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Scientific and Technical Aerospace Reports Volume 39 April 6, 2001

Scientific and Technical Aerospace Reports Volume 39 April 6, 2001

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a recently identified cell survival gene that interacts with Bcl-2, providing a possible molecular basis for interaction between retinoid<br />

<strong>and</strong> apoptosis signaling. In studying regulation of RAR-beta expression, we demonstrate that two retinoid signaling pathways,<br />

i.e., the RXR-dependent pathway <strong>and</strong> the RAR-dependent pathway, can induce RAR-beta expression <strong>and</strong> growth inhibition.<br />

In addition, we have found that lack of COUP-TF expression is mainly responsible for loss of RAR-beta expression in retinoidresistant<br />

breast cancer cells. These results largely enhance our underst<strong>and</strong>ing of the mechanism of retinoid action in breast cancer<br />

cells <strong>and</strong> also point to a possibility of restoring or enhancing retinoid activity in breast cancer cells.<br />

DTIC<br />

Retinene; Apoptosis; Cancer; Estrogens<br />

<strong>2001</strong>0025740 BBN Systems <strong>and</strong> Technologies Corp., Cambridge, MA USA<br />

Stereoscopic Digital Mammography: Improving Cancer Diagnosis Final Report, 17 Jun. 1996-16 Jun. 2000<br />

Getty, David J.; Jul. 2000; 62p; In English<br />

Contract(s)/Grant(s): DAMD17-96-C-6079<br />

Report No.(s): AD-A385848; No Copyright; Avail: CASI; A04, Hardcopy; A01, Microfiche<br />

The subject of study in this project was the potential benefit of using stereoscopic digital mammography as an adjunct to st<strong>and</strong>ard<br />

film mammography to improve the detection <strong>and</strong> diagnosis of breast cancer. We sought to determine whether stereo mammography<br />

might bring significant gains - either in earlier detection of worrisome lesions, or in more accurate discrimination of<br />

lesions as benign or malignant. Several main activities were required to accomplish this evaluation. We further developed <strong>and</strong><br />

refined a system for capturing <strong>and</strong> viewing stereo mammograms, using state-of-the-art digital methods. Over the duration of the<br />

project, stereo mammograms <strong>and</strong> film studies were acquired on a large number of path-proven cases. Three experienced<br />

mammographers served as consultants, <strong>and</strong> an extensive effort was devoted to developing with them a comprehensive list of visual<br />

features to consider in reading the stereo mammograms. In a final reading study with 137 cases, we measured diagnostic accuracy<br />

obtained with st<strong>and</strong>ard film mammograms alone compared to that obtained with film combined with the stereo mammogram. We<br />

found that the stereo mammogram significantly improved diagnostic accuracy. A second, exciting finding was that new, additional<br />

lesions, mostly masses, were detected in the stereo mammogram but were not visible in the film study, in 30% of the cases.<br />

DTIC<br />

Mammary Gl<strong>and</strong>s; Cancer; Diagnosis<br />

<strong>2001</strong>0025744 Johns Hopkins Univ., School of Medicine, Baltimore, MD USA<br />

Combined Use of Tissue Morphology, Neural Network Analysis of Chromatin Texture & Clinical Variables to Predict<br />

Prostate Cancer Agressiveness from Biopsy Material Annual Report, 1 Oct. 1998-30 Sep. 1999<br />

Partin, Alan; Oct. 1999; 25p; In English<br />

Contract(s)/Grant(s): DAMD17-98-1-8468<br />

Report No.(s): AD-A385853; No Copyright; Avail: CASI; A03, Hardcopy; A01, Microfiche<br />

the purpose of this report is to combine clinical, serum, pathological <strong>and</strong> computer derived information into an artificial neural<br />

network to develop/validate a model to predict prostate cancer tumor aggressiveness in both a retrospective <strong>and</strong> prospective cohort<br />

of men with clinically localized prostate cancer both prior to <strong>and</strong> after radical prostatectomy. Prospective enrollment of 500 men<br />

who are scheduled to undergo radical prostatectomy (year 01). Development of a artificial neural network model (year 02). Prospective<br />

validation of this model (projected year 03). All models will be tested <strong>and</strong> developed for biopsy <strong>and</strong> prostatectomy material.<br />

to date, we have completed prospective enrollment of 527 men, collected tissue, serum <strong>and</strong> clinical/pathological information<br />

for 387 <strong>and</strong> completed computer image data analysis of 171 samples. No model has been developed to date <strong>and</strong> awaits final enrollment.<br />

We anticipate final prospective data to be complete <strong>and</strong> model developed by 1/4/2000. At this time we will begin enrollment<br />

of prospective validation samples.<br />

DTIC<br />

Morphology; Prostate Gl<strong>and</strong>; Cancer; Image Analysis; Network Analysis<br />

<strong>2001</strong>0025745 Yale Univ., New Haven, CT USA<br />

Predoctoral Training Program in Breast Cancer Research Annual Report, 1 Aug. 1999-31 Jul. 00<br />

Stern, David; Aug. 2000; 15p; In English<br />

Report No.(s): AD-A385858; No Copyright; Avail: CASI; A03, Hardcopy; A01, Microfiche<br />

Breast cancer is one of the leading causes of cancer deaths of women in the USA. Fortunately, this disease is no longer a ”black<br />

box” that can only be studied empirically. Rather, recent advances in underst<strong>and</strong>ing of normal mammary development <strong>and</strong> carcinogenic<br />

processes have identified a number of specific genes <strong>and</strong> processes that are dysregulated in breast cancer. This means<br />

that research on breast cancer has finally advanced to the stage where a concentrated effort in translational research will yield great<br />

228

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