Bicyclic triterpenoid Iripallidal induces apoptosis and inhibits Akt/mTOR pathway in glioma cells
© Koul et al. 2010
Received: 5 January 2010
Accepted: 24 June 2010
Published: 24 June 2010
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© Koul et al. 2010
Received: 5 January 2010
Accepted: 24 June 2010
Published: 24 June 2010
The highly resistant nature of glioblastoma multiforme (GBM) to chemotherapy prompted us to evaluate the efficacy of bicyclic triterpenoid Iripallidal against GBM in vitro.
The effect of Iripallidal on proliferation and apoptosis in glioma cell lines was evaluated by MTS, colony formation and caspase-3 activity. The effect of iripallidal to regulate (i) Akt/mTOR and STAT3 signaling (ii) molecules associated with cell cycle and DNA damage was evaluated by Western blot analysis. The effect of Iripallidal on telomerase activity was also determined.
Iripallidal (i) induced apoptosis, (ii) inhibited Akt/mTOR and STAT3 signaling, (iii) altered molecules associated with cell cycle and DNA damage, (iv) inhibited telomerase activity and colony forming efficiency of glioma cells. In addition, Iripallidal displayed anti-proliferative activity against non-glioma cancer cell lines of diverse origin.
The ability of Iripallidal to serve as a dual-inhibitor of Akt/mTOR and STAT3 signaling warrants further investigation into its role as a therapeutic strategy against GBM.
Iripallidal [(-) (6R,10S,11S,18R,22S)-26-Hydroxy-22-α-methylcycloirid-16-enal NSC 631939]- a bicyclic triterpenoid isolated from Iris pallida belongs to the terpenoid family as Paclitaxel. Paclitaxel is an effective chemotherapy for several types of neoplasms . Iripallidal inhibited cell growth in a NCI 60 cell line screen  and induced cytotoxicity in human tumor cell lines . Besides the fact that Iridals are ligands for phorbol ester receptors with modest selectivity for RasGRP3 , not much is known regarding its mechanism of action.
Despite recent advances in understanding molecular mechanisms involved in GBM progression, the prognosis of the most malignant brain tumor continues to be dismal. Ras activation occurs in GBMs  and this high level of active Ras has been a target for glioma therapy. RasGRP3- is an exchange factor that catalyzes the formation of the active GTP-bound form of Ras-like small GTPases . Importantly, Ras activation stimulates its downstream effector Akt that plays a major role in glioblastoma development as ~80% of GBM cases express high Akt levels . Akt activates mammalian target of rapamycin (mTOR), which is deregulated in glioblastoma . mTOR phosphorylates p70 ribosomal S6 kinase (p70S6 kinase) that regulates translation of proteins involved in cellular proliferation and formation. Moreover, blocking mTOR signaling reduces glioma cell proliferation . Given the importance of Akt/mTOR signaling in glioma cell survival, significant efforts are being invested in identifying inhibitors that target this pathway [8–10]. In addition to aberrant PI3K/Akt signaling; heightened STAT3 activation plays a critical role in glioblastoma and STAT3 inhibitors have shown promise as therapeutics for GBM [11–13]. In addition to RasGRP3 Iripallidal also binds to PKCα  which is known to induce cells ectopically expressing hyperactive Ras to undergo apoptosis . Not only is STAT3 essential for Ras transformation  but constitutively activated STAT3 is negatively regulated by PKC-activated tyrosine phosphatase(s) . As Iridals interacts with PKCα and RasGRP3-molecules that regulate Akt and STAT3 signaling, and since inhibition of Akt/mTOR and STAT3 signaling are being targeted for GBM treatment we evaluated the effect of Iripallidal on glioma cell proliferation and these signaling pathways.
Glioblastoma cell lines A172, LN229, T98G and U87MG were obtained from American Type Culture Collection and cultured in DMEM supplemented with 10% fetal bovine serum. Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll/Histopaque density gradient centrifugation. Adherent monocytes were purified from PBMC following adherence on glass petri-dish for three hours after flushing the non-adherent cells by extensive washing with PBS. All experiments with human PBMC were conducted under an approved institutional Human Ethics Committee protocol.
On attaining semi-confluence, cells were switched to serum free media and after 6 hours, cells were treated with different concentration of Iripallidal (in Dimethyl sulphoxide, DMSO) in serum free media for 24 hours. DMSO treated cells were used as controls. Iripallidal was purchased from Calbiochem, USA. All reagents were purchased from Sigma unless otherwise stated. Colon cancer cell line HT29, breast cancer line MCF-7, cervical cancer cell line HeLa, hepatocellular carcinoma cell line HepG2, acute myeloid leukemic cell line THP1 and human monocytes were similarly treated with Iripallidal.
Viability of Iripallidal treated monocytes and cancer cell lines was assessed using the [3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxy-phenyl)-2-(4-sulfophenyl)- 2H-tetrazolium, inner salt] (MTS) (Promega) as described earlier .
The Colorimetric Assay kits for caspase 3 (Sigma) were used to determine its enzymatic activity in Iripallidal treated glioma cells as described previously .
Protein from whole cell lysates were isolated as described previously . Protein (20-50 μg) isolated from control and Iripallidal treated cells was electrophoresed on 6% to 10% polyacrylamide gel and Western blotting performed as described . Antibodies were purchased from Cell Signaling Technology (Danvers, MA) unless otherwise mentioned. The following antibodies were used: p21 (BD Biosciences), p27 (Abcam), pSTAT3 (Tyr705), pmTOR (Ser2448), mTOR, Akt, pAkt (Ser473), Cyclin D1 (Abcam), phospho-p70S6K (Thr389), cMyc (Santa Cruz), phospho-S6K (Ser235/236), pH2AX Ser139 (Upstate), cleaved-PARP and β actin. Secondary antibodies were purchased from Vector Laboratories. After addition of chemiluminescence reagent (Amersham), blots were exposed to Chemigenius, Bioimaging System (Syngene, UK) for developing and images were captured using Genesnap software (Syngene). The blots were stripped and reprobed with anti-β-actin to determine equivalent loading as described .
Telomerase activity was determined using the TeloTAGGG Telomerase PCR ELISA PLUS kit (Roche, Germany) as described previously .
The soft agar colony formation assay was performed using CytoSelect™ 96-Well Cell Transformation Assay kit (Cell Biolabs, Inc), as described previously .
All comparisons between groups were performed using two-tailed Paired student's t-Test. All values of p less than 0.05 were taken as significant.
mTOR activation results in phosphorylation of effector molecule p70S6K and S6 ribosomal protein, which subsequently leads to mTOR-dependent gene transcription that regulates cell growth, protein synthesis, and metabolism. We therefore determined the effect of Iripallidal on the status of p70S6K and pS6 kinase. Iripallidal inhibited phosphorylation of mTOR targets 70S6K and ribosomal protein S6 (Fig. 2). These results indicate that iripallidal acts as a dual inhibitor of Akt/mTOR pathway.
As maintained DNA breaks induce apoptosis  and since H2AX is phosphorylated at sites of DNA double-strand breaks , we determined the expression of γ-H2AX in Iripallidal treated cells. While an increased γ-H2AX expression was observed in Iripallidal treated cells (Fig. 4b), the levels of total H2AX was unaffected (Fig. 4b).
In vitro screening of compounds with anticancer properties by NCI identified Iridals for their anti-proliferative activity. Besides its ability to bind PKCα and RasGRP3 , nothing is known regarding the mechanism of action or bioavailability of Iripallidal. Our studies suggest that Iripallidal induce apoptosis in glioma cells and inhibits the Akt/mTOR pathway. The efficacy of mTOR inhibitors in glioblastoma cell lines [8, 10] has prompted their clinical trials for GBM [9, 34]. As rapamycin activates Akt pathway by a negative feedback loop involving phosphorylation of insulin receptor substrate (IRS) by mTOR effector molecule S6 kinase [35, 36], it was therefore not surprising that Rapamycin treatment induced Akt activation in some GBM patients in a Phase I clinical trial . Moreover, dual inhibition of Akt and mTOR has proven effective in pre-clinical model of GBM , suggesting that dual Akt/mTOR inhibitor can effectively overcome the effects of feeback loop efficiently than a single inhibitor selectively targeting mTOR. As mTOR blockade is a biomarker of therapeutic efficacy in glioma , the unique ability of Iripallidal to inhibit both Akt and mTOR can be exploited as novel anti-glioma therapy. In addition to inhibiting Akt/mTOR axis, Iripallidal also inhibited STAT3 signaling. PKC inhibitor attenuates Ras activation and this attenuation correlates with an inhibition of RasGRP3 phosphorylation . Interestingly, PKCα regulates mTOR  as well as STAT3 activation . It is possible that Iripallidal effects Akt/mTOR and STAT3 signaling pathways through its ability to bind PKC.
Iripallidal mediated decrease in STAT3 activation was concurrent with decreased cyclin D1 and increased p21 expression. While cyclin D1 overexpression and STAT3 activation are mutually exclusive events , p21 inhibits STAT3 signaling . Besides, inhibition of mTOR signaling induces cell cycle arrest through regulation of Cyclin D and p27 . As telomerase inhibition is known to cause apoptosis in human cancers , the ability of Iripallidal to down-regulate telomerase activity may also represent a mechanism for its anti-proliferative effect on glioma cells. Besides glioma cell lines, Iripallidal also decreased the viability of several other cancer cell types although to different extents. It is known that cytotoxic responses is a reflection of an integrated readout of all targets and/or biochemical pathways affected upon drug exposure . As strong co-relation exists between chemo-responsiveness and gene expression , it is likely that differential expression of cellular pathways in cancer cell types of diverse origin could have resulted in differences in sensitivity to Iripallidal.
Taken together our studies suggest that (i) Iripallidal induces glioma cell apoptosis and (ii) inhibits Akt/mTOR and STAT3 pathway. This ability of Iripallidal to act as a multi-inhibitor that blocks Akt/mTOR and STAT3 pathways suggest that its potential as a chemotherapeutic agent against GBM should be further evaluated. Importantly, Iripallidal is not only a promising candidate for the treatment of GBM but a wide variety of malignancies, since it elicits cell death in many tumor cell types.
"Bicyclic triterpenoid Iripallidal as a novel anti-glioma and anti-neoplastic therapy in vitro" has been filed for Indian patent (#2915/DEL/2008) and International Patent (PCT/IN09/000336) through Department of Biotechnology, Govt. of India.
This work was supported by core grant from DBT to the National Brain Research Centre, Manesar. DD, VS and NK are supported by a research fellowship from Council of Scientific and Industrial Research (CSIR, Government of India). The authors thank Mr Uttam Kumar Saini for technical assistance.
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.