High Expression of Macrophage Colony-Stimulating Factor in Peritumoral Liver Tissue Is Associated With Poor Survival After Curative Resection of Hepatocellular Carcinoma

医学 肝细胞癌 病理 内科学 巨噬细胞 癌症研究 肿瘤科 切除术 体外 外科 生物 生物化学
作者
Xiao-Dong Zhu,Ju-Bo Zhang,Peng-Yuan Zhuang,Hong-Guang Zhu,Wei Zhang,Yu-Quan Xiong,Wei-zhong Wu,Lu Wang,Zhao-You Tang,Hui-Chuan Sun
出处
期刊:Journal of Clinical Oncology [American Society of Clinical Oncology]
卷期号:26 (16): 2707-2716 被引量:545
标识
DOI:10.1200/jco.2007.15.6521
摘要

Purpose To investigate prognostic values of the intratumoral and peritumoral expression of macrophage colony-stimulating factors (M-CSF) in hepatocellular carcinoma (HCC) patients after curative resection. Patients and Methods Expression of M-CSF and density of macrophages (MΦ) were assessed by immunohistochemistry in tissue microarrays containing paired tumor and peritumoral liver tissue from 105 patients who had undergone hepatectomy for histologically proven HCC. Prognostic value of these and other clinicopathologic factors was evaluated. Results Neither intratumoral M-CSF nor MΦ density was associated with overall survival (OS) or disease-free survival (DFS). High peritumoral M-CSF and MΦ density, which correlated with large tumor size, presence of intrahepatic metastasis, and high TNM stage, were independent prognostic factors for both OS (P = .001 and P < .001, respectively) and DFS (P = .001 and P = .003, respectively) and affected incidence of early recurrence. In a small HCC subset, peritumoral M-CSF was also correlated with both OS and DFS (P = .038 and P = .001, respectively). The combination of peritumoral M-CSF and MΦ had a better power to predict the patients' death and disease recurrence (P < .001 for both). Conclusion High peritumoral M-CSF and MΦ were associated with HCC progression, disease recurrence, and poor survival after hepatectomy, highlighting the importance of peritumoral tissue in the recurrence and metastasis of HCC. M-CSF and MΦ may be targets of postoperative adjuvant therapy.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
去银行整点金条完成签到,获得积分10
1秒前
1秒前
aaaaaa应助美好斓采纳,获得30
1秒前
2秒前
2秒前
哈哈哈完成签到 ,获得积分10
3秒前
iota应助Pavel采纳,获得10
4秒前
jialin完成签到 ,获得积分10
5秒前
科研发布了新的文献求助10
5秒前
111完成签到,获得积分10
6秒前
6秒前
abner发布了新的文献求助10
7秒前
LY发布了新的文献求助10
7秒前
7秒前
8秒前
he完成签到,获得积分10
8秒前
auguscai发布了新的文献求助10
8秒前
英俊qiang发布了新的文献求助10
8秒前
炼丹师完成签到,获得积分10
9秒前
太叔白易完成签到,获得积分0
11秒前
光亮绮山完成签到 ,获得积分10
11秒前
11秒前
13秒前
yorkson境发布了新的文献求助10
13秒前
盛夏夜未眠完成签到,获得积分10
14秒前
吃瓜米吃瓜米完成签到 ,获得积分10
14秒前
酷爱小飞完成签到,获得积分10
14秒前
绵杨完成签到,获得积分10
14秒前
萧晓完成签到 ,获得积分10
15秒前
15秒前
科研通AI6.1应助杨武天一采纳,获得10
16秒前
科研通AI6.2应助杨武天一采纳,获得10
16秒前
ll应助杨武天一采纳,获得10
16秒前
16秒前
高冷的小白完成签到 ,获得积分10
17秒前
18秒前
18秒前
大力的灵雁应助熊猫海采纳,获得20
19秒前
荔枝发布了新的文献求助10
20秒前
qqwwe完成签到,获得积分10
20秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Kinesiophobia : a new view of chronic pain behavior 3000
Les Mantodea de guyane 2500
Molecular Biology of Cancer: Mechanisms, Targets, and Therapeutics 2000
Signals, Systems, and Signal Processing 510
Discrete-Time Signals and Systems 510
Brittle Fracture in Welded Ships 500
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 计算机科学 有机化学 物理 生物化学 纳米技术 复合材料 内科学 化学工程 人工智能 催化作用 遗传学 数学 基因 量子力学 物理化学
热门帖子
关注 科研通微信公众号,转发送积分 5944942
求助须知:如何正确求助?哪些是违规求助? 7095602
关于积分的说明 15897749
捐赠科研通 5076784
什么是DOI,文献DOI怎么找? 2730186
邀请新用户注册赠送积分活动 1690027
关于科研通互助平台的介绍 1614500