|
Cervix carcinoma
|
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 |
|
Cervix carcinoma
|
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 |
|
Cervix carcinoma
|
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 |
|
Cervix carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
This is the first study indicating a correlation between the promoter methylation of FHIT and RASSF1A genes and the clinical stage and histological grading of cervical carcinoma in Indian women.
|
18608185 |
2008 |
|
Cervix carcinoma
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
Regulation of DNA methylation on the expression of the FHIT gene contributes to cervical carcinoma cell tumorigenesis.
|
16865265 |
2006 |
|
Cervix carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
The effect of codon 98 of the FHIT gene on cervical cancer in Korean women.
|
14675322 |
2004 |
|
Cervix carcinoma
|
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 |
|
Cervix carcinoma
|
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 |
|
Cervix carcinoma
|
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 |
|
Cervix carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
Human papillomaviruses (HPVs) are the major cause of cervical carcinoma and have been found to be able to integrate its genes into the chromosome 3 fragile site of cultured cells, deleting a piece of DNA which includes the FHIT gene.
|
12355215 |
2002 |
|
Cervix carcinoma
|
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 |
|
Cervix carcinoma
|
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 |
|
Cervix carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
The FHIT gene is a candidate tumor suppressor gene that has been implicated in the development of cervical carcinoma.
|
11389064 |
2001 |
|
Cervix carcinoma
|
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 |
|
Cervix carcinoma
|
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 |
|
Cervix carcinoma
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
There was a strong association of impaired fhit protein expression with the disruption of normal fhit transcript in cervical carcinoma.
|
10585575 |
2000 |
|
Cervix carcinoma
|
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 |
|
Cervix carcinoma
|
0.100 |
PosttranslationalModification
|
disease |
BEFREE |
These data indicate that the aberrant expression of the FHIT gene is observed in precursor lesions of cervical carcinoma as well as invasive carcinomas, with its incidence not increasing with advance of clinical stage.
|
10027335 |
1999 |
|
Cervix carcinoma
|
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 |
|
Cervix carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
To our knowledge, this is the first report of HDs encompassing the FHIT gene region in primary tumor samples and underscores the usefulness of high resolution genetic analysis of tumor genomes in determining the chromosomal aberrations underlying the malignant progression of CC.
|
9307297 |
1997 |
|
Cervix carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
To study the molecular abnormalities involved in the multistage development of cervical carcinoma (CC), we investigated the presence of oncogenic human papillomavirus (HPV) sequences, loss of heterozygosity (LOH), and microsatellite alterations at several genes/loci at 3p (3p14.2 at the FHIT gene, 3p14.3-21.1, 3p21, and 3p22-24.2), 9p21, RB and P53, and P53 gene point mutations in precisely microdissected archival tissues from 20 CCs and their accompanying precursor lesions (cervical intraepithelial neoplasia, CIN; n = 40) and normal epithelia (n = 20).
|
9242443 |
1997 |
|
Cervix carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
We further show that an area of frequent gaps and breaks within FRA3B, defined by a lambda contig, coincides with a previously characterized site of HPV16 integration in a primary cervical carcinoma.
|
8824874 |
1996 |