SemperFi said:
</p><p>
Sciroxx said:
</p><p>Simple medline search will yield endless linkages between testosterone levels and prostate cancer, the treatment of prostate tumors is anti-testosterone/anti-dehydrotestosterone(which is a direct derivate of testosterone) whatsoever no one claimed that testosterone cause by itself the cancer, not at all ! it's obvious there are multiple parameter in role, some of them u mentioned. Same for breath cancer - first aid measure, and constant measure actually is an anti estrogen for a reason.</p><p>Now dear brother - prostate (or breath) cancer is not my expertise, neither yours, I'm not sure why you're so eager to post on this matter on this thread, and more ever things which are simply not valid.</p><p> This is the only forum to encounter such negative crowed reaction (by couple of guys with obvious agenda) when posting such valuable in</p><p> </p><p>So first, and you're probably aware to it, <strong>testosterone is the main factor</strong> in the most common cancer in males (prostate), same as estrogen is responsible on the most common cancer at women (breath cancer).</p><p>
</p><p>I am eager to post on this matter because your are stating things concerning prostate cancer that are just not proven true. It certainly can be considered a mute issue by you but I am emphatical when it comes to requesting accurate information and unfortunately you are not the sole source of information in our free form forum. If you want to be the only source of information/opinion and dictate the direction of a a debate start a blog or an editorial page.
Again your last sentence based on the known science is a fabrication in an attempt to prove an unprovable point. I have no idea what the main factor (but I did state an opinion on this) of prostate cancer is and neither does $300 million in annual research but for some strange reason you believe that you do.</p><p>The suppression of testosterone in prostate patients and estrogen in breast cancer patients is simply removing the fuel from a fire that has been started by an unknown catalyst. Does hormone treatment that you stated cure the disease? In both diseases a cure remains very controversial. But based on your belief there should be no question that they are both curable with hormone treatment alone because the main factors (your words, not mine) are removed from the equation.</p><p>Fortunately for me I come from a family of physicians and have many long discussions on this subject with them on regular basis. To date not one has said anything other than that the literature for testosterone supplementation has not shown any uptick in prostate cancer. Although every man may be at risk- on steroids or not! One cousin, who is a urologist, has diagnosed 100's of men with prostate cancer. He stated that only a handful have been on supplemental testosterone and very few show signs of elevated testosterone levels. He assumes because the cause of prostrate cancer is unknown that these unlucky men had microscopic prostate cancer cells when they went on testosterone which accelerated the growth of the cancer cells that would have otherwise developed into the disease on their own.</p><p>Why would a normal male with normal testosterone levels be diagnosed with prostate cancer? While another male with elevated testosterone levels have no signs of prostate cancer? Simple; Testosterone is NOT the main factor in prostate cancer as you state.</p><p>I openly rebuke you for saying that I or any other contributing member of this thread has an agenda. It's time to face the truth of the matter- We obviously disagree, you fail to see the inaccuracy in your statements, and you are upset at me for pointing it out.</p><p>Someday you might be 100% correct in your assumptions concerning this matter but as of today you are not.</p><p>I am also sorry that you could not provide sufficient evidence concerning a greater benefit of combining IGF and GH other than an increase in insulin sensitivity because it simply proves that I blew a ton of money on something that I was previously told would be a waste of money. Shame on me.
</p><p>With overpowering positive energy containing no hidden agendas,</p><p>SEMPER FI</p><p>
</p><p> </p><p>It's crystal clear that testosterone levels are one of the main factors whether in inducing or catalyzing prostate tumors of any kin, anyhow it was brought by chance as an example to the "propaganda of be aware this or that causes cancer" and has nothing to do with the subject or this section, so I officially state - first and above all you're right, second you're right, you're always right, and will be right for ever so help me god regarding prostate cancer, life and the universe</p><p>Now it's clear that you love to listen to your self, but has never bothered to look at the sscientific literature and explanations I showed, but what freinds are for ?! so I'll repeat on it briefly for u -</p><p>There is a distinct synergistic effect between IGF1 and GH, and experts endocrinologists experimented, tested, concluded and reported - </p><p>In a nutshell there is a synergistic anabolic effect of GH and IGF1 as shown in increased protein synthesis in multiple tissues and additive increase in nitrogen balance,.</p><p>IGF1 show distincy anti catabolic effects which GH doesn't posses as shows from reduced corticosteone levels and negating highly potent catabolic hormore on the articles below.</p><p> </p><p>There is multi paths metabolic synergistic benefits in combining GH and IGF concerning fat mobilization and usage, increased energy expenditure , and finally distinct balanced of insulin sensitivity not observed by other aids, at least not to such degree</p><p>ncbi.nlm.nih.gov/pubmed/9129466<br style="color: #ffffff; font-family: Verdana, Arial, Tahoma, Calibri, Geneva, sans-serif; font-size: 13px; background-color: #000000;" /><br style="color: #ffffff; font-family: Verdana, Arial, Tahoma, Calibri, Geneva, sans-serif; font-size: 13px; background-color: #000000;" />GH and IGF-I combined further enhanced fat oxidation while reducing protein catabolism. Serum insulin concentrations were significantly increased by GH but decreased by IGF-I. GH significantly decreased serum total triiodothyronine concentrations and IGF-I significantly decreased serum corticosterone concentrations.</p><p>=========================================</p><p>ncbi.nlm.nih.gov/pubmed/10571453</p><p>RESULTS:<br style="color: #ffffff; font-family: Verdana, Arial, Tahoma, Calibri, Geneva, sans-serif; font-size: 13px; background-color: #000000;" />Administration of IGF-I, but not GH, attenuates dexamethasone-induced protein catabolism and increases insulin sensitivity. Simultaneous treatment with GH and IGF-I additively increases the serum concentration of IGF-I, whole-body anabolism, and lipid oxidation. GH or IGF-I when given alone produces similar increases in the serum concentration of IGF-I. However, GH selectively increases skeletal muscle mass whereas IGF-I selectively attenuates the intestinal atrophy and abnormal intestinal ion transport induced by TPN. These tissue-selective anabolic effects of GH and IGF-I are associated with differential increases in protein synthesis in skeletal muscle and jejunum, respectively.<br style="color: #ffffff; font-family: Verdana, Arial, Tahoma, Calibri, Geneva, sans-serif; font-size: 13px; background-color: #000000;" />CONCLUSIONS:<br style="color: #ffffff; font-family: Verdana, Arial, Tahoma, Calibri, Geneva, sans-serif; font-size: 13px; background-color: #000000;" />Simultaneous treatment with GH and IGF-I may offer the greatest clinical efficacy because of improved nitrogen retention in association with enhanced lipid oxidation and stimulation of protein synthesis in multiple tissue types.<br style="color: #ffffff; font-family: Verdana, Arial, Tahoma, Calibri, Geneva, sans-serif; font-size: 13px; background-color: #000000;" />==============================</p><p>==============================================</p><p>ncbi.nlm.nih.gov/pubmed/8853443<br style="color: #ffffff; font-family: Verdana, Arial, Tahoma, Calibri, Geneva, sans-serif; font-size: 13px; background-color: #000000;" />===================================<br style="color: #ffffff; font-family: Verdana, Arial, Tahoma, Calibri, Geneva, sans-serif; font-size: 13px; background-color: #000000;" /><br style="color: #ffffff; font-family: Verdana, Arial, Tahoma, Calibri, Geneva, sans-serif; font-size: 13px; background-color: #000000;" />GH may exert metabolic effects either directly or indirectly through increased production of IGF-I. GH administration increases circulating IGF-I levels via stimulation of hepatic synthesis and secretion of IGF-I; it may also enhance local IGF-I synthesis, which exerts paracrine or autocrine effects. Figure 2 summarizes the metabolic effects of GH and IGF-I. Administration of GH and IGF-I in adult humans has been demonstrated to enhance protein anabolism. Combined administration of GH and IGF-I was observed to be more anabolic than either IGF-I or GH alone. Evidence is presented that protein accretion results mainly from direct effects of GH on tissues; additional indirect effects via IGF-I production are also likely. Administration of GH has been reported to produce carbohydrate intolerance with elevated plasma insulin levels, resulting from insulin resistance. in contrast, insulin sensitivity increased during administration of IGF-I, which exerts hypoglycaemic effects even with concomitant suppression of insulin secretion. A major direct metabolic effect of GH is to increase fat mobilization and oxidation, and thereby to reduce total body fat; there is no evidence that IGF-I acts directly on adipose tissue in vivo. GH administration results in sodium retention via stimulation of Na-K-ATPase. It is suggested that part of the effects of GH on tubular function (e.g. phosphate reabsorption) are mediated via IGF-I. Energy expenditure may be increased by administration of either GH or relatively high doses of IGF-I. One of the reasons for this phenomenon is an increase in lean body mass; GH may increase energy expenditure additionally be enhancing the production of T3 and by increasing lipid oxidation<br style="color: #ffffff; font-family: Verdana, Arial, Tahoma, Calibri, Geneva, sans-serif; font-size: 13px; background-color: #000000;" />===================================</p><p> </p><p> </p>