Tissue Engineering Scaffolds Loaded With a Variety of Plant Extracts: Novel Model in Breast Cancer Therapy.

Despite recent improvements in detecting and managing breast cancer (BC), it continues to be a major worldwide health concern that annually affects millions of people. Exploring the anti-BC potentials of natural compounds has received a lot of scientific attention due to their multi-target mode of action and good safety profiles because of these unmet needs. Drugs made from herbs are secure and have a lot fewer negative effects than those made from synthetic materials. Early stage patients benefit from breast-conserving surgery, but the risk of local recurrence remains, necessitating implanted scaffolds. These scaffolds provide residual cancer cell killing and tailored drug delivery. This review looks at plant extract-infused tissue engineering scaffolds, which provide a novel approach to treating BC. By offering patient individualized, safer treatments, these scaffolds could completely change how BC is treated.

The effect of Scrophularia striata on cell attachment and biocompatibility of decellularized bovine pericardia.

Since using tissue transplantation has faced limitations all over the world, regenerative medicine has introduced decellularized tissues as natural scaffolds and researchers are trying to improve their efficiency and function. In this study, to increase cell attachment and ultimately cell proliferation on decellularized bovine pericardia, scrophularia striata extract was used. Scrophularia striata is an Iranian traditional medicinal plant. For this aim after decellularization of bovine pericardium and analysis of its morphology, it was incubated in scrophularia striata solution. Next, isolated human adipose-derived mesenchymal stem cells were cultured on the tissue. Finally, MTT assay, nitric oxide assay, and scanning electron microscopy observation were performed. MTT showed an increase in cell survival after treating the tissue with the plant extract after 48 h in a dose dependent manner significantly. The survival of cells in 0.5%, 2.5%, and 5% groups was about 5, 10 and 15 folds higher in comparison to control groups, respectively. Additionally, nitric oxide secretion in 2.5% and 5% samples was three and five folds higher than that in control group, respectively. Moreover, SEM observation indicated an impressive and dose-dependent effect of using Scrophularia striata on tissue biocompatibility. The results of this study showed that using Scrophularia striata increased cell viability and cell attachment on decellularized pericardia which could pave the way for the use of natural extracts of medicinal plants to reduce unwanted effects and make desired changes in decellularized tissues.

Phosphate-solubilizing bacteria and silicon synergistically augment phosphorus (P) uptake by wheat (Triticum aestivum L.) plant fertilized with soluble or insoluble P source.

Phosphorus (P) deficiency is one of the major problems in agricultural soils for crop production around the world. Use of silicon (Si) and phosphate-solubilizing bacteria (PSB) is known as one of the most effective and economical ways for increasing P availability and improving P use efficiency under low P conditions. However, little is known about the alleviative role of Si and PSB together in mitigating P-deficiency stress and in improving P use efficiency in Triticum aestivum L. (wheat), as one of the most important crop plants worldwide. Consequently, aim of the research was to study the combined and single effects of Si (0, 150, 300, and 600 mg kg-1 added as silicic acid) and PSB (B0, Bacillus simplex UT1, and Pseudomonas sp. FA1) on P uptake by wheat plant fertilized with soluble or insoluble P (Esfordi rock phosphate, RP) in a completely randomized design with factorial arrangement through a perlite potted experiment. In addition, the effects of various treatments on wheat shoot and root dry weight, activity of catalase, superoxide dismutase, and peroxidase enzymes, and the uptake of Si and potassium (K) by this plant were also investigated. Both shoot and root biomass of wheat plants were markedly reduced when grown in RP-fertilized medium compared with those grown in soluble P-fertilized medium. The PSB strains and Si levels independently improved all the aforementioned parameters. Application of Si to wheat plants grown in soluble P or insoluble P medium markedly enhanced P use efficiency. According to the results of this study, Si not only increased the uptake of P from sparingly soluble-P source (RP), but also enhanced uptake of P from water-soluble P source. Both Pseudomonas sp. FA1 and B. simplex UT1 showed a considerable role in improvement of root and shoot biomass and uptake of P (and K and Si) under both soluble and insoluble P fertilization conditions with Pseudomonas sp. FA1 being more effective than B. simplex UT1. However, the combined application of the PSB with Si resulted in the greatest enhancement in wheat plant P uptake and other measured parameters. Addition of 600 mg Si kg-1 and Pseudomonas sp. FA1 significantly increased the P shoot concentration of wheat plant fertilized with RP to an adequate level (>0.3%) in the range of P-fertilized plants. Therefore, in addition to PSB application, Si should be considered as soil amendment in agricultural soils deficient in plant available Si as a means of sustainable agriculture with respect to possible savings of scarce P resources (P-fertilizers). The information on the availability of P following PSB and Si addition to plant growth medium may help in better management of P fertilization.

In vitro inhibitory effect of crab shell extract on human umbilical vein endothelial cell.

Angiogenesis plays an important role in the tissue repair, rheumatoid arthritis, retinopathies, and growth and metastasis of cancer. Endothelial cell proliferation has been introduced as a model of angiogenesis. Crab sell was suggested for cancer treatment in traditional medicine. The aim of the present study was to investigate the in vitro effect of crab shell hydroethanolic extract on the human umbilical vein endothelial cell (HUVEC) proliferation. Crab sell extract was prepared and the effect of its various concentrations (0, 100, 200, 400, 800, 1000 µg/ml) on HUVECs were surveyed in three periods of 24, 48 and 72 h. HUVEC viability, Nitric oxide (NO) secretion and apoptosis were assessed by MTT, Griess and Tunnel methods, respectively. Data were compared by one-way ANOVA. In this study we found HUVECs viability was reduced in dose and time depended manner significantly and HUVECs NO production decreased significantly, too. Apoptosis index was increased significantly. These findings reveal that high concentrations of crab shell extract have anti-proliferative effects on HUVECs and can be used for cancer treatment.

Antiproliferatory Effects of Crab Shell Extract on Breast Cancer Cell Line (MCF7).

PURPOSE: Breast cancer is the most common type of cancer in women. Despite various pharmacological developments, the identification of new therapies is still required for treating breast cancer. Crab is often recommended as a traditional medicine for cancer. This study aimed to determine the in vitro effect of a hydroalcoholic crab shell extract on a breast cancer cell line. METHODS: In this experimental study, MCF7 breast cancer cell line was used. Crab shell was powdered and a hydroalcoholic (70° ethanol) extract was prepared. Five concentrations (100, 200, 400, 800, and 1,000 µg/mL) were added to the cells for three periods, 24, 48, and 72 hours. The viability of the cells were evaluated using trypan blue and 3-(4, 5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assays. Cell apoptosis was determined using the terminal deoxynucleotidyl transferase dUTP nick end labeling method. Nitric oxide (NO) level was assessed using the Griess method. Data were analyzed using analysis of variance, and p<0.05 was considered significant. RESULTS: Cell viability decreased depending on dose and time, and was significantly different in the groups that were treated with 400, 800, and 1,000 µg/mL doses compared to that in the control group (p<0.001). Increasing the dose significantly increased apoptosis (p<0.001). NO secretion from MCF7 cells significantly decreased in response to different concentrations of the extract in a dose- and time-dependent manner (p<0.050). CONCLUSION: The crab shell extract inhibited the proliferation of MCF7 cells by increasing apoptosis and decreasing NO production.