In vitro and in vivo modulation by rhizoxin of non-P-glycoprotein-mediated vindesine resistance

H Arioka, K Nishio, Y Heike, S Abe, N Saijo - Journal of cancer research …, 1997 - Springer
Rhizoxin is an antineoplastic drug that inhibits tubulin polymerization. In this study, we
demonstrated that rhizoxin was approximately twice as active in vitro against a human small …

Preclinical antitumour activity and animal toxicology studies of rhizoxin, a novel tubulin-interacting agent

HR Hendriks, J Plowman, DP Berger, KD Paull… - Annals of oncology, 1992 - Elsevier
Rhizoxin is a 16-membered antifungal macro-cyclic lactone isolated from the plant
pathogenic fungus Rhizopus chinensis. The compound binds to tubulin, preventing …

Characterisation of a vindesine-resistant human small-cell lung cancer cell line

S Ohta, K Nishio, S Kubo, M Nishio, T Ohmori… - British journal of …, 1993 - nature.com
We established a vindesine-resistant (x 11.6) human small-cell lung cancer cell line
(H69/VDS) by stepwise exposure of parent line H69 to vindesine. H69/VDS showed cross …

Antimicrotubular drugs binding to vinca domain of tubulin

S Gupta, B Bhattacharyya - Molecular and cellular biochemistry, 2003 - Springer
Studies on vinca domain binding drugs were done in great details by a number of workers
as it is recognized as a potential target for anticancer drug development. Their structures …

F-XA7, a novel derivative of vinca alkaloid with potent antitumor activity, efficiently overrides P-glycoprotein-mediated drug resistance both in vitro and in vivo.

H Quan, Y Xu, L Hu, L Lou - Cancer Research, 2013 - AACR
Vinorelbine, a semi-synthetic vinca alkaloid, is widely used for the treatment of non-small
cell lung cancer, metastatic breast cancer and ovarian cancer by inhibiting microtubule …

Assessment of antitumor activity rhizoxin for human lung cancer cell lines: a potent new drug for drug-resistant lung cancer

N Takigawa, T Ohnoshi, H Ueoka… - Gan to Kagaku ryoho …, 1993 - europepmc.org
Rhizoxin is a new macrocyclic lactone isolated from the fungus Rhizopus chinensis. In an
attempt to predict the effectiveness of rhizoxin in the treatment of lung cancer, we compared …

[HTML][HTML] A phase I study of rhizoxin (NSC 332598) by 72-hour continuous intravenous infusion in patients with advanced solid tumors

AW Tolcher, C Aylesworth, J Rizzo, E Izbicka… - Annals of oncology, 2000 - Elsevier
Background Rhizoxin (NSC 332598) is a novel macrolide antitumor antibiotic that inhibits
microtubule assembly and also depolymerizes preformed microtubules. In preclinical …

Antiproliferative effects of halichondrin B analog eribulin mesylate (E7389) against paclitaxel-resistant human cancer cells in vitro

G Kuznetsov, K TenDyke, M Yu, B Littlefield - Molecular Cancer Therapeutics, 2007 - AACR
Abstract C58 Eribulin (E7389, ER-086526, NSC-707389), a structurally-simplified synthetic
analog of the biologically active macrocyclic portion of the marine natural product …

Effects of cytoskeletal inhibitors on the accumulation of vincristine in a resistant human lung cancer cell line with high level of polymerized tubulin.

MW Chan, CD Chiang, EJ Song… - Cancer biochemistry …, 1998 - europepmc.org
We have previously established a vincristine resistant human lung cancer cell line (PC-
9/VCR) by a stepwise exposure of parental line PC-9 to vincristine. In this study the resistant …

Purification and characterization of tubulin from parental and vincristine-resistant HOB1 lymphoma cells

WP Lee - Archives of biochemistry and biophysics, 1995 - Elsevier
A multidrug-resistant lymphoma cell line resistant to 1.0 μM vincristine (designated
HOB1/VCR1. 0) was established. The tubulins of parental and resistant cell Lines mere …