NEU neuren pharmaceuticals limited

Pipeline-in-a-drug, page-191

  1. 717 Posts.
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    Hi @baldwidx, your interesting post touches on the area and several concepts of precision medicine which, as you may have surmised from some of my previous posts, is the area I work in. Your post contains several interesting points which I could write several pages on smile.png, but in the interests of time and space I will just summarise an answer to your question regarding 2591 and cancer (although happy to expand on other elements if you have specific questions).

    The first important thing to consider here is how 2591 works. It upregulates IGF-1 by competitively binding to IGF Binding Protein 3 (IGFBP-3), hence increasing the bioavailability of IGF-1. Here is a schematic from Neuren explaining this.

    https://hotcopper.com.au/data/attachments/6689/6689901-35e7092cece659b3d48bfbe11cde332d.jpg

    IGF-1 then binds to its receptor on the surface of cells to activate the signalling pathways shown in the bottom left of the diagram. These pathways generally promote cell growth by promoting cell cycle progression and inhibiting apoptosis (programmed cell death). In the brain they play a role in maintaining and repairing brain cells and synapses, which is how 2591 works from the neurological perspective. IGF-1 is also produced in the liver and influences physiology and metabolism elsewhere in the body as you have alluded to, but hat is another story...

    So, IGF-1 is an anabolic hormone that promotes cell growth and survival. The aim of cancer therapeutics is generally to kill or halt the growth of cancer cells, which implies downregulating the pathways activated by IGF-1. Therefore, most therapeutic activity has been focussed on molecules that inhibit IGF-1's receptor, IGF-1R, hence preventing pathway activation. 2591 to the best of my knowledge, and considering its mechanism of action described above, does not downregulate IGF-1, although IGF-1 will ultimately regulate itself as it reaches a homeostatic state competing with 2591 for binding to IGFBP-3, hence 2591 being state dependent.

    So, in conclusion, I can't see 2591 having any potential as a cancer therapeutic as it effectively works in the wrong direction with regards to regulating IGF-1 and the pathways it activates.

 
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