scholarly journals EpCAM- and/or NCAM-Expressing Hepatocellular Carcinoma in Which Behavior of Hepatic Progenitor Cell Marker-Positive Cells Are Followed

2019 ◽  
Vol 13 (1) ◽  
pp. 118-124 ◽  
Author(s):  
Atsunori Tsuchiya ◽  
Takeshi Suda ◽  
Chiyumi Oda ◽  
Atsushi Kimura ◽  
Kazunori Hosaka ◽  
...  

Hepatic progenitor cell (HPC) marker-positive hepatocellular carcinomas (HCCs) have recently been extensively analyzed, and their prognosis has been reported as poor compared to HPC marker-negative HCCs. However, previous studies have analyzed the existence of HPC marker-positive cancer cells only in primary lesions, as well as the recurrence rate and prognosis of such tumors. Here, we are the first to report the behavior of HPC marker-positive cancer cells during vascular invasion and metastasis of an HCC. We concurrently analyzed EpCAM- and/or NCAM-expressing cancer cells in the primary, vascular invasion, and metastatic lesions of an HCC. An HCC which includes EpCAM- and/or NCAM-expressing cancer cells has not been previously reported. EpCAM- and/or NCAM-positive cancer cells invaded the vessels and formed heterogeneous populations of these HPC marker-positive cancer cells with HPC marker-negative cancer cells. The frequency of HPC marker-positive cancer colonies and cells in vessels was higher than that in the primary HCC. In the metastatic lesions, EpCAM-positive cancer cells were more frequently detected than NCAM-positive cancer cells, indicating that EpCAM may be more important than NCAM for cancer cell settlement in the metastatic lesions. Furthermore, bigger metastatic tumors tended to include HPC marker-positive cancer cells, suggesting that HPC marker-positive cancer cells have a growth advantage in the metastatic lesions. These results showed that HPC marker-positive cancer cells would be important for vascular invasion and metastasis and suggested that HPC marker-positive cancer cells are an important target in HCC treatment.

2015 ◽  
Vol 62 ◽  
pp. S431-S432
Author(s):  
A. Tsuchiya ◽  
Y. Kojima ◽  
S. Seino ◽  
Y. Watanabe ◽  
M. Nomoto ◽  
...  

Author(s):  
Bo Lin ◽  
Xu Dong ◽  
Qiujiao Wang ◽  
Wei Li ◽  
Mingyue Zhu ◽  
...  

Alpha fetoprotein (AFP) plays a key role in stimulating the growth, metastasis and drug resistance of hepatocellular carcinoma (HCC). AFP is an important target molecule in the treatment of HCC. The application of AFP-derived peptides, AFP fragments and recombinant AFP (AFP-inhibiting fragments, AIFs) to inhibit the binding of AFP to intracellular proteins or its receptors is the basis of a new strategy for the treatment of HCC and other cancers. In addition, AIFs can be combined with drugs and delivery agents to target treatments to cancer. AIFs conjugated to anticancer drugs not only destroy cancer cells with these drugs but also activate immune cells to kill cancer cells. Furthermore, AIF delivery of drugs relieves immunosuppression and enhances chemotherapy effects. The synergism of immunotherapy and targeted chemotherapy is expected to play an important role in enhancing the treatment effect of patients with cancer. AIF delivery of drugs will be an available strategy for the targeted treatment of cancer in the future.


PLoS ONE ◽  
2015 ◽  
Vol 10 (3) ◽  
pp. e0122528 ◽  
Author(s):  
Yu-Wen Huang ◽  
Chien-Chang Chiu ◽  
Ja-Der Liang ◽  
Ling-Ling Chiou ◽  
Guan-Tarn Huang ◽  
...  

2005 ◽  
Vol 22 (5) ◽  
pp. 364-370 ◽  
Author(s):  
Takatsugu Yamamoto ◽  
Takahiro Uenishi ◽  
Masao Ogawa ◽  
Tsuyoshi Ichikawa ◽  
Seikan Hai ◽  
...  

2018 ◽  
Vol 47 (6) ◽  
pp. 2340-2349 ◽  
Author(s):  
Chuan-Zhong Huang ◽  
Ai-Min Huang ◽  
Jing-Feng Liu ◽  
Bin Wang ◽  
Ke-Can Lin ◽  
...  

Background/Aims: Hepatocellular carcinoma (HCC) is a major threat to human health. The condition carries a high risk of death; 45% of new cases occur in China. Surgical resection is the first choice for treatment of HCC, but 30.9% of patients experience recurrence within 6 months after the operation. To improve patient survival, we must determine how to reduce the probability of recurrence and metastasis and elucidate the underlying mechanism of disease. We therefore studied the effect of somatostatin octapeptide (octreotide) on the invasion and metastasis of HCC. Methods: The migration and invasion cytological tests were used to detect the effect of octreotide on liver cancer cells (SK-Hep-1 and HepG2). PEBP1 RNAi was used to knockdown expression. Invasion and metastasis were measured with transwell migration and wound-healing assays. Western blotting was used to detect changes in levels of PEBP1 and invasion pathway proteins after octreotide treatment. The effect of octreotide was studied in vivo by establishing a pulmonary metastasis model using SK-Hep-1 cells in nude mice. In-vivo bioluminescence imaging and hematoxylin and eosin staining of lung tissue were used to verify the results. Results: Increasing concentrations of octreotide were progressively more effective in halting the invasion and metastasis of liver cancer cells. Octreotide may upregulate PEBP1, TIMP-2, and E-cadherin while downregulating MMP-2 and Twist to inhibit cell invasion and metastasis. And downregulation of PEBP1 would also change the expression of MMP-2, TIMP-2 and Twist. The in-vivo experiments showed no cancer cell metastasis in 4 of the 6 mice in the octreotide-treatment group, while all of the mice in the control group displayed pulmonary metastasis of human HCC cells. And the survival period of the mice in the octreotide-treatment group was significantly prolonged. Conclusions: Octreotide may weaken invasion and metastasis through the upregulation of PEBP1. Octreotide may reduce the risk of recurrence and metastasis after surgery for liver cancer.


2011 ◽  
Vol 309 (1) ◽  
pp. 95-103 ◽  
Author(s):  
Atsunori Tsuchiya ◽  
Hiroteru Kamimura ◽  
Yasushi Tamura ◽  
Masaaki Takamura ◽  
Satoshi Yamagiwa ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document