Trastuzumab in combination with paclitaxel enhances antitumor activity by promoting apoptosis in human epidermal growth factor receptor 2-positive trastuzumab-resistant gastric cancer xenograft models
| Autor: | Sei Shu, Yasuhiro Kodera, Naoki Harada, Yoriko Yamashita-Kashima, Mieko Yanagisawa, Hayao Nakanishi, Yasushi Yoshimura |
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| Rok vydání: | 2019 |
| Předmět: |
0301 basic medicine
Male Cancer Research Paclitaxel Class I Phosphatidylinositol 3-Kinases Receptor ErbB-2 Apoptosis 03 medical and health sciences chemistry.chemical_compound Mice 0302 clinical medicine Breast cancer Trastuzumab Stomach Neoplasms Cell Line Tumor Antineoplastic Combined Chemotherapy Protocols medicine Animals Humans Pharmacology (medical) Epidermal growth factor receptor skin and connective tissue diseases Receptor neoplasms Cyclin-Dependent Kinase Inhibitor Proteins Pharmacology Mice Inbred BALB C biology Kinase business.industry Cancer medicine.disease Xenograft Model Antitumor Assays 030104 developmental biology Oncology chemistry Drug Resistance Neoplasm 030220 oncology & carcinogenesis Cancer research biology.protein business medicine.drug |
| Zdroj: | Anti-cancer drugs. 31(3) |
| ISSN: | 1473-5741 |
| Popis: | Trastuzumab, a humanized anti-human epidermal growth factor receptor 2 antibody drug, is the first-line therapy for human epidermal growth factor receptor 2-positive breast and gastric cancer. For breast cancer, the benefit of continuous treatment with trastuzumab after it becomes refractory to first-line therapy has been demonstrated. However, it is unclear whether trastuzumab can show similar efficacy as a second-line treatment for gastric cancer. Here, we report that trastuzumab in combination with paclitaxel exhibits increased antitumor efficacy even for trastuzumab-resistant xenografted tumors. We derived the trastuzumab-resistant models from previously established human epidermal growth factor receptor 2-positive gastric cancer patient-derived cells. Human epidermal growth factor receptor 2 expression, PIK3CA mutation, and phosphatase and tensin homolog expression in these resistant models was equivalent to those in the trastuzumab-sensitive parental model, whereas cyclin-dependent kinase inhibitors, such as p16, p15, and p21, were downregulated. Trastuzumab in combination with paclitaxel enhanced antitumor activity in both the sensitive and resistant models. In the trastuzumab-sensitive model, the combination of trastuzumab and paclitaxel resulted in suppression of the AKT-p27-retinoblastoma protein pathway and induction of apoptosis. Although this combination did not suppress retinoblastoma protein phosphorylation in the trastuzumab-resistant model, it did markedly decrease epidermal growth factor receptor and human epidermal growth factor receptor 2 phosphorylation and further enhance paclitaxel-mediated apoptosis. These results suggested that trastuzumab in combination with paclitaxel can still exert more potent antitumor efficacy than each agent alone in trastuzumab-resistant models, providing evidence that trastuzumab remains beneficial in the treatment of trastuzumab-resistant tumors. |
| Databáze: | OpenAIRE |
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