insulin-detemir and Colorectal-Neoplasms

insulin-detemir has been researched along with Colorectal-Neoplasms* in 1 studies

Other Studies

1 other study(ies) available for insulin-detemir and Colorectal-Neoplasms

ArticleYear
Insulin analogues display IGF-I-like mitogenic and anti-apoptotic activities in cultured cancer cells.
    Diabetes/metabolism research and reviews, 2009, Volume: 25, Issue:1

    Insulin analogues are widely used in the treatment of diabetes mellitus. Some insulin analogues were reported to display atypical activities in vitro that resemble those of insulin-like growth factor-I (IGF-I). The aim of this study was to investigate whether two long-acting insulin analogues [glargine (Lantus, Sanofi Aventis, Germany) and detemir (Levemir, Novo Nordisk, Denmark)] and two short-acting analogues [lispro (Humalog, Eli Lilly, Indianapolis, USA) and aspart (Novolog, Novo Nordisk, Denmark)] exhibit IGF-I-like activities on cultured cancer cells in comparison with IGF-I and regular human insulin.. HCT-116 (colorectal cancer), PC-3 (prostate cancer) and MCF-7 (breast adenocarcinoma) cell lines were treated with insulin, IGF-I or insulin analogues, and proliferation and protection from apoptosis were measured by cell counting and fluorescent-activated cell sorter (FACS) analysis, respectively. In addition, Western blots were used to identify signalling molecules activated by the analogues.. Glargine, detemir and lispro had proliferative effects that resemble IGF-I action. Insulin, however, did not stimulate cellular proliferation. In addition, glargine and detemir displayed an IGF-I-like anti-apoptotic activity. Glargine, like insulin and IGF-I, induced phosphorylation of both ERK and AKT, suggesting that the analogue is able to stimulate both the ras-raf-mitogen-activated protein kinase (MAPK) and PI3K-AKT pathways. Furthermore, glargine induced both insulin receptor (IR) and IGF-IR phosphorylation.. Glargine, detemir and lispro, unlike regular insulin, exhibit in vitro proliferative and anti-apoptotic activities in a number of cancer cell lines. These actions resemble some of the effects of IGF-I, a growth factor involved in cancer initiation and progression. Insulin had no increased IGF-I activity. The specific receptor/s involved in mediating analogues actions remains to be identified.

    Topics: Adenocarcinoma; Apoptosis; Breast Neoplasms; Cell Division; Cell Line, Tumor; Colorectal Neoplasms; Dose-Response Relationship, Drug; Female; Humans; Insulin; Insulin Detemir; Insulin Glargine; Insulin Lispro; Insulin-Like Growth Factor I; Insulin, Long-Acting; Male; Prostatic Neoplasms; Tumor Cells, Cultured

2009