The comparison between the effect of curcumin and its naturally occurring analogues including its demethoxy derivatives (demethoxycurcumin, bisdemethoxycurcumin) and its active hydrogenated metabolites (tetrahydrocurcumin, hexahydrocurcumin and octahydrocurcumin) (Figure 1) pointed out possible structure-activity relationships.

It was reported that the high anti-inflammatory and anti-tumoral potential of curcuminoids are related to low level of hydrogenation and high level of methoxylation but also to the high level of unsaturation of the diketone moiety [15]. On the other hand, the radical scavenging potential of the curcuminoids was linked to the number of ortho-methoxy substitutions and to the level of hydrogenation of the heptadiene moiety of curcumin [16,17]. Indeed, glycosylation of curcumin aromatic ring provides a more water-soluble compound with a greater kinetic stability and a good therapeutic index [18].

Due to the multiple therapeutic potential of curcumin, various formulations were tested in order to enhance its bioavailability and to bring this natural compound to the forefront of therapeutic agents [19]. On one hand, formulation of curcumin in nanoparticles [20,21], liposomes [22,23], micelles [24] and phospholipid complexes decreases its hydrophobicity and increase its circulation time, its permeability through membrane barriers, its solubility as well as its resistance to metabolic stress [11]. On the other hand, the use of an adjuvant like piperine isolated from black pepper (that inhibits UGTs and p450s) [25], quercetin derived from soy beans (that inhibits sulfotransferases) and genistein (that inhibits alcohol dehydrogenase) counteracts detoxification enzymes implicated in curcumin metabolism. This leads to the increase of curcumin absorption, serum concentration and subsequently to the increase of curcumin bioavailability [19,26].

Over the past decades, experimental studies were performed to understand the intracellular mechanisms targeted by curcumin that implicated in the promising therapeutic potential of this natural compound used since centuries in traditional medicine. Aggarwal and coworkers firstly described curcumin as a potent modulator of inflammatory cell signaling [31]. This finding was promising as inflammation is highly involved in the promotion step of tumorigenesis, through the induction of survival, proliferation, invasion, angiogenesis and metastasis [32]. Aggarwal pointed out that this effect on inflammation was mainly due to inhibition of the nuclear factor-kB (NF-κB) signaling pathway [33]. Subsequent studies revealed that this natural compound acts on several components of this pathway. In fact, curcumin was shown to suppress the activation of IkBa kinase (IKK), the phosphorylation and degradation of IkBa and the subsequent phophorylation and nuclear translocation of the p65 subunit in several cancer and premalignant cell types [34,35,36,37,38,39,40]. This prevention of NF-κB activation is also related to the ability of curcumin to inhibit the proteasome function [41,42,43]. Such an inhibition of NF-κB was also induced after treatment with curcumin analogs such as demethoxycurcumin, bisdemethoxycurcumin, tetrahydrocurcumin and 3,5-bis(2-flurobenzylidene)-piperidin-4-one (EF24) [16,44]. Similar results were also observed in primary cells issued from multiple myeloma patients [45] and in patients with advanced pancreatic cancer [46]. It is important to notify that NF-κB regulates the expression of more the 450 genes implicated in all main signaling pathways [47] such as tumor cell proliferation (cyclins), invasion potential (matrix metalloproteinases (MMP), adhesion molecules), angiogenesis (vascular endothelial growth factor (VEGF)) [48] but also growth factors (epidermal growth factor (EGF), tumor necrosis factor (TNFa)) and most of the anti-apoptotic genes (Bcl-2 and X linked inhibitor of apoptosis (XIAP)) [49] as well as numerous oncogenes [50]. The down-regulation of the NF-κB pathway by curcumin could thus impact other related signaling pathways as demonstrated in several studies [51,52,53,54,55] and provide opportunities for both prevention and treatment [56].

In addition to its impact on NF-κB, curcumin also affects other molecular events implicated in inflammation and subsequent tumor promotion [31,57] such as inflammatory cytokines (TNFa, interleukines IL-1, IL-6 and IL-8) [58,59], inflammatory transcription factors (STATs), and inflammatory enzymes (Cyclooxygenase (COX)-2, 5-lipoxygenase (LOX)) [60].

It is reported in the literature that persistent activation of STATs also mediates tumor-promoting inflammation through their collaboration with other transcription factors [31,61,62]. Again, the inhibition of this transcription factor represents a promising tool both for prevention and therapy. We reported that curcumin alone inhibits STATs expression, especially the decrease of nuclear STAT-3, -5a and -5b, without affecting neither STAT1 nor the phosphorylation state of STAT1, -3 or -5 in human chronic K562 leukemia cells. When used as a pre-treatment, curcumin inhibits interferon-gamma-induced phosphorylation of nuclear STAT1 and -3 [63,64]. Similar suppression of STAT3 activation was also observed in Hodgkin’s lymphoma [52], T-cell leukemia [65], head and neck squamous cell carcinoma [66], multiple myeloma cells [52,67] and in CD138⁺ cells derived from multiple myeloma patients [45] following curcumin treatment but also after treatment with curcumin analogs such as GO-Y030 [68], FLLL1 and FLLL12 [69] or a curcumin-phospholipid complex [70]. The interferon-a-induced activation of STAT1 was also inhibited by curcumin in human lung A549 carcinoma and melanoma cells [71]. This inhibition of STAT1 as well as the inhibition of NF-κB were suggested to be implicated in the inhibition of COX-2, an important reactive-oxygen-generating enzymes implicated in inflammatory processes [55,72,73,74]. In fact, it was reported that curcumin is a potent inhibitor of COX-2 in several cancer types [37,73,75,76,77,78,79,80,81]. Moreover, studies performed on mononuclear cells from peripheral blood of patients with pancreatic cancer [46] and on oral premalignant cells [40] reported an inhibition of COX-2 expression after curcumin treatment. More recently, fluorocurcumin, a curcumin analog presenting a higher bioavailability than curcumin, was also shown to down-regulate NF-κB and prostaglandin (PG)E2 level so that it was suggested to be a potential agent against COX-2 overexpressing tumors [82]. All of these in vitro as well as preclinical studies suggested that targeting components of the inflammatory pathways provide good opportunities for prevention and therapy of cancer [56].

Carcinogenesis is a multistage process with three successive steps, initiation, promotion and progression. This process is often linked to oxidative stress, chronic inflammation and hormonal imbalance. The chemopreventive effect of curcumin is mainly based on its effectiveness to inhibit tumorigenesis through the decrease of cancer cell proliferation.

A way for curcumin to counteract cancer cell proliferation consists in the arrest of the cell cycle. This antiproliferative effect was observed in several cancer cell types (prostate, lung, breast and head and neck cancer but also lymphoma and leukemia). In fact, curcumin induces the expression of cyclin-dependent kinase (CDK) inhibitors p16, p21 and p27, and inhibits the expression of cyclin E and cyclin D1 as well as the hyperphosphorylation of retinoblastoma (Rb) protein. This leads to the disruption of cell cycle and to the death of cells by apoptosis [83,84,85].

The modulation of cyclins could be related to the impact of curcumin on the Wingless (Wnt) signaling pathway [86,87], especially through the modulation of the b-catenin/T-cell factor (TCF)/lymphoid enhancer factor (LEF) as observed in osteosarcoma [88], colon cancer cells [89,90], breast stem and cancer cells [91,92]. The observed decrease of the b-catenin/Tcf transcriptional activity was due to the decrease of the nuclear level of expression of b-catenin and Tcf-4 [89]. Similar decrease of b-catenin expression was also shown to be responsible of the inhibition of intestinal tumor growth in an animal model of familial adenomatous polyposis [93]. Gene expression profiling by microarray revealed that curcumin was also able to attenuate the expression of Frizzled-1, a Wnt receptor [94]. Demethoxycurcumin and bisdemethoxycurcumin, two curcumin analogs, were also reported to decrease the b-catenin transcriptional activity with a comparable potency as curcumin in colorectal cancer, through the down-regulation of p300, which is a positive regulator of the Wnt signaling pathway. As the tetrahydrocurcumin metabolite exhibits a much lesser impact on the Wnt pathway, it was suggested that the conjugated bonds in the central seven-carbon chain of curcuminoids are essential for the anti-proliferative activity of curcuminoids [95].

Dysregulations of phosphatidylinositol 3-kinase (PI3K)/Akt signaling pathways were also shown to play an important role in cancer cell growth and survival. Thus the targeting of these pathways may provide new anti-cancer strategies [96,97]. Curcumin was reported to be a good inhibitor of phosphoinositol (PI)3/Akt/mammalian target of rapamycin (mTOR) signaling pathway through the modulation of their expression and phosphorylation in a panel of cancer cell lines derived from leukemia [55,98], cervical cancer [99], colorectal carcinoma [100], renal carcinoma [101], breast cancer [102], Ewing’s sarcoma [103], prostate cancer cells and xenografts [104,105,106,107]. This leads to cell death by apoptosis and to the down-regulation of downstream effector proteins and genes such as p53, NF-κB and eukaryotic initiation factors (eIFs) which play an important role in the initiation of protein synthesis [108,109]. Such an inhibition of PI3/Akt/NF-κB signaling pathway by curcumin was also suggested to be implicated in the down-regulation of the expression of P-glycoprotein (P-gp) implicated in the multidrug resistance (mdr) 1b gene-mediated multidrug resistance [110].

Curcumin analogues such as FLLL11, FLLL12 and 4-hydroxy-3-methybenzoic acid methyl ester (HMBME) were also described as good inhibitors of cell proliferation of breast and prostate cancer though the modulation of PI3/Akt/ mTOR signaling [69,100,111].

The proliferation of solid tumors is also highly linked to their potential to establish metastasis and invade surrounding tissues. This phenomenon is based on the ability of tumor cells to produce growth factors such as EGF, VEGF and MMPs.

Matrix metalloproteinases (MMPs) play a major role in this phenomenon by mediating neovascularization, endothelial cell migration and tube formation [112]. The alteration of MMP-1, membrane type-1 matrix metalloproteinase (MT1-MMP), MMP-2, MMP-9 expression was observed after curcumin treatment in vitro and in vivo in melanoma [113], prostate [114,115], lung [116] and breast cancer cells [117,118].

Over-expression of epidermal growth factor receptor (EGFR) is highly implicated in cancer cell proliferation [119,120]. Curcumin was shown to down-regulate the EGFR expression in pancreatic and lung adenocarcinoma expressing COX-2 [81]. This natural compound also inhibits the EGFR intrinsic kinase activity in human epidermoid carcinoma [121], breast [122], prostate [123,124] and colon cancer cells [125]. This decrease of EGFR expression and activity could be subsequent to the inhibition of the ligand-induced activation of EGFR [126], to the peroxisome proliferator-activated receptor-g (PPAR-g) activation [127], to the suppression of EGFR phosphorylation [128] or to the decrease of the early growth factor-1 (Egr-1) transcriptional activity [129] observed after curcumin treatment. A similar decrease of the EGFR expression level was also observed in estrogen receptor negative breast cancer treated with derivatives of curcumin issued from the replacement of phenyl group of cyclohexanone derived curcumin by heterocyclic rings [122].

Curcumin also appears to be a direct in vitro and in vivo inhibitor of VEGF and fibroblast growth factor (FGF) [48,77,116,130,131,132,133,134], that are usually elevated in many human cancer and that correlate with enhanced microvessel density and metastatic spread. The molecular mechanisms, implicated in curcumin-inhibition of angiogenesis, consist also in the down regulation of the expression of pro-angiogenic components such as angiopoietin 1 and 2 genes, Kinase Domain Region (KDR) [131] and cell surface expression of vascular adhesion molecules (VCAM-1) [135]. Curcumin and its metabolite tetrahydrocurcumin were also reported to decrease the microvascular dilatation, tortuosity and hyper-permeability in hepatocellular carcinoma implanted in nude mouse [136].

Telomeres are specialized heterochromatic structures localized at the end of human chromosomes. They consist of tandem repeats that play structural and functional roles and allow maintaining genome stability. In healthy cells, telomeres are shortened during each cell division so that the cells stop replicating once the telomeres become too short. In contrast, the majority of solid tumors and leukemia acquire elevated telomerase activity to overcome such limitations ensuring thus their immortality and unlimited proliferative potential through the bypass of senescence [137,138]. Telomerase inhibition emerges thus as an attractive target for cancer therapy [139,140]. Treatment of cancer cells with curcumin revealed that this natural compound inhibits telomerase activity by down-regulating the human telomerase reverse transcriptase (hTERT), the catalytic core of telomerase which leads thus to the suppression of cell viability and to the induction of apoptosis [141,142,143,144,145]. Recent findings suggest that such a down-regulation of hTERT could be explained by a decrease of the association of hTERT and p23, a component of the molecular chaperone complex Hsp90-p23 that normally interacts with the rate-limiting catalytic subunit of telomerase [146].

In order to specifically target telomerase, Kappor et al., have taken advantage of the RNA subunit conformation of telomerase. They linked a tetraglycine conjugate of curcumin to an 11-mer DNA sequence complementary to a telomerase RNA sequence. Treatment of oral KB cancer cells with such a construct leads to the a significant reduction of cancer cell growth [147].

In addition to genetic alterations, cancer development and progression are also linked to epigenetic modifications [148], which consist mainly in DNA methylation and posttranslational histone modifications (acetylation, methylation, ubiquitylation, phosphorylation and sumoylation). DNA methylation is mediated by DNA methyltransferases (DNMTs). Aberrant hypermethylation of promoter CpG islands of tumor suppressor genes results in their transcriptional silencing and tumor survival [149]. Curcumin as well as tetrahydrocurcumin were reported to block covalently the catalytic thiolate of the C1226 of DNMT1 leading thus to DNA hypomethylation and suggesting a subsequent death of tumor cells [150].

On the other hand, the level of histone acetylation, resulting from the balance of histone acetyltransferase (HAT) and histone deacetylase (HDAC) activities, plays a crucial role in chromatin remodeling and in the regulation of gene transcription [151]. The impact of curcumin on these implicated epigenetic mechanisms was evaluated and revealed that this natural compound is able to induce histone hypoacetylation by blocking the HAT activity in vitro and in vivo without affecting HDAC [152]. In fact, curcumin was reported to be a potent and specific inhibitor of p300/CREB Binding Protein (CBP) histone acetyltransferase activity in several cancer types by promoting their proteasomal degradation, whereas its tetrahydrocurcumin metabolite does not affect p300 [153,154,155]. Molecular docking carried out for the human HDAC8 enzyme, pointed out that curcumin could also be considered as a potent HDAC inhibitor [156] and other studies showed that it can also significantly decrease the amount of HDAC1 and HDAC3 [157].

More recently, several studies pointed out that deregulation of microRNAs, a category on small noncoding RNAs that function as genes regulators, were also involved in tumorigenesis and related to epigenetics alterations. In fact, the microRNA network is implicated in the regulation of many basic cellular processes such as proliferation, differentiation and cell death [158,159,160,161,162]. Evidence has been provided that dietary compounds such as curcumin could exert their chemopreventive effect through the modulation of miRNAs expression [163]. Indeed, curcumin was reported to alter miRNA expression by up-regulating miRNA-22 and down-regulating miRNA-199a* in human pancreatic cells [164]. On the other hand, this natural compound was also able to up-regulate the expression of miRNA-15a and miRNA-16 which leads to the reduction of the expression of the anti-apoptotic Bcl-2 gene [165].

Apoptosis is a tightly regulated mechanism of cell death that can be initiated by intracellular stress signals and extracellular ligands following curcumin treatment in several cancer types [166,168]. The intrinsic induction of apoptosis is triggered in response to cellular signals including stress and DNA damage. Curcumin was reported to induce the up-regulation of pro-apoptotic proteins from the Bcl-2 family (Bim, Bax, Bak, Puma and Noxa) and the down-regulation of anti-apoptotic proteins (XIAP, Bcl-2, Bcl-xL) [101,105]. This leads to the opening of mitochondrial permeability transition pores, the release of cytochrome c, the activation of the apoptosome (caspase-9/apaf-1/cytochrome c) and the subsequent cleavage of caspase-3, -6 and -7, Poly (ADP-ribose) polymerase (PARP) and finally to the death of tumor cells [169,170,171]. Pre-clinical studies pointed out that curcumin has similar pro-apoptotic effect on primary chronic lymphocytic leukemia B cells but that this effect is inhibited in the presence of stromal cells. In order to overcome this protective effect mediated by stromal cells, curcumin needs to be administered simultaneously with epigallocatechin-3 gallate (EGCG) [172].

On the other hand, apoptosis may also be induced by the extrinsic pathway at the cell surface through the activation of cell membrane receptors (Fas, TRAIL) [173,174,175]. This pathway leads to the assembly of the death- inducing signaling complex (DISC) containing Fas, FAD and caspase-8 and -10. The extrinsic pathway converges then to the intrinsic one by the induction of Bid cleavage, the subsequent release of cytochrome c and the activation of the cascade of caspases.

This induction of cell death by apoptosis after curcumin or curcumin analogs treatment [176] supports the idea of their possible implication for cancer therapy [16,177].

Mitotic catastrophe (MC) is a type of cell death resulting from aberrant mitosis. In fact, this process results from a combination of deficient cell-cycle checkpoints (DNA structure and spindle assembly checkpoints) and cellular damage. Moreover, it has been reported that the intrinsic mitochondrial apoptotic machinery (chromatin condensation, mitochondrial release of proapoptotic proteins, caspase-2 activation and DNA degradation) is highly implicated in the execution of mitotic catastrophe, which occurs at the metaphase level, in a p53 independent manner [178,179]. This type of mitosis leads to the formation of large non-viable cells with several micronuclei and uncondensed chromosomes [179,180]. The disruption of mitotic spindle structure and the appearance of micronucleation after curcumin treatment were firstly described in MCF-7 human breast cancer cells and were related to curcumin-induced cell cycle arrest in G2/M [181]. Mitotic catastrophe was also a way for curcumin to overcome the resistance of tumor cells to apoptosis. In the case of curcumin, the induction of MC was related to the inhibition of survivin, a modulator of cell division and apoptosis in cancer [182,183]. Moreover, curcumin-induced cytotoxicity observed in a panel of oesophageal cancer cell lines after 24h of treatment was associated to MC induction related to an accumulation of the mitotic regulator cyclin B1 and of poly-ubiquitinated proteins [184]. Other publications underline the fact that curcumin metabolites, derivatives and products of degradation were unable to induce G2/M cell cycle arrest and MC compared to the original curcumin compound [185,186].

Mitotic catastrophe induction should be considered for clinical approaches, as a correlation was found between poor prognosis of treatment and inability of cells to induce MC. Moreover an increase of MC induction could compensate impaired induction of apoptosis [167].

Autophagy is a highly regulated process characterized by sequestration of bulk cytoplasm, long-lived proteins and cellular organelles in double-membrane vesicles (autophagosomes), which are subsequently degraded in lysosomes. The final role of autophagy as a tumor suppressor or a protector of cancer cells from anti-cancer therapy is still under investigation [187,188,189]. In the case of curcumin, it was recently reported that this natural compound suppresses the growth of malignant gliomas in vitro and in vivo through cell cycle arrest in G2/M transition phase and induction of autophagy. This phenomenon has been associated to the inhibition of the Akt/mTOR kinase and to the activation of the extracellular signal-regulated kinases (ERK) 1/2 and to the increase of LC-3 II expression [190,191]. Such an induction of autophagy was also observed concomitantly with mitotic catastrophe in oesophageal cancer after curcumin treatment [184].

Curcumin was reported to have a synergistic effect with genistein, a natural compound derived from soy beans. When combined, they are able to reduce the proliferation of the human breast MCF-7 oestrogen-positive cells induced by environmental pesticides [192]. Moreover, combination of curcumin with 1,25-dihydroxyvitamin D3 (calcitrol) treatment, a well known inducer of monocytic differentiation, was able to stimulate monocytic differentiation of the human promyelocytic HL-60 cells [193] and to abolish resistance of calcitrol-differentiated HL60 cells to DNA damage-induced apoptosis by activating other cell signaling pathways leading to cell death [194]. Diet containing both curcumin and omega-3 fatty acids (fish oil diet) leads to the prevention and treatment of pancreatic tumor xenografts through the down-regulation of the expression and activity of iNOS, COX-2 and 5-LOX and up-regulation of p21 [78]. Coadministration of curcumin with embellin, a natural benzoquinone derived from Embelia ribes berries, prevents lipid peroxidation, histological alterations and oxidative tissue damage occurring usually during chemically-induced hepatocarcinogenesis in Wistar albino rats [195]. An additive inhibitory effect on cell proliferation was also observed in human prostate cancer PC-3 cells in vitro and in vivo in human PC-3 xenografts mice treated concomitantly with curcumin and b-phenylethyl isothiocyanate (PEITC), a natural compound issued from cruciferous vegetables. This inhibitory effect was related to the suppression of epidermal growth factor (EGFR), Akt and PI3K phosphorylations and the inhibition of the NF-κB signaling pathway [128,196]. A similar cascade of events was also pointed out following the combination of curcumin and resveratrol in vitro in HCT116 colon cancer cells and in vivo in colon cancer xenografts [197]. Synergistic interactions of curcumin with epigallocatechin-3-gallate (EGCG), a polyphenolic compound found in green tea leads to the reduction of their respective dose index in normal, premalignant and malignant human oral epithelial cells [198]. In the case of chronic lymphocytic leukemia cells (CLL), synergism between EGCG and curcumin allows to overcome the stromal-mediated protection of the CLL cells in the case of sequential therapy. By this way, EGCG sensitizes the cells to curcumin effects and is able to increase strongly cell death in leukemic cells [172]. Curcumin administrated in combination with piperine, an alkaloid from black pepper, inhibits breast stem cell self-renewal without inducing toxicity to differentiated cells. This inhibitory effect is mediated by the inhibition of mammosphere formation and Wnt signaling pathway, but without causing toxicity to differentiated cells [91].

A clinical approach revealed that the combination of curcumin with quercetin, a plant derived flavonoid, reduces the number and size of ileal and adenomas in patients with familial adenomatous polyposis without appreciable toxicity [199]. Most of the natural compounds cited above to have synergestic effect with curcumin in vitro or in vivo are included in ongoing clinical trials in patients affected by cancer.

Due to frequent failure of conventional treatment alone (radiotherapy, chemotherapy and hormonotherapy), novel clinical strategies, based on the combination of different treatments together or in conjunction with chemopreventive agents, are emerging.

The combination of curcumin with radiation enhances significantly the radiation-induced clonogenic inhibition and induces cell death by apoptosis. This combination of treatment reduces the TNFa-mediated NF-κB activity, alters the Bax/Bcl-2 ratio and activates cytochrome c, caspase-9 and caspase-3 in PC-3 prostate cancer cells [200], but also in colorectal cancer cells [53]. Pretreatment of cervical carcinoma cells results in a significant dose-dependent radiosensitization of these cells. This involves an increase of reactive oxygen species (ROS) and extracellular signal-regulated kinase (ERK) 1/2 activation [201]. Altogether these data suggest that curcumin can be considered as a potent radiosensitizer in prostate and cervical cancer.

Several studies have also been performed in order to evaluate the potential synergistic activity of curcumin in combination with synthetic agents commonly used in chemotherapy. We will first focus on the combination of curcumin with chemotherapeutic agents from natural origin and currently used in clinic such as Taxol^® (paclitaxel), derived from Taxus brevifolia. Curcumin was shown to potentiate the effect of paclitaxel-mediated chemotherapy in advanced breast cancer in vitro and in vivo and is able to inhibit lung metastasis. Such a sensitization of taxol-induced cell death by curcumin was also observed in cervical HeLa cancer cells. In both case, the potentiation of chemotherapy by curcumin was related to the down-regulation of NF-κB and serine/threonine Akt pathways, to the suppression of cyclooxygenase 2 (COX-2) and matrix metalloproteinase-9 (MMP-9) but also to the activation of caspases and cytochrome c release [117,202,203]. On the other hand, curcumin appears to be a good adjuvant to enhance the induction of apoptosis and the subsequent chemotherapeutic efficacy of vinorelbine for the treatment of advanced non-small lung H520 carcinoma cells [204] and of celecoxib, a well known COX-2 inhibitor, in pancreatic adenocarcinoma cells [205,206]. This synergism of curcumin and celecoxib is responsible for the down-regulation of the COX-2 signaling pathway. Such a reduction of COX-2 is also observed in human colon cancer HT-29 cell lines when curcumin is associated with the antimetabolite 5-fluorouracil (5-FU) chemotherapeutic agent [207]. The combination of curcumin and 5-FU was also reported for the eradication of human gastric adenocarcinoma cells through the induction of cell cycle arrest in G2/M transition phase [208]. Furthermore, curcumin is able to potentiate the antiproliferative effect of 5-FU associated with oxaliplatin or oxoplatin alone and to stimulate cell death by apoptosis through the attenuation of epidermal growth factors (EGF) and insuline-like growth factor (IGF) signaling pathways in colon cancer HCT-116 and HT-29 cells [209,210].

In addition to its ability to enhance the antitumoral effect of conventional chemotherapy, curcumin is also able to circumvent chemoresistance. Resistance to conventional chemotherapy often appears in the case of treatment with platinium (Pt) drugs such as cisplatin and oxaliplatin [211,212]. Several reports revealed that combination of curcumin with Pt drugs treatment inhibits the growth of cancer cells by modulating EGF and IGF receptors expression and by inducing G2/M cell cycle arrest through the modulation of Akt and p38 MAPK [209,210,213,214]. This combination also leads to the induction of cancer cell death by apoptosis through the increase of p53 tumor suppressor gene expression, through the proteasomal degradation of Bcl-2 mediating cisplatin resistance and through the reduction of interleukin-6 production [215,216]. In the case of colon cancer, the emergence of a subset of self-renewing cells, called cancer stem cells (CSCs), is highly implicated in the failure of oxaliplatin treatment. Treatment of oxaliplatin resistant CSCs cells with curcumin results in a marked reduction of CSCs cells accompanied by alterations of the level of DNA methyltransferase 1 [217]. These findings underline the fact that curcumin is able to increase the sensitivity of resistant cancer cells to Platinium drugs and to prevent the emergence of chemoresistant colon cancer cells due to the enrichment of cancer stem cells. Sung et al., showed that curcumin overcomes chemoresistance and potentiates the effect of thalidomide and bortezomib by down-regulating NF-κB and its target genes (e.g., cyclin D1, Bcl-xL, Bcl-2, XIAP, survivin and VEGF) in human multiple myeloma in vitro and in vivo [218]. More recently, curcumin was also found to potentiate the anti-tumor effect of gemcitabine, another pyrimidine antimetabolite, by suppressing proliferative and angiogenic biomarkers and by modulating the NF-κB signaling pathway in vitro in human bladder cancer 253JBV cells and in vivo in an orthotopic human bladder cancer [134]. Similar results were observed after combination of curcumin with capecitabine in the case of advanced metastatic colorectal cancer in an orthotopic mouse model. This combination was also highly effective in suppressing acites and distant metastasis in other organs [77].

Venkatesan et al. also reported that curcumin is able to attenuate the myocardial toxicity usually observed after adriamycin (doxorubicin) treatment of Wistar rats. In fact, such a pre-treatment with curcumin decreases the level of creatinine kinase and lactate deshydrogenase as well as lipid peroxidation and it increases the level of endogenous antioxidants in order to counteract the side effects of anthracycline chemotherapeutic agents [219]. Such combination of treatment could thus limit free radical-mediated organ injury normally observed after adriamycin treatment.

Curcumin, alone or in combination with docetaxel, was also shown to be highly potent in mice with multidrug-resistant tumors, by decreasing both proliferation, microvessel density and by increasing tumor cell apoptosis [48]. Recently, the results of a phase I dose escalation trial including fourteen patients with advanced or metastatic breast cancer pointed out that curcumin could be used in combination with docetaxel. This study allows to determine the maximal tolerated dose (6 mg/mL curcumin for seven consecutive days every three weeks in combination with a standard dose of docetaxel) as well as their toxicity, safety and effects on tumor marker [220]. Thanks to the encouraging data obtained by clinical trial, a comparative phase II clinical trial study is now under investigation.

Curcumin also appeared to be a good candidate to sensitize prostate cancer cells for TRAIL-mediated immunotherapy. TNFa related apoptosis-inducing ligand (TRAIL) is an inducer of apoptosis in many cancer cells and is an attractive cytokine for the treatment of advanced cancers including prostate cancer. Although prostate cancer cells (DU145, PC-3 and LNCaP) are mostly resistant to TRAIL, they can be sensitized with curcumin to TRAIL-induced apoptosis. This combination induces the inhibition of constitutively active NF-κB, DNA fragmentation, the cleavage of pro-caspase-3, pro-caspase-8 and pro-caspase-9, as well as the truncation of Bid and cytochrome c release. It also leads to the inhibition of the anti-apoptotic proteins Bcl-2, Bcl-xL and XIAP [38,105,221,222,223]. These results were confirmed in vivo by pre-clinical studies performed in PC-3 xenografts [224] and in TRAIL-resistant LNCaP xenografts [225].