## Background: Dna fragmentation factor 45 (dff45)/inhibotor of caspase activated dnase (icad) forms a complex with dff40/cad and inhibits its dna cleaving function during apoptosis. dff45 also functions as a chaperone for native dff40 and is necessary for its function. it has been indicated that d
Decreased expression of methyl methansulfonate and ultraviolet-sensitive gene clone 81 (Mus81) is correlated with a poor prognosis in patients with hepatocellular carcinoma
✍ Scribed by Fan Wu; Si-Yu Liu; Yi-Ming Tao; Di-Peng Ou; Feng Fang; Lian-Yue Yang
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 385 KB
- Volume
- 112
- Category
- Article
- ISSN
- 0008-543X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
BACKGROUND.
Recent work has demonstrated that methyl methansulfonate and ultraviolet‐sensitive gene clone 81 (Mus81) is critical in the maintenance of chromosome stability and tumor suppression in mice. To investigate its role in human hepatocellular carcinoma (HCC), which currently is unknown, the authors examined the correlation between Mus81 expression and prognosis in patients with HCC.
METHODS.
Reverse transcriptase‐polymersase chain reaction and Western blot analyses were used to determine Mus81 expression levels in 41 paired HCC and paracarcinomatous liver tissue (PCLT) specimens. Immunohistochemistry analysis was also performed on 104 HCC specimens from patients with follow‐up information.
RESULTS.
Both Mus81 messenger RNA and protein expression levels were decreased significantly in HCC specimens. Moreover, lower Mus81 expression levels were detected in nodular HCC (NHCC) than in solitary large HCC (SLHCC) specimens. Among 104 specimens of HCC, the positive rate of Mus81 was significantly lower than the rate in PCLT (P = .017), and the decreased Mus81expression was correlated significantly with high Edmondson‐Steiner grade, multiple tumor nodes, and venous invasion. Patients with HCC who had low Mus81 expression had either poorer disease‐free survival or poorer overall survival than patients who had with high Mus81 expression (P = .0027 and P = .0001, respectively). Multivariate Cox regression analysis revealed that low Mus81 expression was an independent prognostic factor for patients with HCC (risk ratio, 5.74; P = .012).
CONCLUSIONS.
Mus81 expression levels were decreased significantly in HCC specimens, and the decreased levels were correlated with a poor prognosis in patients with HCC, implicating Mus81 as a candidate prognostic marker in HCC. Cancer 2008. © 2008 American Cancer Society.
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