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Plastic is considered one of the most indispensable commodities in our daily life. At the end of life, the huge ever-growing pile of plastic waste (PW) causes serious concerns for our environment, including agricultural farmlands, groundwater quality, marine and land ecosystems, food toxicity and human health hazards. Lack of proper infrastructure, financial backup, and technological advancement turn this hazardous waste plastic management into a serious threat to developing countries, especially for Bangladesh. A comprehensive review of PW generation and its consequences on environment in both global and Bangladesh contexts is presented. The dispersion routes of PW from different sources in different forms (microplastic, macroplastic, nanoplastic) and its adverse effect on agriculture, marine life and terrestrial ecosystems are illustrated in this work. The key challenges to mitigate PW pollution and tackle down the climate change issue is discussed in this work. Moreover, way forward toward the design and implementation of proper PW management strategies are highlighted in this study.
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This study was conducted to assess the accumulation and sources of harmful metals and associated public health risk from the usage of underground mine water of Barapukuria coal mine in Bangladesh, keeping in mind the optimum reuse. Thirty underground mine water samples had been analyzed for assessing temperature, pH, EC, TC, DO, BOD, COD, Ca, K, S, Ti, Mn, V, Fe, Co, Ni, Cu, Zn, Br, Rb, Sr, and Pb. Numerous pollution evaluation and health risk assessment indices along with multivariate statistical tools were employed in this study to apprise the pollution scenario, controlling factors, and probable health risk. The chronic or persistent health risk of metals via oral and dermal exposure of adults and children was determined using the hazard quotient (HQ) and hazard index (HI). The results showed that the content of physicochemical parameters and potentially harmful elements in water samples was many folds higher than the national and international standards. The results of pollution evaluation indices indicate that coal seam-leached mine water is highly concentrated by potentially harmful metals and not suitable for drinking, agriculture, and aquatic lives. The correlation coefficients and multivariate analysis illustrate both the geological and anthropogenic factors controlling the variability of metals in mine water. Results of HQoral value suggest that V, Co, and Pb are significant health risk for adults and Mn, V, Co, Cu, and Pb are for children. Vanadium is found potential for dermal effects, and HIdermal value directs 33%, and 70% samples exceed the safe limit for adults and children, respectively. The HI value suggests that oral exposure to harmful metals creates more harm than dermal absorption, and children are more vulnerable than adults. It is anticipated that the outcomes of this study would deliver expedient insights to initiate necessary steps to minimize the public health risk by applying appropriate environmental protocols.
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Metais Pesados , Adulto , Bangladesh , Criança , Carvão Mineral/análise , Monitoramento Ambiental , Humanos , Metais Pesados/análise , Saúde Pública , Medição de Risco , ÁguaRESUMO
Rapid urbanization and industrial growth have triggered heavy metal contamination in agricultural soil in Dhaka, which is a serious concern for ecological risk and public health issues. In this study, fifty-four soil samples from agricultural lands of Dhaka had been analyzed for assessing accumulation, spatial enrichment, ecological risk and sources apportionment of heavy metals using a combined approach of self-organizing map (SOM), positive matrix factorization (PMF), geographical information system (GIS), and enrichment factor (EF). The results of the enrichment factor, geoaccumulation index and contamination factor index showed that more than 90% of the soil samples were polluted by higher levels of Cr and Cd. The mean pollution load index (PLI) results demonstrated that about 73% of soil samples were moderately polluted by heavy metals. Based on SOM and PMF analysis, four potential sources of heavy metals were found in this study area: (i) agrochemical and sewage irrigation (Cd-As); (ii) combined effect of agriculture, industrial and natural sources (Mn, Co, Ni and Zn); (iii) atmospheric deposition and industrial emission (As-Pb); (iv) chemical and leather tanning industries (Cr). The ecological risk index demonstrated that in terms of Cd content, about 75% of soil samples were moderate to high risk, and 20% were moderate to considerable ecological risk, which was the serious environmental, ecological, and public health concern. The spatial projection of ecological risk values showed that the southern part of Dhaka (Keraniganj Upazila) is a high ecological risk in terms of heavy metal pollution. These risk maps in agricultural soils may play a vital role in reducing pollution sources; so that zonal pollution control, as well as ecological protection, may be achieved in this resource-based agricultural land.
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Metais Pesados , Poluentes do Solo , Agricultura , Bangladesh , China , Monitoramento Ambiental , Sistemas de Informação Geográfica , Metais Pesados/análise , Medição de Risco , Solo , Poluentes do Solo/análiseRESUMO
In embryonic development and throughout life, there are some cells can exhibit phenotypic plasticity. Phenotypic plasticity is the ability of cells to differentiate into multiple lineages. In normal development, plasticity is highly regulated whereas cancer cells re-activate this dynamic ability for their own progression. The re-activation of these mechanisms enables cancer cells to acquire a cancer stem cell (CSC) phenotype- a subpopulation of cells with increased ability to survive in a hostile environment and resist therapeutic insults. There are several contributors fuel CSC plasticity in different stages of disease progression such as a complex network of tumour stroma, epidermal microenvironment and different sub-compartments within tumour. These factors play a key role in the transformation of tumour cells from a stable condition to a progressive state. In addition, flexibility in the metabolic state of CSCs helps in disease progression. Moreover, epigenetic changes such as chromatin, DNA methylation could stimulate the phenotypic change of CSCs. Development of resistance to therapy due to highly plastic behaviour of CSCs is a major cause of treatment failure in cancers. However, recent studies explored that plasticity can also expose the weaknesses in CSCs, thereby could be utilized for future therapeutic development. Therefore, in this review, we discuss how cancer cells acquire the plasticity, especially the role of the normal developmental process, tumour microenvironment, and epigenetic changes in the development of plasticity. We further highlight the therapeutic resistance property of CSCs attributed by plasticity. Also, outline some potential therapeutic options against plasticity of CSCs. Graphical Abstract .
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Plasticidade Celular , Progressão da Doença , Resistencia a Medicamentos Antineoplásicos , Células-Tronco Neoplásicas/patologia , Plasticidade Celular/genética , Resistencia a Medicamentos Antineoplásicos/genética , Epigênese Genética , Humanos , Células-Tronco Neoplásicas/metabolismo , Microambiente Tumoral/genéticaRESUMO
Reactivation of the stem cell programme in breast cancer is significantly associated with persistent cancer progression and therapeutic failure. Breast cancer stem cells (BCSCs) are involved in the process of breast cancer initiation, metastasis and cancer relapse. Among the various important cues found in the formation and progression of BCSCs, microRNAs (miRNAs or miRs) play a pivotal role by regulating the expression of various tumour suppressor genes or oncogenes. Accordingly, there is evidence that miRNAs are associated with BCSC self-renewal, differentiation, invasion, metastasis and therapy resistance, and therefore cancer recurrence. miRNAs execute their roles by regulating the expression of stemness markers, activation of signalling pathways or their components and regulation of transcription networks in BCSCs. Therefore, a better understanding of the association between BCSCs and miRNAs has the potential to help design more effective and safer therapeutic solutions against breast cancer. Thus, an miRNA-based therapeutic strategy may open up new horizons for the treatment of breast cancer in the future. In view of this, we present the progress to date of miRNA research associated with stemness marker expression, signalling pathways and activation of transcription networks to regulate the self-renewal, differentiation and therapy resistance properties of BCSCs.
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Neoplasias da Mama/genética , MicroRNAs/genética , Células-Tronco Neoplásicas/metabolismo , Apoptose/genética , Biomarcadores Tumorais , Neoplasias da Mama/metabolismo , Neoplasias da Mama/patologia , Suscetibilidade a Doenças , Feminino , Regulação Neoplásica da Expressão Gênica , Redes Reguladoras de Genes , Humanos , Fenótipo , Interferência de RNA , Transdução de Sinais , Fatores de Transcrição/metabolismo , Transcrição GênicaRESUMO
The inhibition of angiotensin converting enzyme (ACE) activity was determined in vitro by mushroom-derived eritadenine (EA), which was analyzed in 11 principal Korean edible mushrooms. EA inhibited ACE activity with 0.091 µM IC50, whereas the IC50 of captopril (CP), which is a reference compound, was 0.025 µM. Kinetic measurements of ACE reaction in the substrate of hippuryl-l-histidyl-l-leucine (HHL) with or without EA revealed that the Vmax (0.0465 O.D/30 min) was unchanged, but the the Km increased from 2.063 to 3.887 mM, indicating that EA competes with HHL for the active site. When EA was analyzed by HPLC, Lentinus edodes with a soft cap contained the highest amount EA (642.8 mg%); however, Phellinus linteus with a hard cap contained the least amount of EA (9.4 mg%). These results indicate that EA was a strong competitive inhibitor for ACE, and edible mushrooms with soft caps contained a significant amount of EA.
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Adenina/análogos & derivados , Inibidores da Enzima Conversora de Angiotensina/farmacologia , Cogumelos Shiitake/química , Adenina/isolamento & purificação , Adenina/metabolismo , Adenina/farmacologia , Ligação Competitiva , Domínio Catalítico , Cinética , Oligopeptídeos/metabolismo , Peptidil Dipeptidase A/metabolismoRESUMO
The major conjugated linoleic acid (CLA) isomers, c9,t11-CLA and t10,c12-CLA, have anticancer effects; however, the exact mechanisms underlying these effects are unknown. Evidence suggests that reversal of reduced gap junctional intercellular communication (GJIC) in cancer cells inhibits cell growth and induces cell death. Hence, we determined that CLA isomers enhance GJIC in human MCF-7 breast cancer cells and investigated the underlying molecular mechanisms. The CLA isomers significantly enhanced GJIC of MCF-7 cells at 40 µ M concentration, whereas CLA inhibited cell growth and induced caspase-dependent apoptosis. CLA increased connexin43 (Cx43) expression both at the transcriptional and translational levels. CLA inhibited nuclear factor- κ B (NF- κ B) activity and enhanced reactive oxygen species (ROS) generation. No significant difference was observed in the efficacy of c9,t11-CLA and t10,c12-CLA. These results suggest that the anticancer effect of CLA is associated with upregulation of GJIC mediated by enhanced Cx43 expression through inactivation of NF- κ B and generation of ROS in MCF-7 cells.
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The anti-tumor promotional effects of t9,t11-conjugated linoleic acid (t9,t11-CLA) and t10,t12-CLA were evaluated on the 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced inhibition of gap junctional intercellular communication (GJIC) in the human mammary epithelial cell line MCF-10A. The results were compared to those obtained from c9,t11-CLA, which is a more effective anti-tumor promoter on TPA-induced GJIC inhibition in MCF-10A cells than t10,c12-CLA. Cells were treated with 20 µM t9,t11-CLA, t10,t12-CLA, or c9,t11-CLA for 24 h followed by 60 nM TPA for 1 h. Both t9,t11-CLA and t10,t12-CLA equally protected MCF-10A cells from TPA-induced inhibition of GJIC with inferior efficacy to c9,t11-CLA.The protection was due to the ameliorated phosphorylation of connexin43 via suppression of extracellular signal-regulated kinases (ERK1/2) activation. Suppression of TPA-induced reactive oxygen species (ROS) generation by t9,t11-CLA and t10,t12-CLA was less effective, relative to c9,t11-CLA. The results suggest that the anti-promotional activities of t9,t11-CLA and t10,t12-CLA are equal but less potent than c9,t11-CLA in TPA-treated MCF-10A cells. The activity might be mediated by the attenuation of ROS production in MCF-10A cells by preventing the downregulation of GJIC during the cancer promotion stage.
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Junções Comunicantes/efeitos dos fármacos , Ácido Linoleico/farmacologia , Acetato de Tetradecanoilforbol/farmacologia , Linhagem Celular , HumanosRESUMO
A lectin (termed NNTL) was purified from the extracts of Nymphaea nouchali tuber followed by anion-exchange chromatography on DEAE-cellulose, hydrophobic chromatography on HiTrap Phenyl HP and by repeated anion-exchange chromatography on HiTrap Q FF column. The molecular mass of the purified lectin was 27.0 ± 1.0 kDa, as estimated by SDS/PAGE both in the presence and in the absence of 2-mercaptoethanol. NNTL was an o-nitrophenyl ß-D-galactopyranoside sugar-specific lectin that agglutinated rat, chicken and different groups of human blood cells and exhibited high agglutination activity over the pH range 5-9 and temperatures of 30-60 °C. The N-terminal sequence of NNTL did not show sequence similarity with any other lectin and the amino acid analysis revealed that NNTL was rich in leucine, methionine and glycine residues. NNTL was a glycoprotein containing 8% neutral sugar and showed toxicity against brine shrimp nauplii with an LC(50) value of 120 ± 29 µg/ml and exerted strong agglutination activity against four pathogenic bacteria (Bacillus subtilis, Sarcina lutea, Shigella shiga and Shigella sonnei). In addition, antiproliferative activity of this lectin against EAC (Ehrlich ascites carcinoma) cells showed 56% and 76% inhibition in vivo in mice at 1.5 and 3 mg·kg(-1)·day(-1) respectively. NNTL was a divalent ion-dependent glycoprotein, which lost its activity markedly in the presence of denaturants. Furthermore, measurement of fluorescence spectra in the presence and absence of urea and CaCl(2) indicated the requirement of Ca(2+) for the stability of NNTL.
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Carcinoma de Ehrlich/patologia , Morte Celular/efeitos dos fármacos , Proliferação de Células/efeitos dos fármacos , Glicoproteínas/isolamento & purificação , Glicoproteínas/farmacologia , Lectinas/isolamento & purificação , Lectinas/farmacologia , Nymphaea/química , Tubérculos/química , Animais , Cálcio/química , Galinhas , Cromatografia por Troca Iônica , Detergentes/química , Glicoproteínas/química , Hemaglutinação/efeitos dos fármacos , Humanos , Concentração de Íons de Hidrogênio , Íons/química , Lectinas/química , Camundongos , Ratos , Espectrometria de Fluorescência , Temperatura , Células Tumorais Cultivadas/patologiaRESUMO
The protective effect of c9,t11-conjugated linoleic acid (CLA) on the inhibition of gap junctional intercellular communication (GJIC) was examined in a human mammary epithelial cell line (MCF-10A) treated with 12-O-tetradecanoylphorbol-13-acetate (TPA), relative to t10,c12-CLA isomer. TPA inhibited GJIC in a dose-dependent and reversible manner and was associated with connexin 43 phosphorylation. Pretreatment of 20 µM c9,t11-CLA for 24 h prior to 60 nM TPA for 1 h prevented the inhibition of GJIC by reducing the phosphorylation of connexin 43 via suppressing extracellular signal-regulated kinases (ERK1/2) activation. Reactive oxygen species (ROS) accumulation by TPA was attenuated by c9,t11-CLA. The efficacy of c9,t11-CLA in protecting inhibition of GJIC, connexin 43 phosphorylation, and ROS production was superior to that of t10,c12-CLA. These results suggest that c9,t11-CLA, including t10,c12-CLA, prevents the carcinogenesis of MCF-10A cells by protecting down-regulation of GJIC during the cancer promotion stage, and lack of their toxicities could be an excellent indicator for the chemoprevention of breast cancer.