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Mutation analysis of p53, K-ras, and BRAF genes in colorectal cancer progression.
J Cell Physiol. 2005 Aug; 204(2):484-8.JC

Abstract

Gene mutations in APC, K-ras, and p53 are thought to be essential events for colorectal cancer development. Recent data seem to indicate that K-ras and p53 mutations rarely co-exist in the same tumor, indicating that these alterations do not represent a synergistic evolutionary pathway. Moreover, an inverse relation between K-ras gene activation and BRAF mutations has been demonstrated, suggesting alternative pathways for colorectal cancer transformation. To reconstruct the chronological modulation of these gene mutations during cell transformation and colorectal cancer progression, mutations of p53, K-ras, and BRAF genes were analyzed by Single Strand Conformation Polymorphism (SSCP) or sequencing analysis in 100 colorectal cancer samples, evenly distributed among different Dukes' stages. We found mutations in p53, K-ras, and BRAF genes in 35%, 30%, and 4% of tumors, respectively, and observed a minimal or no co-presence of these gene alterations. Moreover, the frequency of molecular p53 mutations increased as tumor stage increased, suggesting an important role for this gene in the progression of colorectal cancer. Conversely, K-ras or BRAF genes were not related to tumor stage or location. These data seem to indicate the absence of a co-presence of the genes, highlighting the possibility of multiple pathways for colorectal tumor progression. Moreover, mutations in p53, K-ras, and BRAF are not present in about one-third of colorectal cancers and therefore other gene mutations need to be investigated to better understand molecular mechanisms at the basis of cell transformation and the progression of colorectal cancer.

Authors+Show Affiliations

Division of Oncology and Diagnostics, Morgagni-Pierantoni Hospital, Forlì, Italy. biomolec@ausl.fo.itNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

15702478

Citation

Calistri, Daniele, et al. "Mutation Analysis of P53, K-ras, and BRAF Genes in Colorectal Cancer Progression." Journal of Cellular Physiology, vol. 204, no. 2, 2005, pp. 484-8.
Calistri D, Rengucci C, Seymour I, et al. Mutation analysis of p53, K-ras, and BRAF genes in colorectal cancer progression. J Cell Physiol. 2005;204(2):484-8.
Calistri, D., Rengucci, C., Seymour, I., Lattuneddu, A., Polifemo, A. M., Monti, F., Saragoni, L., & Amadori, D. (2005). Mutation analysis of p53, K-ras, and BRAF genes in colorectal cancer progression. Journal of Cellular Physiology, 204(2), 484-8.
Calistri D, et al. Mutation Analysis of P53, K-ras, and BRAF Genes in Colorectal Cancer Progression. J Cell Physiol. 2005;204(2):484-8. PubMed PMID: 15702478.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Mutation analysis of p53, K-ras, and BRAF genes in colorectal cancer progression. AU - Calistri,Daniele, AU - Rengucci,Claudia, AU - Seymour,Ian, AU - Lattuneddu,Arturo, AU - Polifemo,Anna Maria, AU - Monti,Franco, AU - Saragoni,Luca, AU - Amadori,Dino, PY - 2005/2/11/pubmed PY - 2005/8/27/medline PY - 2005/2/11/entrez SP - 484 EP - 8 JF - Journal of cellular physiology JO - J. Cell. Physiol. VL - 204 IS - 2 N2 - Gene mutations in APC, K-ras, and p53 are thought to be essential events for colorectal cancer development. Recent data seem to indicate that K-ras and p53 mutations rarely co-exist in the same tumor, indicating that these alterations do not represent a synergistic evolutionary pathway. Moreover, an inverse relation between K-ras gene activation and BRAF mutations has been demonstrated, suggesting alternative pathways for colorectal cancer transformation. To reconstruct the chronological modulation of these gene mutations during cell transformation and colorectal cancer progression, mutations of p53, K-ras, and BRAF genes were analyzed by Single Strand Conformation Polymorphism (SSCP) or sequencing analysis in 100 colorectal cancer samples, evenly distributed among different Dukes' stages. We found mutations in p53, K-ras, and BRAF genes in 35%, 30%, and 4% of tumors, respectively, and observed a minimal or no co-presence of these gene alterations. Moreover, the frequency of molecular p53 mutations increased as tumor stage increased, suggesting an important role for this gene in the progression of colorectal cancer. Conversely, K-ras or BRAF genes were not related to tumor stage or location. These data seem to indicate the absence of a co-presence of the genes, highlighting the possibility of multiple pathways for colorectal tumor progression. Moreover, mutations in p53, K-ras, and BRAF are not present in about one-third of colorectal cancers and therefore other gene mutations need to be investigated to better understand molecular mechanisms at the basis of cell transformation and the progression of colorectal cancer. SN - 0021-9541 UR - https://www.unboundmedicine.com/medline/citation/15702478/Mutation_analysis_of_p53_K_ras_and_BRAF_genes_in_colorectal_cancer_progression_ L2 - https://doi.org/10.1002/jcp.20310 DB - PRIME DP - Unbound Medicine ER -