Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.400 AlteredExpression group BEFREE Expression of FHIT (quick score 98.7 vs. 206.4) and p27 (QS 187.3 vs. 244.8) was significantly lower in carcinomas compared to non-tumor control tissue. 30673867 2019
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.400 Biomarker group BEFREE The mean number of TRGs (<i>FHIT, E-cadherin, MLH1</i>/<i>MSH2</i>, and <i>COX-2</i>) that exhibited reduced or absent expression in LGIN, HGIN/CIS and invasive cancer specimens was 1.12±0.61, 1.66±0.93 and 2.09±0.96, respectively, demonstrating a significant stepwise increment from LGIN to HGIN/CIS and then to invasive cancer (P<0.05). p53 overexpression was frequently detected in ESN with head and neck carcinomas. 28693228 2017
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.400 PosttranslationalModification group BEFREE The fragile histidine triad (FHIT) gene plays an important role in anti-cancer and the abnormal methylation of FHIT gene is found in many carcinomas. 18367246 2008
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.400 AlteredExpression group BEFREE Our results suggest that hypermethylation of the FHIT 5'CpG island may be responsible for inactivation of the FHIT gene in clear cell renal carcinomas. 18378390 2008
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.400 Biomarker group BEFREE The FHIT gene encompassing the most active common human fragile region, FRA3B, has been proposed as a tumour suppressor gene for important common human carcinomas. 16763940 2006
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.400 Biomarker group CTD_human Lung cancer susceptibility in Fhit-deficient mice is increased by Vhl haploinsufficiency. 16061637 2005
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.400 GeneticVariation group BEFREE The fragile histidine triad (FHIT) gene, encompassing the FRA3B fragile site at chromosome 3p14.2, is a candidate tumour suppressor gene involved in a variety of tumours, including gastric carcinomas. 14760383 2004
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.400 PosttranslationalModification group BEFREE Of the 16 cervical carcinomas with 5'-CpG island methylation of the FHIT gene by PCR, 15 showed reduced FHIT protein expression. 14660280 2004
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.400 Biomarker group BEFREE The fragile histidine triad (FHIT) gene is a candidate tumor suppressor gene located at 3p14.2, and the absence or reduction of Fhit protein expression has recently been reported in various carcinomas. 12926121 2003
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.400 GeneticVariation group 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: C0007097
Disease: Carcinoma
Carcinoma
0.400 AlteredExpression group BEFREE Loss of expression of the Fhit protein is often associated with the development of many human epithelial cancers, including lung and cervical carcinomas. 11891319 2002
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.400 Biomarker group BEFREE Poorly differentiated carcinomas showed absent or decreased FHIT. 12090476 2002
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.400 Biomarker group BEFREE Aberration of FHIT gene is associated with increased tumor proliferation and decreased apoptosis-clinical evidence in lung and head and neck carcinomas. 11683369 2001
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.400 GeneticVariation group BEFREE Genomic alterations and abnormal expression of the fragile histidine triad (FHIT) gene in gastric carcinomas were examined to determine whether the FHIT gene is actually a frequent target for alteration during gastric carcinogenesis. 11396980 2001
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.400 GeneticVariation group BEFREE The present study of 67 NSCLCs investigated the allelic imbalance (AIm) within the FHIT locus and its relationship with p53 abnormalities, kinetic parameters [proliferative activity or proliferation index (PI) and apoptotic index (AI)], and ploidy status of the carcinomas. 11169516 2001
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.400 Biomarker group BEFREE These observations are consistent with the observed role of FHIT as a tumor suppressor gene in the pathogenesis of specific subsets of carcinomas. 10717620 2000
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.400 AlteredExpression group BEFREE Loss or impaired expression of the fhit-gene product was detected in 13 of 30 (43%) cervical carcinomas by immunohistochemistry, whereas all 6 normal cervical epithelia, or 22 CINs, expressed fhit protein. 10585575 2000
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.400 AlteredExpression group BEFREE The results confirm that Fhit protein expression is reduced or absent in the majority of cervical carcinomas and suggest that loss of Fhit expression often accompanies cervical tumor progression. 10999736 2000
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.400 GeneticVariation group BEFREE We have analyzed 79 primary cervical carcinomas for allelic imbalance (AI) at 17 chromosome 3 loci, including 3 within the FHIT gene. 11004671 2000
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.400 GeneticVariation group BEFREE In contrast, FHIT alterations were found in the three RER(+) pancreatic carcinomas screened; two had FHIT homozygous deletions affecting exon 5 and the third had a heterozygous missense mutation (H76N). 10679912 2000
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.400 Biomarker group BEFREE We evaluated FHIT gene involvement in 39 esophageal carcinomas (18 adenocarcinomas [AC¿, 21 squamous cell carcinomas [SCC]) by both reverse transcriptase-polymerase chain reaction (RT-PCR) amplification and loss of heterozygosity analysis (LOH). 10812172 2000
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.400 GeneticVariation group BEFREE These findings suggest that LOH of the FHIT gene represents an event in the tumourigenesis of only a small subset of gastric carcinomas and does not correlate with tumour progression or prognosis. 10440747 1999
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.400 AlteredExpression group 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
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.400 Biomarker group BEFREE The 3p14.2 chromosome region, which contains the FHIT gene and the FRA3B fragile site, is frequently altered in carcinomas. 10331745 1999
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.400 GeneticVariation group BEFREE In the group of non-smoking subjects p53 mutations and LOH at the FHIT locus were present in seven (20%) cases, and the two alterations were constantly associated (P < 0.0001), whereas they were not related in the series of carcinomas caused by smoking. 9662254 1998