Premium
Spindle Microtubule Dysfunction and Cancer Predisposition
Author(s) -
Stumpff Jason,
Ghule Prachi N.,
Shimamura Akiko,
Stein Janet L.,
Greenblatt Marc
Publication year - 2014
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.24691
Subject(s) - biology , mitosis , spindle apparatus , microtubule , multipolar spindles , chromosome instability , spindle checkpoint , genome instability , carcinogenesis , chromosome segregation , microbiology and biotechnology , genetics , adenomatous polyposis coli , spindle pole body , cancer , cancer research , microtubule organizing center , cell cycle , cell division , chromosome , cell , gene , centrosome , dna damage , colorectal cancer , dna
Chromosome segregation and spindle microtubule dynamics are strictly coordinated during cell division in order to preserve genomic integrity. Alterations in the genome that affect microtubule stability and spindle assembly during mitosis may contribute to genomic instability and cancer predisposition, but directly testing this potential link poses a significant challenge. Germ‐line mutations in tumor suppressor genes that predispose patients to cancer and alter spindle microtubule dynamics offer unique opportunities to investigate the relationship between spindle dysfunction and carcinogenesis. Mutations in two such tumor suppressors, adenomatous polyposis coli (APC) and Shwachman–Bodian–Diamond syndrome (SBDS), affect multifunctional proteins that have been well characterized for their roles in Wnt signaling and interphase ribosome assembly, respectively. Less understood, however, is how their shared involvement in stabilizing the microtubules that comprise the mitotic spindle contributes to cancer predisposition. Here, we briefly discuss the potential for mutations in APC and SBDS as informative tools for studying the impact of mitotic spindle dysfunction on cellular transformation. J. Cell. Physiol. 229: 1881–1883, 2014. © 2014 Wiley Periodicals, Inc.