Antibody-DM1 conjugates as cancer therapeutics.

Manu Lopus

Department of Molecular, Cellular, and Developmental Biology, and the Neuroscience Research Institute, University of California, Santa Barbara, CA 93106, USA.

Journal Article: Cancer letters (impact factor: 3.74). 08/2011; 307(2):113-8. DOI: 10.1016/j.canlet.2011.03.017

Abstract

Synthetic derivatives of the microtubule-targeted agent maytansine, commonly known as drug maytansinoids or DMs, are emerging as potential cancer therapeutics. DM1 is an antibody-conjugatable maytansinoid that was developed to overcome systemic toxicity associated with maytansine and to enhance tumor-specific delivery. Antibody-DM1 conjugates showed promising results in preclinical and clinical evaluations. However, the molecular mechanism of the drug component DM1 was largely unknown. Recently, researchers have examined the mechanism of DM1 at molecular and cellular levels. According to their findings, DM1 binds at the tips of microtubules and suppresses the dynamicity of microtubules. The antibody-DM1 conjugate cleaves inside cells and releases the active drug in a time-dependent manner. The suppression of microtubule dynamics by DM1 induces mitotic arrest and cell death.

Source: PubMed

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Keywords

active drug
 
antibody-DM1 conjugate cleaves
 
Antibody-DM1 conjugates
 
cell death
 
cellular levels
 
clinical evaluations
 
DM1 induces mitotic arrest
 
drug maytansinoids
 
microtubule dynamics
 
molecular
 
molecular mechanism
 
potential cancer therapeutics
 
preclinical
 
promising results
 
releases
 
suppresses
 
systemic toxicity
 
time-dependent manner
 
tumor-specific delivery