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[In vitro comparison of podophyllotoxin analogues; etoposide, teniposide and NK 611 using human lung cancer cell lines].

Abstract
In an attempt to predict the antitumor activity of a new podophyllotoxin analogue, NK 611, in the treatment of lung cancer, we compared the drug with etoposide and teniposide using four human small cell lung cancer (SCLC) cell lines, SBC-2, -3, -4, -7, and two non-small cell lung cancer cell lines, ABC-1, EBC-1. In terms of the fifty percent tumor growth inhibitory concentration (IC 50) determined by MTT assay, teniposide was most potent among the drugs. The degree of cross-resistance of each drug was investigated using an etoposide-resistant SCLC subline (SBC-3/ETP), an adriamycin-resistant subline (SBC-3/ADM 100), and a cisplatin-resistant subline (SBC-3/CDDP). As for relative resistant (the ratio of IC 50 for resistant subline to that for the parent subline), NK 611 was least cross-resistant to etoposide, adriamycin, and cisplatin among drugs tested. These results indicate that NK 611 may play a role in a salvage chemotherapy for patients with resistant SCLC.
AuthorsN Takigawa, T Ohnoshi, H Ueoka, K Kiura, T Moritaka, M Tabata, Y Segawa, T Shibayama, K Gemba, T Matsumura
JournalGan to kagaku ryoho. Cancer & chemotherapy (Gan To Kagaku Ryoho) Vol. 20 Issue 4 Pg. 473-7 (Mar 1993) ISSN: 0385-0684 [Print] Japan
PMID8383949 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • Antineoplastic Agents
  • Tetrazolium Salts
  • Thiazoles
  • NK 611
  • Etoposide
  • Teniposide
  • thiazolyl blue
  • Podophyllotoxin
Topics
  • Adenocarcinoma (pathology)
  • Antineoplastic Agents (pharmacology)
  • Carcinoma, Small Cell (pathology)
  • Carcinoma, Squamous Cell (pathology)
  • Cell Division (drug effects)
  • Drug Resistance
  • Drug Screening Assays, Antitumor
  • Etoposide (pharmacology)
  • Humans
  • Lung Neoplasms (pathology)
  • Podophyllotoxin (analogs & derivatives, pharmacology)
  • Teniposide (pharmacology)
  • Tetrazolium Salts (pharmacology)
  • Thiazoles (pharmacology)
  • Tumor Cells, Cultured

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