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mRNA expression signature of Gleason grade predicts lethal prostate cancer

Penney, K. L. (author)
Sinnott, J. A. (author)
Fall, Katja, 1971- (author)
Uppsala universitet,Örebro universitet,Institutionen för medicinska vetenskaper,Institutionen för immunologi, genetik och patologi
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Pawitan, Y. (author)
Karolinska Institutet
Hoshida, Y. (author)
Kraft, P. (author)
Stark, J. R. (author)
Fiorentino, M. (author)
Perner, S. (author)
Finn, S. (author)
Calza, S. (author)
Karolinska Institutet
Flavin, R. (author)
Freedman, M. L. (author)
Setlur, S. (author)
Sesso, H. D. (author)
Andersson, Swen-Olof, 1949- (author)
Örebro universitet,Hälsoakademin
Martin, N. (author)
Kantoff, P. W. (author)
Johansson, Jan-Erik, 1946- (author)
Örebro universitet,Hälsoakademin
Adami, H. O. (author)
Karolinska Institutet
Rubin, M. (author)
Loda, M. (author)
Golub, T. R. (author)
Andrén, Ove, 1963- (author)
Örebro universitet,Hälsoakademin,Urologen
Stampfer, M. J. (author)
Mucci, L. A. (author)
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 (creator_code:org_t)
American Society of Clinical Oncology, 2011
2011
English.
In: Journal of Clinical Oncology. - : American Society of Clinical Oncology. - 0732-183X .- 1527-7755. ; 29:17, s. 2391-2396
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • PURPOSE: Prostate-specific antigen screening has led to enormous overtreatment of prostate cancer because of the inability to distinguish potentially lethal disease at diagnosis. We reasoned that by identifying an mRNA signature of Gleason grade, the best predictor of prognosis, we could improve prediction of lethal disease among men with moderate Gleason 7 tumors, the most common grade, and the most indeterminate in terms of prognosis.PATIENTS AND METHODS: Using the complementary DNA-mediated annealing, selection, extension, and ligation assay, we measured the mRNA expression of 6,100 genes in prostate tumor tissue in the Swedish Watchful Waiting cohort (n = 358) and Physicians' Health Study (PHS; n = 109). We developed an mRNA signature of Gleason grade comparing individuals with Gleason ≤ 6 to those with Gleason ≥ 8 tumors and applied the model among patients with Gleason 7 to discriminate lethal cases.RESULTS: We built a 157-gene signature using the Swedish data that predicted Gleason with low misclassification (area under the curve [AUC] = 0.91); when this signature was tested in the PHS, the discriminatory ability remained high (AUC = 0.94). In men with Gleason 7 tumors, who were excluded from the model building, the signature significantly improved the prediction of lethal disease beyond knowing whether the Gleason score was 4 + 3 or 3 + 4 (P = .006).CONCLUSION: Our expression signature and the genes identified may improve our understanding of the de-differentiation process of prostate tumors. Additionally, the signature may have clinical applications among men with Gleason 7, by further estimating their risk of lethal prostate cancer and thereby guiding therapy decisions to improve outcomes and reduce overtreatment.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

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