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Survivin gene silencing sensitizes prostate cancer cells to selenium growth inhibition
© Liu et al; licensee BioMed Central Ltd. 2010
Received: 7 July 2009
Accepted: 10 August 2010
Published: 10 August 2010
Prostate cancer is a leading cause of cancer-related death in men worldwide. Survivin is a member of the inhibitor of apoptosis (IAP) protein family that is expressed in the majority of human tumors including prostate cancer, but is barely detectable in terminally differentiated normal cells. Downregulation of survivin could sensitize prostate cancer cells to chemotherapeutic agents in vitro and in vivo. Selenium is an essential trace element. Several studies have shown that selenium compounds inhibit the growth of prostate cancer cells. The objective of this study is to investigate whether survivin gene silencing in conjunction with selenium treatment could enhance the therapeutic efficacy for prostate cancer and to elucidate the underlying mechanisms.
Expression of survivin was analyzed in a collection of normal and malignant prostatic tissues by immunohistochemical staining. In vitro studies were conducted in PC-3M, C4-2B, and 22Rv1 prostate cancer cells. The effect of selenium on survivin expression was analyzed by Western blotting and semi-quantitative RT-PCR. Survivin gene knockdown was carried out by transfecting cells with a short hairpin RNA (shRNA) designed against survivin. Cell proliferation was quantitated by the 3-(4,5-Dimethylthiazol-2-yl)- 2,5-Diphenyltetrazolium Bromide (MTT) assay and apoptosis by propidium iodide staining followed by flow cytometry analysis. Finally, in vivo tumor growth assay was performed by establishing PC-3M xenograft in nude mice and monitoring tumor growth following transfection and treatment.
We found that survivin was undetectable in normal prostatic tissues but was highly expressed in prostate cancers. Survivin knockdown or selenium treatment inhibited the growth of prostate cancer cells, but the selenium effect was modest. In contrast to what have been observed in other cell lines, selenium treatment had little or no effect on survivin expression in several androgen-independent prostate cancer cell lines. Survivin knockdown sensitized these cells to selenium growth inhibition and apoptosis induction. In nude mice bearing PC-3M xenografts, survivin knockdown synergizes with selenium in inhibiting tumor growth.
Selenium could inhibit the growth of hormone-refractory prostate cancer cells both in vitro and in vivo, but the effects were modest. The growth inhibition was not mediated by downregulating survivin expression. Survivin silencing greatly enhanced the growth inhibitory effects of selenium.
Prostate cancer (PCa) is the second most commonly diagnosed cancer and the second leading cause of cancer deaths in men in the United States . Surgery and radiation therapy are effective for localized disease , but there is no effective treatment strategy for recurrent or metastatic PCa that has failed surgery, radiation or hormonal therapy. Chemotherapeutic drugs could only extend the lives of men with advanced prostate cancer by months, and they are also associated with dose-limiting toxicity. With the recent advances in the understanding of molecular pathways involved in prostate cancer progression, targeted therapies that are designed to interfere with the way cancer cells grow and survive offer new hope in prostate cancer therapeutics.
Survivin, a structurally unique member of the inhibitor of apoptosis (IAP) protein family, is involved in the control of mitotic progression and inhibition of apoptosis . It is abundantly expressed in cancer tissues but is undetectable in normal, differentiated adult tissues. Survivin expression is associated with poor prognosis in many cancer types . The expression of survivin increases gradually from normal prostate tissue, to primary low-grade prostate carcinoma, and to primary high-grade carcinoma, with the highest expression observed in foci of prostate cancer metastasized to the lymph nodes . This pattern of gene expression suggests that survivin is associated with disease progression, and therefore making survivin an attractive target for prostate cancer therapeutics.
Selenium is an essential trace element. Several case control studies have demonstrated an inverse correlation between serum selenium level and the risk of developing prostate cancer [6–8]. The Nutritional Prevention of Cancer (NPC) trial demonstrated that supplementation of selenium, in the form of selenized yeast, could reduce the incidence of prostate cancer by ~50% [9, 10]. Although the interim analysis of the Selenium and Vitamin E Chemoprevention Trial (SELECT) indicated no reduction in prostate cancer risk associated with selenium supplementation , the finding should not be simply interpreted as selenium is ineffective against prostate cancer. In the Discussion, we provide several potential explanations for the discrepancy of the findings in SELECT and the NPC trial. The negative SELECT finding makes it more important and imperative to study the efficacy of new selenium compounds [12–14], including the compounds used in the study, methylseleninic acid (MSA) and methylselenocysteine (MSC), for prostate cancer intervention.
One of mechanisms proposed for the anticancer activity of selenium is apoptosis induction. Due to the role of survivin in conferring cytoprotection against apoptosis in cancer cells, we set out to examine the effect of selenium on the expression of survivin in several hormone refractory prostate cancer cell lines. To our surprise, selenium treatment did not affect survivin expression in these cells. Based on this finding, we hypothesize that selenium treatment and survivin knockdown would complement the action of each other, leading to a greater anticancer effect. The present study was designed to test this hypothesis, and to explore the underlying mechanisms.
MSA and MSC were obtained from PharmaSe (Lubbock, TX). The rabbit anti-human polyclonal antibodies against survivin and caspase 3 were from Santa Cruz Biotech (Santa Cruz, CA). The rabbit anti-human Ki-67 polyclonal antibody was obtained from Neomarker (Fremont, CA). Trizol, RPMI 1640, fetal bovine serum (FBS), and lipofectamine 2000 were purchased from Invitrogen (Carlsbad, CA). Acridine orange (AO) and ethidium bromide (EB) were from Sigma (St. Louis, MO).
Prostate tissue acquisition and immunohistochemical (IHC) analysis
Prostate cancer specimens were obtained from patients undergoing prostatectomy in the Second and the Third Affiliated Hospitals of Jilin University. Normal prostate tissues were obtained from patients undergoing surgery for benign prostatic hyperplasia (BPH) in these hospitals. This study was approved by the Research Ethics Committee of Norman Bethune College of Medicine, Jilin University and was in compliance with the Helsinki Declaration. The tissues were examined by the pathologists to confirm the diagnosis before IHC analyses. All specimens were fixed in 10% formalin, embedded in paraffin, and cut into 4 μm-thick slides. The slides were dewaxed, and the endogenous peroxidase activity was blocked by treatment with 3% hydrogen peroxide solution in methanol for 20 min. Epitope retrieval was performed by treating the slides with 10 mM sodium citrate buffer (pH 6.0) and heating in a microwave oven for two times at the high power for 6 min each. Non-specific binding was prevented by blocking with normal goat serum (1:10) for 10 min. Immunostaining of survivin was performed using a rabbit anti-human survivin polyclonal antibody. Goat anti-rabbit IgG conjugated with horseradish peroxidase was used as the secondary antibody. The staining procedure was carried out manually at room temperature, using an avidin-biotin-peroxidase complex method. The presence of survivin and Ki-67 was evaluated by staining with rabbit anti-survivin and anti-Ki-67 antibody, respectively. After incubation with the primary antibody for 60 min, the slides were incubated with the biotinylated goat anti-rabbit IgG (H+L) (DAKO, Carpinteria, CA) at 37°C for 30 min, followed by incubation with a 1:200 streptavidin-biotin-peroxidase complex (Sigma, St. Louis) for 30 min. Reactive products were visualized with 3,3'-diaminobenzidene (DAB) as the chromogen, and the slides were counterstained with hematoxylin and coverslipped. Sections previously known to express survivin and Ki-67 were included in each run, receiving either the primary antibody as the positive control, or a mouse IgG as the negative control. The stained slides were analyzed with a microscope at 200× magnification. The slides were examined by two independent pathologists who had no knowledge of the clinical outcomes and of the results obtained by the other. Differences in interpretation were reconciled by reviewing the slides jointly. Cellular brownish staining was scored as positive and the threshold was set at 10%. The proliferation index was defined as percent of tumor cells stained positively for Ki-67.
Construction of the short hairpin RNA (shRNA) vectors for survivin silencing
Oligonucleotides for anti-survivin shRNA expression were designed, synthesized, and cloned into the pGCsilencer-U6/Neo/GFP plasmid (GeneChem Co, Shanghai, China). The sequences are: sense, 5'-gatcccGCAGTTTGAAGAATTAACCttcaagaga GGTTAATTCTTCAAACTGCtttttggat-3'; and antisense, 5'-agctatccaaaaaGCAGTTTGAAGAATTAACCtctcttgaaGGTTAATTCTTCAAATGCgg-3'. Sequences in uppercase letters indicate nucleotides 394-412 of the survivin cDNA. BLAST searches of the human genome database were carried out to ensure that the sequences would not target any other transcripts. The recombinant plasmid was named pGCsh-survivin (referred to as sh-survivin hereafter). Recombinant pGCsh-scrambled plasmid (referred to as sh-scrambled hereafter), which used a scrambled sequence that has no significant homology to any mouse or human gene sequences, was constructed as the negative control.
Cell culture and transfection
The PC-3M, C4-2B, and 22Rv1 cells were cultured in RPMI 1640 medium supplemented with 10% FBS, 100 unit/ml of penicillin, 100 μg/ml of streptomycin, and 2 mM of L-glutamine and incubated at 37°C in 5% CO2. For transfection, 5 × 105 cells were plated onto 6-well plates 24 hours before transfection. Transfection was performed using Lipofectamine 2000 according to the manufacturer's instructions. Transfection media were removed 6 hours after transfection and replaced with fresh complete medium containing 10% FBS. Controls included lipofectamine 2000 treated cells and sh-scrambled transfected cells.
Gene expression analysis by semi-quantitative reverse-transcription PCR (RT-PCR) and Western analysis
The effects of survivin shRNA and MSA, alone or in combination, on cellular expression of survivin were measured by semi-quantitative RT-PCR and Western blot analysis. PC-3M cells were divided into 5 groups: (a) control (mock-transfected); (b) scrambled (transfected with sh-scrambled); (c) sh-survivin (transfected with sh-survivin); (d) MSA (treated with 5 μM MSA); (e) combination (transfected with sh-survivin and treated with 5 μM MSA), and cells were harvested after 66 hours following transfection and treatment. Total RNA was isolated using the Trizol reagent according to the manufacturer's instructions. Survivin gene expression was determined by semi-quantitative RT-PCR, using the primer pairs 5'-GAATTCATGGGTGCCCCGACGTTGCC-3' and 5'-AGATCTTTCTTCTTATTGTTGGTTTCC-3'. The housekeeping gene β-actin was amplified as an internal standard.
For Western blot analysis, cells were lysed with HEPES lysis buffer (30 mM HEPES, 1% Triton X-100, 10% glycerol, 5 mM MgCl2, 25 mM NaF, 1 mM EDTA and 10 mM NaCl). Fifty micrograms of protein were electrophoresed on a 10% SDS-PAGE gel, transferred onto a PVDF membrane (Millipore, Bedford, MA), and probed with the anti-survivin or the anti-caspase-3 antibody. A goat anti-rabbit antibody labeled with horseradish peroxidase (Amersham) was added as the secondary antibody. Immunoblots were developed using a chemiluminescence detection system (Amersham Pharmacia Biotech).
Cell proliferation and apoptosis assays
Cell numbers were determined at 66 hours after treatment using the 3-(4,5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide (MTT) assay and quantified by using a microplate reader (Bio-Rad). For apoptosis, 106 cells were fixed in 70% (v/v) ethanol, stained with PBS containing 50 μg/mL propidium iodide, 10 mg/mL RNase, and 0.1% (v/v) Tween-20 for 30 minutes at room temperature, and analyzed for cell apoptosis with a FACScan flow cytometer (Becton Dickinson). For AP/EB staining, PC-3M cells were collected by trypsinization, washed with PBS (pH 7.4), and fixed in 4% paraformaldehyde. Fixed cells were washed twice with PBS and resuspended in PBS containing 16 μg/ml AO and 16 μg/ml EB, then mounted on a glass slide and observed under a fluorescent microscope.
Antitumor effect of survivin siRNA and selenium in vivo
Five-week-old pathogen-free athymic nude mice were purchased from the Institute of Laboratory Animal Science, Chinese Academy of Medical Sciences (Beijing, China). PC-3M cells in exponential growth phase were harvested and single-cell suspensions (2 × 106 cells in 100 μl PBS) were injected subcutaneously (s.c.) into the right dorsal flank of nude mice. Tumor size was measured every 2 to 3 days, and tumor volume calculated as 0.5236 × width 2 × length. After palpable tumors had developed, the mice were divided randomly into five groups (six mice per group): (a) control (mock-transfected); (b) scrambled (transfected with sh-scrambled); (c) sh-survivin (transfected with sh-survivin); (d) MSC (given MSC at 100 μg/mouse/day); (e) combination (transfected with sh-survivin and given MSC). Transfection of the siRNAs was performed by an electroporation method. Twenty micrograms of plasmid suspended in 50 μl PBS was injected percutaneously into the tumors by using a syringe with a 27-gauge needle. Immediately after injection, tumors were pulsed with an electroporation generator (ECM830, BTX, Holliston, MA). Pulses were delivered at a frequency of 1 pulse/sec, 150 V/cm, for 50 milliseconds. This process was performed twice, first on day 15 and then on day 25. For selenium treatment, MSC was given by daily intragastric administration starting at day 15. Mice were sacrificed on day 35 when tumor burden in the control group approaching 10% of body weight. Tumors were excised, fixed in 4% buffered formalin, and embedded in paraffin. The animal study was conducted following internationally recognized guidelines and was approved by the Animal Research Committee of Norman Bethune College of Medicine, Jilin University.
Terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end labeling (TUNEL) assay
Apoptotic cells in tissues were determined by using the TUNEL assay (Roche Diagnostics, Indianapolis, IN) according to the manufacturer's instructions. Briefly, after deparaffinization and rehydration, sections were incubated with proteinase K (16.2 μg/mL in 10 mM Tris·HCL, pH 7.4) for 20 min at 37°C. Slides were rinsed with PBS and incubated with 3% H2O2 in methanol for 10 min at room temperature to block endogenous peroxidase activity, followed by PBS washing and incubation in 0.1% Triton X-100 in 0.1% sodium citrate for 2 min on ice. Sections were then incubated with a mixture of terminal deoxynucleotidyl transferase (TdT) solution and biotin-dUTP solution in a humidified chamber at 37°C for 60 min, followed by washing with PBS and incubation with peroxidase-conjugated streptavidin in a humidified chamber for 30 min at room temperature. After an additional wash with PBS, the slides were incubated in DAB and counterstained with hematoxylin. Paraffin-embedded sections of normal tonsils were used as positive control. Negative control was obtained by replacing the TdT solution with distilled water. The presence of clear nuclear staining was indicative of apoptotic cells. At least 1,000 tumor cell nuclei were randomly selected and examined. The number of TUNEL-positive tumor cell nuclei was counted and the apoptotic index was calculated as follows: apoptotic index = (number of apoptotic cells/total cell number) × 100%.
Chi-square test was used to analyze the difference in survivin expression between normal and cancerous prostate tissues. Pearson correlation analysis was performed to test the correlation of Gleason Score and survivin expression in the prostate cancer cases. Data were presented as mean ± standard deviation (SD) when appropriate. Two-tailed Student's t-test was used to evaluate the differences between treatment and control values, and P < 0.05 was considered statistically significant.
Survivin is overexpressed in prostate cancer tissues
Expression of survivin in normal and cancerous prostatic tissues.
survivin staining status
positive N (%)
negative N (%)
MSA induces apoptosis in PC-3M cells but has little effect on survivin expression
Survivin gene silencing sensitizes prostate cancer cells to growth inhibition by MSA
Based on the data from the previous experiments, we hypothesized that survivin knockdown will sensitize prostate cancer cells to growth inhibition by MSA. To test this hypothesis, we designed a plasmid-based shRNA vector for survivin gene silencing and tested its efficacy. As shown in Fig. 3A, sh-survivin effectively reduced the level of the survivin transcript, whereas the scrambled shRNA had no effect. Western blotting analysis confirmed the down-regulation of survivin expression by sh-survivin in all 3 cell lines (Fig. 3B). Quantitation by volume densitometry showed the knockdown efficiency at the protein level is in the range of 60-70% in these cell lines.
Survivin gene silencing enhances selenium's efficacy on apoptosis induction
Caspases are important mediators of apoptosis. Activation of caspase-3 by enzymatic cleavage is a hallmark event in caspase-dependent apoptosis. We investigated caspase-3 activation by Western blotting and the results are shown in Fig. 5B. Cleaved caspase-3 (19 KDa) was induced similarly by sh-survivin and MSA, whereas their combination led to a modestly but significantly stronger activation (P < 0.05). The changes in caspase-3 activation did not involve changes in gene expression, as the band intensity for procaspase-3 (32 KDa) was not changed by either sh-survivin, or MSA, or their combination. The modest increase in caspase-3 activation in the combined group suggest that the synergistic effect on apoptosis induction could also be mediated by caspase-independent mechanisms, since survivin has also been shown to inhibit both caspase-independent apoptosis . In general, the apoptosis data are in agreement with the MTT results, showing that survivin gene knockdown greatly enhances the anticancer effect of selenium in prostate cancer cells.
Inhibition of tumor growth in vivoby survivin knockdown and selenium
Cell proliferation and apoptosis indices from PC-3M xenografts.
Group (n = 6)
86.75 ± 9.43
3.64 ± 1.66
81.64 ± 9.25
4.45 ± 1.86
16.82 ± 5.32*
31.3 ± 3.64*
56.2 ± 8.65*
14.7 ± 2.23*
6.8 ± 1.64*#
48.6 ± 2.67*#
Soon after the development of the RNA interference (RNAi) technology a few years ago, the potential of using this highly specific and powerful gene silencing approach in treating cancer has generated a great deal of interest. Obviously, the key to the success of this approach is to identify a gene which is expressed universally in cancer cells, but not in normal cells. Survivin appears to be such a candidate. As a member of the IAP family, survivin has been reported to be up-regulated in human cancers of various origins. Consistent with previous reports [5, 20], we found in the present study that survivin is highly expressed in the majority of cancerous prostate tissues, but not in normal prostatic tissues. Silencing of survivin expression in PC-3M cells by a specific shRNA led to decreased cell growth and increased cell death. Elevated survivin expression has been associated with resistance to chemotherapeutic agents [21–24]. Therefore, targeted suppression of survivin expression represents a potential therapeutic strategy for prostate cancer, either being used alone or in a neoadjuvant setting.
Several potential reasons have been discussed to explain the discrepancy of the findings in SELECT and the NPC trial. One important consideration is the baseline selenium level. The NPC trial showed that the protective effect of selenium was limited to patients with baseline serum selenium in the lower 2 tertiles . The average baseline selenium level of the participants in SELECT was much higher than that observed in the NPC study. In fact, 78% of men in SELECT had baseline selenium above the range that selenium provided protection in the NPC trial (<121.6 ng/ml) . Another important consideration is how selenium exerts its anticancer activity. By using a nested case-control design within a prospective study (the Physicians' Health Study) among 586 men diagnosed with prostate cancer during 13 years of follow-up and 577 control subjects, Li et al. showed a ~50% reduction in risk of advanced prostate cancer in individuals within the highest quintile of selenium level compared to those within the lowest quintile . Such association was not observed for localized prostate cancer, suggesting that selenium might function by slowing down tumor progression . In view of the above information, we believe that the negative finding by SELECT should not be simply interpreted as selenium is ineffective against prostate cancer; instead, it raises the hypothesis of whether selenium might only be effective only in selected subsets of men with lower selenium levels at baseline.
The formulation and dose of selenium used in the SELECT study have also been hot topics of debate. The compounds used in the current study, MSA and MSC, are monomethylated forms of selenium and are considered second-generation selenium compounds. Metabolically, they are very different from selenomethionine, the formulation used in the SELECT. MSA and MSC can be easily converted to methylselenol, which is considered to be the critical metabolite for the anticancer activity of selenium [14, 27]. Selenomethionine, on the other hand, can be incorporated nonspecifically into proteins in place of methionine . Due to its compartmentation into tissue proteins, selenomethionine is not as readily available as MSA or MSC for further metabolism. The metabolism of selenomethionine to methylselenol requires at least 5 transsulfuration steps and the action of thiol methyltransferase [12–14]. Studies published prior to and after the start of the SELECT study have showed that MSA and MSC have stronger anticancer activities than selenomethionine [28–30].
Several studies have shown that selenium induces growth arrest and cell death in prostate cancer cells and inhibits the growth of prostate cancer xenografts [15, 16, 31, 32], leading support to the idea that selenium could be used in the treatment of prostate cancer. In the present study, we confirmed the anticancer activity of selenium in the androgen-independent human prostate cancer cells. In contrast to a report that selenium suppresses survivin expression in a number of PCa cell lines, including the parental PC-3 and LNCaP lines , our in vitro and in vivo data both showed that MSA treatment had little or no effect on survivin expression in PC-3M, C4-2B, and 22Rv1 cells. This is consistent with results published by Azrak et al showing at similar doses, selenium treatment did not affect survivin expression in mouse prostate cancer cells or ovarian cancer cells [33, 34]. When used alone, MSA had a modest effect on growth inhibition and apoptosis induction in PC-3M cells cultured in vitro. Similarly, MSC inhibited the growth of PC-3M xenografts but the efficacy appears to be inferior to its inhibitory effect against PC-3 xenografts . The insensitivity of PC-3M cells to selenium could be related to its inability to suppress survivin expression in these cells. In support of the notion, we found that the effect of selenium was greatly enhanced when survivin expression was silenced. Indeed, in nude mice bearing PC-3M xenografts, survivin knockdown in combination with selenium treatment stopped tumor growth completely. In the study by Azrak et al which showed MSA did not inhibit survivin expression in skov3 ovarian cancer cells, survivin knockdown greatly enhanced the efficacy of combination therapy by MSA and paclitaxel, converting the interaction between these two agents from antagonistic to synergistic .
Survivin was highly expressed in clinical prostate cancers but not in normal prostates. In prostate cancer cells where selenium had no effect on survivin expression, growth inhibition and apoptosis induction effects of selenium were modest. Both the in vitro and in vivo efficacies of selenium were greatly enhanced when survivin expression was silenced. The current study suffers from the limitation that the results are obtained mainly from cell culture and animal experiments. Nonetheless, the results suggest a potential mechanism of cancer cell resistance to the cytotoxic effect of selenium compounds and a strategy to improve the efficacy of selenium. This is important, especially in the context of the negative findings of the SELECT trial with regard to the anticancer activity of selenium. Further preclinical studies are needed to confirm the findings before these results can be incorporated into clinical practice.
This work was supported by DOD New Investigator grant no. W81XWH-05-1-0598 (H. Zhang), National Cancer Institute grant no. K01 CA114252 and American Cancer Society Grant No. RSG-07-218-01-TBE (Y. Dong), Specialized Programs of Research in Prostate Cancer grant 2004DFB02000 from the Ministry of Science and Technology of the People's Republic of China (X. Zhao), Japan International Cooperation Agency (X. Zhao), and Jilin Provincial Scholarship for Outstanding Scientists from Jilin Province, China (Y. Dong), and start-up fund from the Louisiana Cancer Research Consortium (H. Zhang). The authors thank Dr. Sudesh K. Srivastav for help with statistical analyses.
- Jemal A, Siegel R, Ward E, Murray T, Xu J, Smigal C, Thun MJ: Cancer statistics, 2006. CA Cancer J Clin. 2006, 56: 106-130. 10.3322/canjclin.56.2.106.View ArticlePubMedGoogle Scholar
- Klein EA, Kupelian PA: Localized prostate cancer: radiation or surgery?. Urol Clin North Am. 2003, 30: 315-30ix. 10.1016/S0094-0143(02)00179-9.View ArticlePubMedGoogle Scholar
- Altieri DC, Marchisio PC: Survivin apoptosis: an interloper between cell death and cell proliferation in cancer. Lab Invest. 1999, 79: 1327-1333.PubMedGoogle Scholar
- Altieri DC: Survivin, versatile modulation of cell division and apoptosis in cancer. Oncogene. 2003, 22: 8581-8589. 10.1038/sj.onc.1207113.View ArticlePubMedGoogle Scholar
- Shariat SF, Lotan Y, Saboorian H, Khoddami SM, Roehrborn CG, Slawin KM, Ashfaq R: Survivin expression is associated with features of biologically aggressive prostate carcinoma. Cancer. 2004, 100: 751-757. 10.1002/cncr.20039.View ArticlePubMedGoogle Scholar
- Brooks JD, Metter EJ, Chan DW, Sokoll LJ, Landis P, Nelson WG, Muller D, Andres R, Carter HB: Plasma selenium level before diagnosis and the risk of prostate cancer development. J Urol. 2001, 166: 2034-2038. 10.1016/S0022-5347(05)65500-0.View ArticlePubMedGoogle Scholar
- Helzlsouer KJ, Huang HY, Alberg AJ, Hoffman S, Burke A, Norkus EP, Morris JS, Comstock GW: Association between alpha-tocopherol, gamma-tocopherol, selenium, and subsequent prostate cancer. J Natl Cancer Inst. 2000, 92: 2018-2023. 10.1093/jnci/92.24.2018.View ArticlePubMedGoogle Scholar
- Nomura AM, Lee J, Stemmermann GN, Combs GF: Serum selenium and subsequent risk of prostate cancer. Cancer Epidemiol Biomarkers Prev. 2000, 9: 883-887.PubMedGoogle Scholar
- Clark LC, Combs GF, Turnbull BW, Slate EH, Chalker DK, Chow J, Davis LS, Glover RA, Graham GF, Gross EG, et al: Effects of selenium supplementation for cancer prevention in patients with carcinoma of the skin. A randomized controlled trial. Nutritional Prevention of Cancer Study Group. JAMA. 1996, 276: 1957-1963. 10.1001/jama.276.24.1957.View ArticlePubMedGoogle Scholar
- Duffield-Lillico AJ, Dalkin BL, Reid ME, Turnbull BW, Slate EH, Jacobs ET, Marshall JR, Clark LC: Selenium supplementation, baseline plasma selenium status and incidence of prostate cancer: an analysis of the complete treatment period of the Nutritional Prevention of Cancer Trial. BJU Int. 2003, 91: 608-612. 10.1046/j.1464-410X.2003.04167.x.View ArticlePubMedGoogle Scholar
- Lippman SM, Klein EA, Goodman PJ, Lucia MS, Thompson IM, Ford LG, Parnes HL, Minasian LM, Gaziano JM, Hartline JA, et al: Effect of selenium and vitamin E on risk of prostate cancer and other cancers: the Selenium and Vitamin E Cancer Prevention Trial (SELECT). JAMA. 2009, 301: 39-51. 10.1001/jama.2008.864.View ArticlePubMedGoogle Scholar
- Ip C, Ganther HE: Activity of methylated forms of selenium in cancer prevention. Cancer Res. 1990, 50: 1206-1211.PubMedGoogle Scholar
- Ip C, Hayes C, Budnick RM, Ganther HE: Chemical form of selenium, critical metabolites, and cancer prevention. Cancer Res. 1991, 51: 595-600.PubMedGoogle Scholar
- Ip C: Lessons from basic research in selenium and cancer prevention. J Nutr. 1998, 128: 1845-1854.PubMedGoogle Scholar
- Yamaguchi K, Uzzo RG, Pimkina J, Makhov P, Golovine K, Crispen P, Kolenko VM: Methylseleninic acid sensitizes prostate cancer cells to TRAIL-mediated apoptosis. Oncogene. 2005, 24: 5868-5877. 10.1038/sj.onc.1208742.View ArticlePubMedGoogle Scholar
- Zu K, Ip C: Synergy between selenium and vitamin E in apoptosis induction is associated with activation of distinctive initiator caspases in human prostate cancer cells. Cancer Res. 2003, 63: 6988-6995.PubMedGoogle Scholar
- Burk RF, Hill KE, Motley AK, Austin LM, Norsworthy BK: Deletion of selenoprotein P upregulates urinary selenium excretion and depresses whole-body selenium content. Biochim Biophys Acta. 2006, 1760: 1789-1793.View ArticlePubMedPubMed CentralGoogle Scholar
- Chun JY, Hu Y, Pinder E, Wu J, Li F, Gao AC: Selenium inhibition of survivin expression by preventing Sp1 binding to its promoter. Mol Cancer Ther. 2007, 6: 2572-2580. 10.1158/1535-7163.MCT-07-0172.View ArticlePubMedPubMed CentralGoogle Scholar
- Liu T, Brouha B, Grossman D: Rapid induction of mitochondrial events and caspase-independent apoptosis in Survivin-targeted melanoma cells. Oncogene. 2004, 23: 39-48. 10.1038/sj.onc.1206978.View ArticlePubMedPubMed CentralGoogle Scholar
- Kaur P, Kallakury BS, Sheehan CE, Fisher HA, Kaufman RP, Ross JS: Survivin and Bcl-2 expression in prostatic adenocarcinomas. Arch Pathol Lab Med. 2004, 128: 39-43.PubMedGoogle Scholar
- Virrey JJ, Guan S, Li W, Schonthal AH, Chen TC, Hofman FM: Increased survivin expression confers chemoresistance to tumor-associated endothelial cells. Am J Pathol. 2008, 173: 575-585. 10.2353/ajpath.2008.071079.View ArticlePubMedPubMed CentralGoogle Scholar
- Zhang M, Mukherjee N, Bermudez RS, Latham DE, Delaney MA, Zietman AL, Shipley WU, Chakravarti A: Adenovirus-mediated inhibition of survivin expression sensitizes human prostate cancer cells to paclitaxel in vitro and in vivo. Prostate. 2005, 64: 293-302. 10.1002/pros.20263.View ArticlePubMedGoogle Scholar
- Zhang M, Latham DE, Delaney MA, Chakravarti A: Survivin mediates resistance to antiandrogen therapy in prostate cancer. Oncogene. 2005, 24: 2474-2482. 10.1038/sj.onc.1208490.View ArticlePubMedGoogle Scholar
- Yang H, Fu JH, Hu Y, Huang WZ, Zheng B, Wang G, Zhang X, Wen J: Influence of SiRNA Targeting Survivin on Chemosensitivity of H460/cDDP Lung Cancer Cells. J Int Med Res. 2008, 36: 734-747.View ArticlePubMedGoogle Scholar
- Duffield-Lillico AJ, Reid ME, Turnbull BW, Combs GF, Slate EH, Fischbach LA, Marshall JR, Clark LC: Baseline characteristics and the effect of selenium supplementation on cancer incidence in a randomized clinical trial: A summary report of the nuritional prevention of cancer trial. Cancer Epidemiol Biomarkers Prev. 2002, 11: 630-639.PubMedGoogle Scholar
- Li H, Stampfer MJ, Giovannucci EL, Morris JS, Willett WC, Gaziano JM, Ma J: A prospective study of plasma selenium levels and prostate cancer risk. J Natl Cancer Inst. 2004, 96: 696-703. 10.1093/jnci/djh125.View ArticlePubMedGoogle Scholar
- Ip C, Thompson HJ, Zhu Z, Ganther HE: In vitro and in vivo studies of methylseleninic acid: evidence that a monomethylated selenium metabolite is critical for cancer chemoprevention. Cancer Res. 2000, 60: 2882-2886.PubMedGoogle Scholar
- Ip C, Birringer M, Block E, Kotrebai M, Tyson JF, Uden PC, Lisk DJ: Chemical speciation influences comparative activity of selenium-enriched garlic and yeast in mammary cancer prevention. J Agric Food Chem. 2000, 48: 2062-2070. 10.1021/jf000051f.View ArticlePubMedGoogle Scholar
- Li GX, Lee HJ, Wang Z, Hu H, Liao JD, Watts JC, Combs GF, Lu J: Superior in vivo inhibitory efficacy of methylseleninic acid against human prostate cancer over selenomethionine or selenite. Carcinogenesis. 2008, 29: 1005-1012. 10.1093/carcin/bgn007.View ArticlePubMedPubMed CentralGoogle Scholar
- Medina D, Thompson H, Ganther H, Ip C: Se-methylselenocysteine: a new compound for chemoprevention of breast cancer. Nutr Cancer. 2001, 40: 12-17. 10.1207/S15327914NC401_5.View ArticlePubMedGoogle Scholar
- Dong Y, Lee SO, Zhang H, Marshall J, Gao AC, Ip C: Prostate specific antigen expression is down-regulated by selenium through disruption of androgen receptor signaling. Cancer Res. 2004, 64: 19-22. 10.1158/0008-5472.CAN-03-2789.View ArticlePubMedGoogle Scholar
- Dong Y, Zhang H, Gao AC, Marshall JR, Ip C: Androgen receptor signaling intensity is a key factor in determining the sensitivity of prostate cancer cells to selenium inhibition of growth and cancer-specific biomarkers. Mol Cancer Ther. 2005, 4: 1047-1055. 10.1158/1535-7163.MCT-05-0124.View ArticlePubMedGoogle Scholar
- Azrak RG, Frank CL, Ling X, Slocum HK, Li F, Foster BA, Rustum YM: The mechanism of methylselenocysteine and docetaxel synergistic activity in prostate cancer cells. Mol Cancer Ther. 2006, 5: 2540-2548. 10.1158/1535-7163.MCT-05-0546.View ArticlePubMedPubMed CentralGoogle Scholar
- Azrak RG, Frank CL, Ghadersohi A, Rustum YM: Silencing survivin results in synergy between methylseleninic acid and paclitaxel against skov3 ovarian cancer cells. Cancer Biol Ther. 2008, 7: 1901-1908.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/10/418/prepub
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