Stathmin expression and its relationship to microtubule-associated protein tau and outcome in breast cancer.
Stathmin expression and its relationship to microtubule-associated protein tau and outcome in breast cancer.
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DOI:
10.1002/cncr.27453
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发表时间:
2012-10-01
期刊:
影响因子:
6.2
通讯作者:
Rimm, David L.
中科院分区:
文献类型:
--
作者:
Baquero, Maria T.;Hanna, Jason A.;Neumeister, Veronique;Cheng, Huan;Molinaro, Annette M.;Harris, Lyndsay N.;Rimm, David L.
关键词:
Microtubule associated proteins (MAPs) endogenously regulate microtubule stability. Here we assess the prognostic value of stathmin, a destabilizing protein in combination with MAP-tau, a stabilizing protein, in order to assess microtubule stabilization as a potential biomarker. Stathmin and MAP-tau expression levels were measured in a breast cancer cohort (n = 651) using the tissue microarray format and quantitative immunofluorescence (AQUA) technology, then correlated with clinical and pathological characteristics and disease free survival. Univariate Cox proportional hazards (PH) models indicated that high stathmin expression predicts worse overall survival (HR = 1.48; 95% CI = 1.119–1.966; P = 0.0061). Survival analysis showed 10-year survival of 53.1% for patients with high stathmin expression versus 67% for low expressers (log rank, P<.003). Cox multivariate analysis showed high stathmin expression was independent of age, menopausal status, nodal status, nuclear grade, tumor size, ER, PR, and HER2 expression (HR = 1.19; 95% CI= 1.03–1.37; P = 0.01). The ratio of MAP-tau to stathmin expression showed a positive correlation to disease free survival (HR = 0.679; 95% CI = 0.517–0.891; P = 0.0053) with a 10-year survival of 65.4% for patients with high MAP-tau to stathmin ratio versus 52.5% survival rate for low ratio (log rank, P = 0.0009). Cox multivariate showed MAP-tau to stathmin ratio was an independent predictor of overall survival (HR = 0.609; 95% CI = 0.422–0.879; P = 0.008). Low stathmin and high MAP-tau are associated with increased microtubule stability and better prognosis in breast cancer.
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DOI:
10.1083/jcb.138.5.1067
发表时间:
1997-09-08
期刊:
The Journal of cell biology
影响因子:
--
作者:
Felgner H;Frank R;Biernat J;Mandelkow EM;Mandelkow E;Ludin B;Matus A;Schliwa M
通讯作者:
Schliwa M
影响因子:
3.4
作者:
Choi, M. C.;Raviv, U.;Safinya, C. R.
通讯作者:
Safinya, C. R.
影响因子:
6.2
作者:
Giltnane, Jennifer M.;Moeder, Christopher B.;Rimm, David L.
通讯作者:
Rimm, David L.
影响因子:
4.8
作者:
LARSSON, N;MELANDER, H;GULLBERG, M
通讯作者:
GULLBERG, M
影响因子:
7.8
作者:
Al-Bassam, Jawdat;Ozer, Rachel S;Safer, Daniel;Halpain, Shelley;Milligan, Ronald A
通讯作者:
Milligan, Ronald A