• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[Experimental study of the expression of c-myc, c-fos and proto-oncogenes on hypertrophic and scars].

作者信息

Hu Zhenfu, Lou Lisheng, Luo Shengkang

机构信息

Department of Plastic Surgery, Nanfang Hospital, First Military Medical University, Guangzhou 510515, China.

出版信息

Zhonghua Zheng Xing Wai Ke Za Zhi. 2002 May;18(3):165-7.

PMID:12189705
Abstract

OBJECTIVE

To investigate the correlation between the expression of key proto-oncogenes playing major roles in tumorigenic process and abnormal sarring.

METHODS

Immunohistochemical technique was performed to detect the expressions of c-myc, c-fos and ras p21 proteins on hypertrophic scars, keloids and normal skin. Image analysis was used to compare their quantitative difference of expression.

RESULTS

C-myc and c-fos expressions on the nucleus of fibroblasts of hypertrophic and keloid scars were significantly higher than normal skin controls, and there was no difference between the two lesions. Ras p21 expression was not detected on the fibroblasts of hypertrophic and keloid scars.

CONCLUSION

  1. c-myc and c-fos oncogenes are activated on hypertrophic and keloid scars, which may contribute to proliferation and differentiation of fibroblasts, synthesis and degradation of collagen and regulation of cytokines and induce abnormal scarring, the mechanisms of their effects remain to be further studied. 2. Ras gene may not mutate or its mutations may not play a major role in the process of abnormal scarring. 3. Only part of proto-oncogenes moderately expressed on abnormal scars. The expression of multiple oncogenes does not coexist in abnormal scars may be the cause of their less chances to induce malignant transformation.
摘要

相似文献

1
[Experimental study of the expression of c-myc, c-fos and proto-oncogenes on hypertrophic and scars].
Zhonghua Zheng Xing Wai Ke Za Zhi. 2002 May;18(3):165-7.
2
Expression of oncoproteins c-fos and c-jun in hypertrophic scars and chronic dermal ulcers and their regulation of basic fibroblast growth factor.癌蛋白c-fos和c-jun在增生性瘢痕和慢性皮肤溃疡中的表达及其对碱性成纤维细胞生长因子的调控
Chin Med J (Engl). 2001 Aug;114(8):852-6.
3
Correlation between successful heterotransplantation of lung tumors in nude mice, poor prognosis of patients and expression of Fos, Jun, ErbB1, and Ras.裸鼠肺肿瘤异种移植成功、患者预后不良与Fos、Jun、ErbB1和Ras表达之间的相关性
Anticancer Res. 1993 Nov-Dec;13(6A):2021-5.
4
Ras, C-myc and C-erbB-2 oncoprotein expression in non-AIDS Mediterranean Kaposi's sarcoma.非艾滋病相关地中海型卡波西肉瘤中Ras、C-myc和C-erbB-2癌蛋白的表达
Anticancer Res. 1990 Nov-Dec;10(6):1619-25.
5
Heterogeneous immunoreactivity of frozen human benign and malignant breast lesions to C-MYC and C-Ha-ras cellular oncogenes.冷冻保存的人类乳腺良恶性病变对C-MYC和C-Ha-ras细胞癌基因的异质性免疫反应性。
Histol Histopathol. 1994 Jan;9(1):35-44.
6
Increased nuclear proto-oncogene expression in hypertrophic cardiomyopathy.肥厚型心肌病中核原癌基因表达增加。
Cardioscience. 1993 Mar;4(1):15-20.
7
Expression of ras p21 and myc p62 oncoproteins in small cell and non small cell carcinoma of the lung.ras p21和myc p62癌蛋白在肺小细胞癌和非小细胞癌中的表达
Anticancer Res. 1990 Sep-Oct;10(5A):1105-14.
8
The effect of afterload and angiotensin II on proto-oncogene mRNA levels in the isolated working rat heart.后负荷和血管紧张素II对离体工作大鼠心脏原癌基因mRNA水平的影响。
Cardiovasc Res. 1996 Jun;31(6):907-16.
9
[Effects of Huoxue Qianyang Formula on expressions of proto-oncogenes c-fos and c-myc in spontaneous hypertensive rats with ventricular hypertrophy].活血潜阳方对自发性高血压心室肥厚大鼠原癌基因c-fos和c-myc表达的影响
Zhong Xi Yi Jie He Xue Bao. 2008 Apr;6(4):387-91. doi: 10.3736/jcim20080412.
10
Effects of fluid shear stress on expression of proto-oncogenes c-fos and c-myc in cultured human umbilical vein endothelial cells.
Clin Hemorheol Microcirc. 2002;26(2):117-23.

引用本文的文献

1
MYC: there is more to it than cancer.MYC:其意义远不止于癌症。
Front Cell Dev Biol. 2024 Mar 6;12:1342872. doi: 10.3389/fcell.2024.1342872. eCollection 2024.
2
Hydrogel Loaded with Components for Therapeutic Applications in Hypertrophic Scars and Keloids.水凝胶负载用于治疗增生性瘢痕和瘢痕疙瘩的药物成分。
Int J Nanomedicine. 2024 Jan 25;19:883-899. doi: 10.2147/IJN.S448667. eCollection 2024.
3
Advances in the pathogenesis and clinical application prospects of tumor biomolecules in keloid.瘢痕疙瘩中肿瘤生物分子的发病机制及临床应用前景研究进展
Burns Trauma. 2022 Jun 25;10:tkac025. doi: 10.1093/burnst/tkac025. eCollection 2022.
4
Long non-coding RNA H19 promotes the proliferation of fibroblasts in keloid scarring.长链非编码RNA H19促进瘢痕疙瘩中成纤维细胞的增殖。
Oncol Lett. 2016 Oct;12(4):2835-2839. doi: 10.3892/ol.2016.4931. Epub 2016 Aug 2.
5
Analysis of c-myc, PAI-1 and uPAR in patients with incisional hernias.
Hernia. 2008 Jun;12(3):285-8. doi: 10.1007/s10029-007-0311-7. Epub 2007 Dec 4.