@article {12375,
	title = {K- Mutations as the Earliest Driving Force in a Subset of Colorectal Carcinomas.},
	journal = {In Vivo},
	volume = {31},
	year = {2017},
	month = {2017 Jul-Aug},
	pages = {527-542},
	abstract = {K-ras oncogene is a key factor in colorectal cancer. Based on published and our data we propose that K-ras could be the oncogene responsible for the inactivation of the tumor-suppressor gene APC, currently considered as the initial step in colorectal tumorigenesis. K-ras fulfills the criteria of the oncogene-induced DNA damage model, as it can provoke well-established causes for inactivating tumor-suppressors, i.e. DNA double-strand breaks (causing allele deletion) and ROS production (responsible for point mutation). The model we propose is a variation of the currently existing model and hypothesizes that, in a subgroup of colorectal carcinomas, K-ras mutation may precede APC inactivation, representing the earliest driving force and, probably, an early biomarker of colorectal carcinogenesis. This observation is clinically useful, since it may modify the preventive colorectal cancer strategy, restricting numerically patients undergoing colonoscopies to those bearing K-ras mutation in their colorectum, either in benign polyps or the normal accompanying mucosa.},
	keywords = {Adenomatous Polyposis Coli Protein, Cell Transformation, Neoplastic, Colon, Colorectal Neoplasms, DNA Breaks, Double-Stranded, Humans, Mutation, Proto-Oncogene Proteins p21(ras), Reactive Oxygen Species},
	issn = {1791-7549},
	doi = {10.21873/invivo.11091},
	author = {Margetis, Nikolaos and Kouloukoussa, Myrsini and Pavlou, Kyriaki and Vrakas, Spyridon and Mariolis-Sapsakos, Theodoros}
}
