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DOI 10.18632/oncotarget.12667

Медицинская библиотека · Oncotarget · 2016

Ino80 promotes cervical cancer tumorigenesis by activating Nanog expression.

Hu Jing, Liu Jie, Chen Aozheng, Lyu Jia, Ai Guihai, Zeng Qiongjing, Sun Yi, Chen Chunxia, Wang Jinbo, Qiu Jin, Wu Yi, Cheng Jiajing, Shi Xiujuan, Song Liwen

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Аннотация

BACKGROUND

End-stage renal disease (ESRD) conveys high mortality risk by complex mechanisms not fully elucidated but possibly linked to hormonal abnormalities, including cortisol. Whereas a high serum cortisol level has recently been linked with increased mortality in the general population, there is scarce information on the clinical associates and prognostic value of cortisol levels in ESRD.

PATIENTS AND

METHODS

Prospective study of prevalent hemodialysis patients (n = 75), mostly non-diabetic (76%), where cortisol levels were assessed and patients were afterwards followed for a median of 20 (interquartile range (IQR) 8 - 31) months.

RESULTS

Cortisol levels were negatively correlated with plasma sodium (Rho = -0.26. p < 0.025) and positively correlated with C-reactive protein (CRP; Rho = 0.26, p = 0.027). The association with CRP remained independent of multiple confounders. Baseline cortisol levels of those who died were higher than of those who survived (19.8 ± 6.9 vs. 15.3 ± 5.7 mcg/dL, p = 0.0083). Kaplan-Meier analysis showed that patients with cortisol levels within the highest tertile (≥ 18 mcg/dL) were at increased risk of death. Cortisol was associated with risk of death both in crude and adjusted Cox proportional hazards models (HR 1.09 (1.021 - 1.167) p = 0.011; and 1.16 (1.027 - 1.309), p = 0.01, respectively)).

CONCLUSIONS

High serum concentrations of cortisol were associated with a state of inflammation and independently identified a subgroup of chronic hemodialysis patients at a high mortality risk.

Для цитирования: Hu Jing, Liu Jie, Chen Aozheng, Lyu Jia, Ai Guihai, Zeng Qiongjing, Sun Yi, Chen Chunxia, Wang Jinbo, Qiu Jin, Wu Yi, Cheng Jiajing, Shi Xiujuan, Song Liwen. Ino80 promotes cervical cancer tumorigenesis by activating Nanog expression.. Oncotarget. 2016. DOI: 10.18632/oncotarget.12667.

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