320 Simultaneous hyperthermic-chemotherapy using a single anti-cancer compound with magnetism in glioblastoma animal model

2015 ◽  
Vol 51 ◽  
pp. S61
Author(s):  
M. Ohtake ◽  
M. Umemura ◽  
I. Sato ◽  
K. Oda ◽  
A. Nagasako ◽  
...  
Blood ◽  
2011 ◽  
Vol 118 (21) ◽  
pp. 4879-4879
Author(s):  
Myoung Woo Lee ◽  
Hye Jin Kim ◽  
Dae Seong Kim ◽  
Meong Hi Son ◽  
Soo Hyun Lee ◽  
...  

Abstract Abstract 4879 Background. A hematological malignant animal model is an essential tool for evaluating efficacy of anti-cancer drugs and elucidating underlying mechanism of leukemogenesis. Intraperitoneal (IP) and intravenous (IV) xenograft of acute lymphoblastic leukemia (ALL) cells have limited capacity as in vivo anti-cancer drug screening system. Purpose. In this study, we aimed to establish an ALL animal model using NOD/SCID mouse and evaluate efficiency and sensitivity of the model as a preclinical drug screening system. Materials and Methods. Firefly luciferase (fLuc)-gene introduced ALL (ALL/fLuc) cell line and patient-originated ALL cells were transplanted into a tibia of NOD/SCID mouse. We conducted a comparative analysis of intra-bone marrow (IBMT) transplanted leukemia model with IP and IV transplantation of leukemic cells. Results. IBMT of ALL/fLuc cells effectively established a bioluminescent leukemia NOD/SCID mouse model. Upon comparison of IBMT model with IP and IV transplantation models, infusing identical number of ALL/fLuc cells into NOD/SCID mice resulted in IBMT model with evaluable bioluminescent signal, but not in IP and IV models. In IBMT model, bioluminescent signals of ALL/fLuc cells emitted from peripheral blood, tibia and infiltrated organs indicated that leukemia model was established. The changes in these signals' strength reflected dose-dependent cytotoxic effects of vincristine, which allowed leukemia model with evaluable bioluminescent signal to be utilized as a preclinical drug screening system. IBMT leukemia model was also established using primary ALL cells that can provide additional insights for the development of leukemia therapeutics. Conclusion. IBMT of ALL/fLuc cells enables development of leukemia mouse model with the greater bioluminescent sensitivity than IP and IV in NOD/SCID to evaluate candidate for development of anti-cancer drug. Disclosures: No relevant conflicts of interest to declare.


2016 ◽  
Vol 1 (1) ◽  
Author(s):  
Kenta Shinozaki ◽  
Tetsuo Ajiki ◽  
Sae Murakami ◽  
Taku Matsumoto ◽  
Masayuki Akita ◽  
...  

<p>Biliary tract cancer still has a poor prognosis with approximately 8,000 cases reported annually in USA. The most promising therapy for the patients with BTC is surgical resection. Chemotherapy is also significant to improve the prognosis, but the available chemotherapeutic agents and anti-cancer effects are limited so far. Thus, novel anti-cancer drugs and regimens are urgent issue. We established a novel cell line from human intraductal papillary neoplasm of the bile duct, which is a novel biliary tract malignant entity. We also developed an orthotopic engraft model by inoculating human gallbladder cancer cells into nude mice. In this review, we summarized characteristics of a novel cell line and an animal model of human BTC.</p>


2020 ◽  
Vol 41 (10) ◽  
pp. 1385-1394
Author(s):  
Priyanka Sharma ◽  
Tadanobu Shimura ◽  
Jasjit K Banwait ◽  
Ajay Goel

Abstract Colorectal cancer (CRC) remains one of the leading causes of cancer-related mortality in the USA. As much as 50–60% of CRC patients develop resistance to 5-fluorouracil (5FU)-based chemotherapeutic regimens, attributing the increased overall morbidity and mortality. In view of the growing evidence that active principles in various naturally occurring botanicals can facilitate chemosensitization in cancer cells, herein, we undertook a comprehensive effort in interrogating the activity of one such botanical—andrographis—by analyzing its activity in CRC cell lines [both sensitive and 5FU resistant (5FUR)], a xenograft animal model and patient-derived tumor organoids. We observed that combined treatment with andrographis was synergistic and resulted in a significant and dose-dependent increase in the efficacy of 5FU in HCT116 and SW480 5FUR cells (P &lt; 0.05), reduced clonogenic formation (P &lt; 0.01) and increased rates of caspase-9-mediated apoptosis (P &lt; 0.05). The genomewide expression analysis in cell lines led us to uncover that activation of ferroptosis and suppression of β-catenin/Wnt-signaling pathways were the key mediators for the anti-cancer and chemosensitizing effects of andrographis. Subsequently, we validated our findings in a xenograft animal model, as well as two independent CRC patient-derived organoids—which confirmed that combined treatment with andrographis was significantly more effective than 5FU and andrographis alone and that these effects were in part orchestrated through dysregulated expression of key genes (including HMOX1, GCLC, GCLM and TCF7L2) within the ferroptosis and Wnt-signaling pathways. Collectively, our data highlight that andrographis might offer a safe and inexpensive adjunctive therapeutic option in the management of CRC patients.


2016 ◽  
Vol 25 (2) ◽  
pp. 132-139 ◽  
Author(s):  
Binna Oh ◽  
Hojung Song ◽  
Dahee Lee ◽  
Jungju Oh ◽  
Gyeungyun Kim ◽  
...  

2020 ◽  
Vol 31 (8) ◽  
pp. 785-791 ◽  
Author(s):  
Chao Yang ◽  
Feng Li ◽  
Jianbin Ma ◽  
Hai-Bao Zhang ◽  
Jing Jia ◽  
...  

Author(s):  
Modje Kazemi ◽  
Abdollah Jafarzadeh ◽  
Maryam Nemati ◽  
Fereshteh Taghipour ◽  
Omolbanin Oladpour ◽  
...  

Abstract Objectives The potent anti-tumorigenic effects were attributed to ginger and there are some reports regarding the anti-cancer and immunomodulatory properties ginger-derived components. This study aimed to investigate the effects of zingerone on some immune-related parameters in an animal model of breast cancer. Methods The breast cancer was established in female BALB/c mice using a carcinogenic 4T1 cell line. At day 10 after cancer induction, tumor-bearing mice were divided into five groups and treated intraperitoneal (daily from days 11–30) with saline or zingerone (at doses 10, 20, 50 and 100 mg/kg/day). The mice were sacrificed on day 31 and the number of splenic Th1- and Treg cells, the expression of IFN-γ and TGF-β in the blood mononuclear cells, the antibody production against sheep red blood cell (SRBC) were determined using flow cytometry, real time-PCR and a standard hemagglutination assay, respectively. Results Zingerone at doses 50 and 100 mg/kg enhanced the number of splenic Th1 cells (p<0.03 and 0.007, respectively); at doses 10, 20, 50 and 100 mg/kg reduced the number of splenic Treg cells (p<0.02, 0.01, and 0.01, respectively), at doses 50 and 100 mg/kg enhanced the expression of IFN-γ (p<0.03), at doses 50 and 100 mg/kg reduced the expression of TGF-β, at doses 50 mg/kg reduced the titer of anti-SRBC antibody (p<0.05). Conclusions Zingerone improve the T cell-mediated and antibody responses in a mouse model of breast cancer. The immunotherapeutic potentials of zingerone in cancers need more considerations.


2021 ◽  
Author(s):  
Vidya Devanathadesikan Seshadri

Abstract Melanoma is an extremely malignant skin cancer with a probability of metastasis and accountable for the mainstream skin associated mortality. In the present study, we described the novel usage of Stachytarpheta cayennensis mediated copper nanoparticles and its anti-cancer activity in both in vitro and in vivo model of skin cancer. The synthesis of Cu-NPs was confirmed using UV-absorbance peak values ranging from 325-345 nm. The size of the nanoparticles was around 90nm, as deduced by the dynamic light scattering study.Furthermore, transmission electron microscopy (TEM) established that the morphology of the copper particles. Cytotoxicity of Cu-NPs of Stachytarpheta cayennensis illustrates the toxicity level of Stachytarpheta cayennensis. Also, the anti-cancer potential of Cu-NPs was evaluated in A375 cells. In experimental animals, body biochemical parameters like SOD, CAT, GSH were diminished in DMBA induced animals while Cu-NPs treatment raised the levels of the aforementioned enzymatic antioxidants compared to the control animals. Additionally, cytotoxicity assay, mitochondrial membrane potential (MMP), cell adhesion analysis, and the estimation of reactive oxygen species (ROS) in the presence of Cu-NPs was evaluated by standard protocols. The present study's outcomes confirm the defensive and valuable effects of copper loaded Stachytarpheta cayennensis against DMBA induced skin melanoma, animal model.


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