Previously, we reported that α-quaternary chiral lactam derivatives have broad spectrum anticancer activity. However, the underlying molecular mechanisms and its relevance are largely unknown. In the present study, we report progress on α-quaternary chiral lactam analogues that address this, focusing on the novel analogue YH-304 as a candidate to broadly target human cancer cells. The effect of YH-304 on cell transformation was assessed by clonogenic assay in non-small cell lung cancer cells (NSCLCs) A549 and 226B. Proapoptotic activity of YH-304 was determined by TUNEL assay and cleaved PARP, cleaved caspase-9, and Bax as markers for apoptosis. The p53-dependency and therapeutic spectrum of YH-304 was assessed by western blot analysis, real-time PCR, and cell viability assays in cells expressing endogenous wild or mutant p53. The effect of YH-304 on angiogenesis in vivo was examined by bFGF-mediated angiogenesis assay in zebrafish. Finally, the effect of YH-304 on AKT and ERK activation (phosphorylation) as a putative mechanism underlying the effect of YH-304 on bFGF-mediated angiogenesis was assessed using western blotting. We found that YH-304 significantly decreases the colony-forming activities of both A549 and 226B cells, inducing cellular apoptosis. Unlike nutlin-3 (p53 pathway activator), YH-304 did not affect the expression levels of p53 and its target gene such as p21 and thus showed p53-independent anticancer activity with broad spectrum. In addition, YH-304 inhibited bFGF-induced angiogenesis in vivo through mediating AKT and ERK signaling pathway, which plays an important role in bFGF activation and angiogenesis. Taken together, our data indicate that YH-304 may represent a novel therapeutic option for the treatment of cancer in a p53-independent manner.
Cancer is a world-wide disease urgently requiring novel therapeutic agents having a new class of structure (1–3). An oxindole structure possessing a bicyclic aromatic heterocycle with a benzene ring fused to γ-lactam is one of the structural classes (4). Diverse derivatives based on oxindole have been reported for development of new type anticancer candidates (5–8). Representative natural product possessing oxindole is spirotryprostatin A, which is well known for its anticancer activities through blockade of the G2/M progression in mouse mammary carcinoma cells (4,9). The other oxindole small molecule, sunitinib was developed as a multi-targeted receptor tyrosine kinase inhibitor and has been widely used in the treatment of renal cell carcinoma and imatinib-resistant gastrointestinal stromal tumors (10,11). In 2005, Ding et al (13) developed the MDM2 inhibitor from spiro-oxindole structure of spirotryprostatin A and the IC50 value of MDM2 inhibitor was 0.83 μM in LNCaP prostate cancer cells (12–14). In a previous study, we developed a series of oxindole derivatives having simplified α-quaternary chiral lactam and evaluated their anticancer efficacy (2,15). However, the mechanisms of action underlying its anticancer effects are largely unknown and need to be better understood to allow this therapy to be used for clinical trials. This prompted us to study further the anti-tumorigenic effects of YH-304, including its underlying molecular mechanisms.
The p53 tumor suppressor mediates growth arrest, senescence, and apoptosis in response to a broad array of cellular damage and protects the organism against the propagation of cells with damaged DNA (16). In unstressed cells, MDM2 acts as an p53-antagonist by inducing ubiquitination of p53, which results in p53 degradation (17). Therefore, inhibition of the p53-MDM2 interaction using chemical or biological inhibitors becomes an attractive strategy for cancer therapy (18). Many MDM2 inhibitors have been developed and evaluated in a large panel of tumors, including lymphomas (19,20). Nutlin-3 is one of the specific inhibitors of the MDM2-p53 interaction and leads to stabilization and activation of the p53 (21,22). However, recently, several studies reported the limitation of the efficacy of nutlin-3 such as resistance formation (23). Therefore, there is an urgent need to develop novel MDM2 inhibitors or p53 activators.
Zebrafish has become a widely used model in pre-clinical drug screening and the mechanistic studies of angiogenesis, since its embryo is small and optically transparent to visualize the whole vessels (24,25). Especially, the use of vascular specific transgene allows for the detection of individual growing cells or vessel formation (26). To date, many types of cancer models have been developed in zebrafish and providing excellent tools for anticancer drug discovery through candidate drug testing (27,28).
In the present study, we used transgenic fluorescent zebrafish tg(fli1:EGFP) to evaluate the anti-angiogenic efficacy of YH-304 in live zebrafish embryos. In the present study, we showed the anti-tumorigenic effect of YH-304 using in vitro clonogenic assay, TUNEL assay, and cell viability assay, as well as the effect on bFGF-induced in vivo angiogenesis. At the molecular level, we found that YH-304 increases the number of TUNEL-positive cells and the expression level of cleaved PARP, cleaved caspase-9 and Bax, resulting in apoptotic cell death. YH-304 did not alter the p53 or its target gene expression levels. In addition, YH-304 potently inhibited angiogenesis of bFGF-mediated AKT and ERK phosphorylation. The anti-tumorigenic and anti-angiogenic potential of YH-304 to induce apoptosis with broad spectrum and downregulate ERK/AKT activity suggests a putative use in anticancer therapy.
Materials and methodsCell cultures
HeLa (human cervical carcinoma cell line), HCT-116 (human colon carcinoma cell line), A549, 226B (human non-small lung cancer cell lines), and MDA-MB-231 (human breast cancer cell line) were purchased from the American Type Culture Collection (ATCC; Manassas, VA, USA) and maintained at 37°C in a humidified 5% CO2 atmosphere. HeLa, HCT-116 and MDA-MB-231 cells were cultured in Dulbecco’s modified Eagle’s medium and A549 and 226B cells were cultured in RPMI-1640 medium supplemented with 10% fetal bovine serum (FBS) and 1% antibiotics (Invitrogen, Carlsbad, CA, USA).
Reagents
Recombinant bFGF was purchased from BD Biosciences (Franklin Lakes, NJ, USA), whereas the anti-GAPDH, α-Tubulin, PARP and p53 antibodies were purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA) and the anti-Akt, p-Akt, cleaved caspase-9, Bax, ERK and p-ERK antibodies used were purchased from Cell Signaling Technology (Boston, MA, USA). Nutlin-3 was purchased from Sigma-Aldrich (St. Louis, MO, USA). YH-304 [(S)-Methyl 1-benzhydryl-3-(4-methylbenzyl)-2-oxopiperidine-3-carboxylate] was produced as previously described (2).
Clonogenic assay
In brief, A549 and 226B cells were seeded at 2×103 cells/well on a 6-well plate and allowed to attach overnight. The next day, medium was replaced with fresh medium containing different concentrations (0.5 and 2 μM) of YH-304 and incubated for 2 h. Following incubation, cells were harvested by trypsinization and counted. For clonogenic assay, 4 ml of cell suspension (50 cells/ml) was seeded in a 6-well plate and were incubated at 37°C for 14 days without any disturbance. Following incubation, the medium was removed and colonies were fixed and stained with 0.01% (w/v) crystal violet for 30 min. A colony consisting of at least 50 cells was counted with ImageJ software (NIH, Bethesda, MD, USA). The experiment was carried out twice in triplicate.
Western blot analysis
Western blot analyses were performed as previously described using the antibodies mentioned above. The respective protein bands were detected by chemiluminescence (FUSION SL4; Vilber Lourmat, Marne la Vallée, France).
Real-time PCR analysis
Total RNA was isolated from cells using TRIzol® reagent (Invitrogen) and transcribed using a PrimeScript First Strand cDNA Synthesis kit (Takara, Shiga, Japan) according to the manufacturers’ protocols. Quantitative real-time PCR was performed in triplicate on Rotor-Gene® Q (Roche Diagnostics, Indianapolis, IN, USA) using LightCycler® SYBR-Green I Master (Roche Diagnostics), and data were analyzed on the basis of threshold cycle values of each sample and normalized with β-actin. The PCR primers used in this study are listed below and were purchased from Bioneer: forward p53 5′-GCCCAACAACACCAGCTCCT-3′ and reverse p53 5′-GCCCAACAACACCAGCTCCT-3′; forward p21 5′-GGCCTCCTGACCCACAGCAG-3′ and reverse p21 5′-GGGCTCAACTCAACACCCACC-3′; forward β-actin 5′-AGAGGGAAATCGTGC-3′ and reverse β-actin 5′-GGC CGTCAGGCAGCTCATAG-3′.
Cell death assays by TUNEL staining
DNA strand breaks during apoptosis were detected by TUNEL of free 3′-OH ends of cleaved DNA. Following YH-304 treatment for 24 h, 226B cells were fixed in 4% (v/v) paraformaldehyde for 30 min on ice. Fixed cells were washed once in phosphate-buffered saline (PBS) and incubated for 60 min at 37°C in 50 μl of TdT-containing solution (Roche Diagnostics, Mannheim, Germany). Following TUNEL staining, all samples were washed once in PBS and nuclei were stained using 4′-6-Diamidino-2-phenylindole (DAPI; Invitrogen). Images were obtained with an Axiovert M200 microscope (Carl Zeiss AG, Oberkochen, Germany).
Cell viability assay
HCT-116, HeLa, A549 and MDA-MB-231 cells were treated with different concentration of YH-304 as indicated. After 24 h, 20 μl of CellTiter 96® Aqueous One solution reagent (Promega, Madison, WI, USA) was added and then read at 490 nm. Dose-response curves were plotted to determine half-maximal inhibitory concentrations (IC50) for the compounds with SigmaPlot software.
Zebrafish angiogenesis assay
Fertilized zebrafish (Danio rerio) eggs of the transgenic strain expressing green fluorescent protein (GFP) under the flk-1 promoter (flk-1:GFP) were used for in vivo imaging of embryonic vascular development. At 24 h post-fertilization (hpf), EGFP-expressing tg(fli1:EGFP) embryos were manually dechorionated and anesthetized with 0.003% tricaine. Anesthetized embryos were then transferred onto a 4% agarose gel for microinjection. Approximately 5 nl of Matrigel containing either PBS or basic fibroblast growth factor (bFGF, 25 ng/ml) was injected into the yolk sac of each embryo using microinjector (Narishige International, Inc., East Meadow, NY, USA). Non-filamentous borosilicate glass capillary needles were used for the microinjection (0.75 mm internal- and 1.0 mm external-diameter). Embryos were transferred into housing-keeping water immediately after injection and incubated with 0.003% 1-phenyl-2-thiourea (Sigma-Aldrich) at 28.5°C to prevent pigmentation. YH-304 treatment was carried out immediately after Matrigel injection and embryos were examined for angiogenesis using a fluorescent microscope (Carl Zeiss) 24 h later.
Statistical analysis
All values are expressed as means ± SE. Statistical significance was set at P<0.05; P<0.05; P<0.001.
ResultsYH-304 inhibits proliferation and colony formation of A549 and 226B NSCLC cells
To investigate the effect of YH-304 on the cancer cell proliferation, A549 and 226B NSCLC cells were pretreated with or without YH-304 ranging from 0.625 to 10 μM for 24 h and then measured by 3-[4,5-methylthiazol-2-yl]-2,5-diphenyl-tetrazolium bromide (MTT) assay. We found that YH-304 inhibited cancer cell proliferation in both A549 (Fig. 1A) and 226B (Fig. 1B) NSCLC cells in a dose-dependent manner. The anticancer effect of YH-304 was subsequently confirmed by clonogenic assay in A549 and 226B NSCLC cells. As observed above, we found that YH-304 suppresses colony formation ability of both A549 (Fig. 1C) and 226B (Fig. 1D) NSCLC cells. This suggests that YH-304 has potential for anticancer efficacy in NSCLC cells.
YH-304 induces apoptosis of A549 NSCLC cells
We next set out to determine whether YH-304 is involved in apoptosis using TUNEL assay. When A549 cells were treated with 0.5 or 2.0 μM YH-304, TUNEL-positive cells were increased as measured by fluorescence microscopy at individual cell level (Fig. 2A). From these cell images, it is clear that the red fluorescence intensity of individual cells increased in a concentration-dependent manner indicating apoptosis by YH-304. Additionally, we evaluated whether YH-304 can induce apoptotic cell death using apoptotic markers such as cleaved poly(ADP-ribose) polymerase (PARP), cleaved caspase-9 and Bax. When A549 cells were treated with 0.5 or 2.0 μM YH-304 for 24 h, the expression of intact PARP was decreased and that of cleaved PARP was detected as compared with control group (Fig. 2B). Also, cleaved caspase-9 and Bax were increased by YH-304 treatment in a dose-dependent manner (Fig. 2B). Together, these results suggest that YH-304 may induce apoptosis of A549 cells.
YH-304 does not affect p53 expression levels in HCT-116 and MDA-MB-231 cells
We previously reported that YH-304 is a simplified spiro-oxindole alkaloid which shares structural similarity with MDM2 inhibitor (an active anticancer agent) (2). Based on structural characteristics, we hypothesized that YH-304 might show the anticancer activity through MDM2 inhibition, resulting in p53 stabilization. To investigate whether the cytotoxic effect of YH-304 is dependent on MDM2-mediated p53 modulation, we determined whether YH-304 induces p53 expression through inhibition of MDM2. We treated either YH-304 or nutlin-3 (a well-known MDM2 inhibitor) in p53 wild-type cells (HCT-116) as well as p53 mutant cells (MDA-MB-231) and then evaluated the expression levels of p53 protein and p53-dependent mRNAs including p21. As expected, nutlin-3 induced both p53 protein expression level (Fig. 3A) and p21 mRNA levels (Fig. 3B) significantly in HCT-116 cells, but not in MDA-MB-231 cells (Fig. 3C and D). However, YH-304 did not alter the mRNA or protein expression levels of p53 in the HCT-116 (Fig. 3A and E) or MDA-MB-231 cells (Fig. 3C and F). Our preliminary mechanistic studies of YH-304 suggested that it has anticancer activities via p53-independent pathway. Further investigations of mechanistic studies for anticancer activities are now in progress.
YH-304 shows broad spectrum anticancer activity in a MDM2-p53-independent manner
The efficacy of YH-304 was investigated in four different cancer cell lines including HCT-116 (colon cancer), HeLa (cervix cancer), A549 (lung cancer), and MDA-MB-231 (breast cancer) cells and compared with a well-known chemotherapy agent, 5-FU and nutlin-3. Compared to 5-FU, YH-304 showed potent efficacy in four different cancer cells lines, showing broad spectrum anticancer effect (Fig. 4). Especially, IC50 values of YH-304 were significantly lower than 5-FU in HCT-116, A549 and MDA-MB-231 cells (Fig. 4). Nutlin-3, a specific MDM-2 inhibitor, exerted anticancer effect in p53 wild-type cancer cells having wild-type p53 but did not affect cell viability of MDA-MB-231 cells possessing mutant p53. However, YH-304 also showed good efficacy in both p53 wild-type and p53-mutant cancer cells, suggesting that YH-304 might be a potent anticancer agent with broad-spectrum in a p53-independent fashion.
YH-304 inhibits in vivo bFGF-induced angiogenesis through suppression of AKT and ERK
To investigate the effect of YH-304 on angiogenesis in vivo, we performed matrigel plug assay with transgenic fluorescent zebrafish tg(fli1:EGFP) which expresses enhanced GFP in the entire vasculature under the control of the fli1 promoter to visualize vascular formation in live zebrafish embryos (26). In plugs with bFGF (200 ng/ml) appeared newly formed vessels (Fig. 5A). In contrast, there was less or no blood vessel formation in plugs with Matrigel alone or mixed with YH-304 (2 μM) (Fig. 5A).
To further assess how YH-304 blocks bFGF-mediated angiogenesis, we tested whether YH-304 can affect AKT and/or ERK activation, two proteins known to play an important role in the bFGF signaling pathway. As shown in Fig. 5B, bFGF increased the phosphorylation of both AKT and ERK, whereas the addition of 0.5 or 2.0 μM YH-304 significantly reduced the phosphorylated AKT and phosphorylated ERK. Instead of bFGF, when treated with 10% FBS, YH-304 showed similar inhibition of phosphorylation of both AKT and ERK (Fig. 5C). Therefore, these data suggest that YH-304 suppresses bFGF-induced angiogenesis in vivo, at least partly through blocking AKT/ERK activation.
Discussion
Cancer is now one of the leading causes of mortality worldwide, causing 7.6 million deaths in 2008 (3). Anticancer drugs are required with novel structural features to overcome multidrug resistance and severe side-effects and to enhance the effectiveness of cancer treatment (29,30). Oxindole derivatives are specialized structures and exerted various biological activities, ranging from MDM2 antagonists (31,32), ion channel blockers (33) and anti-inflammatory agents (34,35) to various protein kinase inhibitors. A number of indole-based compounds inhibit various protein kinase families such as receptor tyrosine kinases (RTKs) and serine/threonine-specific protein kinases (5,10,36,37). As a kinase inhibitor, oxindole sunitinib was used for the treatment of advanced renal carcinoma and gastrointestinal stromal tumors (10,11,36,37). We previously reported the potential use of oxindole derivatives having simplified α-quaternary chiral lactam as anticancer agents. Among them, YH-304 had the strongest cell cytotoxicity against several cancer cell lines. However, the mechanisms of action underlying its anticancer effects are largely unknown and need to be better understood to allow this therapy to be used for clinical applications. This prompted us to study further the anti-tumorigenic effects of YH-304, including its underlying molecular mechanisms. Therefore, the aim of the present study was to further clarify the anticancer mechanism of YH-304 itself, which may offer an opportunity to design effective safe drugs with minimal toxicity for the treatment of carcinoma.
The p53 tumor suppressor has been implicated as a mediator of programmed cell death (16). Loss of wild-type p53 activity is regarded as a major predictor of failure to respond to chemotherapy in various human cancers (17,19,38). Therefore, patients with mutated p53 tend to be less responsive to common chemotherapeutics (39). Since p53 is the most frequently mutated in malignant cancers, therapies that do not depend on functional p53 are in general clinically preferable (39). Notably, although the structure of YH-304 is designed as a kind of oxindole derivatives similar to that of MDM2 inhibitor (a p53 activator), it did not alter the expression of p53 in p53 wild-type (HCT-116) or p53 mutant cells (MDA-MB-231), unlike nutlin-3 (MDM2 inhibitor) (Fig. 3A, C, E and F). Also, YH-304 showed similar or better efficacy in four different cancer cell lines compared to 5-FU (Fig. 4), indicating a p53-independent broad spectrum. Based on p53-independency and broad spectrum, therefore, YH-304 might be clinically preferable after further studies such as toxicity and clinical trials.
Our findings also indicate that YH-304 interferes with AKT and ERK phosphorylation in response to angiogenic factors such as bFGF or serum. Since AKT and ERK activities are required for proliferation and tube formation of vascular endothelial cells, the AKT and ERK pathways are considered as one of the most promising targets for anti-angiogenic therapy (40,41). Taken together, it is reasonable to assume that YH-304-mediated inhibition of AKT and ERK phosphorylation may be responsible for the inhibitory effect of YH-304 on angiogenesis as well as on clonogenic growth. Moreover, growing knowledge on cellular signaling networks in cancer opens up the opportunity to combine AKT and ERK inhibitors with other pathway specific inhibitors. Since synergistic effects between such inhibitors are known to exist, further studies are warranted combining YH-304 with other targeted inhibitors.
Our current data provide experimental evidence for a novel anticancer activity of YH-304 through suppression of AKT and ERK phosphorylation and, thereby, their downstream signaling cascade. Further studies are required to delineate the exact role and mode of action of YH-304, i.e., whether and how blood vessels regress in YH-304-treated Matrigel plugs. The present study provides a proof-of-principle for the development of YH-304 as an anti-angiogenic agent.
Acknowledgements
The present study was supported by the Basic Science Research Program through the National Research Foundation of Korea funded by the Ministry of Science, ICT and Future Planning (NRF-2016R1C1B2012270, NRF-2013R1A1A1059709 and NRF-2014R1A1A1002151).
ReferencesChenLYangJZhengMKongXHuangTCaiYDThe use of chemical-chemical interaction and chemical structure to identify new candidate chemicals related to lung cancerPLoS One10e0128696201510.1371/journal.pone.0128696260475144457841LeeHHwangSJJungJHongSLeeMParkHGLeeHJParkYAsymmetric synthesis and evaluation of α-quaternary chiral lactam derivatives as novel anticancer agentsArch Pharm Res3712641270201410.1007/s12272-013-0274-4JemalASiegelRWardEHaoYXuJMurrayTThunMJCancer statistics, 2008CA Cancer J Clin587196200810.3322/CA.2007.001018287387GallifordCVScheidtKAPyrrolidinyl-spirooxindole natural products as inspirations for the development of potential therapeutic agentsAngew Chem Int Ed Engl4687488758200710.1002/anie.20070134217943924ChenGWengQFuLWangZYuPLiuZLiXZhangHLiangGSynthesis and biological evaluation of novel oxindole-based RTK inhibitors as anti-cancer agentsBioorg Med Chem2269536960201410.1016/j.bmc.2014.10.01725456085NatarajanAGuoYHarbinskiFFanYHChenHLuusLDiercksJAktasHChorevMHalperinJANovel arylsulfoanilide-oxindole hybrid as an anticancer agent that inhibits translation initiationJ Med Chem4749794982200410.1021/jm049623415456240SilvaBVRibeiroNMVargasMDLanznasterMCarneiroJWKroghRAndricopuloADDiasLCPintoACSynthesis, electrochemical studies and anticancer activity of ferrocenyl oxindolesDalton Trans3973387344201010.1039/c002983a20601979KamalARamakrishnaGRajuPRaoAVViswanathANayakVLRamakrishnaSSynthesis and anticancer activity of oxindole derived imidazo[1,5-a]pyrazinesEur J Med Chem4624272435201110.1016/j.ejmech.2011.03.02721481986CuiCBKakeyaHOsadaHSpirotryprostatin B, a novel mammalian cell cycle inhibitor produced by Aspergillus fumigatusJ Antibiot (Tokyo)49832835199610.7164/antibiotics.49.832PapaetisGSSyrigosKNSunitinib: A multitargeted receptor tyrosine kinase inhibitor in the era of molecular cancer therapiesBioDrugs23377389200910.2165/11318860-000000000-0000019894779WangWLConleyAReynosoDNoldenLLazarAJGeorgeSTrentJCMechanisms of resistance to imatinib and sunitinib in gastrointestinal stromal tumorCancer Chemother Pharmacol67Suppl 1S15S24201110.1007/s00280-010-1513-8KussiePHGorinaSMarechalVElenbaasBMoreauJLevineAJPavletichNPStructure of the MDM2 oncoprotein bound to the p53 tumor suppressor transactivation domainScience274948953199610.1126/science.274.5289.9488875929DingKLuYNikolovska-ColeskaZQiuSDingYGaoWStuckeyJKrajewskiKRollerPPTomitaYStructure-based design of potent non-peptide MDM2 inhibitorsJ Am Chem Soc1271013010131200510.1021/ja051147z16028899DingKLuYNikolovska-ColeskaZWangGQiuSShangarySGaoWQinDStuckeyJKrajewskiKStructure-based design of spiro-oxindoles as potent, specific small-molecule inhibitors of the MDM2-p53 interactionJ Med Chem4934323435200610.1021/jm051122a16759082ParkYLeeYJHongSLeeMParkHGHighly enantioselective total synthesis of (+)-isonitramineOrg Lett14852854201210.1021/ol203304222251163ReedSMQuelleDEp53 Acetylation: Regulation and consequencesCancers (Basel)73069201410.3390/cancers7010030MelvinATDumbergerLDWossGSWatersMLAllbrittonNLIdentification of a p53-based portable degron based on the MDM2-p53 binding regionAnalyst (Lond)141570578201610.1039/C5AN01429HHuangKYWengJTLeeTYWengSLA new scheme to discover functional associations and regulatory networks of E3 ubiquitin ligasesBMC Syst Biol10Suppl 13201610.1186/s12918-015-0244-1268181154895279RichmondJCarolHEvansKHighLMendomoARobbinsAMeyerCVennNCMarschalekRHendersonMEffective targeting of the P53-MDM2 axis in preclinical models of infant MLL-rearranged acute lymphoblastic leukemiaClin Cancer Res2113951405201510.1158/1078-0432.CCR-14-2300255733814359964SaikiAYCaenepeelSCosgroveESuCBoedigheimerMOlinerJDIdentifying the determinants of response to MDM2 inhibitionOncotarget677017712201510.18632/oncotarget.3116257309034480710DebenCWoutersAOp de BeeckKvan Den BosscheJJacobsJZwaenepoelKPeetersMVan MeerbeeckJLardonFRolfoCThe MDM2-inhibitor Nutlin-3 synergizes with cisplatin to induce p53 dependent tumor cell apoptosis in non-small cell lung cancerOncotarget62266622679201510.18632/oncotarget.4433261252304673190ZanjirbandMEdmondsonRJLunecJPre-clinical efficacy and synergistic potential of the MDM2-p53 antagonists, Nutlin-3 and RG7388, as single agents and in combined treatment with cisplatin in ovarian cancerOncotargetMay202016(Epub ahead of print)10.18632/oncotarget.949927223080MichaelisMRothweilerFBarthSCinatlJvan RikxoortMLöschmannNVogesYBreitlingRvon DeimlingARödelFAdaptation of cancer cells from different entities to the MDM2 inhibitor nutlin-3 results in the emergence of p53-mutated multi-drug-resistant cancer cellsCell Death Dis2e243201110.1038/cddis.2011.129221700993252738RennekampAJPetersonRT15 years of zebrafish chemical screeningCurr Opin Chem Biol245870201510.1016/j.cbpa.2014.10.025SunYShengZMaCTangKZhuRWuZShenRFengJWuDHuangDCombining genomic and network characteristics for extended capability in predicting synergistic drugs for cancerNat Commun68481201510.1038/ncomms9481264124664598846LiuZLiuFCautious use of fli1a:EGFP transgenic zebrafish in vascular researchBiochem Biophys Res Commun427223226201210.1016/j.bbrc.2012.09.06422995292BarriusoJNagarajuRHurlstoneAZebrafish: A new companion for translational research in oncologyClin Cancer Res21969975201510.1158/1078-0432.CCR-14-2921255733825034890EdenCJJuBMurugesanMPhoenixTNNimmervollBTongYEllisonDWFinkelsteinDWrightKBoulosNOrthotopic models of pediatric brain tumors in zebrafishOncogene3417361742201510.1038/onc.2014.107GonçalvesASMacedoASSoutoEBTherapeutic nanosystems for oncology nanomedicineClin Transl Oncol14883890201210.1007/s12094-012-0912-122855194YinQShenJZhangZYuHChenLGuWLiYMulti-functional nanoparticles improve therapeutic effect for breast cancer by simultaneously antagonizing multiple mechanisms of multidrug resistanceBiomacromolecules1422422252201310.1021/bm400378x23682680RibeiroCJAmaralJDRodriguesCMMoreiraRSantosMMSynthesis and evaluation of spiroisoxazoline oxindoles as anticancer agentsBioorg Med Chem22577584201410.1016/j.bmc.2013.10.048ShangarySDingKQiuSNikolovska-ColeskaZBauerJALiuMWangGLuYMcEachernDBernardDReactivation of p53 by a specific MDM2 antagonist (MI-43) leads to p21-mediated cell cycle arrest and selective cell death in colon cancerMol Cancer Ther715331542200810.1158/1535-7163.MCT-08-0140185662242494594JensenBSBMS-204352: A potassium channel opener developed for the treatment of strokeCNS Drug Rev8353360200210.1111/j.1527-3458.2002.tb00233.x12481191ChenGJiangLDongLWangZXuFDingTFuLFangQLiuZShanXSynthesis and biological evaluation of novel indole-2-one and 7-aza-2-oxindole derivatives as anti-inflammatory agentsDrug Des Devel Ther8186918922014253789064207570SunYLiuJJiangXSunTLiuLZhangXDingSLiJZhuangYWangYOne-step synthesis of chiral oxindole-type analogues with potent anti-inflammatory and analgesic activitiesSci Rep513699201510.1038/srep13699263240654555174HoHKChuaBTWongWLimKSTeoVOngHTChenXZhangWHuiKMGoMLBenzylidene-indolinones are effective as multi-targeted kinase inhibitor therapeutics against hepatocellular carcinomaMol Oncol812661277201410.1016/j.molonc.2014.04.00824839937IzzedineHBuhaescuIRixeODerayGSunitinib malateCancer Chemother Pharmacol60357364200710.1007/s00280-006-0376-5EngelandKSimplify p53: Just an activatorOncotarget6342015255758184381574KoshinoAGoto-KoshinoYSetoguchiAOhnoKTsujimotoHMutation of p53 gene and its correlation with the clinical outcome in dogs with lymphomaJ Vet Intern Med30223229201610.1111/jvim.138074913626HellesøyMLorensJBCellular context-mediated Akt dynamics regulates MAP kinase signaling thresholds during angiogenesisMol Biol Cell2626982711201510.1091/mbc.E14-09-1378260230894501366HuangJJShiYQLiRLHuALuZYWengLWangSQHanYPZhangLLiBAngiogenesis effect of therapeutic ultrasound on HUVECs through activation of the PI3K-Akt-eNOS signal pathwayAm J Transl Res7110611152015262797544532743
YH-304 inhibits proliferation and colony formation of A549 and 226B NSCLCs. (A and B) After incubation with YH-304 ranging from 0.625 to 10 μM for 24 h, MTT was added and the absorbance was measured at 570 nm in an ELISA reader. (A) Effect of YH-304 on cellular proliferation in A549 cells. (B) Effect of YH-304 on cellular proliferation in 226B cells. (C and D) Cells were pretreated with 0.5 or 2 μM of YH-304 and then were seeded (2,000 cells/well) in triplicate onto 6-well plates and treated with 0.5 or 2 μM of YH-304. After 2 weeks, the colonies formed were stained using crystal violet and counted. (C) Colony formation by YH-304 in A549 cells. (D) Colony formation by YH-304 in 226B cells. Values are expressed relative to vehicle-treated cells, normalized to 100% ± standard deviation (SD), and were obtained from three independent experiments. *P<0.05, **P<0.01.
YH-304 induces apoptosis of A549 cells. (A) The TUNEL assay of 0.5 or 2 μM YH-304-treated A549 cells. Apoptotic cell death was evaluated by TUNEL staining (red, ×40 objective lens) after 24-h treatment of YH-304. Representative images of three independent experiments show the effect of YH-304 on TUNEL-positive programmed cell death. Scale bar is 10 μm. (B) Effect of YH-304 on PARP cleavage, cleaved caspase-9 and Bax in A549 cells. A549 cells were treated with YH-304 ranging from 0.5 to 2 μM for 24 h. Western blotting was performed to evaluate the cleaved PARP, intact PARP, cleaved caspase-9, Bax and α-tubulin expression levels. α-tubulin was used as an internal control.
YH-304 did not affect p53 expression levels in HCT-116 and MDA-MB-231 cells. Cells were treated with either 10 μM nutlin-3 (a well-known MDM2 antagonist) or 10 μM of YH-304 for 24 h. (A) Effect of p53 protein expression in HCT-116 (expressing wild-type p53) cells. (B) Effect of p21 mRNA expression in HCT-116 cells. (C) Effect of p53 protein expression in MDA-MB-231 (expressing mutant-type p53) cells. (D) Effect of p21 mRNA expression in MDA-MB-231 cells. (E) Effect of YH-304 on p53 mRNA expression in HCT-116 cells. (F) Effect of YH-304 on p53 mRNA expression in MDA-MB-231 cells. GAPDH and β-actin were used as internal controls.
YH-304 shows broad spectrum anticancer activity via a p53-independent manner. The p53-independent effectiveness of YH-304 against four different types of cancer cells. The average IC50 values of YH-304, 5-FU (5-fluorouracil), and nutlin-3 (a well-known MDM2 inhibitor) were analyzed against three cancer cell lines (HCT-116, HeLa and A549) expressing wild-type p53 and MDA-MB-231 expressing mutant-type p53. Cells were treated with YH-304 ranging from 0.039 to 10 μM for 24 h. Cells treated with DMSO (equivalent volume) were used as vehicle control. N.D., not determined.
YH-304 inhibits bFGF-induced angiogenesis through inhibition of AKT and ERK. (A) Inhibitory effect of YH-304 in Matrigel plug assay in vivo. A total of 5 nl of matrigel containing either PBS or bFGF (25 ng/ml) was injected into the yolk sac of each embryo of zebrafish (Danio rerio) eggs expressing green fluorescent protein (GFP) under the flk-1 promoter (flk-1:GFP) using microinjector. YH-304 was treated immediately after Matrigel injection and embryos were examined for angiogenesis using a fluorescent microscope 24 h later. Scale bar is 100 μm. (B) Effect of YH-304 on AKT and ERK signaling mediated by recombinant bFGF. Western blots show p-AKT, total AKT, p-ERK and total ERK expression levels in A549 cells treated with YH-304 for 24 h. Results from a representative experiment (n=3) are shown. (C) Effect of YH-304 on AKT and ERK signaling mediated by 10% FBS. Western blots show p-AKT, total AKT, p-ERK and total ERK expression levels in A549 cells treated with YH-304 for 24 h.