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全球组蛋白修饰模式与胃腺癌的癌症复发及总生存期相关。

The global histone modification pattern correlates with cancer recurrence and overall survival in gastric adenocarcinoma.

作者信息

Park Young Soo, Jin Min Young, Kim Yong Jin, Yook Jeong Hwan, Kim Byung Sik, Jang Se Jin

机构信息

Department of Pathology, Asan Medical Center, University of Ulsan College of Medicine, 388-1, Poongnap-Dong, Songpa-Gu, 138-736, Seoul, Republic of Korea.

出版信息

Ann Surg Oncol. 2008 Jul;15(7):1968-76. doi: 10.1245/s10434-008-9927-9. Epub 2008 May 10.

Abstract

BACKGROUND

Epigenetic alterations such as DNA methylation and histone modification play important roles in carcinogenesis. It has been recently suggested that global histone modification patterns are independent predictors of cancer recurrence. In this study, we used immunohistochemistry to evaluate the patterns of histone H3 and H4 acetylation and trimethylation in gastric adenocarcinomas.

METHODS

Double 2-mm core tissue microarrays were made from 261 paraffin-embedded gastric adenocarcinoma samples and examined by immunohistochemistry for histone H3 lysine 9 (H3K9) acetylation and trimethylation, histone H4 lysine 16 acetylation, and histone H4 lysine 20 trimethylation. Sections were graded according to the proportion of tumor cells showing nuclear staining.

RESULTS

Trimethylation of H3K9 positively correlated with tumor stage (P = 0.043); lymphovascular invasion (P = 0.029), cancer recurrence (P = 0.043), and higher level of H3K9 trimethylation correlated with a poor survival rate (P = 0.008). Multivariate survival analysis showed that H3K9 trimethylation status is an independent prognostic factor (P = 0.014). After categorizing cases according to the dominant modification pattern, we found that methylation dominance was associated with lymphovascular invasion (P = 0.001), cancer recurrence (P = 0.001), and poor survival rate (P = 0.028). Methylation dominance was also an independent prognostic factor (P = 0.026) in multivariate survival analysis.

CONCLUSION

The pattern of histone modification as detected by immunohistochemistry may be useful as a predictor for the recurrence of cancer and may be an independent prognostic factor in gastric adenocarcinomas.

摘要

背景

DNA甲基化和组蛋白修饰等表观遗传改变在癌症发生过程中起重要作用。最近有研究表明,整体组蛋白修饰模式是癌症复发的独立预测指标。在本研究中,我们采用免疫组织化学方法评估胃腺癌中组蛋白H3和H4的乙酰化及三甲基化模式。

方法

从261例石蜡包埋的胃腺癌样本制作2毫米厚的双芯组织微阵列,通过免疫组织化学检测组蛋白H3赖氨酸9(H3K9)的乙酰化和三甲基化、组蛋白H4赖氨酸16乙酰化以及组蛋白H4赖氨酸20三甲基化。根据显示核染色的肿瘤细胞比例对切片进行分级。

结果

H3K9三甲基化与肿瘤分期呈正相关(P = 0.043);与淋巴管浸润相关(P = 0.029)、癌症复发相关(P = 0.043),且H3K9三甲基化水平越高与生存率越低相关(P = 0.008)。多因素生存分析显示,H3K9三甲基化状态是一个独立的预后因素(P = 0.014)。根据主要修饰模式对病例进行分类后,我们发现甲基化优势与淋巴管浸润相关(P = 0.001)、癌症复发相关(P = 0.001)以及生存率低相关(P = 0.028)。在多因素生存分析中,甲基化优势也是一个独立的预后因素(P = 0.026)。

结论

通过免疫组织化学检测到的组蛋白修饰模式可能作为癌症复发的预测指标,并且可能是胃腺癌的一个独立预后因素。

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