiforme.

PGI 2 Signaling
PGI 2 is synthesized in vascular endothelial cells by prostacyclin synthase (PGIS) through the catalysis of PGH 2 .The PGI 2 receptor (IP) is a rhodopsin-like GPCR that signals via Gα s to activate cAMP synthesis.PGI 2 may also signal through Gα q , Gα i and the PPARδ pathways [13].A recent mouse model has shown that maternal PGI 2 signaling through fetal PPARδ is key for blastocyst hatching and subsequent implantation [95].

PGI 2 in Systemic Cancers
The PGI 2 analogue iloprost has been investigated as a potential agent for lung cancer prevention.A phase II placebo-controlled randomized study showed that iloprost significantly reduced dysplasia in lung tissue biopsies obtained from former smokers [96].Whether PGI 2 signaling levels have a meaningful effect on cancer survival remains unclear.An observational study of patients in Ireland with various forms of lung cancer showed that overall PGI 2 synthase (PGIS) expression was decreased in lung cancer, but PGIS expression levels did not correlate with survival [97].On the other hand, a recent case study showed that a patient with lung cancer treated with iloprost showed no evidence of cancer progression in the absence of conventional chemotherapy [98].

PGI 2 in Glioma
The role of PGI 2 signaling in gliomas is not well understood.Many CNS tumors express endogenous PGI 2 receptors (IP).PGI 2 signaling results in cAMP and cGMP accumulation in N4TG3 murine neuroblastoma cells, but notin 1321N1 human astrocytoma cells [99].Angiotensin is known to induce release of PGI 2 from rat C6 glioma cells [100] and the IP receptor can generate inward Ca 2+ currents in hybrid rodent NG108-15 glioma-neuroblastoma cells [101].Activation of the IP receptor, however, is subject to desensitization in response to prolonged stimulation in these cells [102].Surprisingly, the IP receptor in NG108-15 cells does not activate the ERK1/2 pathways, as would be expected from IP-driven cAMP production [103].In these experiments, PI3K-and PKC-dependent currents were observed in CHO but not glioma cells.Further work is needed to determine whether PGI 2 signaling has functional relevance in glioblastoma.

TxA 2 Signaling
Thromboxane A 2 (TxA 2 ) is produced by the thromboxane synthesis enzyme (TXAS) and signals via the TP receptor, a GPCR linked to Gα q .Like some of the other prostaglandin receptors, TP exerts its effects by mobilizing Ca 2+ stores, most notably in the processes of coagulation and regulation of vascular smooth muscle tone [104].

TxA 2 in Systemic Cancers
Binding of TxA 2 to the TP receptor results in enhanced activity of the protein kinase C-related kinase (PRK)1.PRK1 signals downstream of RhoA and is implicated in the development and progression of prostate cancer [6].Though not as extensively described as a therapeutic target as PGE 2 , TxA 2 has shown promise for as a target for investigation in lung [105] and prostate [6] cancers.

TxA 2 in Glioma
TxA 2 synthesis is known to be elevated in gliomas, and increases with increasing tumor grade [106].TxA 2 signaling results in CREB-dependent induction of IL-6 by human 1321N1 astrocytoma cells through activation of the p38 MAPK and PKA pathways [107].Furthermore, TxA 2 induces cell swelling in 1321N1 cells in a mechanism dependent on Gα q , RhoA, the Na + /H + exchange pump, and aquaporins [108].Since aquaporins are known to be involved in migration and proliferation of human glioma cell lines (D54, D65, STTG1, U87, U251) [109], this discovery regarding the role of TxA 2 in astrocytoma cells raises the question of whether TxA 2 inhibition could be used to inhibit glioma invasion.Inhibition of TxA 2 signaling by blocking TXAS also renders glioma cells more sensitive to apoptosis when subjected to -radiation [110] or alkylating chemotherapy (U87 glioblastoma cells) [111].Thus, inhibition of TxA 2 signaling may be a valuable adjunct to radiation therapy in glioma.

Conclusion
The 2-series eicosanoids have diverse roles in the biology of systemic cancers and glioma.These effects vary drastically in a cancer-and context-specific manner.The list of cancer cell processes affected by prostaglandin signaling is impressive and includes modulation of the immune system, induction of the EMT, modulation of tumor cell migration and invasion, changes in the cell metabolic state, and alterations in the balance between oncogene and tumor-suppressor activity.New therapies based on eicosanoid biology could provide valuable therapies to currently intractable cancers.One possible strategy would be to combine the purported anti-proliferative and pro-apoptotic effects of PGD 2 , PGI 2 and PGJ 2 while inhibiting the oncogenic effects of the other 2-series eicosanoids.Our current knowledge suggests that the 2-series eicosanoids merit further study as possible therapeutic targets in patients with glioblastoma and other cancers.