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An interferon-related gene signature for DNA damage resistance is a predictive marker for chemotherapy and radiation for breast cancer

Weichselbaum, RR (author)
Ishwaran, H (author)
Yoon, T (author)
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Nuyten, DSA (author)
Baker, SW (author)
Khodarev, N (author)
Su, AW (author)
Shaikh, AY (author)
Roach, P (author)
Kreike, B (author)
Roizman, B (author)
Bergh, J (author)
Karolinska Institutet
Pawitan, Y (author)
Karolinska Institutet
de Vijver, MJV (author)
Minn, AJ (author)
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 (creator_code:org_t)
2008-11-25
2008
English.
In: Proceedings of the National Academy of Sciences of the United States of America. - : Proceedings of the National Academy of Sciences. - 1091-6490. ; 105:47, s. 18490-18495
  • Journal article (peer-reviewed)
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  • Individualization of cancer management requires prognostic markers and therapy-predictive markers. Prognostic markers assess risk of disease progression independent of therapy, whereas therapy-predictive markers identify patients whose disease is sensitive or resistant to treatment. We show that an experimentally derived IFN-related DNA damage resistance signature (IRDS) is associated with resistance to chemotherapy and/or radiation across different cancer cell lines. The IRDS genes STAT1, ISG15, and IFIT1 all mediate experimental resistance. Clinical analyses reveal that IRDS(+) and IRDS(−) states exist among common human cancers. In breast cancer, a seven–gene-pair classifier predicts for efficacy of adjuvant chemotherapy and for local-regional control after radiation. By providing information on treatment sensitivity or resistance, the IRDS improves outcome prediction when combined with standard markers, risk groups, or other genomic classifiers.

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