Abstract

Dietary compounds that possess the properties of altering epigenetic processes are gaining popularity as targets for cancer prevention studies. These compounds when administered at optimal concentrations and especially in combination can have enhanced effects in cancer prevention or therapy. It is important to study the interaction of two or more compounds in order to assess their role in enhancing prevention. Genistein (GEN), found in soy, has been extensively studied for its role as an epigenetic modifier especially as a DNA methyltransferase (DNMT) inhibitor and sulforaphane (SFN), found in cruciferous vegetables, is known as a histone deacetylase (HDAC) inhibitor. However, very little is known about the effects of these two compounds in conjunction in breast cancer prevention or therapy. In our current study, we determined that, at certain doses, the compounds have synergistic effects in decreasing cellular viability of breast cancer cell lines. Our results indicate that the combination of GEN and SFN is much more effective than their single doses in increasing the rate of apoptosis and lowering the colony forming potential of these cells. We determined that these compounds inhibit cell cycle progression to G2 phase in MDA-MB-231 and G1 phase in MCF-7 breast cancer cell lines. Additionally, we determined that the combination is effective as an HDAC and histone methyltransferase (HMT) inhibitor. Furthermore, we demonstrated that this combination downregulates the levels of HDAC2 and HDAC3 both at the mRNA and protein levels. We also found that these compounds have the potential to downregulate KLF4 levels, which plays an important role in stem cell formation. The combination of GEN and SFN is also effective in downregulating hTERT levels, which is known to be activated when KLF4 binds to its promoter region. Our hypothesis is further strengthened by in vivo studies, where the combination is administered to transgenic mice in the form of genistein and SFN-enriched broccoli sprouts. We have demonstrated that the combination is more effective in preventing or treating mammary cancer via extending tumor latency and reducing tumor volumes/sizes than either of these dietary components administered alone. These results are consistent with our in vitro study suggesting potential preventive and therapeutic effects of this novel dietary combinatorial approach against breast cancer.

Highlights

  • AccoKredyiwnogrdtso: greencisetneitn;sstualtfiosrtaipcsh,anteh;oburegahst ctahnecebr;reepaisgtenceatincsc;eHrDdAeCa;thKLrFa4t;ecohmabsindateiocnre; saysneedrgyo;ver the years, ovberroaclclolbi;rteraansstgceanniccmerouinsecmidoednecl e rates have increased among most races [1]

  • The combination has downregulated KLF4, which acts as an oncogene in breast cancer

  • The combination was effective in downregulating hkinstoownne DdNeaAcetylase (HDAC) activity, especially HDAC2 and HDAC3, which act in concert with KLF4

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Summary

Introduction

AccoKredyiwnogrdtso: greencisetneitn;sstualtfiosrtaipcsh,anteh;oburegahst ctahnecebr;reepaisgtenceatincsc;eHrDdAeCa;thKLrFa4t;ecohmabsindateiocnre; saysneedrgyo;ver the years, ovberroaclclolbi;rteraansstgceanniccmerouinsecmidoednecl e rates have increased among most races [1]. The cause for breast cancer is still unknown though most of the evidence points toward genetic and epigenetic abnormalities. Epigenetic gene alterations are an important hallmark of breast cancer. Enome and playEpaingeancettiivcegeroneleailntercaatniocnesraprereavneinmtipoonrtaanntdhtahllemraarpkyo[f4b].reSaesvt ecarnacledr.ieAtacroymcmomonpcoauunsedosfabdremasint istered singly ocrainncecroins jeupnigcetnioetnicwmiotdhifoictahteiornds,ieestapreyciaclolyminpcoreuansidnsg oDrNoAthmeerthcyhleamtioontahnedrahpisetounteicdaegaceentytslactiaonn.reverse abnormBnauliomgaecetnrioveueasdcstiteiuvtdaairetyisohcnoamvoerpsosuuiglnegdnessctieandrgethionaft ctshapenescceieadrliecinteatlrelysrec[so5tm]b.peocauunsdes of their can alter anticancer properties and abnormal epigenetic states. Genthiasttecainn co(GnfEerNpo),tenfotiualnsdideienffecntsa.tLuorwaler sdooysebseoafnth, e sisingalencoimsopflouanvdosnine cotmhabtinaitsionamkaynohawvne DNA methyltarabnetstfeerrcahseem(oDprNevMenTti)veinphoitebnittioarl awndhtirleanssulaltfioonraalpimhapnacet.(SFN), which is enriched in cruciferous vegetables sGuecnhistaesinbr(GocEcNo)l,i fsopurnodutisn (BnSatpu)raal nsdoykbaelaen,, hisasabneeisnofslahvoownen tthoathaisvea hkinstoownne DdNeaAcetylase (HDAC)mienthhyibltirtainnsgfeprarsoep(eDrNtiMesT[)1i1n,h1i2b]it.oFrigwuhrilee 1suslhfoorwapshathnee s(StrFuNc)t, uwrheicohf GisEeNnriachneddSinFNcr.uTcihfeeroinushibitory effects ovfeGgeEtaNblaesndsuSchFNasinbrtouccmoloi rspinrohuitbsit(iBoSnp)maanyd bkealae,tthraibsubteeedn tsohomwondtuolahtaivnegheisptiogneendeetaicceptyaltahswe ays by altering(eeHfpfDeicgAtseCno)feiGntihEciNbmitaiannrgdkpsSrFionNpecirnatniteucsme[r1o1cr,e1in2ll]hs.i.FbOiigtiuuorrnepm1rsaehyvobiwoeusatsthtrseitbsuutrdtueicedtsutorhemaovofedGusEhlNaotiwanngndetSphFigaNet.naTehctieocmipnahbtihibnwiatoatyroysrial diet consistinbgy aolfteDrinNgMepTigaenndetiHc mDaArkCs iinnhcainbciteorrcselclsa.nOaulrtperretvhieouespsitguednieesthicavmeaschhowinnerthyavt aiacodmirbeicntaatonrdialindirect inhibitiodnietocfoDnsNisMtinTgsoafnDdNHMDT AanCdsH, tDhAerCebinyhilbeiatodrisncgantoalmterodthueleaptingegnaetbicermractihoinnesryinvDiaNdiArecmt aenthdylation and histionndeireaccteitnyhliabtiitoionn/odfeDacNeMtyTlas taiondn HinDtAuCmso, rth-reerleabtyedleagdeinnegsto[1m3–o1d5u]l.aStiFngNaibsearrnatiinonhsibiintoDrNoAf HDAC activity,mwehthicyhlatrieosnulatnsdinhaisntoinnecraecaestyelaintiognl/odbeaalceatnyldatlioocnailnhitsutmonore-raeclaetteydlagtieonneso[f1a3–n1u5]m. We hypothesized that the optimal concentration of the two compounds should be effective in synergistically decreasing cancer cell viability. The correct combination of two or more dietary compounds that act synergistically can be very effective in preventing and treating breast cancer. Previous studies have shown that SFN exhibits chemopreventive activity by inducing cell cycle arrest and induction of cyclin-dependent kinase inhibitor 1A (p21 waf1/cip1) via KLF4 transcription factor mediation [17]

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