乳腺癌組織Notch1和JAG1蛋白表達與分子分型相關性研究
發(fā)布時間:2018-04-18 10:39
本文選題:乳腺腫瘤 + 分子分型; 參考:《中華腫瘤防治雜志》2017年05期
【摘要】:目的 Notch信號通路在乳腺癌中存在異常表達,但在不同分子分型乳腺癌中的表達情況鮮見報道。本研究將探討不同分子分型乳腺浸潤性導管癌組織中Notch1和JAG1蛋白表達及其與臨床病理特征之間的關系。方法收集濱州醫(yī)學院附屬醫(yī)院病理科2012-01-06-2014-12-30存檔的乳腺浸潤性導管癌病例240例,根據ER、PR、HER2、Ki-67免疫組化結果分為管腔A型、管腔B型、HER2過表達型及三陰性型4組,每組60例,采用免疫組化En-Vision法檢測不同分子分型乳腺癌中Notch1、JAG1蛋白的表達情況,對各分型乳腺癌組織的陽性表達率進行統計學分析。結果各分型乳腺癌組織中Notch1的陽性表達差異有統計學意義(P=0.010,P0.05),其中三陰性乳腺癌(86.67%)與管腔A型(56.67%)比較(P0.001),HER2過表達型(83.33%)與管腔A型(56.67%)比較,差異均有統計學意義,P0.001;Notch1的陽性表達與淋巴結轉移相關(P=0.017,P0.05),與臨床分期(P=0.005,P0.01)、組織學分級(P=0.009,P0.01)顯著相關,與ER表達(r_s=-0.206,P=0.001,P0.01)、PR表達(r_s=-0.187,P=0.005,P0.01)顯著負相關,而與患者年齡、腫塊大小無關。各分型乳腺癌組織中JAG1的陽性表達差異有統計學意義(P=0.035,P0.05),以三陰性乳腺癌陽性表達率最高,但各組間兩兩比較差異無統計學意義;JAG1陽性表達與ER表達(r_s=-0.142,P=0.015,P0.05)、PR表達(r_s=-0.127,P=0.035,P0.05)呈負相關;Notch1和JAG1之間無明顯相關性。結論 Notch1陽性表達與ER、PR表達顯著負相關,與乳腺癌的組織學分級、淋巴結轉移及臨床分期密切相關,并在HER2過表達型,尤其是三陰性乳腺癌組織中存在高表達,有可能成為三陰性乳腺癌新的治療靶點。
[Abstract]:Objective there is abnormal expression of Notch signaling pathway in breast cancer, but it is rarely reported in different molecular types of breast cancer.The purpose of this study was to investigate the expression of Notch1 and JAG1 in breast invasive ductal carcinoma with different molecular types and their relationship with clinicopathological features.Methods 240 cases of invasive ductal carcinoma of breast were collected from Department of Pathology, affiliated Hospital of Binzhou Medical College, from January to June 2014-12-30. According to the immunohistochemical results of ERB HER2 Ki-67, 240 cases were divided into 4 groups: type A, type B, and type B, with 60 cases in each group.Immunohistochemical En-Vision method was used to detect the expression of Notch1 and JAG1 protein in different molecular types of breast cancer, and the positive expression rate of Notch1 and JAG1 protein was analyzed statistically.Results there were significant differences in the positive expression of Notch1 between the three negative breast cancer tissues (P 0.010 and P 0.05, including three negative breast cancer (86.67)) and the lumen A (56.67) (P 0.001 HER2 overexpression type (83.33) and the lumen A (56.67)).There was significant correlation between the positive expression of P0.001ntch1 and lymph node metastasis (P0. 017 / P0. 05), clinical stage P0. 005 / P0. 01, histological grade P0. 009 / P0. 01), and the positive expression of P0. 001- 0. 206P0. 001p0. 01PR was negatively correlated with the age of the patients and the size of the tumor, but it was not correlated with the age of the patients and the size of the tumor. The positive expression of P0. 001ntch1 was significantly correlated with the expression of P0. 017 and P0. 005P0. 01, but not correlated with the age of the patients and the size of the tumor.The positive expression of JAG1 in breast cancer was significantly different among the three types of breast cancer, and the positive expression rate of JAG1 was the highest in triple-negative breast cancer.But there was no significant difference between the two groups. There was no significant correlation between the positive expression of JAG1 and the expression of ER, rstch1 and JAG1. There was no significant correlation between the positive expression of JAG1 and the expression of rsser-0.127 P0. 035 and JAG1.Conclusion the positive expression of Notch1 is negatively correlated with the expression of ERP PR, and is closely related to the histological grade, lymph node metastasis and clinical stage of breast cancer, and is highly expressed in the overexpression of HER2, especially in triple-negative breast cancer.It is possible to become a new therapeutic target for triple negative breast cancer.
【作者單位】: 濱州醫(yī)學院附屬醫(yī)院病理科;濱州醫(yī)學院病理學教研室;
【基金】:山東省自然科學基金(ZR2010HM096)
【分類號】:R737.9
【相似文獻】
相關期刊論文 前10條
1 趙春霞;李棟梁;曹玉文;付欣鴿;李鋒;;Notch1基因單核苷酸多態(tài)性與乳腺癌和增生性病變的相關性研究[J];農墾醫(yī)學;2011年02期
2 趙麗;張姣;付麗;馬勇杰;谷峰;;乳腺癌細胞Notch1蛋白表達及其與紫杉醇敏感性的關系[J];中國腫瘤臨床;2012年09期
3 牛煥付;李瑞梅;李德軍;王文龍;;乳腺癌組織Notch1信號的表達及其臨床意義[J];中國病原生物學雜志;2010年10期
4 李傳偉;李連宏;柳雅玲;范姝君;王波;孫杰;;Notch1信號在乳腺癌干細胞分化中的作用[J];臨床與實驗病理學雜志;2008年02期
5 逯,
本文編號:1768008
本文鏈接:http://sikaile.net/yixuelunwen/zlx/1768008.html
最近更新
教材專著