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Progenics Pharmaceuticals, Inc. Message Board

  • jimturner54321 jimturner54321 Mar 31, 2014 3:14 AM Flag

    Presentation April 6th at American Association for Cancer Research

    http://www.abstractsonline.com/Plan/ViewAbstract.aspx?sKey=80ee3b0c-3fa4-42f6-9b37-af3fd1772cb0&cKey=e6e07be2-b6de-437f-a6f2-bf51f9e73bb4&mKey=6ffe1446-a164-476a-92e7-c26446874d93

    Abstract Number: 798
    Presentation Title: Androgen receptor, PI3K/mTOR and PSMA: Exploring and exploiting the interplay between therapeutic targets in prostate cancer
    Presentation Time: Sunday, Apr 06, 2014, 1:00 PM - 5:00 PM
    Location: Hall A-E, Poster Section 33
    Poster Board Number: 12
    Author Block: Jose D. Murga, Wells W. Magargal, II, Sameer M. Moorji, Vincent A. DiPippo, William C. Olson. Progenics Pharmaceuticals, Inc, Tarrytown, NY
    Abstract Body: Introduction: Androgen receptor (AR), the PI3K/mTOR signaling pathway and prostate-specific membrane antigen (PSMA) represent significant potential targets for prostate cancer therapy. The present study examined the cross-regulation and co-targeting of these molecular pathways.
    Methods: Cytotoxicity and the kinetics of antigen expression were evaluated in prostate cancer cell lines (LNCaP and C4-2) that vary according to androgen dependence. Expression of PSMA, prostate-specific antigen (PSA), and AR was evaluated in cells cultured in rapamycin and AR inhibitors. Cells were tested for susceptibility to PI3K/mTOR inhibitors used alone and in combination with PSMA ADC, a fully human PSMA monoclonal antibody conjugated to the microtubule disrupting agent monomethyl auristatin E (MMAE). Potential drug synergy or antagonism was evaluated using the Bliss independence method.
    Results: In androgen-dependent LNCaP cells, rapamycin exerted antiproliferative effects that were accompanied by an increase in AR expression and signaling in the absence of any significant effect on PSMA expression. In androgen-independent C4-2 cells, rapamycin increased AR expression/signaling and PSMA expression in the absence of any significant anti-proliferative effect. AR inhibitors synergized with PSMA ADC in LNCaP and C4-2 cells, but PI3K/mTOR pathway inhibitors synergized with PSMA ADC in C4-2 cells only. More modest synergy was observed by combining non-targeted microtubule inhibitors with inhibitors of AR or mTOR. Compared with rapamycin, GDC0941 (PI3K inhibitor) and MK-2206 (Akt inhibitor), both upstream of mTOR, synergized less strongly with PSMA ADC in C4-2 cells.
    Conclusions: In this study, AR and PI3K/mTOR pathways exhibited cross-regulation impacting PSMA expression. PSMA ADC synergized with AR and mTOR inhibitors via a multimodal mechanism involving increased PSMA expression and disruption of microtubule function. The findings support clinical exploration of regimens combining PSMA-targeted therapies with inhibitors of the AR and/or PI3K/mTOR signaling pathways.

    American Association for Cancer Research
    615 Chestnut St. 17th Floor
    Philadelphia, PA 19106

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