Search bioRxiv⌕ Search

bioRxiv · 10.1101/2022.01.25.477792

Comparative study of the effect of neutrons emitted from neutron source 241Am-Be and curcumin on MCF-7 breast cancer cells in 3D culture medium

Abstract

IntroductionCancer is one of the major medical problems threatening human health. Breast cancer is the most prevalent type of cancer in women. Reports indicate that treatments such as surgery, chemotherapy, biotherapy, and radiotherapy play a limited but important role in treating the disease. For more efficient treatment, new treatment strategies have been evolved based on combination therapy in which two or more different methods are exploited for this aim. In the present study, a combination therapy based on radiotherapy (using neutron radiation emitted from a 241Am-Be neutron source) and biotherapy (using curcumin) is applied to investigate the treatment efficiency of MCF-7 breast cancer in a three-dimensional culture medium. materials and methodsThe neutron dose rate in the 241Am-Be source was measured using BF3 detection and MCNPX simulation methods, and then the results of both methods were compared. MTT, neutral red uptake assay, nitric oxide, glutathione assay, catalase, cytochrome c, comet assay, and caspase-3 were used to determine the effect and type of mortality due to neutron effect as well as the combined effect of neutron and curcumin in cancer cells. ResultsCalculating the fast neutron flux around the source with two methods of simulation with MCNPX and detection with BF3 showed that with increasing distance from the source, the fast neutron flux decreased exponentially. The results of neutron dose rate measurement in the 241Am-Be source also showed that if the test cells in the vial are located at a distance of 22 cm from the inlet of the collimator and are exposed to neutron radiation for 5, 10, 15, and 20 hours, the neutron dose received by breast cancer cells will be 3, 6, 9, and 12 mGy/h, respectively. The results of cytotoxicity due to neutron irradiation as well as the combined effect of neutron and curcumin (80 M concentration) showed that neutron irradiation with or without curcumin at 5, 10, 15, and 20 hours reduced the survival of tumor cells. According to the results, the rate of apoptosis due to the neutron effect at irradiation times has increased with increasing time. Statistical analysis also showed that the rate of apoptosis due to the combined effect of neutrons and curcumin was not significant compared to the effect of neutrons only. The results of studying the effect of neutrons and the combination of neutrons and curcumin on the production of nitric oxide, catalase, and GSH also showed that curcumin has an antioxidant effect by reducing the amount of nitric oxide and increasing the production of catalase and glutathione in cells. However, neutrons, alone, lacked this effect. ConclusionOverall, this study showed that the neutron source 241Am-Be with the applied doses was able to destroy the c-o, and c-h bonds of curcumin, resulting in cell death and apoptosis induction in breast cancer cells. It was caused by neutron radiation. On the other hand, according to the results of the comet assay and caspase-3 experiments, although neutrons induced apoptosis in breast cancer cells, the death rate due to necrosis was much higher than apoptosis. Due to the significant anti-cancer effect of curcumin in 3D culture, the use of this molecule before or after neutron therapy is recommended. HighlightsO_LIThe results of neutron dose rate measurement in the 241Am-Be source showed that if the test cells in the vial are located at a distance of 22 cm from the inlet of the collimator and are exposed to neutron radiation for 5, 10, 15, and 20 hours, the neutron dose received by breast cancer cells will be 3, 6, 9, and 12 mGy/h, respectively. C_LIO_LIThe results of cytotoxicity due to neutron irradiation as well as the combined effect of neutron and curcumin (80 M concentration) showed that neutron irradiation with or without curcumin at 5, 10, 15, and 20 hours reduced the survival of tumor cells. C_LIO_LIAccording to the results, the rate of apoptosis due to the neutron effect at irradiation times has increased with increasing time. The results of studying the effect of neutrons and the combination of neutrons and curcumin on the production of nitric oxide, catalase, and GSH also showed that curcumin has an antioxidant effect by reducing the amount of nitric oxide and increasing the production of catalase and glutathione in cells. However, neutrons, alone, lacked this effect. C_LIO_LIthis study showed that the neutron source 241Am-Be with the applied doses was able to destroy the c-o, and c-h bonds of curcumin, resulting in cell death and apoptosis induction in breast cancer cells. It was caused by neutron radiation. C_LIO_LIaccording to the results of the comet assay and caspase-3 experiments, although neutrons induced apoptosis in breast cancer cells, the death rate due to necrosis was much higher than apoptosis. C_LI

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Zargan, S., Salehi Barough, M., Zargan, J., Shayesteh, M., Mousavi, M., Keshavarz, H., Haji Nor Mohamadi, A.. 2022-01-28. Comparative study of the effect of neutrons emitted from neutron source 241Am-Be and curcumin on MCF-7 breast cancer cells in 3D culture medium. https://doi.org/10.1101/2022.01.25.477792

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Expression-System Biases Compromise the Functional Assessment of KCNH2 Variants and Clinical Risk Assessment

Background: Functional characterization of KCNH2 variants is essential for assessing pathogenicity in long QT syndrome type 2. Because hERG channels assemble as tetramers, the relative expression of wild-type (WT) and variant subunits critically influences channel function and pathogenicity assessment. However, commonly used experimental systems may not reproduce the balanced allelic expression observed in heterozygous patients. Methods: Allele-specific KCNH2 expression was analyzed in two independent RNA-sequencing datasets from human left ventricular tissue. Using the dominant-negative T74R hERG variant as a model, we calibrated the relationship between WT-to-variant expression ratios and hERG current amplitude. Using automated patch-clamp electrophysiology, we compared 3 dual-expression strategies: internal ribosome entry site (IRES), P2A-linked tandem constructs, and dual cytomegalovirus promoter (dCMV) constructs. Co-electroporation of WT and variant plasmids in different ratios was the reference. Results: Allele-specific expression analysis supported balanced KCNH2 expression in human left ventricular tissue. At a 1:1 WT-to-T74R expression ratio, hERG current amplitude was reduced to 31.0% of WT, consistent with a dominant-negative mechanism in which incorporation of 2 or more T74R subunits renders the channel nonfunctional. All 3 dual-expression strategies produced substantial expression imbalances, with the first cassette consistently favored. IRES constructs showed the greatest asymmetry. P2A constructs partially improved expression balance but introduced an additional N-terminal proline in the second cassette altering T74R-associated trafficking and channel biophysics. The dCMV system also failed to achieve balanced expression, including after stable integration. Co-electroporation of separate WT and variant plasmids provided the most reliable means of controlling their relative expression. Conclusions: Commonly used dual-expression constructs do not reliably reproduce balanced WT and variant hERG expression, potentially distorting assessments of dominant-negative effects and variant pathogenicity. Co-electroporation of separate plasmids provides a robust approach for high-throughput functional phenotyping under heterozygous conditions, with implications for the interpretation of KCNH2 variants and potentially other genes encoding multimeric ion channels.

biophysics↗

Learning from Hi-C reveals nuclear dynamical reorganization in budding yeast across the cell cycle

Hi-C contact maps provide population-averaged measurements of chromosomal contacts. Converting these measurements, however, into three-dimensional structures and associated dynamics remains an underdetermined problem. Existing approaches broadly fall into two classes. Data-driven reconstruction methods that infer either a consensus structure or an ensemble of conformations, but do not inform on chromosome dynamics. Physics-based models, which generate dynamical trajectories, but require prior assumptions about nuclear geometry, chromatin mechanics, tethering, or molecular interactions. Here, we bridge these approaches using the Full-Inversion Chromatin model, a data-driven whole-genome polymer framework that learns an effective force field directly from Hi-C contact probabilities, integrated with Serpentine, a tool to quantify contact-map discrepancies while accounting for differences in sequencing coverage and sparsity. This generates structural ensembles of chromosomes and effective chromatin dynamics. We apply this method at 5-kb resolution to Saccharomyces cerevisiae in G1, mid-S, S/G2, G2/M, anaphase, and quiescence. Without explicitly imposing the spindle pole body, centromere or telomere tethering, predefined chromatin states, or nuclear-envelope interactions, the inferred ensembles recover these major features of yeast nuclear organization. Importantly, although dynamical information is not used during model training, the resulting polymer trajectories reproduce the subdiffusive scaling and chromosomal variations of independently measured chromatin motion. The model further predicts heterogeneous mobility along chromosomes and a distinctive telomere-dependent dynamical organization. Thus, population-averaged Hi-C contacts contain sufficient information to infer not only three-dimensional genome organization, but also effective, locus-dependent chromatin dynamics.

biophysics↗

One high-order ion-coupling mechanism generates multiple SLC1A stoichiometries

Human excitatory amino acid transporter 2 (hEAAT2) is a glial transporter that clears glutamate and aspartate from the extracellular space to terminate neurotransmission. When this essential role is disrupted, excess extracellular glutamate causes excitotoxicity and neurological disease. hEAAT2 transports amino acids into cells against their concentration gradients by coupling uptake to the co-transport of Na+ and H+, and counter-transport of K+. Substrate transport also activates a thermodynamically uncoupled Cl- conductance, whose significance is unknown. Here, to dissect the molecular mechanisms underlying coupled and uncoupled ion transport by EAATs, we leverage the tractable Drosophila melanogaster homologue dEAAT2, which transports taurine as well as glutamate and aspartate. By functionally characterising dEAAT2, we confirmed it has features of a canonical EAAT transport cycle, including an uncoupled Cl- conductance. However, it functions an ion-independent electroneutral exchanger, in stark contrast to its ion-coupled electrogenic human counterpart. Cryo-electron microscopy (cryo-EM) and computational simulations confirmed the inability of dEAAT2 to transport cations, but just two point mutations conferred Na+, H+, and K+ dependence, reconstituting the complex ion coupling profile of human transporters in the Drosophila exchanger. We also showed that dEAAT2 transports taurine in a complex with Cl-, bestowing a unique Cl--dependence on taurine transport, independent of uncoupled Cl- flux. Our findings show that ancestral exchangers in the EAAT family preserve the machinery to achieve complex ion-coupled transport, revealing the molecular basis of high-order ion coupling in hEAATs.

biophysics↗