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	<title>Pine Street Foundation &#187; Prostate Cancer</title>
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		<title>Antioxidants &amp; Chemotherapy for Advanced Prostate Cancer: The Latest Research on Specific Interactions</title>
		<link>http://pinestreetfoundation.org/2007/06/21/antioxidants-chemotherapy-for-advanced-prostate-cancer-the-latest-research-on-specific-interactions/</link>
		<comments>http://pinestreetfoundation.org/2007/06/21/antioxidants-chemotherapy-for-advanced-prostate-cancer-the-latest-research-on-specific-interactions/#comments</comments>
		<pubDate>Thu, 21 Jun 2007 20:00:51 +0000</pubDate>
		<dc:creator>PSFJA</dc:creator>
				<category><![CDATA[Avenues]]></category>
		<category><![CDATA[Becoming Your Own Advocate]]></category>
		<category><![CDATA[Chemotherapy & Antioxidants]]></category>
		<category><![CDATA[Antioxidants]]></category>
		<category><![CDATA[Chemotherapy]]></category>
		<category><![CDATA[Prostate Cancer]]></category>

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		<description><![CDATA[While it is true that there are some antioxidants that can hinder chemotherapy's effects, recent research suggests that there are some antioxidants that, when combined with chemotherapy, can increase the effectiveness of treatment by upwards of 30%. In this article, we seek to provide some clarity on this topic by providing useful guidelines that patients and health care providers can use to make better, more informed treatment decisions. Although this article specifically focuses on advanced metastatic prostate cancer, future articles will focus on the use of antioxidants and chemotherapy in the treatment of other cancers. ]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://pinestreetfoundation.org/wp-content/uploads/2009/05/canda2.png"><img class="alignleft size-thumbnail wp-image-126" title="Chemotherapy and Antioxidants" src="http://pinestreetfoundation.org/wp-content/uploads/2009/05/canda2-150x150.png" alt="Chemotherapy and Antioxidants" width="150" height="150" /></a>INTRODUCTION</strong><br />
It has been commonly assumed that all chemotherapy drugs are incompatible           with all antioxidants, but there is a growing body of evidence that           suggests this might not always be the case (Lamson and Brignall 1999).<span id="more-351"></span></p>
<p>While some antioxidants are clearly not beneficial and can even decrease         effectiveness of some chemotherapeutic treatments for certain cancers,         there are many other antioxidants that do not interfere and may even         enhance specific chemotherapy drugs, while also decreasing their side         effects.</p>
<p>For this article, we investigated treatments for advanced metastatic         prostate cancer, for which there are a limited number of chemotherapy           treatments available. Although we focus on metastatic disease, some           of the antioxidants discussed in this article are relevant for men           with localized prostate cancer as well as for those who are at high           risk for developing prostate cancer.</p>
<p><strong>PROSTATE CANCER AND ITS TREATMENT</strong><br />
Prostate cancer is the second most common cancer in men after skin cancer.           The most common form of prostate cancer occurs in men age 65 or older,           and is often a slow growing, localized disease limited to the prostate           gland. For this type of prostate cancer, there are a variety of treatments,           including &#8220;watchful waiting,&#8221; radiation         (including seeds), cryotherapy, surgery, High Intensity Focused Ultrasound         (HIFU), hormone suppressing drugs (Androgen Deprivation Therapy), as         well as other novel treatments. (See Glossary at the end of this article         for brief descriptions of these terms.)</p>
<p>If cancer         of the prostate gland goes untreated or undiagnosed, it can begin to         metastasize, either slowly over many years or, in some cases, very rapidly.         When prostate cancer metastasizes, it can spread locally to the pelvic         bones, bladder, and other nearby organs. Advanced metastatic prostate         cancer commonly progresses to distant sites in the bones but can also         spread to other organs.</p>
<p>The first line of treatment for metastatic prostate cancer is usually         hormone suppression therapy. This is called Androgen Deprivation Therapy         (ADT) and includes drugs such as leuprolide (Lupron), goserelin (Zoladex),         flutamide (Eulexin), bicalutamide (Casodex), nilutamide (Nilandron),         or cyproterone (Androcur, Cyprostat). Secondary hormone therapy may be         used if and when the first treatment does not work. This would include         a combination of the same drugs listed above and may include others as         well.</p>
<p>When Androgen Deprivation Therapy stops working, patients move on to         chemotherapy, starting with drugs such as paclitaxel (Taxol), docetaxel         (Taxotere), or mitoxantrone (Novantrone). Off-label or clinical trial         chemotherapy drugs are sometimes added, such as carboplatin (Paraplatin),           cisplatin (Platinol), satraplatin, epothilone, or doxorubicin (Adriamycin).           Research has shown that chemotherapy has limited potential for controlling           progression of metastatic prostate cancer, leading to the addition           of newer therapies (in combination with chemotherapy or not) and clinical           trials.</p>
<p>Some of the newer therapies, which can be         considered, include: anti-angiogenesis drugs, such as bevacizumab (Avastin)         or sunitinib (Sutent), which stop new blood vessels from growing; immune         therapy, which stimulates the immune system to fight cancer; and gene         therapy, which uses genetic material in the treatment of disease, including         GVAX, ipilimumab (MDX -010), Granulocyte-Macrophage Colony-Stimulating         Factor (GMCSF), and sipuleucel-T (Provenge).</p>
<p><strong>RESEARCH ON HOW ANTIOXIDANTS AND CANCER THERAPIES WORK TOGETHER</strong><br />
As new approaches to treating advanced prostate cancer in conjunction           with chemotherapy are being developed, it becomes more and more useful           to explore approaches that involve increasing the effectiveness of           chemotherapy while decreasing its side effects. There are antioxidants           that, when properly combined with chemotherapy, have been shown to           produce this effect. Although it is not commonly known, these combinations           have been investigated as early as the 1980’s         (Lamson and Brignall 1999) and one published scientific review reported         on the results of over 180 studies specifically investigating antioxidant/chemotherapy         and antioxidant/radiation combinations (Lamson and Brignall 1999).</p>
<p>The following are brief summaries of more recently published evidence         on the combination of antioxidants and chemotherapy specifically for         advanced metastatic prostate cancer:</p>
<p><strong>CURCUMIN</strong><br />
Curcumin is an active component of the Indian curry spice turmeric. Curcumin           is known for its antitumor, antioxidant, anti-amyloid, and anti-inflammatory           properties. It also promotes healthy bile excretion and healthy platelet           function.</p>
<p><em>Curcumin &amp; Chemotherapy</em><br />
Curcumin appears to block a protein that plays a role in the resistance           to the chemotherapy drug mitoxantrone. It therefore may be compatible           with mitoxantrone (Chearwae, Shukla et al. 2006). However, curcumin           appears to block a pathway by which taxol based drugs (taxanes) cause           tumor suppression and therefore should not be taken in combination           with taxanes (Wang and Wieder 2004).</p>
<p><strong>MELATONIN</strong><br />
Melatonin is a hormone released from the pineal gland and helps to improve           quality of sleep. It is also known to reduce metastasis in cancer patients.</p>
<p><em>Melatonin &amp; Chemotherapy</em><br />
Melatonin’s antioxidant activity appears to counteract toxicity         of common chemotherapy treatments for advanced prostate cancer, including         cisplatin, mitoxantrone, and paclitaxel. Melatonin significantly reduces         the frequency of thrombocytopenia, neurotoxicity, cardiotoxicity, stomatitis,         and asthenia related to chemotherapy. Additionally, melatonin promotes         cancer cell death when combined with the same therapies (Lissoni, Barni         et al. 1999). In a human clinical trial, melatonin at a dosage of 20mg         combined with intra-muscular hormone therapy triptorelin (Trelstar, Depot,         Trelstar LA) decreased levels of prostate specific antigen (PSA) and         growth factors for metastatic prostate cancer (Lissoni, Cazzaniga et         al. 1997).</p>
<p><strong>GENISTEIN</strong><br />
Genistein is a soy extract that may help cancer prevention. It also inhibits           proliferation of invasive prostate cancer.</p>
<p><em>Genistein &amp; Chemotherapy</em><br />
Genistein significantly improves the antitumor activity of docetaxel,           doxorubicin, and cisplatin through several different mechanisms. Genistein,           when used alone, also has anticancer activity without toxicity (Li,           Ahmed et al. 2005; Li, Kucuk et al. 2006).</p>
<p><strong>EPIGALLOCATECHIN-GALLATE         (EGCG)</strong><br />
Epigallocatechin-gallate (EGCG) is one of the components of green tea         extract, which is made from the dried leaves of an Asian evergreen shrub.         EGCG is 25 to 100 times more potent an antioxidant than vitamin C. Research         studies have found that in men who are at high risk for prostate cancer,         EGCG reduces the incidence of those men developing the disease.</p>
<p><em>EGCG &amp; Chemotherapy</em><br />
An in vitro study found that when EGCG is used in combination with paclitaxel,           hormone refractory prostate cancer cells developed resistance to treatment           sooner than either paclitaxel or EGCG alone (Axanova, Morre et al.           2005).</p>
<p><strong>CAPSAICIN</strong><br />
Capsaicin is a chili pepper extract, often topically used to reduce pain           and inflammation. It is also used for anticancer treatment.</p>
<p><em>Capsaicin &amp; Chemotherapy</em><br />
An in vitro study showed that when capsaicin is used in combination with           paclitaxel, hormone refractory prostate cancer cells developed resistance         to treatment. When used in combination with cisplatin, it reduces the         effectiveness of the cisplatin (Axanova, Morre et al. 2005).</p>
<p><strong>CAPSIBIOL-T</strong><br />
Capsibiol-T is a combination of EGCG and capsaicin.</p>
<p><em>Capsibiol-T &amp; Chemotherapy</em><br />
In vitro studies show that when hormone refractory prostate cancer cells           are pretreated with Capsibiol-T and then treated with paclitaxel, the           combination has an additive effect in decreasing survival of cancer         cells (Axanova, Morre et al. 2005).</p>
<p><strong>VITAMIN D3</strong><br />
Vitamin D3 is metabolized into calcitriol. In one trial, researchers           used a formulation of calcitriol called DN 101 that does not have as           many problems with toxicity as vitamin D3 when used at high doses.           High doses of calcitriol alone appear to inhibit hormone refractory           metastatic prostate cancer cell growth and stimulate cancer cell death,           as well as inhibit the invasiveness of prostate cancer cells (Schwartz,           Wang et al. 1997). It has also been shown to increase differentiation           of prostate cancer cells (Esquenet, Swinnen et al. 1996; Bauer, Thompson           et al. 2003).</p>
<p><em>Vitamin D3 &amp; Chemotherapy</em><br />
In combination with docetaxel, vitamin D3 has an additive effect. In           a recent study, docetaxel used with a specific formulation of calcitriol         (DN 101) increased survival rate in hormone refractory metastatic prostate         cancer patients (Beer, Ryan et al. 2007).</p>
<p><strong>VITAMIN         A</strong><br />
Vitamin A is an essential nutrient for humans and has many diverse functions         in maintaining normal health. It has various different metabolites that         are similar in structure and, with a few changes, can become vitamin         A with the help of enzymes in the body.</p>
<p><em>Vitamin A &amp; Chemotherapy</em><br />
Retinoic Acid (an acidified form of vitamin A) has a synergistic effect           in combination with docetaxel through two known<br />
mechanisms therefore increasing docetaxel’s ability to stop tumor         growth (Sun, Li et al. 2004).</p>
<p>13-cis-retinoic acid (a vitamin A derivative) has         been shown in in-vitro trials in combination with paclitaxel to have         a synergistic effect in inhibiting the growth of prostate cancer cell         lines (it enhances the effectiveness of paclitaxel in attacking cancer         cells). However, in combination with carboplatin, it has an antagonistic         effect (it diminishes effectiveness of carboplatin) (Cabrespine, Bay         et al. 2005).</p>
<p>All-trans retinoic acid (a vitamin A derivative) helps Taxol-based         drugs (taxanes) to increase cancer cell death (Wang and Wieder 2004).</p>
<p><strong>SILIBININ</strong><br />
Silibinin is an extract from milk thistle seed that is known for its           ability to protect the liver.</p>
<p><em>Silibinin &amp; Chemotherapy</em><br />
Silibinin and platinum-based compounds (cisplatin, carboplatin, satraplatin),           when used together, have a substantially higher ability to inhibit           prostate cancer cell growth and cause prostate cancer cell death, when           compared with platinum-based compounds alone (Dhanalakshmi, Agarwal           et al. 2003).</p>
<p><strong>BETA-GLUCAN</strong><br />
Beta-glucans are natural soluble fiber polysaccharides found in the bran           of cereal grains such as barley, oats, rye, and wheat. Beta-glucans           can also be extracted from maitake mushrooms, as in the following study.</p>
<p><em>Maitake Beta-glucan &amp; Chemotherapy</em><br />
In combination with carmustine (BCNU), maitake beta-glucan enhances           effectiveness of chemotherapy, with a 90% cancer cell viability reduction           (Finkelstein, Aynehchi et al. 2002).</p>
<p><strong>WHAT IF THERE IS INSUFFICIENT EVIDENCE FOR INTERACTIONS BETWEEN SPECIFIC         CHEMOTHERAPY DRUGS AND SPECIFIC ANTIOXIDANTS?</strong><br />
When it is uncertain whether a specific antioxidant and chemotherapy         drug treatment combination would conflict, then the possibility of combining         them largely depends on the timing of their use. It is important to know         that most water-soluble antioxidants usually stay in the blood for one         day or less while oil-soluble antioxidants can stay in the blood for         up to several days. This information, in combination with the known half-life         of chemotherapy drugs (which is generally 72 hours or less), can allow         patients and health care providers, working together in a process of         shared decision-making, to make an informed decision on whether or not         to combine certain antioxidants within the same treatment protocol. If         a decision is made to use antioxidants intermittently, some healthcare         providers will choose to separate their use by at least three days to         allow time for chemotherapy drugs to complete their intended purpose         before being metabolized.</p>
<p><strong>CONCLUSION</strong><br />
Although this article only briefly touches on the possibility of combining           some antioxidants with chemotherapy as an effective way for treating           cancer, our hope is that it encourages both patients and health care           providers to more seriously consider the importance of these various         combinations. One must, of course, be judicial in determining which combinations         are safe, but when the cancer research community is constantly looking         for ways to make cancer treatments more effective and to help people         live longer, antioxidant-chemotherapy combinations are worthy of further         study and deeper understanding.</p>
<p><em>Special thanks to Johanna Altgelt and Jeremy Paster for their significant           contributions to this article.</em></p>
<p><a href="http://pinestreetfoundation.org/avenues/avenues18/byoa18.html#top">Top of Page</a></p>
<p>&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;..</p>
<p><strong>GLOSSARY OF TERMS</strong></p>
<p><strong>Androgen Deprivation Therapy</strong>: Medications that work         by decreasing the amount of testosterone.<br />
<strong>Bevacizumab (Avastin)</strong>: A synthetic antibody often used         along with chemotherapy, first developed to treat colon and rectal cancer         that has spread to other parts of the body. It works by blocking a protein         called vascular endothelial growth factor (VEGF), which decreases the         blood supply to the tumor.<br />
<strong>Bicalutamide (Casodex)</strong>: A drug used in combination with         hormone treatment to treat prostate cancer that has spread to other areas         of the body. It works by blocking the action of testosterone in the prostate.<br />
<strong>Carboplatin (Paraplatin)</strong>: A platinum-containing anticancer         drug that is an analog of cisplatin with somewhat reduced toxicity and         that is used in the treatment of various cancers.<br />
<strong>Chemotherapy</strong>: The use of chemical agents in the treatment         or control of disease, especially cancer.<br />
<strong>Cisplatin (Platinol)</strong>: A platinum-containing anticancer         drug that functions by producing cross links in DNA between and within         strands.<br />
<strong>Cryotherapy</strong>: The therapeutic use of cold, such as in cryosurgery.<br />
<strong>Cyproterone</strong>: A synthetic steroid used in the form of         its acetate to inhibit androgenic secretions (as testosterone).<br />
<strong>Docetaxel (Taxotere)</strong>: A semisynthetic antineoplastic         drug derived from the needles of the yew tree.<br />
<strong>Doxorubicin (Adriamycin)</strong>: An anthracycline antibiotic         with broad antineoplastic activity that is obtained from a bacterium         of the genus Streptomyces (S. peucetius) and is administered in the form         of its hydrochloride.<br />
<strong>Epothilone (Ixabepilone)</strong>: A new type of drug with the         same mechanism as the taxanes, which may have greater potency than paclitaxel,         have activity in tumors that are resistant to paclitaxel, can stay in         cancer cells longer, and can be useful in people who have already had         several different types of aggressive therapies.<br />
<strong>Excretion</strong>: The act or process of separating or eliminating         substances from the body.<br />
<strong>Flutamide</strong>: A nonsteroidal antiandrogen that is used         in the treatment of prostate cancer.<br />
<strong>Goserelin (Zoladex)</strong>: A drug that is similar to luteinizing         hormone releasing hormone (LHRH), which is made by the body. It decreases         the hormone testosterone, which can help slow or stop the growth of prostate         cancer cells.<br />
<strong>Granulocyte-Macrophage Colony-Stimulating Factor         (GM-CSF)</strong>: A hormone essential in augmenting the body’s         immune response to vaccines.<br />
<strong>GVA X</strong>: An immunotherapy for prostate cancer, made from         two genetically-modified prostate cancer cell lines, currently in clinical         trials for advanced-stage prostate cancer.<br />
<strong>Half-life</strong>: The time required for half the amount of         a substance (as a drug or radioactive tracer) in or introduced into a         living system or ecosystem to be eliminated or disintegrated by natural         processes.<br />
<strong>High Intensity Focused Ultrasound (HIFU)</strong>: The therapeutic         use of ultrasound that is much more powerful and focused than ordinary         diagnostic ultrasound.<br />
<strong>Interaction</strong>: The effect of one drug, food, or vitamin         on the effectiveness or metabolism of another drug. This can be synergistic,         in which the effect of the drug is increased, or antagonistic, in which         the effect of the drug is decreased or blocked.<br />
<strong>Leuprolide (Lupron)</strong>: A synthetic analog of gonadotropin-releasing         hormone used to treat cancer of the prostate gland. It works by reducing         the amount of testosterone that the body makes. This can help slow or         stop the growth of prostate cancer cells and helps relieve symptoms like         painful or difficult urination.<br />
<strong>Metabolism</strong>: The sum of the processes by which a particular         substance is handled (as by assimilation and incorporation or by detoxification         and excretion) in the living body.<br />
<strong>Metastatic</strong>: Having to do with the transfer of cancer         from one part of the body to another..<br />
<strong>Mitoxantrone</strong>: An antineoplastic drug that is used in         the form of its dihydrochloride either alone or in combination in the         treatment of some leukemias and carcinomas.<br />
<strong>Nilutamide (Nilandron)</strong>: A drug used in combination with         surgery or other medications to treat prostate cancer. Testosterone,         a natural hormone in men, stimulates the growth of prostate cancer cells.         Nilutamide is an anti-androgen that works by blocking the effects of         testosterone.<br />
<strong>Provenge</strong>: A new vaccine currently in clinical trials         for advanced stage prostate cancer.<br />
<strong>Radiation</strong>: Energy radiated in the form of waves or particles         used, for example, in medicine to stop the growth of cancer cells.<br />
<strong>Sunitinib (Sutent)</strong>: A newly developed drug, which works         by decreasing the blood supply to tumor cells.<br />
<strong>Taxanes</strong>: A group of drugs that includes paclitaxel (Taxol)         and docetaxel (Taxotere), which are used in the treatment of cancer.         Taxanes have a unique way of preventing the growth of cancer cells: they         affect cell structures called microtubules, which play an important role         in cell functions. In normal cell growth, microtubules are formed when         a cell starts dividing. Once the cell stops dividing, the microtubules         are broken down or destroyed. Taxanes stop the microtubules from breaking         down; cancer cells become so clogged with microtubules that they cannot         grow and divide.<br />
<strong>Watchful Waiting</strong>: An approach by which patients are         given no immediate treatment until the tumor shows signs of progressing,         often offered to men diagnosed with early stage prostate cancer. Less         often recommended following recent publication of a study showing better         10-year survival rates in men who received either surgery or radiation         therapy, compared to those who elected for watchful waiting approach.         (Tewari, A., G. Divine, et al. 2007)</p>
<p>&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;&#8230;..</p>
<p><strong>REFERENCES</strong></p>
<p>1. Axanova, L., D. J. Morre, et al. (2005). &#8220;Growth of LNC aP cells     in monoculture and coculture with osteoblasts and response to tNO X inhibitors.&#8221; Cancer     Lett <strong>225</strong>(1):     35-40.<br />
2. Bauer, J. A., T. A. Thompson, et al. (2003). &#8220;Growth inhibition     and differentiation in human prostate carcinoma cells induced by the vitamin     D analog 1alpha,24-dihydroxyvitamin D2.&#8221; Prostate <strong>55</strong>(3):     159-67.<br />
3. Beer, T. M., C. W. Ryan, et al. (2007). &#8220;Double-blinded randomized     study of high-dose calcitriol plus docetaxel compared with placebo plus docetaxel     in androgen-independent prostate cancer: a report from the ASCEN T Investigators.&#8221; J     Clin Oncol <strong>25</strong>(6):     669-74.<br />
4. Cabrespine, A., J. O. Bay, et al. (2005). &#8220;In vitro assessment of     cytotoxic agent combinations for hormone-refractory prostate cancer treatment.&#8221; Anticancer     Drugs <strong>16</strong>(4):     417-22.<br />
5. Chearwae, W., S. Shukla, et al. (2006). &#8220;Modulation of the function     of the multidrug resistancelinked ATP-binding cassette transporter ABCG2     by the cancer chemopreventive agent curcumin.&#8221; Mol Cancer Ther <strong>5</strong>(8):     1995-2006.<br />
6. Dhanalakshmi, S., P. Agarwal, et al. (2003). &#8220;Silibinin sensitizes     human prostate carcinoma DU145 cells to cisplatin- and carboplatin-induced     growth inhibition and apoptotic death.&#8221; Int J Cancer <strong>106</strong>(5):     699-705.<br />
7. Esquenet, M., J. V. Swinnen, et al. (1996). &#8220;Control of LNC aP proliferation     and differentiation: actions and interactions of androgens, 1alpha,25-dihydroxycholecalciferol,     all-trans retinoic acid, 9-cis retinoic acid, and phenylacetate.&#8221; Prostate <strong>28</strong>(3):     182-94.<br />
8. Finkelstein, M. P., S. Aynehchi, et al. (2002). &#8220;Chemosensitization     of carmustine with maitake beta-glucan on androgen-independent prostatic     cancer cells: involvement of glyoxalase I.&#8221; J Altern Complement Med <strong>8</strong>(5):     573-80.<br />
9. Lamson, D. W. and M. S. Brignall (1999). &#8220;Antioxidants in cancer     therapy; their actions and interactions with oncologic therapies.&#8221; Alternative     Medicine Review <strong>4</strong>(5): 304-329.<br />
10. Li, Y., F. Ahmed, et al. (2005). &#8220;Inactivation of nuclear factor     kappaB by soy isoflavone genistein contributes to increased apoptosis induced     by chemotherapeutic agents in human cancer cells.&#8221; Cancer Res <strong>65</strong>(15):     6934-42.<br />
11. Li, Y., O. Kucuk, et al. (2006). &#8220;Antitumor and antimetastatic     activities of docetaxel are enhanced by genistein through regulation of osteoprotegerin/receptor     activator of nuclear factor-kappaB (RAN K)/RAN K ligand/MMP-9 signaling in     prostate cancer.&#8221; Cancer     Res <strong>66</strong>(9): 4816-25.<br />
12. Lissoni, P., S. Barni, et al. (1999). &#8220;Decreased toxicity and increased     efficacy of cancer chemotherapy using the pineal hormone melatonin in metastatic     solid tumour patients with poor clinical status.&#8221; Eur J Cancer <strong>35</strong>(12):     1688-92.<br />
13. Lissoni, P., M. Cazzaniga, et al. (1997). &#8220;Reversal of clinical     resistance to LHRH analogue in metastatic prostate cancer by the pineal hormone     melatonin: efficacy of LHRH analogue plus melatonin in patients progressing     on LHRH analogue alone.&#8221; Eur     Urol     <strong>31</strong>(2): 178-81.<br />
14. Tewari, A., G. Divine, et al. (2007). &#8220;Long-term survival in men     with high grade prostate cancer: a comparison between conservative treatment,     radiation therapy and radical prostatectomy: a propensity scoring approach.&#8221; J     Urol <strong>177</strong>(3):     911-5.<br />
15. Schwartz, G. G., M. H. Wang, et al. (1997). &#8220;1 alpha,25-Dihydroxyvitamin     D (calcitriol) inhibits the invasiveness of human prostate cancer cells.&#8221; Cancer     Epidemiol Biomarkers Prev <strong>6</strong>(9): 727-32.<br />
16. Sun, M., H. Li, et al. (2004). &#8220;[The synergistic effects of docetaxol     and retinoic acid on prostate cancer cell line PC-3].&#8221; Sichuan Da Xue     Xue Bao Yi Xue Ban <strong>35</strong>(6): 797-801.<br />
17. Wang, Q. and R. Wieder (2004). &#8220;All-trans retinoic acid potentiates     Taxotere-induced cell death mediated by Jun N-terminal kinase in breast cancer     cells.&#8221; Oncogene     <strong>23</strong>(2): 426-33.</p>
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