56 research outputs found

    Atmospheric Pressure Photoionization Tandem Mass Spectrometry of Androgens in Prostate Cancer

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    Androgen deprivation therapy is the most common treatment option for advanced prostate cancer. Almost all prostate cancers recur during androgen deprivation therapy, and new evidence suggests that androgen receptor activation persists despite castrate levels of circulating androgens. Quantitation of tissue levels of androgens is critical to understanding the mechanism of recurrence of prostate cancer during androgen deprivation therapy. A liquid chromatography atmospheric pressure photoionization tandem mass spectrometric method was developed for quantitation of tissue levels of androgens. Quantitation of the saturated keto-steroids dihydrotestosterone and 5-α-androstanedione required detection of a novel parent ion, [M + 15]+. The nature of this parent ion was explored, and the method was applied to prostate tissue and cell culture with comparison to results achieved using electrospray ionization

    Flow diagram for the recruitment process of the PCaP study, LA cohort.

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    <p><sup><b>a</b></sup> Diagnosing physicians provided consent to contact 98% of AA and 96% of CA potential subjects in pre-K and 97% of AA and 96% of CA in post-K. <sup>b</sup> The reasons included: i) They changed their mind about enrollment after a visit was scheduled; ii) The scheduled interview ended up being cancelled. <sup>c</sup> The total number of ineligible, enrolled, refused and uncontacted cases were 273, 1234, 754 and 27, respectively.</p

    Individual mouse CWR-R1 tumor volume (cm<sup>3</sup>) trajectories and predicted mean tumor volumes from each cohort.

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    <p>Tumors were measured using digital calipers and volumes calculated from day 14 to day 160 after CWR-R1 cell inoculation. Tumor volumes, LacZ (A, n = 22), LacZ+T (B, n = 21), ARΔTR (C, n = 21) or ARΔTR+T (D, n = 21), are shown from day 21 when growth began through day 96 beyond which only 1 mouse in each group remained. Mixed modeling statistical analysis showed a statistically significant difference among the 4 groups. ARΔTR-transduced CWR-R1 tumor growth rates were reduced compared to LacZ controls in the absence (p = 0.01, panel A vs. C) or presence (p = 0.0004, panel C vs. D) of T. (E) Predicted mean CWR-R1 tumor volumes (cm<sup>3</sup>) were plotted against time of first tumor harvest for the LacZ+T (open squares), LacZ (open diamonds), ARΔTR+T (solid circles) and ARΔTR (open circles) groups. ARΔTR-expressing CWR-R1 tumors (circles) exhibit decreased growth rates compared to LacZ-transduced CWR-R1 control cells.</p
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