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本文引用的文献

1
Identification of c-kit gene mutations in primary adenoid cystic carcinoma of the salivary gland.涎腺原发性腺样囊性癌中c-kit基因突变的鉴定
Mod Pathol. 2009 Oct;22(10):1296-302. doi: 10.1038/modpathol.2009.95. Epub 2009 Jul 17.
2
Overexpression of EGFR and absence of C-KIT expression correlate with poor prognosis in salivary gland carcinomas.表皮生长因子受体(EGFR)的过表达和C-KIT表达的缺失与涎腺癌的不良预后相关。
Histopathology. 2008 Nov;53(5):567-77. doi: 10.1111/j.1365-2559.2008.03159.x.
3
Deletion of 1p32-p36 is the most frequent genetic change and poor prognostic marker in adenoid cystic carcinoma of the salivary glands.1p32-p36缺失是涎腺腺样囊性癌中最常见的基因改变和不良预后标志物。
Clin Cancer Res. 2008 Aug 15;14(16):5181-7. doi: 10.1158/1078-0432.CCR-08-0158.
4
Salivary gland-type lung carcinomas: an EGFR immunohistochemical, molecular genetic, and mutational analysis study.唾液腺型肺癌:一项表皮生长因子受体免疫组织化学、分子遗传学及突变分析研究
Mod Pathol. 2008 Sep;21(9):1168-75. doi: 10.1038/modpathol.2008.113. Epub 2008 Jun 27.
5
Regulation of in situ to invasive breast carcinoma transition.原位乳腺癌向浸润性乳腺癌转变的调控。
Cancer Cell. 2008 May;13(5):394-406. doi: 10.1016/j.ccr.2008.03.007.
6
Microenvironmental regulators of tissue structure and function also regulate tumor induction and progression: the role of extracellular matrix and its degrading enzymes.组织结构与功能的微环境调节因子也调控肿瘤的诱发与进展:细胞外基质及其降解酶的作用
Cold Spring Harb Symp Quant Biol. 2005;70:343-56. doi: 10.1101/sqb.2005.70.013.
7
Myoepithelial cells: autocrine and paracrine suppressors of breast cancer progression.肌上皮细胞:乳腺癌进展的自分泌和旁分泌抑制因子
J Mammary Gland Biol Neoplasia. 2005 Jul;10(3):249-60. doi: 10.1007/s10911-005-9585-5.
8
Parotid carcinoma: expression of kit protein and epidermal growth factor receptor.腮腺癌:c-kit蛋白与表皮生长因子受体的表达
J Oral Pathol Med. 2006 May;35(5):286-91. doi: 10.1111/j.1600-0714.2006.00421.x.
9
Imatinib mesylate in patients with adenoid cystic cancers of the salivary glands expressing c-kit: a Princess Margaret Hospital phase II consortium study.甲磺酸伊马替尼治疗表达c-kit的涎腺腺样囊性癌患者:玛格丽特公主医院II期联合研究
J Clin Oncol. 2005 Jan 20;23(3):585-90. doi: 10.1200/JCO.2005.06.125.
10
Phase II clinical trial data with the epidermal growth factor receptor tyrosine kinase inhibitor erlotinib (OSI-774) in non-small-cell lung cancer.表皮生长因子受体酪氨酸激酶抑制剂厄洛替尼(OSI-774)用于非小细胞肺癌的II期临床试验数据。
Clin Lung Cancer. 2004 Dec;6 Suppl 1:S20-3. doi: 10.3816/clc.2004.s.010.

腺样囊性癌中细胞类型依赖性生物标志物的表达:生物学和治疗意义。

Cell type-dependent biomarker expression in adenoid cystic carcinoma: biologic and therapeutic implications.

作者信息

Bell Diana, Roberts Dianna, Kies Merrill, Rao Pulivarthi, Weber Randal S, El-Naggar Adel K

机构信息

Department of Pathology, The University of Texas M.D. Anderson Cancer Center, Houston, Texas, USA.

出版信息

Cancer. 2010 Dec 15;116(24):5749-56. doi: 10.1002/cncr.25541. Epub 2010 Sep 7.

DOI:10.1002/cncr.25541
PMID:20824717
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2998592/
Abstract

BACKGROUND

Adenoid cystic carcinoma (ACC), a rare and progressive salivary malignancy, is characterized by cellular, morphologic, and clinical heterogeneity. The authors of this report hypothesized that the dual cellular composition of ACC plays an important role in biomarker evaluation, tumor biologic behavior, and response to therapy.

METHODS

To investigate the differential localization and expression of the c-Kit protein and the epidermal growth factor receptor (EGFR) protein, immunohistochemical analyses were performed on tissue arrays that were constructed from 199 tumors, and the results were correlated with clinicopathologic factors.

RESULTS

c-Kit expression was limited to the inner ductal epithelial cells, whereas EGFR expression was limited mainly to the outer myoepithelial cells in the majority of ACCs with tubular and cribriform patterns. In solid ACCs, c-Kit uniformly was positive, whereas EGFR consistently was negative. A significant statistical correlation was observed between c-Kit expression and a poor 3-year outcome, and EGFR expression was correlated with a better 3-year outcome.

CONCLUSIONS

The current findings underscored the importance of cellular subtype localization of biomarkers in the clinical and therapeutic stratification of patients with ACC.

摘要

背景

腺样囊性癌(ACC)是一种罕见的进行性涎腺恶性肿瘤,具有细胞、形态和临床异质性。本报告的作者推测,ACC的双细胞组成在生物标志物评估、肿瘤生物学行为及对治疗的反应中起重要作用。

方法

为研究c-Kit蛋白和表皮生长因子受体(EGFR)蛋白的差异定位及表达,对由199个肿瘤构建的组织芯片进行免疫组化分析,并将结果与临床病理因素相关联。

结果

在大多数呈管状和筛状结构的ACC中,c-Kit表达局限于导管内层上皮细胞,而EGFR表达主要局限于外层肌上皮细胞。在实性ACC中,c-Kit均呈阳性,而EGFR始终呈阴性。观察到c-Kit表达与3年不良预后之间存在显著统计学相关性,而EGFR表达与较好的3年预后相关。

结论

目前的研究结果强调了生物标志物的细胞亚型定位在ACC患者临床和治疗分层中的重要性。