| http://purl.uniprot.org/citations/35364781 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
| http://purl.uniprot.org/citations/35364781 | http://www.w3.org/2000/01/rdf-schema#comment | "Hepatocellular carcinoma (HCC) remains a significant health problem with a substantial genetic predisposition. The liver harbors the largest proportion of macrophages among all the solid organs. There is considerable controversy regarding the relationship between the macrophage receptor with collagenous structure (MARCO) and tumor development and progression. Accordingly, we performed this case-control study to determine whether associations exist between the MARCO single nucleotide polymorphism rs6761637 and HCC susceptibility and clinical characteristics. We successfully genotyped 586 HCC cases and 647 controls using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. The overall genotype distribution of rs6761637 was similar in the HCC and control groups (P = 0.143). However, the CT + CC genotypes of rs6761637 were slightly more common in the HCC group among female (P = 0.021), overweight (body mass index ≥ 24 kg/m2, P = 0.003), and nonsmoking (P = 0.022) individuals. The minor C allele carriers had a 1.47-fold increased risk of developing large tumor nodules (P = 0.041). rs6761637 did not affect the recurrence-free or overall survival rate of patients with HCC (P = 0.247 and 0.304, respectively). In conclusion, this is the first report of the association between MARCO genetic variations and HCC risk. These results suggest that the MARCO rs6761637 polymorphism may play a regulatory role in HCC carcinogenesis, but it does not seem to predict prognosis."xsd:string |
| http://purl.uniprot.org/citations/35364781 | http://purl.org/dc/terms/identifier | "doi:10.1007/s12026-022-09271-2"xsd:string |
| http://purl.uniprot.org/citations/35364781 | http://purl.uniprot.org/core/author | "Liu F."xsd:string |
| http://purl.uniprot.org/citations/35364781 | http://purl.uniprot.org/core/author | "Luo L."xsd:string |
| http://purl.uniprot.org/citations/35364781 | http://purl.uniprot.org/core/author | "Su Z."xsd:string |
| http://purl.uniprot.org/citations/35364781 | http://purl.uniprot.org/core/author | "Wang L."xsd:string |
| http://purl.uniprot.org/citations/35364781 | http://purl.uniprot.org/core/author | "Wu X."xsd:string |
| http://purl.uniprot.org/citations/35364781 | http://purl.uniprot.org/core/author | "Wei B."xsd:string |
| http://purl.uniprot.org/citations/35364781 | http://purl.uniprot.org/core/author | "Cai B."xsd:string |
| http://purl.uniprot.org/citations/35364781 | http://purl.uniprot.org/core/date | "2022"xsd:gYear |
| http://purl.uniprot.org/citations/35364781 | http://purl.uniprot.org/core/name | "Immunol Res"xsd:string |
| http://purl.uniprot.org/citations/35364781 | http://purl.uniprot.org/core/pages | "400-407"xsd:string |
| http://purl.uniprot.org/citations/35364781 | http://purl.uniprot.org/core/title | "Association of the MARCO polymorphism rs6761637 with hepatocellular carcinoma susceptibility and clinical characteristics."xsd:string |
| http://purl.uniprot.org/citations/35364781 | http://purl.uniprot.org/core/volume | "70"xsd:string |
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