Abstract:
:To ascertain whether insulin-like growth factors (IGF-1 and IGF-2) affect the estrogen- and insulin-responsive R3230AC mammary carcinoma, studies of IGF-1 and IGF-2 receptors were conducted on primary-culture tumor cells and on membranes purified from whole tumors. By saturation binding analysis, cells in culture displayed one class of IGF-1 binding sites with an affinity constant, Kd, of 5.5 +/- 0.7 x 10(-9) M, whereas in membrane preparations, high and low affinity IGF-1 binding sites, with Kd's of 5 +/- 1.7 x 10(-9) M and 1 +/- 0.4 x 10(-7) M, respectively, were detected. Specificity of binding was demonstrated by 85% displacement of 125I-IGF-1 with 1,000-fold excess unlabeled IGF-1 and 50% displacement with 6.5 x 10(-9) M IGF-1 or 3 microM insulin. Binding sites for IGF-2 were also demonstrable in cultured cells, having a Kd of 7 +/- 0.8 x 10(-10) M, and 50% displacement was obtained with 1.5 x 10(-9) M IGF-2 or 1.5 x 10(-8) M IGF-1. Cross-linking experiments on cultured cells confirmed the presence of IGF-1 and IGF-2 receptors. In purified tumor membranes, IGF binding proteins (M(r) 28,000-32,000) were also detected; their labeling was not displaced by 10(-5) M insulin. In vitro, the tumor cells secrete one or more IGF binding proteins into the medium. Despite the fact that these cells expressed specific IGF receptors, their growth was apparently independent of these growth factors, since neither IGF-1 nor IGF-2 was mitogenic for R3230AC cells in vitro. Nevertheless, IGF-1 caused concentration-related significant increases in the plating efficiency of these cells. Further studies are necessary to determine the functional role of these growth factors, their receptors, and their binding proteins in the biology of this rodent mammary tumor.
journal_name
Oncol Resjournal_title
Oncology researchauthors
Korc-Grodzicki B,Furlanetto RW,Hilf Rsubject
Has Abstractpub_date
1992-01-01 00:00:00pages
109-19issue
3eissn
0965-0407issn
1555-3906journal_volume
4pub_type
杂志文章abstract::Topotecan, a topoisomerase I poison and water-soluble derivative of camptothecin, has shown promise in treating solid tumors; however, the drug is unstable under physiological conditions and converts to an inactive form within 30 minutes. Encapsulating topotecan in liposomes (LIP-TPT) minimizes inactivation. The effic...
journal_title:Oncology research
pub_type: 杂志文章
doi:
更新日期:1995-01-01 00:00:00
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journal_title:Oncology research
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journal_title:Oncology research
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doi:10.3727/096504018X15199489058224
更新日期:2019-05-07 00:00:00
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journal_title:Oncology research
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doi:10.3727/096504013X13854886566598
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journal_title:Oncology research
pub_type: 杂志文章
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更新日期:1995-01-01 00:00:00
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journal_title:Oncology research
pub_type: 杂志文章
doi:10.3727/096504016X14747335734344
更新日期:2017-03-13 00:00:00
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journal_title:Oncology research
pub_type: 杂志文章
doi:
更新日期:1997-01-01 00:00:00
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journal_title:Oncology research
pub_type: 杂志文章
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更新日期:1998-01-01 00:00:00
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journal_title:Oncology research
pub_type: 杂志文章
doi:
更新日期:1997-01-01 00:00:00
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journal_title:Oncology research
pub_type: 杂志文章
doi:10.3727/096504017X14873430389189
更新日期:2017-09-21 00:00:00
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journal_title:Oncology research
pub_type: 杂志文章
doi:10.3727/096504008785114156
更新日期:2008-01-01 00:00:00
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journal_title:Oncology research
pub_type: 杂志文章
doi:10.3727/096504017X14957939026111
更新日期:2018-04-27 00:00:00
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journal_title:Oncology research
pub_type: 杂志文章
doi:10.3727/096504009789745665
更新日期:2009-01-01 00:00:00
abstract::Osteosarcoma is the most common primary bone malignancy manifested predominantly in children and young adults. Studies indicate that miR-107 is involved in the pathogenesis of osteosarcoma and that tropomyosin 1 (TPM1) acts as a tumor suppressor in many types of cancer. In this study, we analyzed the effect of miR-107...
journal_title:Oncology research
pub_type: 杂志文章
doi:10.3727/096504017X14882829077237
更新日期:2017-09-21 00:00:00
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journal_title:Oncology research
pub_type: 杂志文章
doi:10.3727/096504016X14761811155298
更新日期:2017-04-14 00:00:00
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journal_title:Oncology research
pub_type: 杂志文章
doi:10.3727/096504016X14743337535446
更新日期:2017-03-13 00:00:00
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journal_title:Oncology research
pub_type: 杂志文章
doi:
更新日期:1999-01-01 00:00:00
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journal_title:Oncology research
pub_type: 杂志文章
doi:10.3727/096504018X15220594629967
更新日期:2019-02-21 00:00:00
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journal_title:Oncology research
pub_type: 杂志文章
doi:10.3727/000000003108747983
更新日期:2003-01-01 00:00:00
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journal_title:Oncology research
pub_type: 杂志文章
doi:
更新日期:1994-01-01 00:00:00
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journal_title:Oncology research
pub_type: 杂志文章
doi:
更新日期:1994-01-01 00:00:00
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journal_title:Oncology research
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更新日期:2018-04-10 00:00:00
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journal_title:Oncology research
pub_type: 杂志文章
doi:
更新日期:1997-01-01 00:00:00
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journal_title:Oncology research
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doi:10.3727/096504017X14841698396829
更新日期:2017-08-07 00:00:00
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更新日期:2020-07-08 00:00:00
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journal_title:Oncology research
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journal_title:Oncology research
pub_type: 临床试验,杂志文章,多中心研究
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journal_title:Oncology research
pub_type: 临床试验,杂志文章
doi:
更新日期:1994-01-01 00:00:00
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journal_title:Oncology research
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