Establishment and characterization of a new drug surviving cell line Am1010, derived directly from muscle metastases of a human lung adenocarcinoma patient with multi-drug-resistance tOcisplatin, taxol, and gefitinib
Aim: To Characterize a new human lung cancer cell line Am1010, derived from drug-surviving cells (DSCs). Methods: The Am1010 cell line was established after 4 cycles of chemotherapy from an arm muscle metastasic tumor of a patient diagnosed with lung adenocarcinoma. The cell line has been remained i...
Gespeichert in:
Veröffentlicht in: | Acta pharmacologica Sinica 2010 (5), p.601-608 |
---|---|
1. Verfasser: | |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Aim: To Characterize a new human lung cancer cell line Am1010, derived from drug-surviving cells (DSCs). Methods: The Am1010 cell line was established after 4 cycles of chemotherapy from an arm muscle metastasic tumor of a patient diagnosed with lung adenocarcinoma. The cell line has been remained in continuous culture for more than one year during this study. Results: The Am1010 cell line demonstrated in vitro multi-drug-resistance to cisplatin, taxol, and gefitinib. The Am1010 cell doubling time without drug treatment was 42.395 h. The IC50 value of cisplatin was 4.299 pmol/L and 〉10 IJmol/L for the Am1010 and P0318 (a cell line derived from non-DSCs) cells, respectively. The IC50 value of taxol was 0.067 μmol/L and 〉1 IJmol/L for the Am1010 and P0318 cells, respectively. The IC50 ovalue of gefitinib was 15.233 μmol/L and 〉70 μmol/L for Am1010 and P0318 cells, respectively. 11 genes involved in the focal adhesion and cell adhesion pathways were found to be differentially expressed. The cells of Am1010 have a significantly larger chromosome number than most lung cancer cell lines. Conclusion: This novel DSCs derived lung cancer cell line will be a valuable in vitro tool for the investigation of lung cancer drug resistance and metastasis. |
---|---|
ISSN: | 1671-4083 1745-7254 |