Carcinoma, Hepatocellular ; therapy ; Chemoembolization, Therapeutic ; Humans ; Liver Neoplasms ; therapy

Carcinoma, Hepatocellular ; therapy ; Drug Delivery Systems ; methods ; trends ; Genetic Therapy ; Humans ; Liver Neoplasms ; therapy ; Receptor, Epidermal Growth Factor ; administration & dosage

Antineoplastic Agents ; therapeutic use ; Carcinoma, Hepatocellular ; pathology ; surgery ; therapy ; Catheter Ablation ; methods ; Chemoembolization, Therapeutic ; Combined Modality Therapy ; Hepatectomy ; methods ; Hepatic Artery ; Humans ; Lung Neoplasms ; pathology ; surgery ; therapy ; Neoplasm Staging ; Radiotherapy, Conformal

Carcinoma, Hepatocellular ; therapy ; Humans ; Liver Neoplasms ; therapy

Combined Modality Therapy ; Humans ; Liver Neoplasms ; therapy

Abstract: Objective To detect the polymorphisms of drug resistance-related genes pvcrt-o and pvmdr1 of Plasmodium vivax in lazan city in the China-Myanmar border, in order to guide the treatment plan of Plasmodium vivax. Methods A total of 48 Plasmodium vivax samples were collected from Lazan in the China-Myanmar border in 2007, and fragments of pvcrt-o and pvmdr1 genes were amplified by PCR and sequenced. The sequences were aligned with the Salvador I (Sal-I) strain reference genome sequences to determine the presence of SNPs. Results The target fragments of pvcrt-o gene were amplified from 39 Plasmodium vivax samples, while pvmdr1 genes were amplified from 40 samples. Amongst them, 25 samples had AAG insertion before the 10th amino acid (K10 insertion) of pvcrt-o gene, accounting for 64.1%. Non-synonymous mutations were detected at three loci of pvmdr1 gene (T958M, Y976F, and F1076L), the mutation rates were 100%, 22.5%, and 55.0%, respectively. There were three haplotypes of pvmdr1 gene, of which the triple mutant 958M/976F/1076L accounted for 22.5% (9/40), the double mutant 958M/Y976/1076L accounted for 32.5% (13/40), and the single mutant 958M/Y976/F1076 accounted for 45.0% (18/40). The proportion of strains with pvcrt-o and pvmdr1 gene mutation is 63.16%, which is significantly different from those only with pvmdr1 mutation. Conclusions The proportion of pvcrt-o and pvmdr1 gene mutation of 48 Plasmodium vivax isolates is high in the China-Myanmar border, and there is a certain degree of correlation between the two gene mutations. To assess changes in Plasmodium vivax drug resistance in this region, it is required to improve the surveillance of these two molecular markers.

Carcinoma, Hepatocellular ; Humans ; Liver Neoplasms

Carcinoma, Hepatocellular ; pathology ; therapy ; Chemoembolization, Therapeutic ; Combined Modality Therapy ; Ethanol ; administration & dosage ; Hepatectomy ; Humans ; Injections, Intralesional ; Liver Neoplasms ; pathology ; therapy

Benzenesulfonates ; therapeutic use ; Biomarkers ; blood ; Carcinoma, Hepatocellular ; diagnosis ; therapy ; Catheter Ablation ; methods ; Chemoembolization, Therapeutic ; Congresses as Topic ; Hepatectomy ; methods ; Hepatic Artery ; Humans ; Liver Transplantation ; Lung Neoplasms ; diagnosis ; therapy ; Neoplasm Staging ; Niacinamide ; analogs & derivatives ; Phenylurea Compounds ; Practice Guidelines as Topic ; Pyridines ; therapeutic use ; Radiotherapy, Conformal ; Ultrasonography ; alpha-Fetoproteins ; analysis

Antineoplastic Agents ; pharmacology ; therapeutic use ; Benzenesulfonates ; pharmacology ; therapeutic use ; Carcinoma, Hepatocellular ; diagnosis ; surgery ; therapy ; Diagnosis, Differential ; Humans ; Liver Neoplasms ; diagnosis ; surgery ; therapy ; Liver Transplantation ; Neoplasm Recurrence, Local ; Neoplasm Staging ; Niacinamide ; analogs & derivatives ; Oligonucleotide Array Sequence Analysis ; Phenylurea Compounds ; Polymerase Chain Reaction ; Pyridines ; pharmacology ; therapeutic use ; Retrospective Studies ; Survival Rate