Migration Transition Research Articles

When Bare Life is Bearable: The Life Projects of Rohingya and Hazara Refugees Living in Malaysia

With anti-migrant populism and strict border regimes in many receiving countries, hundreds of thousands of refugees have been entangled in transit situations and face critically vulnerable conditions. While recent research on transit migration has explored “life projects,” including work, studies, and volunteering undertaken by refugees to make their lives more bearable in a context of protracted uncertainty, how refugees describe the country in which they are living and what facilitates their life projects there have remained less understood in a Southeast Asian context and in the Global South more generally. This article addresses this lacuna, drawing on interviews with Rohingya and Hazara refugees living in Malaysia. Rohingya and Hazara refugees described Malaysia as a safer place than their home countries, where they had endured violence and persecution. Examining key conditions underpinning the life projects of Hazara and Rohingya refugees, this article demonstrates that refugee lives are not completely on hold in transit situations, despite what dominant understandings of refugee lives often suggest. As it shows, while Rohingya and Hazara refugees are excluded from legal rights in Malaysia, the Malaysian state has not made them fully subject to laws and, instead, at times, has tacitly supported refugees. This situation has enabled refugees to pursue informal life projects, leading to a bearable bare life.

Mutant p53-microRNA-200c-ZEB2-Axis-Induced CPT1C Elevation Contributes to Metabolic Reprogramming and Tumor Progression in Basal-Like Breast Cancers.

TP53 is mutated in more than 80% of basal-like breast cancers (BLBCs). BLBCs with TP53 mutation are usually high-grade and have worse responses to chemotherapy, leading to poor clinical outcomes. Wild-type p53 (WTp53) is well-accepted to promote fatty acid oxidation (FAO); however, in this study, we demonstrate that mutant p53 (Mutp53) enhances FAO activity through constitutively upregulating CPT1C via dysregulating the miR-200c-ZEB2 axis. Sustained CPT1C expression contributes to the metabolic preference of FAO, epithelial-mesenchymal transition (EMT) phenotypes, migration, invasion, and cancer stemness in BLBC, which is mediated by modulating the redox status. Furthermore, interference of CPT1C expression impairs tumor growth and pulmonary colonization of BLBC cells in vivo, and even postpones the occurrence of spontaneous metastasis, resulting in a prolonged disease-specific survival (DSS). Consistently, clinical validation reveals that high CPT1C is observed in breast cancer patients with metastasis and is correlated with poor overall, disease-free, progression-free, and disease-specific survival in BLBC patients. Together, unlike WTp53 which transiently transactivates CPT1C, Mutp53 provides long-term benefits through sustaining CPT1C expression by disturbing the miR-200c-ZEB2 axis, which potentiates FAO and facilitates tumor progression in BLBC, suggesting that targeting Mutp53-CPT1C-driven metabolic reprogramming is promising to serve as novel therapeutic strategies for BLBC in the future.

CDK1 Promotes Epithelial-Mesenchymal Transition and Migration of Head and Neck Squamous Carcinoma Cells by Repressing ∆Np63α-Mediated Transcriptional Regulation.

∆Np63α is a key transcription factor overexpressed in types of squamous cell carcinomas (SCCs), which represses epithelial–mesenchymal transition (EMT) and cell migration. In this study, we found that CDK1 phosphorylates ∆Np63α at the T123 site, impairing its affinity to the target promoters of its downstream genes and its regulation of them in turn. Database analysis revealed that CDK1 is overexpressed in head and neck squamous cell carcinomas (HNSCCs), especially the metastatic HNSCCs, and is negatively correlated with overall survival. We further found that CDK1 promotes the EMT and migration of HNSCC cells by inhibiting ∆Np63α. Altogether, our study identified CDK1 as a novel regulator of ΔNp63α, which can modulate EMT and cell migration in HNSCCs. Our findings will help to elucidate the migration mechanism of HNSCC cells.

Histone deacetylase 3 promotes alveolar epithelial–mesenchymal transition and fibroblast migration under hypoxic conditions

Epithelial–mesenchymal transition (EMT), a process by which epithelial cells undergo a phenotypic conversion that leads to myofibroblast formation, plays a crucial role in the progression of idiopathic pulmonary fibrosis (IPF). Recently, it was revealed that hypoxia promotes alveolar EMT and that histone deacetylases (HDACs) are abnormally overexpressed in the lung tissues of IPF patients. In this study, we showed that HDAC3 regulated alveolar EMT markers via the AKT pathway during hypoxia and that inhibition of HDAC3 expression by small interfering RNA (siRNA) decreased the migration ability and invasiveness of diseased human lung fibroblasts. Furthermore, we found that HDAC3 enhanced the migratory and invasive properties of fibroblasts by positively affecting the EMT process, which in turn was affected by the increased and decreased levels of microRNA (miR)-224 and Forkhead Box A1 (FOXA1), respectively. Lastly, we found this mechanism to be valid in an in vivo system; HDAC3 siRNA administration inhibited bleomycin-induced pulmonary fibrosis in mice. Thus, it is reasonable to suggest that HDAC3 may accelerate pulmonary fibrosis progression under hypoxic conditions by enhancing EMT in alveolar cells through the regulation of miR-224 and FOXA1. This entire process, we believe, offers a novel therapeutic approach for pulmonary fibrosis.

Investigating unfrozen water and its components during freeze–thaw action in loess using a novel NMR technique

AbstractFrost heave and thaw settlement are primarily caused by water migration. Variations in liquid water and its components during freezing and thawing are crucial variables for investigating water migration. Here, a novel soil layer‐scanning method based on magnetic resonance imaging cryogenic soil‐moisture analysis (MRI‐CSMA) was applied to measure dynamic changes of liquid water and its components in nine layers (each 11.1‐mm thick) of four loess samples with different initial water contents (9.2%, 15.7%, 20.0%, and 30.0%) in freezing–thawing experiments under a closed system. The ice–water phase transition and water migration were key factors that controlled the liquid water and its components. During freezing, the liquid water content of each layer (except layer 7) decreased. In the frozen zone (layers 1–6), the liquid water content decreased with decreasing temperature owing to the water–ice phase transition. The lower the temperature, the higher the fraction of water that transitioned to ice. In the unfrozen zone (layers 8–9), parts of the liquid water migrated upward owing to the suction generated at the freezing front. The farther away the freezing front, the smaller the suction and quantity of water migration. During thawing, the liquid water content of each layer increased owing to the ice–water phase transition in the frozen zone and infiltrated down to the unfrozen zone. The contents of the free and adsorbed water exhibited similar change trends to the liquid water content during freezing. However, the change degree of free water was much larger than that of adsorbed water because the phase transition and migration of free water is easier than that of absorbed water. Notably, the liquid water content near the freezing front (layer 7) increased in the early stage of freezing, owing to the combined effect of soil compression and the water–ice phase transition. These results provide a reference for research on water migration in the soil during freezing–thawing and validate the advantage of MRI‐CSMA when characterising water migration in large soil samples.Highlights A novel device (MRI Cryogenic Soil‐Moisture Analyzer) was used. Variations in unfrozen water and its components during freezing were studied. Soil consolidation and pore pressure affect the liquid water change during freezing.

Chinese Students in Thai Higher Education Institutions and the Transformation of Graduate Migrant: Characteristics, Practices, and Transitional Migration

This research article entitled "Chinese students in Thai higher education institutions and the transformation of graduate migrant: Characteristics, practices, and transitional migration" aims to clarify two objectives. Firstly, to analyze the determinants that motivate Chinese students to enroll in Thai higher education institutions and, secondly, to examine the particular characteristics and patterns of status involved in transitioning from student to graduate labor. Mixed research methods from in-depth interviews and questionnaires are employed in gathering and analyzing the finding. Criticizing Human capital theory, Chinese students in Thailand intend to invest in the Thai language to escalate their socioeconomic status. However, the popularity of the Thai language over the Vietnamese and Myanmese languages, which share a higher trading volume with Yunnan and Guangxi, represents the significance of Thai soft power through social media and healthier cultural linkage. Lastly, the length of stay among transforming Chinese workers depends on individual contentment. Applying social field theory, their economic capital mainly motivates short-term migrants. However, the pursuit of social and cultural contentment is the principal motivating factor attracting graduate migrants to reside long-term in Thailand.

Comprehensive Analysis of hsa-miR-654-5p’s Tumor-Suppressing Functions

The pivotal roles of miRNAs in carcinogenesis, metastasis, and prognosis have been demonstrated recently in various cancers. This study intended to investigate the specific roles of hsa-miR-654-5p in lung cancer, which is, in general, rarely discussed. A series of closed-loop bioinformatic functional analyses were integrated with in vitro experimental validation to explore the overall biological functions and pan-cancer regulation pattern of miR-654-5p. We found that miR-654-5p abundance was significantly elevated in LUAD tissues and correlated with patients’ survival. A total of 275 potential targets of miR-654-5p were then identified and the miR-654-5p-RNF8 regulation axis was validated in vitro as a proof of concept. Furthermore, we revealed the tumor-suppressing roles of miR-654-5p and demonstrated that miR-654-5p inhibited the lung cancer cell epithelial-mesenchymal transition (EMT) process, cell proliferation, and migration using target-based, abundance-based, and ssGSEA-based bioinformatic methods and in vitro validation. Following the construction of a protein–protein interaction network, 11 highly interconnected hub genes were identified and a five-genes risk scoring model was developed to assess their potential prognostic ability. Our study does not only provide a basic miRNA-mRNA-phenotypes reference map for understanding the function of miR-654-5p in different cancers but also reveals the tumor-suppressing roles and prognostic values of miR-654-5p.

Exposure to transit migration: Public attitudes and entrepreneurship

Does exposure to mass migration affect the attitudes and economic behavior of natives in transit countries? In order to answer this question, we use a unique locality-level panel from the 2010 and 2016 rounds of the Life in Transition Survey and data on the main land routes taken by migrants in 18 European countries during the refugee crisis in 2015. To capture the exogenous variation in natives’ exposure to transit migration, we construct an instrument that is based on each locality’s distance to the optimal routes that minimize traveling time between refugees’ main origins and destinations. We find that the entrepreneurial activity of native population falls considerably in localities that are more exposed to mass transit migration, compared to those located farther away. We explore potential mechanisms and find that exposure to mass transit migration results in lower confidence in government, higher perceived political instability, and less willingness to take risks. We also document an increase in anti-migrant sentiment while attitudes towards other minorities remain unchanged.

MiRNA-124 regulates palmitic acid-induced epithelial-mesenchymal transition and cell migration in human retinal pigment epithelial cells by targeting LIN7C.

The present study revealed that palmitic acid (PA) treatment induced epithelial-mesenchymal transition (EMT) of retinal pigment epithelial (RPE) cells, which are involved in the progression of proliferative vitreoretinopathy (PVR). ARPE-19 cells were treated with PA followed by miRNA screening and EMT marker detection using qRT-PCR. Then, miR-124 mimic or inhibitor was transfected into ARPE-19 cells to explore the role of miR-124 on the EMT of ARPE-19 cells using transwell assay. The underlying mechanism of miRNA were predicted by bioinformatics method and confirmed by luciferase activity reporter assay. Furthermore, gain-of-function strategy was also used to explore the role of LIN7C in the EMT of ARPE-19 cells. The expression of miRNA or mRNA expression was determined by qRT-PCR and the protein expression was determined using western blot assay. The result presented that PA reduced the expression of E-cadherin/ZO-1 whilst increasing the expression of fibronectin/α-SMA. In addition, PA treatment enhanced the expression of microRNA (miR)-124 in ARPE-19 cells. Overexpression of miR-124 enhanced PA-induced upregulation of E-cadherin and ZO-1 expression and downregulation of fibronectin and α-SMA. Moreover, miR-124 mimic also enhanced the migration of ARPE-19 cells induced by PA treatment. Inversely, miR-124 inhibitor presented opposite effect on PA-induced EMT and cell migration in ARPE-19 cells. Luciferase activity reporter assay confirmed that Lin-7 homolog C (LIN7C) was a direct target of miR-124 in ARPE-19 cells. Overexpression of LIN7C was found to suppress the migration ability and expression of fibronectin and α-SMA, while increasing expression of E-cadherin and ZO-1; miR-124 mimic abrogated the inhibitive effect of LIN7C on the EMT of ARPE-19 cells and PA further enhanced this abolishment. Collectively, these findings suggest that miR-124/LIN7C can modulate EMT and cell migration in RPE cells, which may have therapeutic implications in the management of PVR diseases.

Autophagy regulates transforming growth factor β signaling and receptor trafficking

Transforming growth factor beta (TGFβ) stimulates tumorigenesis by inducing epithelial to mesenchymal transition (EMT) and cell migration. TGFβ signaling is regulated by the endocytosis of cell surface receptors and their subcellular trafficking into the endo-lysosomal system. Here we investigated how autophagy, a cellular quality control network that delivers material to lysosomes, regulates TGFβ signaling pathways that induce EMT and cell migration. We impaired autophagy in non-small cell lung cancer cells using chloroquine, spautin-1, ULK-101, or small interfering RNA (siRNA) targeting autophagy-related gene (ATG)5 and ATG7 and observed that inhibiting autophagy results in a decrease in TGFβ1-dependent EMT transcription factor and cell marker expression, as well as attenuated stress fiber formation and cell migration. This correlated with decreased internalization of cell surface TGFβ receptors and their trafficking to early/late endosomal and lysosomal compartments. The effects of autophagy inhibition on TGFβ signaling were investigated by Smad2/Smad3 phosphorylation and cellular localization using western blotting, subcellular fractionation, and immunofluorescence microscopy. We observed that inhibiting autophagy decreased the amount and timeframe of Smad2/Smad3 signaling. Taken together, our results suggest that inhibiting autophagy attenuates pro-tumorigenic TGFβ signaling by regulating receptor trafficking, resulting in impaired Smad2/Smad3 phosphorylation and nuclear accumulation.

Stabilizing the Anionic Redox in 4.6 V LiCoO2 Cathode through Adjusting Oxygen Magnetic Moment

AbstractThe irreversible oxygen redox and the resulting structure degradation of LiCoO2 at a high voltage cause very poor cycling performance. Herein, the anionic redox chemistry in 4.6 V LiCoO2 cathode material through manipulating the oxygen magnetic moment (OMM) with oxygen vacancy and V doping is proposed to stabilize, and the relationship between OMM and the oxidation degree of oxygen is revealed. Oxygen vacancy induces the generation of OMM, and the synergy of oxygen vacancy and V doping reduces the change of OMM during charge/discharge processes. This mitigates the oxidation degree of oxygen and improves the reversibility of oxygen redox, which greatly inhibits the irreversible oxygen escape. The oxygen vacancies can further reduce the overlap of the electron clouds and lower the O 2p band center thus decreasing the oxygen redox activity. Moreover, the introduced V also increases the energy barrier of the phase transition and suppresses the irreversible phase transition and Co migration. The irreversible O2 release is significantly inhibited and the cycling stability at 4.6 V is largely enhanced. This study presents the relationship between OMM and the oxidation degree of oxygen and provides some insights into improving the anion redox reversibility through adjusting the oxygen magnetic moment.

MO072: PST3.1A, An Inhibitor of MGAT5 Decreases Renal Fibrosis in a Rat Model of Chronic Kidney Disease

Abstract BACKGROUND AND AIMS Renal fibrosis is a main feature of chronic kidney disease (CKD) that participates in its progression to the end stage.(1) N-acetylglucosaminyltransferase 5 (MGAT5) adds N-acetylglucosamines to newly synthesized glycoproteins and is overexpressed in tumors participating in epithelial–mesenchymal transition (EMT), invasion and cell migration, some of the features observed in fibrosis.(2) PST3.1a is an inhibitor of MGAT5 that has already been shown to be beneficial in the treatment of brain tumors.(3) We presently evaluated the use of PST3.1a on renal fibrosis in CKD. METHOD Six-week-old Sprague-Dawley rats underwent 5/6th subtotal nephrectomy (SNx) (n = 16) or no surgery (Control) (n = 14). PST3.1a (0.2 mg/mL) or placebo was administered in the drinking water from the day of surgery for the entire protocol. Animals were sacrificed 4 weeks after surgery and the kidney was taken to evaluate fibrosis, MGAT5 expression and activity. Fibrosis was determined both by Sirius red staining and by immunohistochemistry (IHC) staining of three types of collagen (I, III and IV). To measure the activity of MGAT5 immunohistochemistry staining of Phaseolus Vulgaris Leucoagglutinine (PHA-L) and galectin 3 were carried out. RESULTS MGAT5 expression (12.2% ± 1.2 control versus 26.7% ± 2.6 SNx) and renal fibrosis (11.5% ± 0.7 control versus 26.9% ± 1.9 SNx) increased significantly in SNx animals in a preliminary study. In the present study, PST3.1atreatment significantly decreased the expression of collagen 1 (col1) (2.1% ± 0.2 SNx versus 1.3% ± 0.2 SNx + PST3.1a; P < 0.05) and collagen 4 (col4) (9.4% ± 1.01 SNx versus 6.4% ± 0.3SNx + PST3.1a; P < 0.05) in kidneys of SNx animals (Fig. 1). Collagen 3 also had a trend to decrease. Sirius red staining showed a decrease in the PST3.1a treated group although it did not reach statistical significance (8.4% ± 1.7SNx versus 6.7% ± 0.2 SNx + PST3.1a). PHA-L and galectin 3 expressions were increased in SNx animals, and the overexpression was blunted in PST3.1a treated animals (9.4% ± 1.5 SNx versus 5.7% ± 0.2 SNx + PST3.1a; P < 0.05 for galectin 3) (Fig. 2). CONCLUSION Fibrosis was observed in SNx animals 4 weeks after surgery. PST3.1a significantly decreased MGAT5 activity. Treatment with PST3.1a decreased fibrosis and significantly downregulated col1 and col4. These data show that PST3.1a treatment through MGAT5 inhibition may be a new treatment for fibrosis in the context of CKD.

Novel Inhibitor for Downstream Targeting of Transforming Growth Factor-β Signaling to Suppress Epithelial to Mesenchymal Transition and Cell Migration.

Cancer metastasis accounts for most of the mortality associated with solid tumors. However, antimetastatic drugs are not available on the market. One of the important biological events leading to metastasis is the epithelial to mesenchymal transition (EMT) induced by cytokines, namely transforming growth-factor-β (TGF-β). Although several classes of inhibitors targeting TGF-β and its receptor have been developed, they have shown profound clinical side effects. We focused on our synthetic compound, HPH-15, which has shown anti-fibrotic activity via the blockade of the TGF-β Smad-dependent signaling. In this study, 10 μM of HPH-15 was found to exhibit anti-cell migration and anti-EMT activities in non-small-cell lung cancer (NSCLC) cells. Although higher concentrations are required, the anti-EMT activity of HPH-15 has also been observed in 3D-cultured NSCLC cells. A mechanistic study showed that HPH-15 inhibits downstream TGF-β signaling. This downstream inhibition blocks the expression of cytokines such as TGF-β, leading to the next cycle of Smad-dependent and -independent signaling. HPH-15 has AMPK-activation activity, but a relationship between AMPK activation and anti-EMT/cell migration was not observed. Taken together, HPH-15 may lead to the development of antimetastatic drugs with a new mechanism of action.

The Role of Scleraxis in Inducing Vascular Stiffness

Vascular fibrosis (VF) is one of the most significant pathologies related to blood vessel dysfunction. VF results in an impairment of vascular tone due to an increase in extracellular matrix proteins (ECM) and vascular smooth muscle synthesis within the vessel wall, thus increasing vascular stiffness and reducing lumen diameter. VF is both caused by and exacerbates numerous vascular diseases including diabetes, atherosclerosis and in particular, hypertension, which accounts for 13% of deaths globally (WHO World Health Report, 2002). Multiple studies have investigated various therapeutic approaches to interfere with VF, but to date this condition remains untreated, thus novel approaches to target fibrosis development and progression are urgently required.Our lab identified the transcription factor scleraxis as a novel master regulator of cellular phenotype conversion. We demonstrated that scleraxis is sufficient to induce fibroblast to myofibroblast phenotype conversion, a critical step in the development of fibrosis in many tissue types. Scleraxis also induces Epithelial to Mesenchymal Transition (EMT) and cell migration as part of development and cell differentiation. Some studies have shown that mechanical stretch in tendons increases expression of scleraxis, while additional studies reported that stretch in rabbit aorta induces the vascular smooth muscle proliferative phenotype. Our preliminary data has revealed that scleraxis is expressed in VSMCs in the arterial wall, and we have found elevated scleraxis expression in high pressure versus low pressure regions of vessels. We thus hypothesize that scleraxis is sufficient and necessary to induce vascular fibrosis.Our data shows that scleraxis overexpression increases thickness of the aortic vascular wall in scleraxis overexpression mice, via histological sections, thus contributing to the progression of vascular fibrosis. In vitro studies show that scleraxis overexpression in Human Aortic Smooth Muscle Cells (HAOSMC) induces their proliferation and migration using different assays (CCk8/Edu+ proliferation assay, Transwell migration assay, gene expression assays). Scleraxis overexpression also induces hypertrophy of HAOSMC shown via immunostaining. This suggests that scleraxis overexpression induces VSMC plasticity from contractile to synthetic‐proliferative phenotype, thus inducing VSMC hyperplasia.New & Noteworthy: Our findings indicate that scleraxis plays a role in VSMC plasticity via scleraxis‐ mediated transcriptional regulation of VSMC proliferation and migration. This work has potential relevance to many related diseases that feature VSMC activation, including atherosclerosis and restenosis.

Exclusion of NUMB Exon12 Controls Cancer Cell Migration through Regulation of Notch1-SMAD3 Crosstalk.

NUMB is an endocytic adaptor protein that contains four isoforms (p65, p66, p71 and p72) due to alternative splicing regulation. Here, we show that NUMB exon12 (E12)-skipping isoforms p65/p66 promote epithelial to mesenchymal transition (EMT) and cancer cell migration in vitro, and facilitate cancer metastasis in mice, whereas E12-included p71/p72 isoforms attenuate these effects. Mechanistically, p65/p66 isoforms significantly increase the sorting of Notch1 through early endosomes (EEs) for enhanced Notch1 activity. In contrast, p71/p72 isoforms act as negative regulators of Notch1 by ubiquitylating the Notch1 intracellular domain (N1ICD) and promoting its degradation. Moreover, we observed that the interaction between N1ICD and SMAD3 is important for their own stabilization, and for NUMB-mediated EMT response and cell migration. Either N1ICD or SMAD3 overexpression could significantly recuse the migration reduction seen in the p65/p66 knockdown, and Notch1 or SMAD3 knockdown rescued the migration advantage seen in the overexpression of p66. Taken all together, our study provides mechanistic insights into the opposite regulation of Notch1-SMAD3 crosstalk by NUMB isoforms and identifies them as critical regulators of EMT and cancer cell migration.

Improving the oxygen redox reversibility of Li-rich battery cathode materials via Coulombic repulsive interactions strategy

The oxygen redox reaction in lithium-rich layered oxide battery cathode materials generates extra capacity at high cell voltages (i.e., >4.5 V). However, the irreversible oxygen release causes transition metal (TM) dissolution, migration and cell voltage decay. To circumvent these issues, we introduce a strategy for tuning the Coulombic interactions in a model Li-rich positive electrode active material, i.e., Li1.2Mn0.6Ni0.2O2. In particular, we tune the Coulombic repulsive interactions to obtain an adaptable crystal structure that enables the reversible distortion of TMO6 octahedron and mitigates TM dissolution and migration. Moreover, this strategy hinders the irreversible release of oxygen and other parasitic reactions (e.g., electrolyte decomposition) commonly occurring at high voltages. When tested in non-aqueous coin cell configuration, the modified Li-rich cathode material, combined with a Li metal anode, enables a stable cell discharge capacity of about 240 mAh g−1 for 120 cycles at 50 mA g−1 and a slower voltage decay compared to the unmodified Li1.2Mn0.6Ni0.2O2.

Dependence of thermal conductivity on the phase transition of gas hydrate in clay sediments

The insufficient heat supply during gas production from hydrate reservoir significantly hinders the efficiency of hydrate exploitation. The effective thermal conductivity (ETC) of hydrate bearing sediment has been recognized as an effective indicator of the heat transfer process. Yet its evaluation could be coupled with the phase transition and components migration; the relevant knowledge on its dependence on the phase transition of gas hydrate in clay sediments still remains limited. Here in this work, a point-heat-source based instrument was used to investigate the change of ETC in fine-grained sediment during ice melting, hydrate formation and decomposition. The result shows that the ETC declined during ice melting and hydrate decomposition; hydrate formation could result in an increase of ETC. The decomposition water in pores could partly facilitate the heat transfer in porous media. Samples with the initial water saturation higher than 18% were more easily affected by hydrate formation and decomposition; this indicates that hydrate reservoir with a high water saturation could face a more varying capacity of heat transfer. The hydrate samples of deionized water and brine water system with similar saturation of nongaseous phase shows a similar behavior of ETC during phase transition. Moreover, typical effective medium model was evaluated with our measured data. A thermal resistance model based on the real distribution of phases in hydrate bearing sediment was proposed; its feasibility was verified by our measured data and those of in-house and field tests in the literature. This study could provide some insight into the energy supply during hydrate exploitation and the enhancement of the gas production process.

Isolation and eradication of ovarian CD44+ cancer stem cells via Notch signaling pathway mediated by ectopic silence of MAML1

Background: Ovarian cancer is the fifth leading cause of cancer-related deaths among women globally. Cancer stem cells (CSCs) are a subpopulation of tumor cells involved in ovarian tumor formation, metastasis, relapse, and chemoresistance. Moreover, the Notch signaling pathway has a pivotal role in CSCs maintenance. This study was designed to isolate CSCs from the A2780 cell line and determine the effectiveness of Mastermind-like transcriptional coactivator 1 (MAML1) inhibition, a key factor of the Notch pathway, in targeted therapy against ovarian CSCs. Methods: The CD44+ or CD133+ CSCs were isolated from the ovarian A2780 cell line using magnetic cell sorting. The isolated CSCs were also evaluated for stemness markers expression, self-renewal capacity, cell cycle progression, and chemoresistance compared to their negative counterparts. Afterward, MAML1-shRNA was used to inhibit the Notch pathway in CD44+CSCs. The role of MAML1 was also evaluated in the CD44+ CSCs epithelial-mesenchymal transition (EMT) process and migration. Results: In addition to the high expression of stemness markers, such as Sox2 and Musashi1, ovarian CD44+ or CD133+ CSCs had a high ability for sphere formation, higher percentage in the G1 phase to S phase, and decreased sensitivity to chemotherapy drug compared to CD44- or CD133- cells. Besides, silencing MAML1 significantly reduced the levels of EMT markers and cell migration in CD44+ CSCs, compared to scramble. Conclusions: Mastermind-like transcriptional coactivator 1 can be considered a pivotal factor in the targeted therapy and eradication of CD44+ CSCs through the inhibition of the Notch signaling pathway in an ovarian cancer patient with a special focus on the ovarian A2780 cell line

MED1 Downregulation Contributes to TGFβ-Induced Metastasis by Inhibiting SMAD2 Ubiquitination Degradation in Cutaneous Melanoma

Metastasis is the main reason for the high mortality of patients and indeed a difficult task in the treatment of cutaneous melanoma. Therefore, it is of great clinical value to explore the molecular mechanism of cutaneous metastatic melanoma and develop novel therapies. MED1, acting as a factor required for activator-dependent transcription, is reported to be involved in carcinogenesis and progression. In this study, we found that MED1 was highly expressed in patients with cutaneous melanoma. MED1 downregulation could induce cellular epithelial-to-mesenchymal transition and promote migration, invasion, and metastasis of cutaneous melanoma invivo and invitro. Further analysis showed that in Med1 knockdown cells, the TGFβ/SMAD2 signaling pathway mediated an increase in epithelial-to-mesenchymal transition phenotype and migration. The opposite results were observed after treatment with TGFβ inhibitors. To further explore the mechanism, we found that MED1 interacted with SMAD2, and MED1 downregulation could protect SMAD2 from degradation by inhibiting SMAD2 ubiquitination. Together, these results suggest that MED1 inhibited TGFβ signaling pathway to reduce cell epithelial-to-mesenchymal transition phenotype and migration through SMAD2 ubiquitination in the metastasis of cutaneous melanoma. Our findings elucidated the role of MED1 in the metastasis of cutaneous melanoma and provided a target for the therapeutic strategies of cutaneous melanoma.

Role of Th17 Cytokines in Airway Remodeling in Asthma and Therapy Perspectives.

Airway remodeling is a frequent pathological feature of severe asthma leading to permanent airway obstruction in up to 50% of cases and to respiratory disability. Although structural changes related to airway remodeling are well-characterized, immunological processes triggering and maintaining this phenomenon are still poorly understood. As a consequence, no biotherapy targeting cytokines are currently efficient to treat airway remodeling and only bronchial thermoplasty may have an effect on bronchial nerves and smooth muscles with uncertain clinical relevance. Th17 cytokines, including interleukin (IL)-17 and IL-22, play a role in neutrophilic inflammation in severe asthma and may be involved in airway remodeling. Indeed, IL-17 is increased in sputum from severe asthmatic patients, induces the expression of “profibrotic” cytokines by epithelial, endothelial cells and fibroblasts, and provokes human airway smooth muscle cell migration in in vitro studies. IL-22 is also increased in asthmatic samples, promotes myofibroblast differentiation, epithelial-mesenchymal transition and proliferation and migration of smooth muscle cells in vitro. Accordingly, we also found high levels of IL-17 and IL-22 in a mouse model of dog-allergen induced asthma characterized by a strong airway remodeling. Clinical trials found no effect of therapy targeting IL-17 in an unselected population of asthmatic patients but showed a potential benefit in a sub-population of patients exhibiting a high level of airway reversibility, suggesting a potential role on airway remodeling. Anti-IL-22 therapies have not been evaluated in asthma yet but were demonstrated efficient in severe atopic dermatitis including an effect on skin remodeling. In this review, we will address the role of Th17 cytokines in airway remodeling through data from in vitro, in vivo and translational studies, and examine the potential place of Th17-targeting therapies in the treatment of asthma with airway remodeling.