• 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

Induction of matrix metalloproteinase 9 expression in breast carcinoma cells by a soluble factor from fibroblasts.

作者信息

Himelstein B P, Muschel R J

机构信息

Division of Oncology, Department of Pediatrics, University of Pennsylvania School of Medicine, Philadelphia, USA.

出版信息

Clin Exp Metastasis. 1996 May;14(3):197-208. doi: 10.1007/BF00053892.

DOI:10.1007/BF00053892
PMID:8674273
Abstract

Tumor-stromal interactions appear to play an important role in the induction of metalloproteinase expression in malignant tumors. We describe a tissue culture system in which expression of MMP-9 (gelatinase B or the 92 kDa type IV collagenase/gelatinase) was induced by co-cultivation of fibroblasts with breast cancer cell lines. While neither the breast cancer cells nor the normal rat embryo fibroblasts made MMP-9 alone in culture, human MMP-9 was made in the co-cultures. The MMP-9 was secreted in a latent form. The induction occurred at least in part through increases in the MMP-9 mRNA levels in the breast cancer cells. These increases did not appear to require protein synthesis. Conditioned medium from the fibroblasts could duplicate the induction of MMP-9 in the breast cancer cell lines. The active factor in the medium was inactivated by heat or by trypsin suggesting that it was a protein. This protein was in the size range of 30-100 kDa. Thus, fibroblasts could secrete a factor which was able to regulate the expression of MMP-9 in breast cancer cells.

摘要

相似文献

1
Induction of matrix metalloproteinase 9 expression in breast carcinoma cells by a soluble factor from fibroblasts.
Clin Exp Metastasis. 1996 May;14(3):197-208. doi: 10.1007/BF00053892.
2
Induction of M(r) 92,000 type IV collagenase expression in a squamous cell carcinoma cell line by fibroblasts.成纤维细胞诱导鳞状细胞癌细胞系中分子量为92,000的IV型胶原酶表达。
Cancer Res. 1995 Feb 15;55(4):963-7.
3
Differential regulation of matrix metalloproteinase-9, tissue inhibitor of metalloproteinase-1 (TIMP-1) and TIMP-2 expression in co-cultures of prostate cancer and stromal cells.前列腺癌与基质细胞共培养中基质金属蛋白酶-9、金属蛋白酶组织抑制剂-1(TIMP-1)和TIMP-2表达的差异调节
Int J Cancer. 2001 Aug 15;93(4):507-15. doi: 10.1002/ijc.1358.
4
Co-culture of human breast adenocarcinoma MCF-7 cells and human dermal fibroblasts enhances the production of matrix metalloproteinases 1, 2 and 3 in fibroblasts.人乳腺腺癌MCF-7细胞与人真皮成纤维细胞的共培养增强了成纤维细胞中基质金属蛋白酶1、2和3的产生。
Br J Cancer. 1995 May;71(5):1039-45. doi: 10.1038/bjc.1995.200.
5
MMP-2 and MMP-9 expression in breast cancer-derived human fibroblasts is differentially regulated by stromal-epithelial interactions.基质-上皮相互作用对乳腺癌来源的人成纤维细胞中MMP-2和MMP-9表达的调控存在差异。
Breast Cancer Res Treat. 2002 Mar;72(1):69-77. doi: 10.1023/a:1014918512569.
6
Induction of fibroblast 92 kDa gelatinase/type IV collagenase expression by direct contact with metastatic tumor cells.通过与转移性肿瘤细胞直接接触诱导成纤维细胞92 kDa明胶酶/IV型胶原酶表达。
J Cell Sci. 1994 Feb;107 ( Pt 2):477-86. doi: 10.1242/jcs.107.2.477.
7
Modulation of the expression of interstitial and type-IV collagenases in coculture of HT1080 fibrosarcoma cells and fibroblasts.
Invasion Metastasis. 1995;15(5-6):169-78.
8
Induction of membrane-type matrix metalloproteinase 1 (MT1-MMP) expression in human fibroblasts by breast adenocarcinoma cells.乳腺腺癌细胞诱导人成纤维细胞中膜型基质金属蛋白酶1(MT1-MMP)的表达。
Clin Exp Metastasis. 1997 Mar;15(2):157-63. doi: 10.1023/a:1018404927753.
9
Fibroblast-directed expression and localization of 92-kDa type IV collagenase along the tumor-stroma interface in an in vitro three-dimensional model of human squamous cell carcinoma.在人鳞状细胞癌的体外三维模型中,成纤维细胞导向的92-kDa IV型胶原酶沿肿瘤-基质界面的表达与定位
Mol Carcinog. 1997 Aug;19(4):258-66. doi: 10.1002/(sici)1098-2744(199708)19:4<258::aid-mc7>3.0.co;2-8.
10
Coordinate enhancement of gelatinase A mRNA and activity levels in human fibroblasts in response to breast-adenocarcinoma cells.人成纤维细胞中明胶酶A信使核糖核酸及活性水平对乳腺腺癌细胞的协同增强作用。
Int J Cancer. 1994 Feb 1;56(3):331-6. doi: 10.1002/ijc.2910560306.

引用本文的文献

1
Migration, invasion, and metastasis are mediated by in neuroblastoma.在神经母细胞瘤中,迁移、侵袭和转移是由……介导的。 (原文此处不完整)
Front Oncol. 2024 May 31;14:1336031. doi: 10.3389/fonc.2024.1336031. eCollection 2024.
2
Recruitment and retention: factors that affect pericyte migration.招募和保留:影响周细胞迁移的因素。
Cell Mol Life Sci. 2014 Jan;71(2):299-309. doi: 10.1007/s00018-013-1432-z. Epub 2013 Aug 4.
3
PEGylation extends circulation half-life while preserving in vitro and in vivo activity of tissue inhibitor of metalloproteinases-1 (TIMP-1).

本文引用的文献

1
Developmental expression of MMP-9 (gelatinase B) mRNA in mouse embryos.基质金属蛋白酶-9(明胶酶B)mRNA在小鼠胚胎中的发育表达。
Dev Dyn. 1995 Sep;204(1):30-40. doi: 10.1002/aja.1002040105.
2
Elevated levels of M(r) 92,000 type IV collagenase in human brain tumors.人脑肿瘤中92,000分子量IV型胶原酶水平升高。
Cancer Res. 1993 May 15;53(10 Suppl):2208-11.
3
Production of matrix metalloproteinase 9 (92-kDa gelatinase) by human oesophageal squamous cell carcinoma in response to epidermal growth factor.人食管鳞状细胞癌对表皮生长因子的反应中基质金属蛋白酶9(92 kDa明胶酶)的产生
聚乙二醇化延长了组织金属蛋白酶抑制剂-1(TIMP-1)的循环半衰期,同时保持了其在体外和体内的活性。
PLoS One. 2012;7(11):e50028. doi: 10.1371/journal.pone.0050028. Epub 2012 Nov 20.
4
Metastatic and non-metastatic colorectal cancer (CRC) cells induce host metalloproteinase production in vivo.转移性和非转移性结直肠癌(CRC)细胞在体内可诱导宿主产生金属蛋白酶。
Clin Exp Metastasis. 1999 Jun;17(4):341-9. doi: 10.1023/a:1006651019335.
5
Significance of membrane type 1 matrix metalloproteinase expression in breast cancer.膜型1基质金属蛋白酶在乳腺癌中的表达意义
Jpn J Cancer Res. 1999 May;90(5):516-22. doi: 10.1111/j.1349-7006.1999.tb00778.x.
6
Increased matrix metalloproteinase-9 activity in human ovarian cancer cells cultured with conditioned medium from human peritoneal tissue.
Clin Exp Metastasis. 1997 Nov;15(6):612-9. doi: 10.1023/a:1018495414975.
Br J Cancer. 1993 Apr;67(4):721-7. doi: 10.1038/bjc.1993.132.
4
Matrix metalloproteinases: a review.基质金属蛋白酶:综述
Crit Rev Oral Biol Med. 1993;4(2):197-250. doi: 10.1177/10454411930040020401.
5
Messenger RNA for two type IV collagenases is located in stromal cells in human colon cancer.两种IV型胶原酶的信使核糖核酸位于人类结肠癌的基质细胞中。
Am J Pathol. 1993 Feb;142(2):359-65.
6
Regulatory mechanism of 92 kDa type IV collagenase gene expression which is associated with invasiveness of tumor cells.与肿瘤细胞侵袭性相关的92kDa IV型胶原酶基因表达的调控机制。
Oncogene. 1993 Feb;8(2):395-405.
7
M(r) 92,000 type IV collagenase is increased in plasma of patients with colon cancer and breast cancer.分子量92,000的IV型胶原酶在结肠癌和乳腺癌患者的血浆中含量升高。
Cancer Res. 1993 Jan 1;53(1):140-6.
8
Expression of 72 kilodalton and 92 kilodalton type IV collagenase in malignant fibrous histiocytomas and dermatofibromas.72千道尔顿和92千道尔顿IV型胶原酶在恶性纤维组织细胞瘤和皮肤纤维瘤中的表达。
Lab Invest. 1993 Sep;69(3):305-11.
9
Interleukin-1 beta and transforming growth factor-alpha/epidermal growth factor induce expression of M(r) 95,000 type IV collagenase/gelatinase and interstitial fibroblast-type collagenase by rat mucosal keratinocytes.白细胞介素-1β以及转化生长因子-α/表皮生长因子可诱导大鼠黏膜角质形成细胞表达分子量为95,000的IV型胶原酶/明胶酶和间质成纤维细胞型胶原酶。
J Biol Chem. 1993 Sep 5;268(25):19143-51.
10
Binding and localization of M(r) 72,000 matrix metalloproteinase at cell surface invadopodia.分子量72,000的基质金属蛋白酶在细胞表面侵袭伪足处的结合与定位
Cancer Res. 1993 Jul 1;53(13):3159-64.