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BMC Cancer. 2010; 10: 276.
Published online Jun 10, 2010. doi:  10.1186/1471-2407-10-276
PMCID: PMC2927993

Epigallocatechin-3-gallate suppresses the expression of HSP70 and HSP90 and exhibits anti-tumor activity in vitro and in vivo

Abstract

Background

Epigallocatechin-3-gallate (EGCG), one of the major catechins in green tea, is a potential chemopreventive agent for various cancers. The aim of this study was to examine the effect of EGCG on the expression of heat shock proteins (HSPs) and tumor suppression.

Methods

Cell colony formation was evaluated by a soft agar assay. Transcriptional activity of HSP70 and HSP90 was determined by luciferase reporter assay. An EGCG-HSPs complex was prepared using EGCG attached to the cyanogen bromide (CNBr)-activated Sepharose 4B. In vivo effect of EGCG on tumor growth was examined in a xenograft model.

Results

Treatment with EGCG decreased cell proliferation and colony formation of MCF-7 human breast cancer cells. EGCG specifically inhibited the expression of HSP70 and HSP90 by inhibiting the promoter activity of HSP70 and HSP90. Pretreatment with EGCG increased the stress sensitivity of MCF-7 cells upon heat shock (44°C for 1 h) or oxidative stress (H2O2, 500 μM for 24 h). Moreover, treatment with EGCG (10 mg/kg) in a xenograft model resulted in delayed tumor incidence and reduced tumor size, as well as the inhibition of HSP70 and HSP90 expression.

Conclusions

Overall, these findings demonstrate that HSP70 and HSP90 are potent molecular targets of EGCG and suggest EGCG as a drug candidate for the treatment of human cancer.

Background

Epigallocatechin-3-gallate (EGCG), one of the most abundant polyphenols in green tea, inhibits cell proliferation and induces apoptosis in a variety of human cancer cells [1-3]. Previous studies have suggested that EGCG produces anti-cancer effect by modulating the activity of mitogen-activated protein kinases (MAPKs), IGF/IGF-1 receptor, Akt, NF-κB, and CDKs [4-7]. EGCG also has other effects such as the inhibition of growth factor receptor, proteasome inhibition, mitochondrial depolarization, and the inhibition of fatty acid synthase [8-11]. Some studies have demonstrated that EGCG can inhibit the transcriptional activity of aryl hydrocarbon receptor (AhR) through the mechanism that involves direct binding of EGCG to the C-terminal region of heat shock protein 90 (HSP90) [12]. EGCG also modifies the association of HSP90 with several co-chaperones such as p23 and Hsc70, and functionally inhibits Glucose-regulated protein 78 (Grp78), a member of HSP70 family, by competing with ATP for binding to Grp78's active site [13,14]. Recent studies have implicated EGCG in the inhibition of estrogen receptor alpha (ERα), multidrug resistance protein 1 (MDR1), and telomerase in human breast cancer cells and drug-resistant breast cancer cells, leading to the suppression of cell viability and induction of apoptosis [15-17]. However, the mechanisms and signaling pathways underlying the potential anti-cancer effects of EGCG in breast cancer cells remain unclear.

Stress response upon variety of physiological and environmental stimulus including hypoxia, radiotherapy, and chemotherapy is important for cell survival [18]. HSPs are a class of stress-inducible proteins that play critical roles in stress response. HSPs function as molecular chaperone and protect cells against proteotoxic damages [19,20]. The overproduction of HSPs results in the increased incidence of cell transformation and is clinically correlated with poor prognosis and resistance to apoptosis in a wide range of human cancers [21-24]. Therefore, understanding the regulatory mechanism of HSPs and its response against anti-cancer therapies is important for the development of anti-cancer strategy.

The aim of this study was to evaluate the effects of EGCG on the expression and activity of HSPs. Here we reports that the anti-tumor activity of EGCG is mediated by the targeting of HSP70 and HSP90 in vitro and in vivo and suggests the potential value of EGCG as a therapeutic agent for cancer treatment.

Methods

Cell culture

The human breast cancer MCF-7 cells, mouse breast cancer 4T1 cells, and mouse colon carcinoma CT26 cells were cultured at 37°C with 5% CO2 in DMEM supplemented with 10% fetal bovine serum, 100 units/ml of penicillin, and 100 μg/ml of streptomycin.

Cell proliferation assay

A total of 3 × 105 MCF-7 cells were cultured in the presence or absence of EGCG (Sigma Chemical Co., Saint Louis, MO) for 24 h. After the respective medium was removed, the cells were incubated with MTT (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide) solution (5 mg/ml in phosphate-buffered saline, PBS) for 3 h, and the absorbance was measured using an auto ELISA plate reader at 570 nm.

Flow cytometric analysis

Cells were harvested and fixed with 70% ethanol for 1 h at 4°C. After washing with cold PBS, cells were incubated with DNase-free RNase and propidium iodide at 37°C for 30 min. Cells were then analyzed by flow cytometry using Cell Lab Quanta™ SC (Beckman Coulter Inc, Fullerton, CA).

Cell colony formation assay

The inhibition of the colony formation of MCF-7 cells following treatment with EGCG was measured by soft agar assay. Briefly, cells (8 × 103 cells/ml) were treated with various concentrations of EGCG in 0.3% Basal Medium Eagle (BME) agar containing 10% FBS, 2 mM L-glutamine, and 25 μg/ml gentamicin. The cultures were maintained at 37°C with 5% CO2 atmosphere for 10 days. Cell colonies were scored using conventional microscope.

Western blotting

Cells were treated with EGCG for 24 h. Cells were then washed with PBS and harvested in lysis buffer. Samples containing an equal amount of proteins were loaded into each lane of a SDS-polyacrylamide gel for electrophoresis and subsequently transferred onto a polyvinylidene difluoride membrane. After blocking, the membranes were incubated with antibodies against HSP27, HSP40, HSP60, HSP70, HSP90, HSP110, HSF1, HSF2, and β-actin (Santa Cruz Biotechnology, Santa Cruz, CA).

Luciferase reporter assay

The promoter region of HSP70 was amplified by PCR according to the published sequence [25] and inserted into pGL3-basic luciferase reporter vector (Promega, Madison, WI). Reporter vector containing HSP90 promoter (pXP2-HSP90) was kindly provided by Wu K.J. (NYMU, Taipei). Plasmids were transfected into MCF-7 cells using FuGene 6 reagent (Roche Molecular Biochemicals, Indianapolis, IN) according to the manufacturer's instructions. After 24 h, cells were heat shocked at 42°C for 1 h. Finally, the cells were treated with or without EGCG for 24 h and lysed using lysis buffer. Luciferase activity was measured using a TriStar LB 941 multimode microplate reader (Berthold Technologies, Germany).

EGCG-Sepharose 4B generation and in vitro EGCG pull-down assay

EGCG was conjugated with cyanogen bromide (CNBr)-activated Sepharose 4B (Sigma Chemical Co.). Briefly, EGCG (2.5 mg) was dissolved in 500 μl of coupling buffer (0.1 M NaHCO3 and 0.5 M NaCl, pH 6.0). The CNBr-activated Sepharose 4B was swelled and washed in 1 mM HCl on a sintered glass filter, then washed with the coupling buffer. CNBr-activated Sepharose 4B beads were added to the EGCG-containing coupling buffer and incubated at 4°C for 24 h. The EGCG-conjugated Sepharose 4B was washed with three cycles of alternating pH wash buffers (buffer 1, 0.1 M acetate and 0.5 M NaCl, pH 4.0; buffer 2, 0.1 M Tris-HCl and 0.5 M NaCl, pH 8.0). EGCG-conjugated beads were then equilibrated with binding buffer (0.05 M Tris-HCl and 0.15 M NaCl, pH 7.5). The control unconjugated CNBr-activated Sepharose 4B beads were prepared as described above in the absence of EGCG. The cell lysate was mixed with EGCG-conjugated Sepharose 4B in the absence or presence of ATP at 4°C for 3 h. The beads were then washed three times with binding buffer. The bound proteins were eluted with SDS loading buffer. The proteins were then resolved by SDS-PAGE followed by immunoblotting with antibodies against HSP70 and HSP90 (Santa Cruz Biotechnology).

Xenograft model and EGCG treatment

Six-week-old male BALB/c mice were obtained from Samtako (Korea). CT26 cells (5 × 106 cells/200 μl) were injected subcutaneously and permitted to grow until palpable (4 days). When tumors reach the size of 50~150 mm3, the mice were randomly grouped and treated with EGCG (10 mg/kg) by daily intraperitoneal injection for 7 days. Control animals received an injection of PBS in volumes equivalent to those used for injection of EGCG (n = 5 for each group). The mice were observed daily for tumor growth. The tumor volume was calculated by the formula: V = (ab2)/2, in which 'a' is the longest diameter and 'b' is the shortest diameter of the tumor.

Immunohistochemistry assay

The excised tumors were fixed in 10% formalin and embedded in paraffin. For immunohistochemical staining, avidin-biotin complex method was performed using anti-HSP70, anti-HSP90, and anti-PCNA antibodies (Santa Cruz Biotechnology). The immune reactions were visualized by immersing the sectioned tissues in 3,3'-diaminobenzidine tetrahydrochloride. Counterstaining was performed with hematoxylin.

Statistical analysis

All statistical analyses were carried out using Excel software. The significance of the differences was determined using an independent-samples t-test. A p-value < 0.05 was regarded as statistically significant.

Results

EGCG induces the G2/M phase cell cycle arrest in MCF-7 cells

The effect of EGCG on MCF-7 human breast cancer cells was examined by increasing concentrations of EGCG. As shown in Figure Figure1A,1A, treatment with EGCG (10 ~ 200 μM) inhibited the growth of MCF-7 cells in a dose-dependent manner with an IC50 of 150 μM. Extensive inhibition of cell growth was observed in the cells treated with high concentration (200 μM) of EGCG. Cell cycle distribution analysis of MCF-7 cells treated with EGCG (100 μM) showed that the cells were mainly arrested at the G2/M phase (Figure (Figure1B1B).

Figure 1
EGCG inhibits cell proliferation and induces the G2/M phase cell cycle arrest in MCF-7 cells. (A) The cells were treated with increasing concentrations of EGCG and cell viability was assessed by MTT assay. Asterisk, P < 0.05, significantly different ...

EGCG inhibits cell colony formation of MCF-7 cells

MCF-7 cells were plated on a soft agar matrix, treated with EGCG, and incubated at 37°C in a 5% CO2 incubator. After 10 days, the number of colonies was counted. As shown in Figure Figure2,2, EGCG inhibited colony formation in a dose-dependent manner, suggesting that EGCG is a critical inhibitor of MCF-7 cell proliferation.

Figure 2
EGCG inhibits colony formation of MCF-7 cells on soft agar. Cell suspensions were mixed with 0.3% agar in the culture medium with EGCG. After 10 days of incubation at 37°C in a 5% CO2 incubator, colonies were counted. Representative phase contrast ...

EGCG inhibits the expression of HSP70 and HSP90 in MCF-7 cells

Several reports have revealed that HSPs are important mediators of chemotherapy resistance. Therefore, we investigated the effect of EGCG on the expression of various HSPs. MCF-7 cells were incubated with increasing concentrations of EGCG (10 ~ 200 μM) for 24 h. As shown in Figure Figure3A3A and and3B,3B, the levels of protein and mRNA of HSP70 and HSP90 were decreased by 100 μM of EGCG, while the other HSPs (HSP110, HSP60, HSP40, and HSP27) were unaffected. In addition, EGCG inhibited the expression of HSP90-regulated Akt and Bcl-2 in MCF-7 cells (Figure (Figure3C3C).

Figure 3
FEGCG suppresses the expression of HSP70 and HSP90 in MCF-7 cells. (A) The cells were treated with EGCG for 24 h and the expression levels of heat shock proteins were determined by Western blot analysis. (B) The levels of HSP90, HSP70, and HSP60 mRNA ...

To examine the effect of EGCG on the promoter activity of HSP70 and HSP90, we performed the luciferase reporter assay. Consistent with the previous studies, heat shock (42°C for 1 h) induced transcriptional activity of HSP70 and HSP90 (Figure (Figure3D3D and and3E).3E). However, heat shock-induced promoter activity was suppressed by EGCG.

To understand the molecular changes associated with HSP70 and HSP90 inhibition, we examined the protein levels of HSP transcription factors. As shown in Figure Figure3F,3F, EGCG significantly decreased the levels of heat shock transcription factor 1 (HSF1) and HSF2 in a dose-dependent manner. These data suggest that EGCG suppresses the expression of HSP70 and HSP90 by inhibiting the expression of their transcription factors, HSF1 and HSF2.

EGCG competes with ATP for binding to the ATPase domain of HSP70 and HSP90

It was previously shown that EGCG antagonizes the function of the HSP70 family protein, Grp78, by directly competing with ATP for binding to the ATPase domain of Grp78 [14]. To investigate this possibility, we assessed the interaction between the HSPs and EGCG using EGCG-conjugated Sepharose 4B beads. EGCG-conjugated Sepharose pull-down assay confirmed that both HSP70 and HSP90 interact efficiently with EGCG (Figure (Figure4A).4A). Then, we examined the competition between EGCG and ATP for the ATPase binding pockets of HSP70 and HSP90. As shown in Figure Figure4B,4B, the binding of EGCG with HSP70 or HSP90 was decreased with increasing amount of ATP. These data demonstrate that EGCG competes with ATP for binding to the ATPase domain of HSP70 and HSP90.

Figure 4
EGCG binds to the ATPase domain of HSP70 and HSP90. (A) Whole cell lysates were incubated with EGCG-conjugated Sepharose 4B. After precipitation, the levels of bound HSP70 or HSP90 were monitored by Western blot analysis. (B) Whole cell lysates were incubated ...

Stress sensitivity is increased in EGCG-treated MCF-7 cells

Next, we examined whether EGCG has effect on the cell viability upon heat shock or H2O2 treatment. MCF-7 cells were pretreated with EGCG for 24 h and the cells were heat shocked (44°C, 1 h) or treated with H2O2 (500 μM, 24 h). Upon stress, cell viability was decreased approximately 20% in MCF-7 cells (Figure (Figure5A5A and and5B).5B). Interestingly, pretreatment of cells with EGCG strongly reduced the cell viability after heat shock or H2O2 treatment compared with single treatment with EGCG or stress (Figure (Figure5A5A and and5B).5B). The inhibition of cell growth was increased depending on the EGCG concentration. In addition, heat shock- and H2O2-induced HSP70 and HSP90 expression were significantly inhibited in the cells pretreated with EGCG (Figure (Figure5C5C and and5D).5D). These results indicate that EGCG increases the stress sensitivity of MCF-7 cells through the suppression of HSP70 and HSP90 expression.

Figure 5
EGCG increases the stress sensitivity of MCF-7 cells. The cells were treated with EGCG for 24 h and then heat shocked (44°C for 1 h) or treated with H2O2 (500 μM, 37°C for 24 h). (A), (B) Cell viability was measured by MTT assay. ...

EGCG suppresses tumor growth in xenograft model

The anti-tumor efficacy of EGCG was examined on a mouse xenograft model using CT26 colon cancer cells. CT26 cells were injected subcutaneously in BALB/c mice. After the palpable tumors were appeared (4 days after injection), EGCG (10 mg/kg) was injected intraperitoneally every day for 7 days. As shown in Figure Figure6A,6A, the administration of EGCG caused a 70% decrease in tumor volume compared with PBS-treated control mice. The toxicity of EGCG was assessed by mouse survival and careful monitoring of body weight. The EGCG treatment did not alter body weight compared with PBS-treated control mice (Figure (Figure6B6B).

Figure 6
EGCG represses the growth of tumor in mice. BALB/c mice were subcutaneously injected with 5 × 106 colon carcinoma CT26 cells into the right flank. After 4 days, the mice were given daily dose of PBS or EGCG (10 mg/kg) through intraperitoneal injection ...

To examine whether EGCG is able to inhibit the expression of HSP70 and HSP90 in vivo, the tumor tissues were excised. Immunohistochemistry assay showed that the levels of HSP70 and HSP90 were decreased in EGCG-treated mice compared with control (Figure (Figure7A).7A). The expression of PCNA, a proliferation biomarker, also significantly decreased (approximately 50%). Western blot analysis showed that the expression levels of HSP70 and HSP90 were decreased in EGCG-treated mice compared with control (Figure (Figure7B7B).

Figure 7
Histological and immunohistochemical appearance of tumors from CT26 cell-injected mice. Mice were subcutaneously injected with CT26 cells into the right flank. Four days later, mice were treated with either PBS (control) or EGCG for 7 days. (A) H & ...

Discussion

EGCG is an anti-oxidant that plays an important role in preventing cancer and cardiovascular disease [26]. Although many different molecules and signaling pathways have been demonstrated in various cell lines, the exact action mechanism of EGCG is unknown.

Ciocca et al. reported that the expression of three main HSPs, HSP27, HSP70, and HSP90, are elevated in breast cancer [21]. It is known that the levels of the HSPs are elevated in many cancers, and elevated HSP expression provides cellular resistance to anti-cancer therapies [21]. Some studies have shown that EGCG inhibits tumor growth by suppressing the HSP27, HSP70, HSP90, and/or HSP90 client proteins [13,27,28]. Grp78, a member of HSP70 family, is one of the target proteins of EGCG. Grp78 plays critical role as a molecular chaperone and promotes tumor cell proliferation, survival, and metastasis [14]. Therefore, HSPs could be a possible candidate to improve the efficacy of anti-cancer therapy.

Our data demonstrated that EGCG has an anti-proliferative effect on MCF-7 cells. In addition, EGCG specifically reduced the expression of HSP70 and HSP90 without affecting the levels of other HSPs. We also observed that EGCG inhibits the expression of HSP90 client protein, Akt. Previously, it was reported that HSP90 directly interacts with Akt and this process is essential for the stability and function of Akt [29]. Although we did not directly observe the inhibition of Akt signaling by HSP90 inhibition, EGCG-induced cell cycle arrest may associate with the inhibition of HSP90/Akt signaling. Additionally, we observed that EGCG binds with HSP70 and HSP90 by using an EGCG-Sepharose 4B pull-down assay. We also found clear evidence that EGCG competes with ATP for binding to the ATP binding pocket of HSP70 and HSP90 in human breast cancer cells. Although Li et al. reported that EGCG has no effect on ATP binding to HSP90 [13], several studies have reported that EGCG interacts with the ATPase domain of HSP90 and Grp78 and inhibits their functions by competing with ATP for binding to the ATP binding domain in hepatoma and pancreatic cancer cells [12,14]. Collectively, these results suggest that EGCG is likely to affect signaling pathways of cell growth and survival by inhibiting the expression of HSP70 and HSP90 and/or by binding to the HSP70 and HSP90.

Here we demonstrated, for the first time, that EGCG suppresses the expression of HSF1 and HSF2. A luciferase reporter assay showed that EGCG inhibits heat shock- or oxidative stress-induced promoter activity of HSP70 and HSP90. These results demonstrate that EGCG can inhibit the upstream regulator of HSP70 and HSP90. Previous studies suggested that the level of HSF1 become elevated in a number of cancer cells, and the elevated HSF1 is implicated in tumorigenesis through the expression of the HSP70 family proteins and the inhibition of apoptotic pathways [30]. Induction of HSPs by HSF1 is essential for the growth of many tumor cells. Furthermore, inhibition of HSF1 leads to the induction of cell death and tumor regression [31-33]. Therefore, HSF1 is an attractive target for cancer treatment. Unlike HSF1, the role of HSF2 in tumor progression is unclear. Recent studies have shown that HSF1 can physically associate with HSF2 and their interaction is enhanced by heat shock [34,35]. Therefore, the interplay between HSF1 and HSF2 may regulate their function and play an important role on tumor progression by activating target genes.

It is widely accepted that HSPs play an important role in cell protection during cellular stress [18,36]. In this study, we examined the effect of EGCG on heat shock- or oxidative stress (H2O2)-treated MCF-7 cells. Heat shock and H2O2 inhibited cell viability approximately 20% and induced the expression of HSP70 and HSP90. Pretreatment with EGCG further suppressed cell viability after heat shock or H2O2 treatment. And the stress-induced expression of HSP70 and HSP90 was suppressed by EGCG pretreatment in a dose-dependent manner. These results suggest that EGCG enhances stress sensitivity of cells by suppressing the expression of HSP70 and HSP90.

Several studies have shown that the anti-tumor activity of EGCG in xenograft model [37,38]. Here we showed that EGCG inhibits tumor formation in CT26 cell inoculated BALB/c mice. Immunohistochemical staining showed decreased levels of PCNA, HSP70, and HSP90 in the tumors from EGCG treated mice. We also examined the effect of EGCG in xenograft model using 4T1 murine breast cancer cells. In our study, CT26 cells were more sensitive to EGCG than 4T1 cells in vivo (data not shown). Because different types of tumor cells have different genetic alterations and characteristics, the molecular targets of EGCG may be different in different cell lines. The role of HSPs in tumorigenesis is supported by the experimental data showing high expression levels of HSPs are required for the growth of tumor xenografts. Furthermore, high level of HSPs correlates with poor therapeutic outcome in human breast cancer suggesting the inhibition of HSPs can be therapeutically useful [39,40].

In this study, we demonstrate that the anti-tumor activity of EGCG is mediated by the inhibition of HSP70 and HSP90 and suggests EGCG as a potent candidate for the anti-tumor agent.

Conclusion

In this study, we demonstrated that the treatment of EGCG decreased cell proliferation and colony formation of MCF-7 human breast cancer cells. In addition, EGCG specifically inhibited the expression of HSP70 and HSP90 by inhibiting their promoter activity. Pretreatment with EGCG increased the stress sensitivity of MCF-7 cells upon heat shock or oxidative stress. Moreover, treatment with EGCG in a xenograft model resulted in delayed tumor incidence and reduced tumor size, as well as the inhibition of HSP70 and HSP90 expression. These results suggest that HSP70 and HSP90 could be a potential molecular target of EGCG.

Abbreviations

EGCG: Epigallocatechin-3-gallate; HSP: heat shock protein; HSF: heat shock transcription factor; MTT: 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide; CNBr: cyanogen bromide; PCNA: proliferating cell nuclear antigen.

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

PLCHBT, and HSD carried out the experiments described in the study. JHY, SAK, and SGA conceived and reviewed the study. All authors read and approved the final manuscript.

Pre-publication history

The pre-publication history for this paper can be accessed here:

http://www.biomedcentral.com/1471-2407/10/276/prepub

Acknowledgements

This study was supported by the Korea Science and Engineering Foundation (KOSEF) grant funded by the Korea government (MOST) (No. R13-2008-010-01001-0). Soo-A Kim was supported by the Korea Research Foundation Grant funded by the Korean Government(MOEHRD) (KRF-2007-531-E00009).

References

  • Asano Y, Okamura S, Ogo T, Eto T, Otsuka T, Niho Y. Effect of (-)-epigallocatechin gallate on leukemic blast cells from patients with acute myeloblastic leukemia. Life Sci. 1997;60:135–142. doi: 10.1016/S0024-3205(96)00603-0. [PubMed] [Cross Ref]
  • Hibasami H, Komiya T, Achiwa Y, Ohnishi K, Kojima T, Nakanishi K, Akashi K, Hara Y. Induction of apoptosis in human stomach cancer cells by green tea catechins. Oncol Rep. 1998;5:527–529. [PubMed]
  • Paschka AG, Butler R, Young CY. Induction of apoptosis in prostate cancer cell lines by the green tea component, (-)-epigallocatechin-3-gallate. Cancer Lett. 1998;130:1–7. doi: 10.1016/S0304-3835(98)00084-6. [PubMed] [Cross Ref]
  • Sah JF, Balasubramanian S, Eckert RL, Rorke EA. Epigallocatechin-3-gallate inhibits epidermal growth factor receptor signaling pathway. Evidence for direct inhibition of ERK1/2 and AKT kinases. J Biol Chem. 2004;279:12755–12762. doi: 10.1074/jbc.M312333200. [PubMed] [Cross Ref]
  • Gupta S, Hastak K, Ahmad N, Lewin JS, Mukhtar H. Inhibition of prostate carcinogenesis in TRAMP mice by oral infusion of green tea polyphenols. Proc Natl Acad Sci USA. 2001;98:10350–10355. doi: 10.1073/pnas.171326098. [PMC free article] [PubMed] [Cross Ref]
  • Liang YC, Lin-Shiau SY, Chen CF, Lin JK. Inhibition of cyclin-dependent kinases 2 and 4 activities as well as induction of Cdk inhibitors p21 and p27 during growth arrest of human breast carcinoma cells by (-)-epigallocatechin-3-gallate. J Cell Biochem. 1999;75:1–12. doi: 10.1002/(SICI)1097-4644(19991001)75:1<1::AID-JCB1>3.0.CO;2-N. [PubMed] [Cross Ref]
  • Vayalil PK, Katiyar SK. Treatment of epigallocatechin-3-gallate inhibits matrix metalloproteinases-2 and -9 via inhibition of activation of mitogen-activated protein kinases, c-jun and NF-kappaB in human prostate carcinoma DU-145 cells. Prostate. 2004;59:33–42. doi: 10.1002/pros.10352. [PubMed] [Cross Ref]
  • Liang YC, Lin-shiau SY, Chen CF, Lin JK. Suppression of extracellular signals and cell proliferation through EGF receptor binding by (-)-epigallocatechin gallate in human A431 epidermoid carcinoma cells. J Cell Biochem. 1997;67:55–65. doi: 10.1002/(SICI)1097-4644(19971001)67:1<55::AID-JCB6>3.0.CO;2-V. [PubMed] [Cross Ref]
  • Nam S, Smith DM, Dou QP. Ester bond-containing tea polyphenols potently inhibit proteasome activity in vitro and in vivo. J Biol Chem. 2001;276:13322–13330. doi: 10.1074/jbc.M004209200. [PubMed] [Cross Ref]
  • Qanungo S, Das M, Haldar S, Basu A. Epigallocatechin-3-gallate induces mitochondrial membrane depolarization and caspase-dependent apoptosis in pancreatic cancer cells. Carcinogenesis. 2005;26:958–967. doi: 10.1093/carcin/bgi040. [PubMed] [Cross Ref]
  • Brusselmans K, De Schrijver E, Heyns W, Verhoeven G, Swinnen JV. Epigallocatechin-3-gallate is a potent natural inhibitor of fatty acid synthase in intact cells and selectively induces apoptosis in prostate cancer cells. Int J Cancer. 2003;106:856–862. doi: 10.1002/ijc.11317. [PubMed] [Cross Ref]
  • Palermo CM, Westlake CA, Gasiewicz TA. Epigallocatechin gallate inhibits aryl hydrocarbon receptor gene transcription through an indirect mechanism involving binding to a 90 kDa heat shock protein. Biochemistry. 2005;44:5041–5052. doi: 10.1021/bi047433p. [PubMed] [Cross Ref]
  • Li Y, Zhang T, Jiang Y, Lee HF, Schwartz SJ, Sun D. (-)-Epigallocatechin-3-gallate inhibits Hsp90 function by impairing Hsp90 association with cochaperones in pancreatic cancer cell line Mia Paca-2. Mol Pharm. 2009;6:1152–1159. doi: 10.1021/mp900037p. [PMC free article] [PubMed] [Cross Ref]
  • Ermakova SP, Kang BS, Choi BY, Choi HS, Schuster TF, Ma WY, Bode AM, Dong Z. (-)-Epigallocatechin gallate overcomes resistance to etoposide-induced cell death by targeting the molecular chaperone glucose-regulated protein 78. Cancer Res. 2006;66:9260–9269. doi: 10.1158/0008-5472.CAN-06-1586. [PubMed] [Cross Ref]
  • Farabegoli F, Barbi C, Lambertini E, Piva R. (-)-Epigallocatechin-3-gallate downregulates estrogen receptor alpha function in MCF-7 breast carcinoma cells. Cancer Detect Prev. 2007;31:499–504. doi: 10.1016/j.cdp.2007.10.018. [PubMed] [Cross Ref]
  • Mittal A, Pate MS, Wylie RC, Tollefsbol TO, Katiyar SK. EGCG down-regulates telomerase in human breast carcinoma MCF-7 cells, leading to suppression of cell viability and induction of apoptosis. Int J Oncol. 2004;24:703–710. [PubMed]
  • Farabegoli F, Papi A, Bartolini G, Ostan R, Orlandi M. (-)-Epigallocatechin-3-gallate downregulates Pg-P and BCRP in a tamoxifen resistant MCF-7 cell line. Phytomedicine. 2010;17:356–362. doi: 10.1016/j.phymed.2010.01.001. [PubMed] [Cross Ref]
  • Lindquist S, Craig EA. The heat-shock proteins. Annu Rev Genet. 1988;22:631–677. doi: 10.1146/annurev.ge.22.120188.003215. [PubMed] [Cross Ref]
  • Georgopoulos C, Welch WJ. Role of the major heat shock proteins as molecular chaperones. Annu Rev Cell Biol. 1993;9:601–634. doi: 10.1146/annurev.cb.09.110193.003125. [PubMed] [Cross Ref]
  • Gething MJ, Sambrook J. Protein folding in the cell. Nature. 1992;355:33–45. doi: 10.1038/355033a0. [PubMed] [Cross Ref]
  • Ciocca DR, Calderwood SK. Heat shock proteins in cancer: diagnostic, prognostic, predictive, and treatment implications. Cell Stress Chaperones. 2005;10:86–103. doi: 10.1379/CSC-99r.1. [PMC free article] [PubMed] [Cross Ref]
  • Ciocca DR, Rozados VR, Cuello Carrion FD, Gervasoni SI, Matar P, Scharovsky OG. Hsp25 and Hsp70 in rodent tumors treated with doxorubicin and lovastatin. Cell Stress Chaperones. 2003;8:26–36. doi: 10.1379/1466-1268(2003)8<26:HAHIRT>2.0.CO;2. [PMC free article] [PubMed] [Cross Ref]
  • Nylandsted J, Brand K, Jaattela M. Heat shock protein 70 is required for the survival of cancer cells. Ann N Y Acad Sci. 2000;926:122–125. [PubMed]
  • Volloch VZ, Sherman MY. Oncogenic potential of Hsp72. Oncogene. 1999;18:3648–3651. doi: 10.1038/sj.onc.1202525. [PubMed] [Cross Ref]
  • Noonan EJ, Place RF, Rasoulpour RJ, Giardina C, Hightower LE. Cell number-dependent regulation of Hsp70B' expression: evidence of an extracellular regulator. J Cell Physiol. 2007;210:201–211. doi: 10.1002/jcp.20875. [PubMed] [Cross Ref]
  • Jagtap S, Meganathan K, Wagh V, Winkler J, Hescheler J, Sachinidis A. Chemoprotective mechanism of the natural compounds, epigallocatechin-3-O-gallate, quercetin and curcumin against cancer and cardiovascular diseases. Curr Med Chem. 2009;16:1451–1462. doi: 10.2174/092986709787909578. [PubMed] [Cross Ref]
  • Tang Y, Zhao DY, Elliott S, Zhao W, Curiel TJ, Beckman BS, Burow ME. Epigallocatechin-3 gallate induces growth inhibition and apoptosis in human breast cancer cells through survivin suppression. Int J Oncol. 2007;31:705–711. [PubMed]
  • Tang XY, Zhu YQ. Epigallocatechin-3-gallate suppressed the over-expression of HSP 70 and MDR1 induced by heat shock in SGC 7901. J Chemother. 2008;20:355–360. [PubMed]
  • Kim S, Kang J, Hu W, Evers BM, Chung DH. Geldanamycin decreases Raf-1 and Akt levels and induces apoptosis in neuroblastomas. Int J Cancer. 2003;103:352–359. doi: 10.1002/ijc.10820. [PubMed] [Cross Ref]
  • Khaleque MA, Bharti A, Sawyer D, Gong J, Benjamin IJ, Stevenson MA, Calderwood SK. Induction of heat shock proteins by heregulin beta1 leads to protection from apoptosis and anchorage-independent growth. Oncogene. 2005;24:6564–6573. [PubMed]
  • Calderwood SK, Khaleque MA, Sawyer DB, Ciocca DR. Heat shock proteins in cancer: chaperones of tumorigenesis. Trends Biochem Sci. 2006;31:164–172. doi: 10.1016/j.tibs.2006.01.006. [PubMed] [Cross Ref]
  • Kim SA, Kwon SM, Yoon JH, Ahn SG. The antitumor effect of PLK1 and HSF1 double knockdown on human oral carcinoma cells. Int J Oncol. 2010;36:867–872. [PubMed]
  • Whitesell L, Lindquist S. Inhibiting the transcription factor HSF1 as an anticancer strategy. Expert Opin Ther Targets. 2009;13:469–478. doi: 10.1517/14728220902832697. [PubMed] [Cross Ref]
  • Ostling P, Björk JK, Roos-Mattjus P, Mezger V, Sistonen L. Heat shock factor 2 (HSF2) contributes to inducible expression of hsp genes through interplay with HSF1. J Biol Chem. 2007;282:7077–7086. doi: 10.1074/jbc.M607556200. [PubMed] [Cross Ref]
  • Sandqvist A, Björk JK, Akerfelt M, Chitikova Z, Grichine A, Vourc'h C, Jolly C, Salminen TA, Nymalm Y, Sistonen L. Heterotrimerization of heat-shock factors 1 and 2 provides a transcriptional switch in response to distinct stimuli. Mol Biol Cell. 2009;20:1340–1347. doi: 10.1091/mbc.E08-08-0864. [PMC free article] [PubMed] [Cross Ref]
  • Kim SA, Chang S, Yoon JH, Ahn SG. TAT-Hsp40 inhibits oxidative stress-mediated cytotoxicity via the inhibition of Hsp70 ubiquitination. FEBS Lett. 2008;582:734–740. doi: 10.1016/j.febslet.2008.01.053. [PubMed] [Cross Ref]
  • Katiyar SK, Mohan RR, Agarwal R, Mukhtar H. Protection against induction of mouse skin papillomas with low and high risk of conversion to malignancy by green tea polyphenols. Carcinogenesis. 1997;18:497–502. doi: 10.1093/carcin/18.3.497. [PubMed] [Cross Ref]
  • Sartippour MR, Heber D, Ma J, Lu Q, Go VL, Nguyen M. Green tea and its catechins inhibit breast cancer xenografts. Nutr Cancer. 2001;40:149–156. doi: 10.1207/S15327914NC402_11. [PubMed] [Cross Ref]
  • Nylandsted J, Wick W, Hirt UA, Brand K, Rohde M, Leist M, Weller M, Jaattela M. Eradication of glioblastoma, and breast and colon carcinoma xenografts by Hsp70 depletion. Cancer Res. 2002;62:7139–7142. [PubMed]
  • Vargas-Roig LM, Gago FE, Tello O, Aznar JC, Ciocca DR. Heat shock protein expression and drug resistance in breast cancer patients treated with induction chemotherapy. Int J Cancer. 1998;79:468–475. doi: 10.1002/(SICI)1097-0215(19981023)79:5<468::AID-IJC4>3.0.CO;2-Z. [PubMed] [Cross Ref]

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