The Target Differences of Anti-Tumorigenesis Potential of Curcumin and its Analogues Against HER-2 Positive and Triple-Negative Breast Cancer Cells

Abstract

[...]PGV-1 was more potent compared to curcumin to suppress the tumor formation of metastatic breast cancer xenograft model in nude mice. Introduction Curcumin ((1E,6E)-1-(4-hydroxy-3-methoxyphenyl)-7-(3-methoxy-4-methylphenyl) hepta-l,6-diene-3,5-dione) (Figure 1A), a symmetric molecule isolated from turmeric (Curcuma longa), exerts potent chemopreventive activities via numerous mechanisms including interfering cell cycle signaling pathway, inhibiting cancer metastasis, and modulating redox homeostasis in cancer cells.1-4 Despite its superior potency, curcumin has not been available for clinical cancer therapy due to its chemical instability and poor bioavailability.5 Namely Pentagamavunon-0 (PGV-0) ((2E,5E)-2-[(4-hydroxy-3-methoxyphenyl) methylidene]-5-[(3-methoxy-4-methylphenyl) methylidene] cyclopentane-l-one) (Figure IB) and Pentagamavunon-1 (PGV-1) ((2E,5E)-2-[(4-hydroxy-3.5-dimethylphenyl) methylidene] -5-[(3-methoxy-4.5-dimethylphenyl) methylidene] cyclop entan-1 - one) (Figure 1C), the curcumin analogues were synthesized by the Faculty of Pharmacy Universitas Gadjah Mada, differ from curcumin in their chemical core in order to improve the physicochemical properties of curcumin.6 Both PGV-0 and PGV-1 have been demonstrated to exhibit better cytotoxic and anti-inflammatory activities compared to curcumin.7,8 Our previous study showed that PGV-0 and PGV-1 possess cytotoxic activities and augment the sensitivity of resistant breast cancer cells to doxorubicin.9 In this concern, we also analyzed the hypothetical interaction between PGV-0 or PGV-1 and HER2 receptor under molecular docking, showing that those compounds bind to HER-2 receptor at ATP binding site. HER2 activates multiple signaling axes, especially in MAPK signaling system and STAT3; leading to rapid tumor proliferation and cancer metastasis.15 HER2 also promotes epithelial-mesenchymal transition (EMT) by upregulating TGFß/SNAIL-ZEB1, activates a Wnt-dependent EMT-like dissemination program, and downregulates E-cadherin expression.16,17 Interestingly, the increase of HER2 expression could be observed in metastatic cancer cells even though the primary tumor is HER2 negative.15,18 In addition, HER2 signaling shows crosstalk with nuclear factor kappa B (NFkB) pathway. HER2 activates NFkB pathway primarily through IkB kinase-a (IKKa), differing from the ordinary activation of NFkB that is primarily through IKKß.19 Reciprocally, NFkB regulates the expression of HER2 through its binding to the promoter of the HER2 gene.20,21 As a powerful transcription factor, NFkB also activates the expression of myriads genes involving in proliferation, invasion, metastasis, and EMT.22 Further, constitutive activation of NFkB in HER2+ cells causes resistance to anti-HER2 drugs.23 Accordingly, HER2 and NFkB signaling are promising pathways to target the aggressive proliferation and metastasis of breast cancer.

Headnote

Keywords:

* Breast cancer

* Curcumin analogues

* HER2

* Metastasis

* NFkB

* Triple-negative breast cancer

Abstract

Purpose: The current study aims to evaluate the in vitro cytotoxic and cell migration effects of synthetic curcumin and its analogues on HER2 and nuclear factor kappa B (NFkB) pathways, as well as the in vivo inhibitory effect on cancer growth of metastatic breast cancer.

Methods: Cell viability, protein expression, and protein localization were determined in vitro using MTT assay, western blotting, and immunofluorescence, respectively. Meanwhile, scratch wound healing assay and gelatin zymography were conducted to investigate the metastasis inhibitory effect. The in vivo anti-tumor ability was evaluated in xenograft mouse model using triple-negative breast cancer (TNBC) cells.

Results: Curcumin, PGV-0, and PGV-1 exhibited cytotoxic effect against HER2-overexpressing breast cancer cells. Although PGV-1 showed the best activity in the single cytotoxic assay, curcumin showed the strongest synergism with doxorubicin. Curcumin and PGV-0 inhibited membrane localization of HER2. In contrast, PGV-1 neither inhibited localization nor decreased the expression of HER2, nonetheless showed the most potent inhibition against nuclear localization of p65 indicating the different mechanisms of curcumin, PGV-0, and PGV-1. Regarding cancer metastasis, curcumin and PGV-1 showed inhibitory activities against cell migration and inhibited MMP-2 and MMP-9 protein expression. Lastly, PGV-1 was more potent compared to curcumin to suppress the tumor formation of metastatic breast cancer xenograft model in nude mice.

Conclusion: Overall, our study strengthens the potency of curcumin analogue, PGV-1, for treating several types of cancer, including metastatic breast cancer.

Introduction

Curcumin ((1E,6E)-1-(4-hydroxy-3-methoxyphenyl)-7-(3-methoxy-4-methylphenyl) hepta-l,6-diene-3,5-dione) (Figure 1A), a symmetric molecule isolated from turmeric (Curcuma longa), exerts potent chemopreventive activities via numerous mechanisms including interfering cell cycle signaling pathway, inhibiting cancer metastasis, and modulating redox homeostasis in cancer cells.1-4 Despite its superior potency, curcumin has not been available for clinical cancer therapy due to its chemical instability and poor bioavailability.5 Namely Pentagamavunon-0 (PGV-0) ((2E,5E)-2-[(4-hydroxy-3-methoxyphenyl) methylidene]-5-[(3-methoxy-4-methylphenyl) methylidene] cyclopentane-l-one) (Figure IB) and Pentagamavunon-1 (PGV-1) ((2E,5E)-2-[(4-hydroxy-3.5-dimethylphenyl) methylidene] -5-[(3-methoxy-4.5-dimethylphenyl) methylidene] cyclop entan-1 - one) (Figure 1C), the curcumin analogues were synthesized by the Faculty of Pharmacy Universitas Gadjah Mada, differ from curcumin in their chemical core in order to improve the physicochemical properties of curcumin.6 Both PGV-0 and PGV-1 have been demonstrated to exhibit better cytotoxic and anti-inflammatory activities compared to curcumin.7,8 Our previous study showed that PGV-0 and PGV-1 possess cytotoxic activities and augment the sensitivity of resistant breast cancer cells to doxorubicin.9 In this concern, we also analyzed the hypothetical interaction between PGV-0 or PGV-1 and HER2 receptor under molecular docking, showing that those compounds bind to HER-2 receptor at ATP binding site. In addition, PGV-0 and PGV-1 also strengthen the cytotoxicity of 5-fluorouracil in colon cancer cells.10,11 In general, PGV-1 performed most potent to inhibit cancer cell growth. Recently, PGV-1 showed a strong inhibitory effect against 4T1 cells, a triple-negative breast cancer (TNBC) cell model, under in vitro experiment through ROS generation.12 These studies warrant the potency of PGV-0 and PGV-1 to be further investigated as anticancer drugs, especially to the specific types of breast cancers, namely HER2 positive and TNBC.

HER2 positivity (HER2+), a subtype of breast cancer characterized by either HER2 protein overexpression or gene amplification, is found in approximately 15%-30% of breast cancers and contributes with low survival and poor clinical outcome in breast cancer patient.13 This reduced survival is closely related to aggressive proliferation of HER2-overexpressing cells14; as well as the occurrence of breast cancer metastasis as HER2 overexpression increases the invasive potential of cancer cells. HER2 activates multiple signaling axes, especially in MAPK signaling system and STAT3; leading to rapid tumor proliferation and cancer metastasis.15 HER2 also promotes epithelial-mesenchymal transition (EMT) by upregulating TGFß/SNAIL-ZEB1, activates a Wnt-dependent EMT-like dissemination program, and downregulates E-cadherin expression.16,17 Interestingly, the increase of HER2 expression could be observed in metastatic cancer cells even though the primary tumor is HER2 negative.15,18

In addition, HER2 signaling shows crosstalk with nuclear factor kappa B (NFkB) pathway. HER2 activates NFkB pathway primarily through IkB kinase-a (IKKa), differing from the ordinary activation of NFkB that is primarily through IKKß.19 Reciprocally, NFkB regulates the expression of HER2 through its binding to the promoter of the HER2 gene.20,21 As a powerful transcription factor, NFkB also activates the expression of myriads genes involving in proliferation, invasion, metastasis, and EMT.22 Further, constitutive activation of NFkB in HER2+ cells causes resistance to anti-HER2 drugs.23 Accordingly, HER2 and NFkB signaling are promising pathways to target the aggressive proliferation and metastasis of breast cancer.

In this study, we utilized HER2-overexpressing breast cancer cells, MCF7/HER2-5, as a model to evaluate the activities of synthetic curcumin analogues, PGV-0 and PGV-1, in HER2 and NFkB signaling pathways. In addition, we also employed 4T1 cells for in vivo tumor implanted model representing the TNBC tumor model. The result of this study is expected to provide more comprehensive evidence of PGV-0 and PGV-1 to be developed as HER2+ or HER2-breast cancer therapy and for more comprehension of TNBC.

Materials and Methods

Chemicals and cell lines

Curcumin, PGV-0, and PGV-1 were synthesized by Curcumin Research Center (CRC), Faculty of Pharmacy, Universitas Gadjah Mada. All cell lines were the collection of Nara Institute of Science and Technology (NAIST), Japan. Mammary carcinoma cells, MCF-7/HER25 5 MCF-7/mock cells were kindly given by Prof. Yoshio Inouye (Department of Surgery, Toho University School of Medicine). HEK293T cells and 4T1 cells were obtained from Prof. Masashi Kawaichi (NAIST). All cells were maintained in Dulbecco's modified Eagle medium (DMEM) medium at 37 °C supplemented with 10% FBS (Sigma), HEPES (Sigma), sodium bicarbonate (Sigma), 150 IU/mL penicillin (Gibco), and 150 pg/mL streptomycin (Gibco), and 1.25 pg/mL fungizone (Gibco).

Cytotoxic assay

MCF-7/HER2-5, MCF-7/mock, and HEK293T cells were plated in 96-well plates at a density of 1 x 104 cells per well and allowed to grow for 24 h. The cells were then treated with a series concentration of curcumin, PGV0, and PGV-1 for 24 h. After treatment, 5 mg/mL of 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT, Sigma) in PBS was diluted in DMEM (1:9), 100 pL of the reagent was added to each well, and incubated for 3 h at 37 °C. The reaction of MTT formazan was stopped by 10% sodium dodecyl sulfate (SDS) in 0.01 N HCl followed by incubation overnight at room temperature. To absorbance at Л 595 nm was measured using an ELISA microplate reader.

Immunofluorescence

MCF-7/HER2-5 cells were seeded in glass coverslips inside the 6-cm dish and cultured to 80% confluence. The cells were then treated with compounds, either alone or in combination with doxorubicin, and incubated for 24 h. After 24 h, the cells were fixed using 70% ethanol and incubated for 15 min at room temperature. After rinsing with PBS, the cells were incubated with the 1% BSA as blocking serum for 30 min at room temperature. Then, the cells were incubated with a primary antibody [mouse anti-p65 (Santa Cruz) or mouse anti-HER2 (Santa Cruz}] overnight at 4°C followed by secondary antibody (Santa Cruz) for 1 h. Then, DAPI staining was used to label nuclei for 10 min at room temperature in the dark. The cells were again rinsed with PBS and placed on sliding glass. The slides were analyzed and photographed using a fluorescence microscope.

Western blotting

MCF-7/HER2-5 cells (2 x 105 cells/mL) were grown to confluence and treated with PGV-1 or curcumin at the indicated concentration for 24 h. After treating with the compounds, the cells were washed with cold PBS. The cells were then lysed in lysis buffer containing 50 mM Tris-HCl (pH 8.0), 150 mM sodium chloride (NaCl), 0.1% SDS, 1.0% NP-40 mM, 100x protease inhibitor cocktail, and 100 mM phenylmethylsulfonyl fluoride in propanol and incubated for 10 min at 4°C. Cells were scraped using a scrapper on the ice and added to a microtube. The cell suspension was sonicated for 10 s and centrifuged at 15 000 rpm for 20 min at 4°C. The supernatant (cell lysate) was used as the protein sample for western blotting. The protein samples were denatured in 5x SDS-PAGE sample buffer and subjected to 10% SDS-polyacrylamide gel electrophoresis. The separated proteins were transferred onto a PVDF membrane, followed by blocking with 5% skim milk powder (w/v) in TBS (20 mM Tris and 133 mM NaCl, 1 N HCl) containing 20% Tween 20 for 1 h at room temperature. The membrane was probed for the protein expression levels using a specific primary antibody of mouse anti-HER2 (Santa Cruz) overnight at 4°C. Equal protein loading was examined by tubulin detection using a mouse anti-tubulin-specific antibody (Santa Cruz). After washing with 1x TBS-T, the membrane was probed with an HRP-conjugated appropriate secondary antibody for 1 h at room temperature and visualized by ECL PRIME or the ECL detection system.

Gelatin zymography

MCF-7/HER2-5 cells (2 x105) on 6 well plate was incubated for 24 h in C02 incubator then treated with curcumin or PGV-1 for 24 h. The media were collected and subjected to gel electrophoresis (SDS-PAGE) using 10 % gel containing 0.1% gelatin running at 100 volts, 50 A for 2 h. The gel was renatured with renaturing solution containing 2.5% Triton X-100 for 30 min and incubated with incubation buffer for 20 h. The gel was then stained with 0.5% Coomassie Brilliant Blue and incubated for 30 min. After 30 min, the gel was de-stained by a destaining solution. The gel is scanned and documented. Band intensities were measured using ImageJ software.

Scratch wound healing assay

MCF-7/HER2-5 cells (8 x104) were seeded into each well of 24 well plates and incubated for 24 h. Cells were then starved by changing the medium into serum-free medium for 18 h. Cells then were scratched with a yellow tip and treated with curcumin, PGV-1, doxorubicin, or the combination treatment. Following the treatment, cells were documented at 0, 24, 48 h. Quantification of the area of wound closures were calculated using ImageJ software.

In vivo experiment

Nude mice bearing metastatic breast cancer cells were generated by subcutaneously (s.c.) implantation of 4T1 cells (5 x 104 cells in 0.2 mL medium) into the four flanks of 6-week-old nude mice on day 0. Starting from the same day, treatments were given with curcumin and PGV1 1 mg/kg BW) in corn oil via intra-peritoneal (i.p) administration every 2 days for 12 days. The untreated mice received corn oil as a vehicle. Tumor sizes were measured during this period.

Data Analysis

The data analysis were conducted according to the previously reported.9,23 All statistical analyses were performed using ANOVA in SPSS 16 software with P value of 0.05 as considered to be significantly different.

Results

Cytotoxic activity of curcumin analogues against MCF7/HER2-5, MCF-7/mock, and HEK293T cells

A single treatment of curcumin, PGV-0, and PGV-1 on MCF-7/HER2-5 and MCF-7/mock showed cytotoxic effects (Figure 2A and 2B) with IC50 values as shown in Table 1. The IC50 of curcumin, PGV-0, and PGV-1 were 52, 32, 14 gM on MCF-7/HER2-5 and 38, 18, 5 gM on MCF-7/mock, respectively. The compounds resulted in higher IC50 values on MCF-7/HER2-5 cells, indicating that the transfection of HER2 genes altered the cell response to the compounds. Among the other compounds, PGV1 1 the strongest cytotoxicity on both mammary carcinoma cells.

Selectivity is an important property of desired chemotherapeutic agents, in which a compound should exhibit higher potency against cancer cells compared to normal cells. Mathematically, selectivity is a ratio that measures the window of cytotoxicity in normal cells, with selectivity index (SI) >3 represents good selectivity of a compound.24 Hence, we also checked the cytotoxic activity of compounds on HEK293T cells (kidney cells that represented normal cell model) and calculate their SI. As shown in Figure 2C and Table 2, only PGV-1 exhibited SI > 3 in both MCF-7/HER2-5 and Мер-7/ mock cells, suggesting its good selectivity and potency to be considered as a chemotherapeutic agent.

Cytotoxic effect of the combination of curcumin analogues with doxorubicin on MCF-7/HER2-5 cells

Here, we used doxorubicin that known to be the standard chemotherapy for breast cancer as a threat against several adverse effects and raising resistance. Therefore, the application of combinatorial therapy is desirable to increase the effectivity of doxorubicin. A combinatorial cytotoxic assay was conducted by combining the curcumin analogues and doxorubicin on MCF-7/HER2-5 cells with serial concentrations of 1/20, 1/8, 1/4, and 1/2 of the IC50 values of both compounds. The combination index (Cl) value was calculated to evaluate the synergistic effect of the combination. A synergistic effect is indicated by a Cl value <0.9. The result showed that the three compounds enhanced the cytotoxicity of doxorubicin (Figure 3). In addition, the combination of curcumin and doxorubicin showed the lowest cell viability among the other combinations, suggesting that curcumin and doxorubicin was the best combination. Furthermore, the Cl value confirmed that the combination of curcumin and doxorubicin at all doses was synergistic and resulted in the lowest Cl value among all combinations (Tables 3, 4, and 5). This finding suggests that curcumin was the best combination with doxorubicin.

Effect of curcumin analogues on the expression and localization of HER2

To confirm whether the cytotoxic activity of curcumin analogues was related to HER2 overexpression of MCF7/HER2-5 cells, the expression of HER2 was observed by western blotting (Figure 4). MCP-7/HER2-5 cells exhibited a higher expression of HER2 compared to the mock cells. Although the cytotoxic effect of PGV-1 was more potent than those of curcumin and PGV-0, PGV1 1 not decrease the expression of HER2. Furthermore, curcumin decreased the levels of 185-kDa HER2 and exhibited two additional bands, which are interesting for further investigation.

Immunofluorescence staining revealed that curcumin, as well as PGV-0 inhibited HER2 localization to the plasma membrane (Figure 5). On the other hand, PGV-1 and its combination with doxorubicin had no effect on the localization of HER2 protein on MCP-7/HER2-5 cells. These findings revealed the different mechanisms of PGV-1 effects than those of curcumin and PGV-0.

Effect of curcumin analogues on p65 localization

The NFkB pathway has been reported to be downstream of HER2 and regulates numerous cellular functions, including those involved in tumorigenesis.19 Therefore, we examined the effect of curcumin analogues on the activation of p65, an active subunit of NFkB, as shown in Figure 6. We found the more localized p65 in the nucleus in doxorubicin treatment, indicating the activation of p65 occurred. Curcumin and its analogues decreased the nucleus expression of p65 and PGV-1 showed the lowest nucleus localization of this protein. This was an interesting finding, considering that PGV-1 did not decrease the expression or the localization of HER2. Thus, the effect of PGV-1 on the localization of p65 was not related to HER2 expression, but maybe due to the inhibition of HER2 activation as reported previously.9 In this regard, PGV-1 showed a unique effect compared to curcumin and PGV-0 and needs for further investigation.

Effect of curcumin and PGV-1 on cancer metastasis

Cancer metastasis involves multistep processes, including cancer cell invasion to surrounding tissue and cell migration.25 Matrix metalloproteinase proteins (MMPs), especially MMP-2 and MMP-9, are key proteins in invasion as these proteins degrade components of extracellular matrix, allowing the cancer cells to invade their surrounding tissues.26 Hence, we checked the effect of PGV-1 and curcumin on the expression of MMP-2 and MMP-9 using gelatin zymography (Figure 7). We found that both curcumin and PGV-1 decreased the level of MMP-2 and MMP-9.

We then checked the effect of compounds on cell migration using scratch wound healing assay to evaluate the potential inhibitory effect of PGV-1 in cancer metastasis (Figure 8). We used doxorubicin at a low dose as an inducer of cell migration and we found that doxorubicin did not inhibit cell migration. Meanwhile, curcumin only inhibited cell migration at higher dose (25 pM). On the other hand, PGV-1 exhibited an inhibitory effect on cell migration at a dose as low as 1.75 pM. Combination of curcumin or PGV-1 with doxorubicin showed similar results with the treatment of each compound alone. These results suggest that curcumin or PGV-1, but not doxorubicin, was the key inhibitor of cell migration and PGV-1 still performed a superior effect.

Effect of curcumin and PGV-1 on tumor progression in vivo

Since we did not find significant differences of the PGV-1 treatment on HER expression profiles, we then evaluated the efficacy focusing on PGV-1 against tumor xenograft using 4T1 cells, a highly tumorigenic HER2- and metastatic cell line, which are suitable for our purpose in developing an anti-metastatic agent.27 We used curcumin as the comparison. Previously, we found that PGV-1 exhibited strong in vitro cytotoxic effect to 4T1 cells with the IC50 value of 4 pM and inhibited cell migration as well as MMP-9 expression in vitro. In this experiment we succeeded in performing a xenograft mouse model using 4T1 cells within 8 days. We administered PGV-1, curcumin, or vehicle (corn oil) every two days for 12 days and evaluated the tumor progression (Figure 9). Tumor nodules were measurable, starting on day 8 after tumor xenograft. Tumor on vehicle-treated mice grew rapidly and reached tumor volume of ~600mm3 only in 4 days after tumor nodules appeared (day 12 after tumor injection). Curcumin slightly inhibits tumor progression, although not-significant statistically. On the other hand, PGV-1 significantly inhibited tumor progression compared to vehicle and curcumin treatments indicating that PGV1 1 better in inhibiting tumor growth in vivo than curcumin.

Discussion

This study was conducted to evaluate the tumor growth inhibitory activities of curcumin and its analogues, PGV-0, and PGV-1. At first, we conducted a new synthesis method for PGV-1 to improve the effectivity of the preparation by employing a high concentration of hydrochloric acid to accelerate the coupling reaction between electrophilic C-carbonyl at the benzaldehyde and the nucleophilic side at the cyclopentanone. This reaction seemed to work effectively to yield 50% PGV-1. Even though this result as not much as the previously reported by Sardjiman et al,28 but still comparable in the optimum yield and much more efficient with only 1h reaction. Therefore, this reaction method is recommended for further PGV-1 preparation.

For the anti-cancer evaluation, we used HER2overexpressing breast cancer cells, MCF-7/HER2-5 for in vitro model, and then 4T1 cells for in vivo model. We found the IC50 value of curcumin analogues against MCF7/HER2-5 cells was higher than that against MCF-7/ mock cells, suggesting the HER2 expression alters in the cell sensitivity to curcumin and its analogues. Still, all the compounds exhibited cytotoxic activity with an IC50 value <20 pM, indicating the high potential of these compounds to be developed as chemotherapeutic agents. PGV-1 was found to be the most potent agent among the other compounds. However, in combination with doxorubicin, curcumin showed the maximum synergistic effect. The molecular mechanism of this combination needs to be elucidated further.

Since HER2 overexpression and NFkB over activation are usually observed in cancer cells, both proteins have been considered as desirable targets for cancer therapy. Moreover, HER2 signaling is related to the NFkB pathway through PI3K/Akt signaling to activate IKK. Merhkofer et al19 reported that the IKK involved in HER2 signaling is IKKa, which functions to phosphorylate IkB, resulting in the degradation of IkB by the proteasome.19 Protein p65 that is released from IkB then translocated to the nucleus to act as a transcription factor. Protein p65 is a transcription factor for HER2 expression; hence, there is a loop-like HER2-NFkB-HER2 pathway that is a probable cause for breast cancer resistance to chemotherapeutic agents.29 In the present study, our data revealed that curcumin inhibited the localization of HER2. This result is not the first report showing that curcumin acts as a HER2 and a tyrosine kinase inhibitor. In 1999, a study conducted by Hong et al. also demonstrated the same result.30 However, the two curcumin analogues exhibited different activities on the localization of HER2. Based on their structure, the difference between PGV-0 and PGV-1 is due to the occurrence of methyl groups on the benzene ring (Figure 1), which may be responsible for their different mechanisms of action on cancer cells. This study revealed that PGV-0 acts like curcumin in inhibiting the localization of HER2, whereas PGV-1 did not have any effect on HER2. In addition, this in vitro assay confirmed our previous finding that PGV-1 exhibits the lowest interaction with EGFR and HER2 in silico.9 Another interesting finding in this study is that curcumin resulted in two additional bands with a higher molecular weight than the 185-kDa HER2. Given that these protein bands were found only in the curcumin-treated cells, it is possible that curcumin affects the post-translational modification of HER2. However, this hypothesis needs further investigation.

In this study, curcumin and PGV-0 were found to inhibit the translocation of p65 to the nucleus caused by doxorubicin, which might be related to their interaction with HER2. However, PGV-1 also inhibited the translocation of p65. There are other pathways in regulating of NFkB in addition to HER2 and PI3K/ Akt, such as mitogen-activated protein kinase 1, NFkBinducing kinase, NFKB-activating kinase, mixed-lineage kinase 3, and TGFß-activated kinase 1.31 The effect of PGV-1 on other upstream molecules of NFkB is worth to be elucidated further. Another phenomenon found was that PGV-1 induced chromatin condensation in the nuclei (Figure 5G). This result is in agreement with our previous study showing that PGV-1 specifically induces prometaphase arrest during mitotic phase of cell cycle.32

Our study, together with other studies, demonstrated that curcumin and PGV-0 target the tyrosine kinase receptor and could block growth signaling in breast cancer, whereas PGV-1 acts directly in the nucleus to abrogate cell mitosis and decrease the localization of p65. These target mechanisms of PGV-1 may significantly contribute to its inhibitory effects of MMPs expression and cells migration which is important to be developed as anti-metastatic agent. In addition, PGV-1 was proven to work in vivo to significantly inhibit the tumor development of 4T1 implanted tumor model but not for curcumin. Since 4T1 cells is a TNBC model which is characterized as metastatic phenomena and supported with our previously finding,12 this in vivo data demonstrated that PGV-1 is suitable to treat more general metastatic cancers much better than curcumin. Overall, this study discovered that curcumin analogues exhibited a synergistic effect with doxorubicin on HER2-overexpressing breast cancer cells. Even that PGV-1 not specifically targets HER2, it still works better than curcumin to halt tumor development, including in in vivo study. Taken together with the strong cytotoxic effect of PGV-1 suggesting that this compound perhaps possesses some additional targets that differ to curcumin and PGV-0. In this regard, the cell cycle modulation may be the most interesting target of PGV-1 that should be more to pay attention.

Conclusion

In conclusion, we showed curcumin and its analogues, PGV-0 and PGV-1 exhibit synergist cytotoxic effect with doxorubicin in HER2-overexpressed breast cancer cells. Curcumin and PGV-0 act at the upstream level of signaling cascade by inhibiting the localization of HER2 tyrosine kinase receptor, while PGV-1 acts at the downstream level by inhibiting nuclear translocation of NFkB subunit, p65. Moreover, PGV-1 show superior potency to inhibit cancer metastasis than curcumin. In in vivo experiment, PGV1 1 more potent anticancer activity against TNBC tumor compared to curcumin; hence, highlighting the potency of PGV-1 to be considered as a chemopreventive agent for metastatic breast cancer.

Ethical Issues

All animal experiments were performed in Animal Experimentation Facility of NAIST-Japan and the experimental procedures were approved by the Institutional Animal Care and Use Committee of NAIST (reference No. 1321) and the Ministry of Education, Culture, Sports, Science and Technology of Japan (Notice No. 71, 2006).

Conflict of Interest

The authors declare that they have no competing financial interests.

Acknowle dgments

We express our gratitude to the International Collaboration Research Grant 2013-2014 Directorate General of Higher Education, Ministry of Education and Culture, Republic of Indonesia, No: 180/SP2H/PL/Dit.litabmas/IV/2012, who funded this research. We also thank Prof. Yoshio Inouye for the MCF7/HER2-5 cells used in this research.

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Article info

Article History:

Received: 19 Dec. 2019

Revised: 2 Apr. 2020

Accepted: 16 Apr. 2020

epublished: 7 Nov. 2020

Footnote

*Corresponding Author: Edy Meiyanto, Tel: [phone], Fax: [phone], E-mail: [email protected]

References

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