Identification of candidate oncogenes in human colorectal cancers with microsatellite instability

56Citations
Citations of this article
89Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Microsatellite instability can be found in approximately 15% of all colorectal cancers. To detect new oncogenes we sequenced the exomes of 25 colorectal tumors and respective healthy colon tissue. Potential mutation hot spots were confirmed in 15 genes; ADAR, DCAF12L2, GLT1D1, ITGA7, MAP1B, MRGPRX4, PSRC1, RANBP2, RPS6KL1, SNCAIP, TCEAL6, TUBB6, WBP5, VEGFB, and ZBTB2; these were validated in 86 tumors with microsatellite instability. ZBTB2, RANBP2, and PSRC1 also were found to contain hot spot mutations in the validation set. The form of ZBTB2 associated with colorectal cancer increased cell proliferation. The mutation hot spots might be used to develop personalized tumor profiling and therapy. © 2013 by the AGA Institute.

Cite

CITATION STYLE

APA

Gylfe, A. E., Kondelin, J., Turunen, M., Ristolainen, H., Katainen, R., Pitkänen, E., … Aaltonen, L. A. (2013). Identification of candidate oncogenes in human colorectal cancers with microsatellite instability. Gastroenterology, 145(3). https://doi.org/10.1053/j.gastro.2013.05.015

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free