24
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Trastuzumab-DM1 (T-DM1) retains all the mechanisms of action of trastuzumab and efficiently inhibits growth of lapatinib insensitive breast cancer.

      Breast Cancer Research and Treatment
      Animals, Antibodies, Monoclonal, therapeutic use, Antibodies, Monoclonal, Humanized, Antibody-Dependent Cell Cytotoxicity, drug effects, Blotting, Western, Breast Neoplasms, drug therapy, metabolism, pathology, Cell Line, Tumor, Cell Survival, Drug Resistance, Neoplasm, Female, Humans, Immunoconjugates, Immunotoxins, Maytansine, analogs & derivatives, Mice, Mice, Nude, Mice, Transgenic, Phosphatidylinositol 3-Kinases, Quinazolines, adverse effects, Receptor, ErbB-2, antagonists & inhibitors, immunology, Signal Transduction

      Read this article at

      ScienceOpenPublisherPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Trastuzumab (Herceptin(®)) is currently used as a treatment for patients whose breast tumors overexpress HER2/ErbB2. Trastuzumab-DM1 (T-DM1, trastuzumab emtansine) is designed to combine the clinical benefits of trastuzumab with a potent microtubule-disrupting drug, DM1 (a maytansine derivative). Currently T-DM1 is being tested in multiple clinical trials. The mechanisms of action for trastuzumab include inhibition of PI3K/AKT signaling pathway, inhibition of HER-2 shedding and Fcγ receptor mediated engagement of immune cells, which may result in antibody-dependent cellular cytotoxicity (ADCC). Here we report that T-DM1 retains the mechanisms of action of unconjugated trastuzumab and is active against lapatinib resistant cell lines and tumors.

          Related collections

          Author and article information

          Comments

          Comment on this article