Association between activated K-ras and c-erbB-2 oncogenes with “high-risk” and “low-risk” Human Papilloma Virus types in preinvasive cervical lesions

2. SILVANA A. MOURÓN, MARTÍN C. ABBA, ALBA GÜERCI, MARÍA A. GÓMEZ, FERNANDO N. DULOUT, CARLOS D. GOLIJOW

MUTATION RESEARCH. GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS

Elsevier Science B.V

Lugar: Leiden. Netherland; Año: 2000 vol. 469 p. 127 - 134

1383-5718

Clinical and epidemiological data have linked cervical cancer to the Human Papiloma Virus (HPV) infection. However, the presence of HPV infection alone is not enough to cause tumorigenesis, suggesting a role for additional host-cell genetic factors. The aim of the present work was to study the association of K-ras and c-erbB-2 mutations in cervical tissue samples with different grades of dysplasia and infected with HPV-6 (“low-risk” type) or HPV-16 and HPV-18 (“high-risk “ types)..Negative HPV-DNA samples were used as controls. The detection of K-ras and c-erbB-2 activation were performed by Artificial Refractory Mutation System (ARMS)-PCR and semiquantitative PCR, respectively. Statistical analysis showed a highly significant difference in  K-ras codon 12 mutation frequency between high-risk and low-risk HPV-infected samples (p < 0,05). On the other hand, amplification of the c-erb-2  oncogene appeared associated to tissue samples infected with HPV-6 (p < 0,003). Cervical carcinoma appears to arise from a series of well-characterized progesive histological changes, but the genetic alterations necessary for cervical tumorigenesis  are not yet clear. These results raise the possibility for a role of certain proto-oncogenes and their activation in cervical neoplasia.