Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.100 PosttranslationalModification disease BEFREE There was more FHIT promoter methylation in cervical cancer than in cervical intraepithelial neoplasia lesions and normal controls (odds ratio = 8.0, p = 0.055; odds ratio = 10.75, p < 0.001, respectively). 28639889 2017
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.100 AlteredExpression disease BEFREE Thus, WWOX may be considered as a novel important genetic marker in cervical cancer and the association between the altered expression of FHIT and WWOX may be a critical event in the progression of this neoplasia. 19700237 2010
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.100 GeneticVariation disease BEFREE Therefore, we made an attempt to find out point mutation of FHIT gene in HPV mediated cervical cancer in Indian women. 19730990 2010
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.100 GeneticVariation disease BEFREE Effect of aberrant promoter methylation of FHIT and RASSF1A genes on susceptibility to cervical cancer in a North Indian population. 18608185 2008
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.100 Biomarker disease BEFREE The purpose of this study was to determine the effect of the FHIT gene on tumorigenesis of cervical cancer. 16865265 2006
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.100 GeneticVariation disease BEFREE The effect of codon 98 of the FHIT gene on cervical cancer in Korean women. 14675322 2004
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.100 Biomarker disease BEFREE We analysed the expression of the fragile histidine triad (FHIT) gene in cervical cancer to evaluate its clinical relevance in relation to human papillomavirus (HPV) infection. 12698186 2003
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.100 GeneticVariation disease BEFREE In this study we investigated FHIT (Fragile Histidine Triad) protein alterations in cervical carcinomas to assess the relation of this gene with cervical cancer. 12657123 2003
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.100 Biomarker disease BEFREE Our findings suggest an association between HPV infection and FHIT gene abnormalities raising the possibility of a mechanistic role for the FHIT gene as a cofactor with HPV in triggering the development of cervical cancer. 12144820 2002
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.100 AlteredExpression disease BEFREE FRA3B is the most frequently expressed common fragile site localized within human chromosomal band 3p14.2, which is frequently deleted in many different cancers, including cervical cancer. 12483524 2002
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.100 GeneticVariation disease BEFREE Our findings suggest essential roles of genes on these 3p loci, particularly the FHIT gene in participating in clonal selection and early development of cervical cancer. 11235906 2001
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.100 AlteredExpression disease BEFREE These findings demonstrate that truncated FHIT transcripts are commonly detected in both normal and tumor tissues, and suggest that these altered transcripts are not causally related to tumorigenesis in cervical cancer. 11498789 2001
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.100 AlteredExpression disease BEFREE The candidate tumor suppressor gene FHIT has been mapped to 3p14.2, and previous studies have demonstrated reduced or aberrant FHIT transcripts and reduced or absent Fhit protein expression in a large percentage of cervical cancer-derived cell lines and primary cervical carcinomas. 10999736 2000
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.100 GeneticVariation disease BEFREE The finding of a statistically significant relationship between FHIT gene LOH and oncogenic HPV infection suggests a link between the integration of viral DNA and subsequent gene deletion in the progression of cervical cancer. 11113868 2000
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.100 GeneticVariation disease BEFREE Our data indicate that alteration of the FHIT gene is an important genetic event associated with cervical cancer and oncogenic 9537577 1998