Toosendanin Affects the Occurrence and Development of Prostate Carcinoma Cells DU145 by Regulating Forkhead Box C2-Antisense RNA 1

2021 ◽  
Vol 11 (3) ◽  
pp. 533-540
Author(s):  
Siyao Shen ◽  
Junhui Xiong ◽  
Zhigang Zeng ◽  
Hong Zhao ◽  
Xiaochun Zeng ◽  
...  

Prostate carcinoma is a common malignant tumor of the male genitourinary system. Toosendanin can inhibit the biological behavior of a variety of malignant tumor cells (such as ovarian carcinoma, lung carcinoma, and breast carcinoma, etc.), but its effect on the malignant behavior of prostate carcinoma cells and its mechanism are not yet understood. Therefore, this article discusses the influence of toosendanin on the multiplication, apoptosis, migration, and invasion of prostate carcinoma cells and its possible mechanism. Different doses (0.125, 0.25, 0.5 ^M) of toosendanin can reduce the cell viability, number of colonies, number of migrating cells, number of invasive cells, and Bcl-2 protein and FOXC2-AS1 levels of prostate carcinoma cells, as well as increase the apoptosis rate and Bax protein level. Overexpression of FOXC2-AS1 can increase the cell viability, number of colonies formed, number of migrating cells, number of invasive cells, and Bcl-2 protein expression, as well as reduce the rate of apoptosis and Bax protein level after toosendanin treatment of prostate carcinoma cells. It was demonstrated that toosendanin may inhibit the multiplication, migration, and invasion of prostate carcinoma cells and promote its apoptosis by down-regulating FOXC2-AS1 expression.

2008 ◽  
Vol 2008 ◽  
pp. 1-8 ◽  
Author(s):  
Dayanand D. Deo ◽  
Ashwin P. Rao ◽  
Saideep S. Bose ◽  
Allal Ouhtit ◽  
Surendra B. Baliga ◽  
...  

Obesity has been linked with an increased risk of prostate cancer. The formation of toxic free oxygen radicals has been implicated in obesity mediated disease processes. Leptin is one of the major cytokines produced by adipocytes and controls body weight homeostasis through food intake and energy expenditure. The rationale of the study was to determine the impact of leptin on the metastatic potential of androgen-sensitive (LNCaP) cells as well as androgen-insensitive (PC-3 and DU-145) cells. At a concentration of 200_nm, LNCaP cells showed a significant increase (20% above control;P<.0001) in cellular proliferation without any effect on androgen-insensitive cells. Furthermore, exposure to leptin caused a significant (P<.01toP<.0001) dose-dependent decrease in migration and invasion of PC3 and Du-145 prostate carcinoma cell lines. At the molecular level, exposure of androgen-independent prostate cancer cells to leptin stimulates the phosphorylation of MAPK at early time point as well as the transcription factor STAT3, suggesting the activation of the intracellular signaling cascade upon leptin binding to its cognate receptor. Taken together, these results suggest that leptin mediates theinvasivepotential of prostate carcinoma cells, and that this effect is dependent on their androgen sensitivity.


2014 ◽  
Vol 2014 ◽  
pp. 1-16 ◽  
Author(s):  
Georgios Chondrogiannis ◽  
Michalis Kastamoulas ◽  
Panagiotis Kanavaros ◽  
Georgios Vartholomatos ◽  
Maria Bai ◽  
...  

We analyzed the effects of IL-13, IFN-γ, and IL-1βon cell viability and death of LNCaP and PC-3 cells and major signaling pathways involved in these effects. Significant increase of LNCaP cell death (apoptotic and necrotic) and increased levels of active caspase 3 were observed in cells treated with inhibitors of ERK 1/2 (UO126) and p38 (SB203580) prior to IL-1βtreatment in comparison to cells treated with UO126, SB203580, or IL-1βalone. Significant increase of LNCaP but not PC-3 cell death was detected after treatment with LY-294002 (inhibitor of phosphatidylinositol 3-kinase). No significant increase of LNCaP and PC-3 cell death was observed after treatment with SP600125 (inhibitor of JNK), SB203580 (inhibitor of p38), UO126 (inhibitor of ERK 1/2), or BAY 11-7082 (inhibitor of NF-κB). Reduced c-FLIPLexpression was observed in LNCaP cells treated with LY-294002. The significant potentiation of LNCaP cell death by inhibition of ERK 1/2, p38, and PI3-K pathways may provide a rationale for therapeutic approach in androgen-dependent prostate cancer.


2019 ◽  
Author(s):  
Chuanjia Yang ◽  
Siyang Zhang ◽  
Xiaoying Chang ◽  
Yonglian Huang ◽  
Dongxu Cui ◽  
...  

Abstract Background Heparanase (HPSE) is an endo-β-D-glucuronidase, which is found overexpressed in various human cancers. The purpose of our work was to investigate the possible role of HPSE and the involved signaling molecules in the development of papillary thyroid carcinoma. Methods In this study, the expression plasmid of HPSE and RNA interference with shRNA specific for HPSE were used to elucidate the effects of HPSE on proliferation, apoptosis, migration and invasion in papillary thyroid carcinoma cells of B-CPAP. The probable downstream signaling molecules of HPSE were also explored. Results The results showed that upregulation of HPSE significantly promoted cell proliferation, migration and invasion of B-CPAP cells, and interfered with cell apoptosis. On the contrary, knockdown of HPSE exhibited the opposite effects. Compared with the parental cells, HPSE silencing cells showed attenuated capabilities of proliferation, migration and invasion, yet the apoptotic rate of transfected cells was increased. The activations of various signaling molecules correlated with cell biological behavior were found to be regulated by HPSE upregulation or knockdown. Conclusions Our results suggested that HPSE probably contributed to the progression and metastasis of papillary thyroid carcinoma, which were associated with multiple signaling pathways. HPSE could be a potent molecular target for the therapeutic strategy of papillary thyroid carcinoma.


2018 ◽  
Vol 8 (11) ◽  
pp. 531 ◽  
Author(s):  
Alexandra Zambrano ◽  
Rosa Raybaudi-Massilia ◽  
Francisco Arvelo ◽  
Felipe Sojo

Background:  There are many kinds of tropical fruit available in Venezuela. Two of these fruits are the focus of our study: blackberry (“mora”) and soursop (“guanábana”). These fruits have extraordinary bioactive components. For example, blackberry has antioxidant compounds such as anthocyanins, which are characteristic of the Rosaceae family. Acetogenins present in the Annonaceae family have been shown to possess cytotoxic properties that act against different types of tumor cells. In previous research, we have discovered how lyophilized soursop pulp has an elevated cytotoxic effect with a IC50 of 7.1940±1.06 in human cervix carcinoma cells (HeLa) and 0.8460±1.29 in human prostate carcinoma cells (PC3).Objective: This study focused on the health benefits and properties of the soursop and the blackberry. Our main focus was to determine the antioxidant and cytotoxic properties in a formulated beverage based on blackberry, soursop, and yogurt containing probiotics and prebiotics.Methods: The research includes the study of soursop pulp (SP), blackberry pulp (BP), and two formulations of the functional beverage selected through a sensorial analysis, F2 (BP + SP + Yogurt + Truvía® + Sacarose) and F3 (BP + SP + Yogurt + Truvía® + Sacarose + Sodium tripolyphosphate). Cell viability of prostate carcinoma cells (PC3), breast carcinoma without over-expression of the HER2/c-erb-2 gene (MCF-7), breast carcinoma in which the HER2/c-erb-2 gene is over-expressed (SKBr3) and healthy cells of human connective tissue used as control (Fibroblasts).  The previous indicated samples were assessed using MTT (3- (4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide). The antioxidant activity of the functional beverage was also done using a freshly preparation of 1,1-diphenyl-2-picrylhydrazyl (DPPH). Results: The BP demonstrated the highest cytotoxicity for both lines of breast cancer cell lines, MCF-7 and SKBR3. The values of the minimum concentration required to inhibit 50 % of the cell population (IC50) was 0.12 ± 1.10 and 1.81 ± 1.68% v / v respectively, followed by SP in MCF-7 and PC3 with values of 1.40 ± 1.03 and 1.34 ± 1.06 respectively. At the same time, the effectiveness of the formulations used found that 3.60 ± 1.04% v / v of F2 beverage was necessary to achieve 50 % inhibition of cell viability of MCF-7 line. For the formulation F3, it was necessary to use a concentration of 5.21 ± 1.04% v / v for that tumor cell line. However, the F2 and F3 formulations demonstrated IC50 values of 3.69 ± 1.08% v / v and 2.50 ± 1.08% v / v respectively for the PC3 cell line. On the other hand, the antioxidant capacity of BP and SP reached elevated values at 30 minutes of exposure to DPPH, obtaining a rate of 85.28 ± 0.11 and 80.94 ± 0.07 % respectively by using a concentration of 12.5 %, F2 and F3 formulations also reached values of 83.97 ± 0.46 and 85.62 ± 0.11 % at 100 % concentration of both drinks respectively.Conclusion: We discovered that the cytotoxic activity of both formulations prepared as well as the pulps were fairly good, revealing highly effective consequences for the inactivation of breast tumor cells MCF-7 and prostate tumor cells PC3. Moreover, BP and SP demonstrated a high antioxidant activity, with a synergistic effect accomplished by the mixture on F2 and F3.Keywords: Functional beverage, cytotoxic, antioxidant, soursop, blackberry, yogurt.


2021 ◽  
Vol 11 (9) ◽  
pp. 1730-1736
Author(s):  
Jinxiao Li ◽  
Xiaoping Chi ◽  
Jinyu Yan ◽  
Qian Yang ◽  
Jun Wu

The clinical prognosis of endometrial cancer is poor. We assessed the influence of IL-17 and FGF2 on HEC-1B cells to provide evidence for the clinical prevention and treatment. HEC-1B cells were assigned into control group, IL-17 group, FGF2 group, and IL-17+FGF2 group followed by analysis of cell viability, IL-17 and FGF2 protein and mRNA content by Western Blot and RT-PCR. Under co-culture, the cell viability, migration and invasion and FGF2 level in IL-17 group, FGF2 group, and IL-17+FGF2 group were found to be significantly higher than those in control Group (P <0.05), but the apoptosis rate was significantly lower than control group. The above changes were more significant in IL-17+ FGF2 group compared to other three groups (P < 0.05). IL-17 and FGF2 treatment in HEC-1B cells can significantly promote the viability, migration and invasion of malignant tumor cells with more significant changes in the IL-17+FGF2 intervention group, suggesting these two have a synergistic effect. In conclusion, IL-17 and FGF2 exerts synergistic effect on promoting endometrial cancer cell migration and invasion, indicating that they might be novel targets for the treatment of endometrial cancer.


2020 ◽  
Vol 34 (7) ◽  
pp. 1629-1637 ◽  
Author(s):  
Zhifeng Han ◽  
Jingzhe Zhang ◽  
Kun Zhang ◽  
Yinghao Zhao

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