Gene amplification and mRNA and protein overexpression of c-erbB-2 (HER-2/neu) in human intrahepatic cholangiocarcinoma as detected by fluorescence in situ hybridization, in situ hybridization, and immunohistochemistry

荧光原位杂交 原位杂交 免疫组织化学 癌变 生物 分子生物学 信使核糖核酸 基因表达 基因复制 癌基因 基因 染色体 细胞周期 遗传学 免疫学
作者
Yoko Ukita,Masako Kato,Tadashi Terada
出处
期刊:Journal of Hepatology [Elsevier]
卷期号:36 (6): 780-785 被引量:52
标识
DOI:10.1016/s0168-8278(02)00057-0
摘要

The human proto-oncogene c-erbB-2 (also called HER-2/neu) is located on chromosome 17q21-22. There have been no studies on gene amplification or mRNA expression of c-erbB-2 in human intrahepatic cholangiocarcinoma (CC) hitherto.We investigated c-erbB-2 gene amplification by fluorescence in situ hybridization (FISH), c-erbB2 mRNA expression by ISH, and c-erbB-2 protein expression by immunohistochemistry in 22 archival cases of CC.FISH revealed that c-erbB-2 gene signals were increased in CC. ISH showed that c-erbB-2 mRNA signals were located in the nuclei and cytoplasms of cancer cells and were increased in cancer cells compared with non-cancerous bile ducts where no signals were present. Immunohistochemistry showed that the c-erbB-2 protein was expressed in the cell membrane of cancer cells, and was increased compared with non-cancerous bile ducts where no expression was found. There was a positive significant correlation between c-erbB-2 mRNA and protein expression. Clinicopathologically, there were no correlations between the c-erbB-2 expression and various pathological features.These data suggest that c-erbB-2 gene amplification does occur in CC, and that there is an overexpressed c-erbB-2 protein through the enhanced mRNA expression. The c-erbB-2 gene amplification may be related to the oncogenesis or tumor progression of CC.

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
眼睛大的擎苍完成签到,获得积分10
2秒前
量子星尘发布了新的文献求助10
3秒前
3秒前
3秒前
CC完成签到 ,获得积分10
6秒前
Caesar发布了新的文献求助10
7秒前
songjiatian发布了新的文献求助10
9秒前
卡卡卡完成签到,获得积分10
9秒前
oyc完成签到,获得积分10
11秒前
Caesar完成签到,获得积分10
12秒前
12秒前
YifanWang应助oneonlycrown采纳,获得10
13秒前
Chief完成签到,获得积分0
13秒前
量子星尘发布了新的文献求助10
14秒前
14秒前
14秒前
Tanya完成签到 ,获得积分10
15秒前
三木小君子完成签到,获得积分10
17秒前
所所应助shenerqing采纳,获得10
19秒前
一颗土豆发布了新的文献求助10
20秒前
科目三应助迅速的冰海采纳,获得10
22秒前
量子星尘发布了新的文献求助10
22秒前
23秒前
24秒前
思源应助上上签采纳,获得10
25秒前
江台风应助lwb采纳,获得10
27秒前
感冒药完成签到 ,获得积分10
28秒前
娄十三发布了新的文献求助10
29秒前
29秒前
科研通AI6.1应助桃子e采纳,获得10
31秒前
32秒前
32秒前
量子星尘发布了新的文献求助10
33秒前
科研通AI2S应助Fxxkme采纳,获得10
36秒前
眼睛大的尔蝶完成签到,获得积分10
36秒前
37秒前
37秒前
shenerqing发布了新的文献求助10
38秒前
Mickey发布了新的文献求助10
40秒前
41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
Encyclopedia of Forensic and Legal Medicine Third Edition 5000
Agyptische Geschichte der 21.30. Dynastie 2000
中国脑卒中防治报告 1000
Variants in Economic Theory 1000
Global Ingredients & Formulations Guide 2014, Hardcover 1000
Research for Social Workers 1000
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 5820324
求助须知:如何正确求助?哪些是违规求助? 5965377
关于积分的说明 15554664
捐赠科研通 4942088
什么是DOI,文献DOI怎么找? 2661775
邀请新用户注册赠送积分活动 1608044
关于科研通互助平台的介绍 1562989