MAC-321, a novel taxane with greater efficacy than paclitaxel and docetaxel in vitro and in vivo

• Published in: Molecular cancer therapeutics 2003-09, Vol.2 (9), p.873
• Main Authors: Sampath, Deepak, Discafani, Carolyn M, Loganzo, Frank, Beyer, Carl, Liu, Hao, Tan, Xingzhi, Musto, Sylvia, Annable, Tami, Gallagher, Patricia, Rios, Carol, Greenberger, Lee M
• Format: Article
• Language: English
• Subjects: Administration, Oral; Animals; Antineoplastic Agents, Phytogenic - pharmacology; ATP Binding Cassette Transporter, Sub-Family B - antagonists & inhibitors; ATP Binding Cassette Transporter, Sub-Family B - metabolism; Cell Division - drug effects; Female; Humans; Inhibitory Concentration 50; Mice; Mice, Nude; Microtubules; Microtubules - drug effects; Multidrug resistance; Neoplasms, Experimental - metabolism; Neoplasms, Experimental - pathology; Oral bioavailability; Paclitaxel - analogs & derivatives; Paclitaxel - pharmacology; Taxane; Taxoids - pharmacology; Tubulin - biosynthesis; Tubulin - drug effects; Tubulin - isolation & purification; Tubulin-targeted agents; Tumor Cells, Cultured
• ISSN: 1535-7163; 1538-8514

The taxanes, paclitaxel (PTX) and docetaxel (DTX), belong to a novel class of anticancer drugs that stabilize microtubules and lead to tumor cell death. While both agents are widely used for the treatment of lung, breast, and ovarian cancer, many tumor types are refractory or develop resistance to these drugs. We describe here a novel analogue of DTX, designated MAC-321 [ M icrotubule/ A poptosis/ C ytotoxic: 5β, 20-epoxy-1, 2α-, 4-, 7β-, 10β-, 13α-hexahydroxytax-11-en-9-one 4 acetate 2 benzoate 7-propionate 13-ester with (2 R ,3 S )- N -tertbutoxycarbonyl-3-(2-furyl)isoserine], that overcomes P-glycoprotein-mediated resistance to PTX and DTX in preclinical model systems. Similar to PTX or DTX, MAC-321 enhanced the rate of tubulin polymerization in vitro and caused the bundling of microtubules in cells. MAC-321 inhibited proliferation of a panel of 14 tumor cell lines with minimal variation in potency (IC 50 = 2.2 ± 1.4 n m ; range = 0.6–5.3 n m ). Unlike PTX or DTX, the IC 50 of MAC-321 did not vary in cells that expressed low to moderate levels of P-glycoprotein. Even under extraordinary conditions in KB-V1 cells, which highly overexpress P-glycoprotein, resistance to MAC-321 was 80-fold compared with that of PTX (1400-fold) and DTX (670-fold). In addition, equivalent or less resistance to MAC-321 compared with PTX or DTX was observed in four cell lines that contain distinct point mutations within the taxane-binding site of β-tubulin. Most importantly, MAC-321 displayed superior in vivo efficacy because: ( a ) MAC-321 either partially or completely inhibited tumor growth in three tumor models that overexpressed P-glycoprotein and were resistant to PTX; and ( b ) unlike PTX or DTX, MAC-321 was highly effective when given orally. MAC-321 was also highly effective when given as single i.v. dose. Our findings suggest that MAC-321, which is currently under clinical evaluation, may have broad therapeutic value.