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Total aglycones from Marsdenia tenacissima increases antitumor efficacy of paclitaxel in nude mice.

Abstract
Marsdeniae tenacissimae Caulis (MTC) is a Chinese herbal medicine used mainly for treatment of cancer, whose pharmacologically active constituents responsible for its in vivo activity and clinical efficacy have not been clearly elucidated. In this study, total aglycones of MTC (ETA) showed the ability to sensitize KB-3-1, HeLa, HepG2 and K562 cells to paclitaxel treatment. More inspiringly, ETA markedly enhanced the antitumor activity of paclitaxel in nude mice bearing HeLa or KB-3-1 xenografts. Compared to treatment with paclitaxel alone, treatment with combination of paclitaxel and ETA achieved significant reduction in volume and weight of HeLa tumors (p<0.05), and remarkable inhibition to the growth of KB-3-1 tumors (p<10⁻⁶). ETA was characterized by the presence of a group of tenacigenin B ester derivatives, among which four reference compounds, 11α-O-tigloyl-12β-O-acetyltenacigenin B, 11α,12β-di-O-tigloyltenacigenin B, 11α-O-2-methylbutanoyl-12β-O-tigloyltenacigenin B, and 11α-O-(2-methylbutanoyl)-12β-O-benzoyltenacigenin B, accounted for 42.14% of the total peak area of 19 detectable components assayed by HPLC. Our study has identified ETA as a promising sensitizer for cancer chemotherapy.
AuthorsRui-Jing Zhu, Xiao-Ling Shen, Ling-Lin Dai, Xiang-Ying Ai, Ru-Hua Tian, Rong Tang, Ying-Jie Hu
JournalMolecules (Basel, Switzerland) (Molecules) Vol. 19 Issue 9 Pg. 13965-75 (Sep 05 2014) ISSN: 1420-3049 [Electronic] Switzerland
PMID25197933 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antineoplastic Agents, Phytogenic
  • Drugs, Chinese Herbal
  • Paclitaxel
Topics
  • Animals
  • Antineoplastic Agents, Phytogenic (pharmacology)
  • Cell Line, Tumor
  • Cell Survival (drug effects)
  • Drug Synergism
  • Drugs, Chinese Herbal (pharmacology)
  • Female
  • Humans
  • Marsdenia (chemistry)
  • Mice, Inbred BALB C
  • Mice, Nude
  • Paclitaxel (pharmacology)
  • Tumor Burden (drug effects)
  • Xenograft Model Antitumor Assays

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