PUBLICATION

Unregulated smooth-muscle myosin in human intestinal neoplasia

Authors
Alhopuro, P., Phichith, D., Tuupanen, S., Sammalkorpi, H., Nybondas, M., Saharinen, J., Robinson, J.P., Yang, Z., Chen, L.Q., Orntoft, T., Mecklin, J.P., Järvinen, H., Eng, C., Moeslein, G., Shibata, D., Houlston, R.S., Lucassen, A., Tomlinson, I.P., Launonen, V., Ristimäki, A., Arango, D., Karhu, A., Sweeney, H.L., and Aaltonen, L.A.
ID
ZDB-PUB-080414-9
Date
2008
Source
Proceedings of the National Academy of Sciences of the United States of America   105(14): 5513-5518 (Journal)
Registered Authors
Keywords
none
MeSH Terms
  • Adenomatous Polyposis Coli/genetics
  • Amino Acid Sequence
  • Case-Control Studies
  • Colorectal Neoplasms/genetics
  • DNA Mutational Analysis
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Intestinal Neoplasms/genetics*
  • Molecular Sequence Data
  • Mutation*
  • Myosin Heavy Chains/genetics*
  • Myosin Type II/genetics*
  • Peutz-Jeghers Syndrome/genetics
  • Smooth Muscle Myosins/genetics*
  • Smooth Muscle Myosins/physiology
PubMed
18391202 Full text @ Proc. Natl. Acad. Sci. USA
Abstract
A recent study described a recessive ATPase activating germ-line mutation in smooth-muscle myosin (smmhc/myh11) underlying the zebrafish meltdown (mlt) phenotype. The mlt zebrafish develops intestinal abnormalities reminiscent of human Peutz-Jeghers syndrome (PJS) and juvenile polyposis (JP). To examine the role of MYH11 in human intestinal neoplasia, we searched for MYH11 mutations in patients with colorectal cancer (CRC), PJS and JP. We found somatic protein-elongating frameshift mutations in 55% of CRCs displaying microsatellite instability and in the germ-line of one individual with PJS. Additionally, two somatic missense mutations were found in one microsatellite stable CRC. These two missense mutations, R501L and K1044N, and the frameshift mutations were functionally evaluated. All mutations resulted in unregulated molecules displaying constitutive motor activity, similar to the mutant myosin underlying mlt. Thus, MYH11 mutations appear to contribute also to human intestinal neoplasia. Unregulated MYH11 may affect the cellular energy balance or disturb cell lineage decisions in tumor progenitor cells. These data challenge our view on MYH11 as a passive differentiation marker functioning in muscle contraction and add to our understanding of intestinal neoplasia.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping