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表皮生长因子受体在恶性浆液性和黏液性卵巢肿瘤中的免疫表达

EGFR Immunoexpression in Malignant Serous and Mucinous Ovarian Tumors.

作者信息

Cîrstea A E, Stepan A E, Zăvoi R E, Simionescu C E

机构信息

PhD Student, University of Medicine and Pharmacy of Craiova, Romania.

Department of Pathology, University of Medicine and Pharmacy of Craiova, Romania.

出版信息

Curr Health Sci J. 2018 Apr-Jun;44(2):129-134. doi: 10.12865/CHSJ.44.02.06. Epub 2018 Mar 27.

DOI:10.12865/CHSJ.44.02.06
PMID:30746159
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6320459/
Abstract

The epithelial growth factor receptor (EGFR) is involved in various stages of cancer growth such as tumor initiation, angiogenesis and metastasis, being an attractive target for oncogenic therapy. The present study aims to evaluate the EGFR expression in 54 cases of serous and mucinous ovarian borderline tumors and carcinomas. EGFR expression was present in more than half of the investigated tumors, more frequently in carcinomas than in borderline tumors, especially in the serous type. The highest values of the final staining score (FSS) were observed only in serous carcinomas in the advanced stages of the disease. As a result of frequent expression of EGFR in ovarian tumors, it is necessary to monitor EGFR inhibitors for ovarian cancer therapy, but probably after establishing more rigorous selection and stratification criteria for patients.

摘要

表皮生长因子受体(EGFR)参与癌症生长的各个阶段,如肿瘤起始、血管生成和转移,是肿瘤治疗的一个有吸引力的靶点。本研究旨在评估54例浆液性和黏液性卵巢交界性肿瘤及癌中EGFR的表达情况。超过半数的被研究肿瘤中存在EGFR表达,癌中的表达比交界性肿瘤更常见,尤其是浆液性类型。仅在疾病晚期的浆液性癌中观察到最终染色评分(FSS)的最高值。由于EGFR在卵巢肿瘤中频繁表达,有必要监测EGFR抑制剂用于卵巢癌治疗,但可能需要先为患者建立更严格的选择和分层标准。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6ce/6320459/84f9613663cc/CHSJ-44-2-129-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6ce/6320459/c10379a6ddcf/CHSJ-44-2-129-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6ce/6320459/4a7125ae1a6d/CHSJ-44-2-129-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6ce/6320459/687e7cd3774e/CHSJ-44-2-129-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6ce/6320459/f9b4d01f1aea/CHSJ-44-2-129-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6ce/6320459/84f9613663cc/CHSJ-44-2-129-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6ce/6320459/c10379a6ddcf/CHSJ-44-2-129-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6ce/6320459/4a7125ae1a6d/CHSJ-44-2-129-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6ce/6320459/687e7cd3774e/CHSJ-44-2-129-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6ce/6320459/f9b4d01f1aea/CHSJ-44-2-129-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6ce/6320459/84f9613663cc/CHSJ-44-2-129-fig5.jpg

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本文引用的文献

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Genes Cancer. 2017 May;8(5-6):589-599. doi: 10.18632/genesandcancer.142.
2
Increased serum level of epidermal growth factor receptor (EGFR) is associated with poor progression-free survival in patients with epithelial ovarian cancer.血清表皮生长因子受体(EGFR)水平升高与上皮性卵巢癌患者无进展生存期不良相关。
Cancer Chemother Pharmacol. 2014 Mar;73(3):631-7. doi: 10.1007/s00280-014-2396-x. Epub 2014 Jan 30.
3
Overexpression of HIF-1α, metallothionein and SLUG is associated with high TNM stage and lymph node metastasis in papillary thyroid carcinoma.
卵巢癌全基因组 DNA 拷贝数谱分析和生物信息学分析揭示了与不同侵袭/迁移能力相关的关键基因和途径。
Aging (Albany NY). 2020 Jan 2;12(1):178-192. doi: 10.18632/aging.102608.
4
Lidocaine inhibits the progression of retinoblastoma in vitro and in vivo by modulating the miR‑520a‑3p/EGFR axis.利多卡因通过调节 miR-520a-3p/EGFR 轴抑制视网膜母细胞瘤的体外和体内进展。
Mol Med Rep. 2019 Aug;20(2):1333-1342. doi: 10.3892/mmr.2019.10363. Epub 2019 Jun 6.
缺氧诱导因子-1α、金属硫蛋白和SLUG的过表达与甲状腺乳头状癌的高TNM分期及淋巴结转移相关。
Int J Clin Exp Pathol. 2013 Dec 15;7(1):322-30. eCollection 2014.
4
Comprehensive profiling of EGFR/HER receptors for personalized treatment of gynecologic cancers.EGFR/HER 受体的综合分析用于妇科癌症的个体化治疗。
Mol Diagn Ther. 2014 Apr;18(2):137-51. doi: 10.1007/s40291-013-0070-3.
5
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