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丝裂原活化蛋白激酶及其上游调节信号在人胃癌中的表达增加。

Increased expression of mitogen-activated protein kinase and its upstream regulating signal in human gastric cancer.

作者信息

Liang Bin, Wang Shan, Zhu Xue-Guang, Yu Yong-Xiang, Cui Zhi-Rong, Yu You-Zhi

机构信息

Division of Surgical Oncology, Peking University People's Hospital, Beijing 100044, China.

出版信息

World J Gastroenterol. 2005 Feb 7;11(5):623-8. doi: 10.3748/wjg.v11.i5.623.

Abstract

AIM

To investigate the expression of mitogen-activated protein kinases (MAPKs) and its upstream protein kinase in human gastric cancer and to evaluate the relationship between protein levels and clinicopathological parameters.

METHODS

Western blot was used to measure the expression of extracellular signal-regulated kinase (ERK)-1, ERK-2, ERK-3, p38 and mitogen or ERK activated protein kinaseMEK-1 proteins in surgically resected gastric carcinoma, adjacent normal mucosa and metastatic lymph nodes from 42 patients. Immunohistochemistry was employed for their localization.

RESULTS

Compared with normal tissues, the protein levels of ERK-1 (integral optical density value 159 526+/-65 760 vs 122 807+/-65 515, P = 0.001), ERK-2 (168 471+/-95 051 vs 120 469+/-72 874, P<0.001), ERK-3 (118 651+/-71 513 vs 70 934+/-68 058, P<0.001), P38 (104 776+/-51 650 vs 82 930+/-40 392, P = 0.048) and MEK-1 (116 486+/-45 725 vs 101 434+/-49 387, P = 0.027) were increased in gastric cancer tissues. Overexpression of ERK-3 was correlated to TNM staging (average ratio of integral optic density (IOD)(tumor): IOD(normal) in TNM I, II, III, IV tumors was 1.43+/-0.34, 5.08+/-3.74, 4.99+/-1.08, 1.44+/-1.02, n = 42, P = 0.023) and serosa invasion (4.31+/-4.34 vs 2.00+/-2.03, P = 0.037). In poorly differentiated cancers (n = 33), the protein levels of ERK-1 and ERK-2 in stage III and IV tumors were higher than those in stage I and II tumors (2.64+/-3.01 vs 1.01+/-0.33, P = 0.022; 2.05+/-1.54 vs 1.24+/-0.40, P = 0.030). Gastric cancer tissues with either lymph node involvement (2.49+/-2.91 vs 1.03+/-0.36, P = 0.023; 1.98+/-1.49 vs 1.24+/-0.44, P = 0.036) or serosa invasion (2.39+/-2.82 vs 1.01+/-0.35, P = 0.022; 1.95+/-1.44 vs 1.14+/-0.36, P = 0.015) expressed higher protein levels of ERK-1 and ERK-2. In Borrmann II tumors, expression of ERK-2 and ERK-3 was increased compared with Borrmann III tumors (2.57+/-1.86 vs 1.23+/-0.60, P = 0.022; 5.50+/-5.05 vs 1.83+/-1.21, P = 0.014). Borrmann IV tumors expressed higher p38 protein levels. No statistically significant difference in expression of MAPKs was found when stratified to tumor size or histological grade (P>0.05). Protein levels of ERK-2, ERK-3 and MEK-1 in metastatic lymph nodes were 2-7 folds higher than those in adjacent normal mucosa. The immunohistochemistry demonstrated that ERK-1, ERK-2, ERK-3, p38 and MEK-1 proteins were mainly localized in cytoplasm. The expression of MEK-1 in gastric cancer cells metastasized to lymph nodes was higher than that of the primary site.

CONCLUSION

MAPKs, particularly ERK subclass are overexpressed in the majority of gastric cancers. Overexpression of ERKs is correlated to TNM staging, serosa invasion, and lymph node involvement. The overexpression of p38 most likely plays a prominent role in certain morphological subtypes of gastric cancers. MEK-1 is also overexpressed in gastric cancer, particularly in metastatic lymph nodes. Upregulation of MAPK signal transduction pathways may play an important role in tumorigenesis and metastatic potential of gastric cancer.

摘要

目的

研究丝裂原活化蛋白激酶(MAPKs)及其上游蛋白激酶在人胃癌中的表达情况,并评估蛋白水平与临床病理参数之间的关系。

方法

采用蛋白质印迹法检测42例手术切除的胃癌组织、癌旁正常黏膜及转移淋巴结中细胞外信号调节激酶(ERK)-1、ERK-2、ERK-3、p38和丝裂原或ERK激活蛋白激酶MEK-1蛋白的表达。采用免疫组织化学法进行定位。

结果

与正常组织相比,胃癌组织中ERK-1(积分光密度值159 526±65 760 vs 122 807±65 515,P = 0.001)、ERK-2(168 471±95 051 vs 120 469±72 874,P<0.001)、ERK-3(118 651±71 513 vs 70 934±68 058,P<0.001)、P38(104 776±51 650 vs 82 930±40 392,P = 0.048)和MEK-1(116 486±45 725 vs 101 434±49 387,P = 0.027)的蛋白水平升高。ERK-3的过表达与TNM分期相关(TNM I、II、III、IV期肿瘤的积分光密度平均比值(IOD)(肿瘤):IOD(正常)分别为1.43±0.34、5.08±3.74、4.99±1.08、1.44±1.02,n = 42,P = 0.023)和浆膜侵犯相关(4.31±4.34 vs 2.00±2.03,P = 0.037)。在低分化癌(n = 33)中,III期和IV期肿瘤的ERK-1和ERK-2蛋白水平高于I期和II期肿瘤(2.64±3.01 vs 1.01±0.33,P = 0.022;2.05±1.54 vs 1.24±0.40,P = 0.030)。有淋巴结转移(2.49±2.91 vs 1.03±0.36,P = 0.023;1.98±1.49 vs 1.24±0.44,P = 0.036)或浆膜侵犯(2.39±2.82 vs 1.01±0.35,P = 0.022;1.9±1.44 vs 1.14±0.36,P = 0.015)的胃癌组织中ERK-1和ERK-2的蛋白水平较高。在Borrmann II型肿瘤中,ERK-2和ERK-3的表达高于Borrmann III型肿瘤(2.57±1.86 vs 1.23±0.60,P = 0.022;5.50±5.05 vs 1.83±±1.21,P = 0.014)。Borrmann IV型肿瘤中p38蛋白水平较高。按肿瘤大小或组织学分级分层时,MAPKs的表达无统计学差异(P>0.05)。转移淋巴结中ERK-2、ERK-3和MEK-1的蛋白水平比癌旁正常黏膜高2-7倍。免疫组织化学显示,ERK-1、ERK-2、ERK-3、p38和MEK-1蛋白主要定位于细胞质。转移至淋巴结的胃癌细胞中MEK-1的表达高于原发部位。

结论

MAPKs,尤其是ERK亚类在大多数胃癌中过表达。ERK的过表达与TNM分期、浆膜侵犯和淋巴结转移相关。p38的过表达很可能在某些形态学亚型的胃癌中起重要作用。MEK-1在胃癌中也过表达,尤其是在转移淋巴结中。MAPK信号转导通路的上调可能在胃癌的发生和转移潜能中起重要作用。

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