• BMB Reports
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• 제52권4호
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• pp.277-282
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• 2019

Currently speaking, it is noted that radiofrequency ablation (RFA) has been the most widely used treatment for hepatocellular carcinoma (HCC) occurring in patients. However, accumulating evidence has demonstrated that the incidence of insufficient RFA (IRFA) may result in the identified rapid progression of residual HCC in the patient, which can greatly hinder the effectiveness and patient reported benefits of utilizing this technique. Although many efforts have been proposed, the underlying mechanisms triggering the rapid progression of residual HCC after IRFA have not yet been fully clarified through current research literature reviews. It was shown in this study that cell proliferation, migration and invasion of residual HepG2 and SMMC7721 cells were significantly increased after the IRFA was simulated in vitro. In other words, it is noted that IRFA could do this by enhancing the image of autophagy of the residual HCC cell via the $HIF-1{\alpha}/BNIP3$ pathway. Consequently, the down-regulation of BNIP3 may result in the inhibition of the residual HCC cell progression and autophagy after IRFA. Our present study results suggest that IRFA could promote residual HCC cell progression in vitro by enhancing autophagy via the $HIF-1{\alpha}/BNIP3$ pathway. For this reason, it is noted that the targeting of the BNIP3 may be useful in preventing the rapid growth and metastasis of residual HCC after IRFA.

• Asian Pacific Journal of Cancer Prevention
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• 제13권12호
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• pp.6217-6220
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• 2012

Introduction: Up to present, EGF $61^*A$/G, TGF-${\beta}1$-$509^*T$/C and TNF-${\alpha}$-$308^*A$/G gene polymorphisms have been analysed in other cancer entities than hepatocellular carcinoma (HCC). We here investigated the frequency of these gene polymorphisms among HCC patients. Materials and Methods: A total of 73 HCC patients and 117 cancer-free healthy people were recruited at the Surgical Department of Zhongshan Hospital. Genomic DNA was isolated from peripheral blood and gene polymorphisms were analyzed by PCR-RFLP. Results: The distribution of EGF $61^*G$/G homozygotes among HCC patients was more frequent than that in the control group (24.7% vs 11.1%, OR=2.618, 95%CI=1.195-5.738). In parallel, the frequency of the "G" allele in the HCC patient group was also higher than that in the control group (45.9% vs 33.3%, OR= 1.696, 95%CI=1.110-2.592). No difference could be found for the TGF-${\beta}1$-509 and TNF-${\alpha}$-308 genotypes. Conclusion: EGF $61^*G$/G genotype and G allele are significantly increased among patients with HCC. TGF-${\beta}1$-$509^*T$/C and TNF-${\alpha}$-$308^*A$/G gene polymorphisms are not related to this cancer entity.

• Journal of Preventive Medicine and Public Health
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• 제30권1호
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• pp.1-15
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• 1997

To investigate the association between hepatocellular carcinema(HCC) and infection of hepatitis B virus(HBV) and hepatitis C virus(HCV) in an HBV endemic area, a case-control study of 254 patients with HCC and of 1,270 age and sex matched health control subjects was done. Among the 254 HCC patients 166(65.4%) were positive for hepatitis B surface antigen(HBsAg), 49(19.3%) were positive for HCV antibody (anti-HCV Ab). The crude odd ratio of patients with HBsAg was 36.1(95% CI :22.4-58.2) and with anti-HCV Ab was 9.0(95% CI :5.5-14.6). In an analysis, which HBsAg(-), HBcAb(-), anti-HCV Ab(-) group was chosen as referent group, odd ratio of HBsAg(+) group was 14.4(95% CI: 7.2-28.9) and of anti- HCV Ab(+) was 10.7(95% CI: 2.9-40.0). odd ratio of anti-HCV Ab(+), HBsAg(+) group and anti-HCV Ab(+), HBsAg(-), HbcAb(+) group for HCC were elevated to 27.3(95% CI : 9.0-82.9), 15.9(95% CI:7.1-35.8) respectly, The odd ratio of anti-HCV Ab(-), HBsAg(-), HBcAb(+) group was 2.4(95% CI : 1.1-5.0). These result suggested that HBV and HCV were associated with HCC. In HBV endemic area patients with HBcAb alone should be considered risk group for HCC.

• Journal of Digestive Cancer Research
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• 제5권1호
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• pp.5-15
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• 2017

Hepatocellular carcinoma (HCC) is the sixth most common cancer and second leading cause of cancer-related death in the world. The aggressive but not always predictable pattern of HCC causes the limited treatment option and poorer outcome. Many researches had already proven the heterogeneity of HCC is one of the major challenges for treatment option and prognosis prediction. Molecular subtyping of HCC and selection of patient based on molecular profile can provide the optimization in the treatment and prognosis prediction. In this review, we have tried to summarize the molecular classification of HCC proposed by different valuable researches presented in the logistic way.

• 대한핵의학회지
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• 제29권4호
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• pp.484-491
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• 1995

간세포암의 원발병소와 전이병소의 간담도 신티그램 소견을 비교 분석하여 서로 다른 경로에 의한 전이병소에서 신티그램 소견의 차이를 알아보고 전이병소와 원발병소에서 방사능 집적빈도와 출현시간의 상호관계를 규명하고자 하였다. 간세포암으로 진단된 환자 9명의 간외 전이 12예를 대상으로 하였고 전이병소 12예는 폐전이 4예, 골 전이 1예, 우심방 전이 1예, 복벽 전이 1예, 복강 및 후복강 임파절 전이 5예였다. 간담도 신티그램은 $^{99m}Tc-DISIDA$ 370MBq를 주사한 후 10분, 30분, 1시간, 2시간과 4-6시간 지연연상을 얻었다. 그 결과는 다음과 같았다. 1) 간세포암 원발병소 9예중 4예(44%) 전이병소 12예중 5예(42%)에서 방사능집적을 관찰하였고 이중 혈행성전이 5예중 3예(60%}, 직접전이는 2예 모두에서 방사능 집적을 볼 수 있었지만 임파절 전이의 경우 5예 모두에서 방사능 직접이 없었다. 2) 혈행성 전이인 폐 전이가 있었던 4예에서는 원발병소 3예와 전이 병소 3예에서 방사능 집적이 있었고 원발병소는 모두 2시간부터, 전이병소 중 2예는 1시간, 나머지 2시간부터 방사능이 직접되었다. 이중 2예는 원발과 전이병소가 함께 양성으로 나타났는데 모두 원발병소에 비해 전이병소에서 먼저 방사능 직접을 볼 수 있었지만 전이병소에는 직접이 없었다. 3) 직접 전이인 우심방과 복벽 전이는 같은 환자에게서 함께 발생했는데 원발과 전이병소에는 모두 30분 영상에서부터 방사능 직접을 관찰하였다. 4) 임파전이가 있었던 5예 중 원발병소 1에서만 방사능 집적이 있었지만 나머지 4예의 원발병소와 전이병소 5예 전부에서는 방사능 집적이 없었다. 이상의 결과로 간담도 신티그램상 혈행성이나 직접전이병소는 임파 전이병소보다 방사능 집적이 잘 되고 원발과 전이병소가 함께 집적이 잘되고 원발과 전이병소가 함께 전이가 집적되는 경향이 있으며 원발병소에 비해 혈행성이나 직접전이 병소에서 방사능 직접율이 높고, 더 빨리 집적됨을 관찰할 수 있었다. 따라서 간담도신티그래프는 간세포암의 원발성병소보다 혈행성이나 직접 전이병소의 진단에 더 유용하게 사용 될 수 있으며 특히 간세포암 전이의 진단이 애매한 경우에는 특이도를 높힐 수 있는 검사 방법이라고 생각된다.

• Asian Pacific Journal of Cancer Prevention
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• 제15권11호
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• pp.4545-4548
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• 2014

Objective: To investigate the changes of serum vascular endothelial growth factor (VEGF), soluble interleukin-2 receptor (SIL-2R) and hepatocyte growth factor (HGF) contents in patients with primary hepatocellular carcinoma (HCC) before and after percutaneous microwave coagulation therapy (PMCT) and determine their clinical significance. Materials and Methods: Fasting venous blood (3 mL) from 81 patients with primary HCC diagnosed by pathology was collected in the mornings 1 day before PMCT, and 1 day, 7 days and 1 month after PMCT, and then the serum was separated and stored in $-70^{\circ}C$. The contents of VEGF, SIL-2R and HGF were detected by enzyme linked immunosorbent assay (ELISA). Results: The serum VEGF, SIL-2R and HGF contents in 81 patients with primary HCC had obviously dynamic changes before and after PMCT. By comparison to 1 day after PMCT with pre-operation, there was no statistical significance regarding VEGF and SIL-2R contents (P>0.05), but HGF content showed significant difference (P<0.01). Compared with pre-operation, VEGF, SIL-2R and HGF contents 7 days and 1 month after PMCT all manifested significant differences (P<0.01). By comparison to 7 days with 1 month after PMCT, there was no statistical significance regarding the VEGF content (P>0.05), whereas SIL-2R and HGF contents showed significant change (P<0.01). Conclusions: The contents of serum VEGF, SIL-2R and HGF have obviously dynamic changes in primary HCC before and after PMCT, and their joint detection is expected to be an effective hematologic evaluation index of PMCT for primary HCC.

• Asian Pacific Journal of Cancer Prevention
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• 제15권17호
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• pp.7069-7077
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• 2014

Background: This retrospective study aimed to validate the safety and effectiveness of hepatectomy for huge hepatocellular carcinoma (HCC). Materials and Methods: Data of patients who underwent hepatectomy for HCC between January 2006 and December 2012 were reviewed. The patients were divided into three groups: huge HCC(${\geq}10cm$ in diameter), large HCC(${\geq}5$ but<10 cm in diameter) and small HCC(<5cm in diameter). Results: Characteristics of pre-operative patients in all three groups were homogeneously distributed except for alpha fetal protein (AFP)(p<0.001).The 30, 60, 90-day post-operative mortality rates were not different among the three groups (p=0.785, p=0.560, and p=0.549). Laboratory data at 1, 3, and 7 days after surgery also did not vary. The 5-year overall survival (OS) and 5-year disease-free survival (DFS) rates in the huge and large HCC groups were lower than that of the small HCC group (OS: 32.5% vs 36.3% vs 71.2%, p=0.000; DFS: 20.0% vs 24.8% vs 40.7%, p=0.039), but there was no difference between the huge and large HCC groups (OS: 32.5% vs 36.3%, p=0.667; DFS: 20.0% vs 24.8%, p=0.540). In multivariate analysis, five independent poor prognostic factors that affected OS were significantly associated with worse survival (p<0.05), namely, AFP level, macrovascular invasion, Edmondsone Steiner grade, surgical margin and Ishak score. AFP level, macrovascular invasion, microvascular invasion, and surgical margin influenced disease-free survival independently (p<0.05). Conclusions: The safety of hepatectomy for huge HCC is similar to that for large and small HCC; and this approach for huge HCC may achieve similar long-term survival and disease-free survival as for large HCC.

• Asian Pacific Journal of Cancer Prevention
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• 제17권5호
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• pp.2539-2543
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• 2016

Background: In the Barcelona Clinic Liver Cancer (BCLC) system, only sorafenib is suggested for HCC patients having performance status (PS) 1 or 2 even if they have treatable lesions. In the current study, we aimed to explore the outcome of using aggressive treatment for HCC patients with PS 1 and 2. Materials and Methods: Five hundred and twenty four patients with HCC were enrolled in this study and divided into 2 groups: 404 PS 1 and 120 PS 2. Of the included 524 patients, 136 recceived non-aggressive supportive treatment and sorafenib, while 388 patients were offered aggressive treatment in the form of surgical resection, transplantation, percutaneous ablation, trans-arterial chemoembolization and/or chemoperfusion. All the patients were followed up for a period of 2 years to determine their survival. Results: Most HCC patients were CHILD A and B grades (89.4% versus 85.0%, for PS1 and PS2, respectively). Patients with PS1 were significantly younger. Out of the enrolled 524 patients, 388 were offered aggressive treatment, 253 (65.2%) having their lesions fully ablated, 94 (24.2%) undergoing partial ablation and 41 patients with no ablation (10.6%). The median survival of the patients with PS 1 who were offered aggressive treatment was 20 months versus 9 months only for those who were offered supportive treatment and sorafenib (p<0.001). Regarding HCC patients with PS 2, the median survivals were similarly 19.7 months versus 8.7 months only (p<0.001). Conclusions: Aggressive treatment of HCC patients with PS 1 and 2 significantly improves their survival. Revising the BCLC guidelines regarding such patients is recommended.

• 한국의학물리학회지:의학물리
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• 제17권4호
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• pp.246-251
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• 2006

본 연구의 목적은 전신 PET/CT영상에서 조영제의 영향에 대한 보정 유 무가 SUV (standard uptake value)에 미치는 영향을 평가하는 것이었다. 영상획득은 GE DSTe PET/CT 시스템을 사용하였으며, 간질환(hepatocellular carcinoma, HCC)과 신장질환(renal cell carcinoma, RCC)이 있는 환자를 대상으로 하여 영상을 평가하였다. 영상 평가는 조영제에 의한 영향을 보정한 영상과 보정하지 않은 영상에서 각각 동일한 위치에 같은 크기의 관심영역을 설정한 후 각 관심영역으로부터 구한 SUV를 비교함으로써 수행하였다. HCC 환자의 경우 조영제에 의한 영향의 보정 유 무에 따른 평균 SUV의 차이는 $1.5{\pm}1.2%$이었고, 최대 4.3%의 SUV 차이를 나타내었다. RCC 환자의 경우 평균 SUV의 차이는 $1.0{\pm}0.9%$이었고, 최대 1.9%의 SUV 차이를 나타내었다. 조영제를 사용한 PET/CT 영상에서 조영제에 의한 영향을 보정하지 않았을 경우는 조영제에 의한 영향을 보정해준 경우에 비해 상대적으로 높은 SUV를 나타내었다. 본 연구의 결과는 HCC 환자와 RCC 환자의 경우 조영제에 의한 영향을 보정한 경우와 보정하지 않은 경우 SUV에 큰 차이를 보이지는 않았으나, 향후 보다 많은 수의 HCC 환자와 RCC 환자를 대상으로 한 추가적인 연구가 필요할 것이라고 생각한다. 또한 다른 질환을 가진 환자의 경우에 대해서도 조영제가 SUV에 미치는 영향을 평가하는 것은 매우 유용하리라 생각한다.

• BMB Reports
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• 제45권11호
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• pp.629-634
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• 2012

The human glycoprotein, stanniocalcin 2 (STC2) plays multiple roles in several tumor types, however, its function and clinical significance in hepatocellular carcinoma (HCC) remain unclear. In this study, we detected STC2 expression by quantitative real-time PCR and found STC2 was upregulated in HCC tissues, correlated with tumor size and multiplicity of HCC. Ectopic expression of STC2 markedly promoted HCC cell proliferation and colony formation, while silencing of endogenous STC2 resulted in a reduced cell growth by cell cycle delay in G0/G1 phase. Western blot analysis demonstrated that STC2 could regulate the expression of cyclin D1 and activate extracellular signal-regulated kinase 1/2 (ERK1/2) in a dominant-positive manner. Transwell chamber assay also indicated altered patterns of STC2 expression had an important effect on cell migration. Our findings suggest that STC2 functions as a potential oncoprotein in the development and progression of HCC as well as a promising molecular target for HCC therapy.