Correlations between IGF-IR Expression and Clinicopathological Factors and Prognosis in Patients with Lung Adenocarcinoma

Background and objective The incidence of lung adenocarcinoma increases rapidly, and IGF-IR is the key mediator of several growth factors signal transduction, therefore it plays an important role in the proliferation and differentiation of cancer cell. The aim of this study is to detect the expression of IGF-IR in lung adenocarcinoma and to evaluate its implication for the clinicopathological factors and prognosis of patients with this disease. Methods The IGF-IR expression was detected by immunohistochemical staining. Correlations between IGF-IR expression with clinicopathological factors were analyzed using the Chi-squared test. The Kaplan-Meier method was used to calculate the overall patient survival rate, and the difference in survival curves was evaluated using a Log-rank test. Univariate and multivariate analysis was carried out using the Cox proportional-hazard model. Results In 126 cases of tumor sections tested, IGF-IR were detected in 89 cases. Statistical analysis revealed that the IGF-IR expression was related to tumor size and T stage, while there were no relations between IGFIR expression and age, gender, smoking, pathological stages, and differentiation. Cox analysis indicated that metastasis and chemotherapy efficacy were the prognostic factors in these patients, while IGF-IR expression was not the independent prognostic factor. Conclusion The IGF-IR expression is related to tumor size and T stage, while there is no relation between IGF-IR expression and prognosis

Analysis of Differential Gel Electrophoresis of Paclitaxol Resistant and Sensitive Lung Adenocarcinoma Cells' Secretome

Background and objective Paclitaxol (PTX) resistance is one of main factors which affect the outcome of chemotherapy of lung adenocarcinoma. The aim of this study is to compare the secreted protein expression profiles between Paclitaxol (PTX) resistant and sensitive lung adenocarcinoma cells by proteomic research method, so as to provide evidence of choosing individual chemotherapy drugs in clinical treatment. Methods Total secreted proteins extracted from a PTX sensitive cell line A549 and a PTX resistant cell line A549-Taxol were separated by fluorscent differential gel electrophoresis (DIGE). High quality 2-DE profiles were obtained and analyzed by Decyder 6.5 analysis software to screen differentially expressed protein spots. Those spots were identified by mass spectrometry. Results 2-DE patterns of lung adenocarcinoma cells with high-resolution and reproducibility were obtained. 76 significantly differentially expressed protein spots were screened, 19 proteins were identified by mass spectrometry. The identified proteins could be classified into different catogories: metabolic enzyme, extracellular matrix (ECM) degradation enzyme, cytokine, signal transducer, cell adhesion, and so on. Conclusion Multiple secreted proteins related to chemoresistance of A549-Taxol cells were identified in this study for the first time. The results presented here would provide clues to identify new serologic chemoresistant biomarkers of NSCLC

Spatiotemporal transcriptomic atlas of mouse organogenesis using DNA nanoball-patterned arrays.

Spatially resolved transcriptomic technologies are promising tools to study complex biological processes such as mammalian embryogenesis. However, the imbalance between resolution, gene capture, and field of view of current methodologies precludes their systematic application to analyze relatively large and three-dimensional mid- and late-gestation embryos. Here, we combined DNA nanoball (DNB)-patterned arrays and in situ RNA capture to create spatial enhanced resolution omics-sequencing (Stereo-seq). We applied Stereo-seq to generate the mouse organogenesis spatiotemporal transcriptomic atlas (MOSTA), which maps with single-cell resolution and high sensitivity the kinetics and directionality of transcriptional variation during mouse organogenesis. We used this information to gain insight into the molecular basis of spatial cell heterogeneity and cell fate specification in developing tissues such as the dorsal midbrain. Our panoramic atlas will facilitate in-depth investigation of longstanding questions concerning normal and abnormal mammalian development.This work is part of the ‘‘SpatioTemporal Omics Consortium’’ (STOC) paper package. A list of STOC members is available at: http://sto-consortium.org. We would like to thank the MOTIC China Group, Rongqin Ke (Huaqiao University, Xiamen, China), Jiazuan Ni (Shenzhen University, Shenzhen, China), Wei Huang (Center for Excellence in Brain Science and Intelligence Technology, Chinese Academy of Sciences, Shanghai, China), and Jonathan S. Weissman (Whitehead Institute, Boston, USA) for their help. This work was supported by the grant of Top Ten Foundamental Research Institutes of Shenzhen, the Shenzhen Key Laboratory of Single-Cell Omics (ZDSYS20190902093613831), and the Guangdong Provincial Key Laboratory of Genome Read and Write (2017B030301011); Longqi Liu was supported by the National Natural Science Foundation of China (31900466) and Miguel A. Esteban’s laboratory at the Guangzhou Institutes of Biomedicine and Health by the Strategic Priority Research Program of the Chinese Academy of Sciences (XDA16030502), National Natural Science Foundation of China (92068106), and the Guangdong Basic and Applied Basic Research Foundation (2021B1515120075).S

Effects of cations on rare earth adsorption and desorption in binding sites of montmorillonite

The exchangeability of rare earth (RE) in weathered crust elution-deposited rare earth ores largely depends on its interaction with clay minerals, which may be significantly influenced by various cations. Therefore, the effects of K+, Ca2+ and Al3+ on RE3+ adsorption and desorption in binding sites of montmorillonite (MMT) were investigated. Through the pre-saturation, the interlayer ions of MMT had been replaced by K+, Ca2+ or Al3+. RE3+ can adsorb on the interlayer sites of Ca-MMT and K-MMT, but nearly not Al-MMT. The basal spacing of Ca-MMT is larger than K-MMT, which provides a smaller hinder effect of interlayer collapse for the interlayer diffusion of RE3+. The adsorption capacity followed the order: Ca-MMT＞K-MMT＞Al-MMT and La3+＞Y3+＞Eu3+. It can predict that the grade of the exchangeable RE in ores abundant in Ca2+ is the most, followed by the ore rich in K+ and Al3+ the least. Clay minerals tend to adsorb light RE and hard to adsorb middle and heavy RE. The reversibility of RE adsorbed in interlayers, especially in collapsed interlayers, is far worse than that on externals. The desorption rates of RE were in the order of RE-Al-MMT＞RE-K-MMT＞RE-Ca-MMT and Eu3+＞Y3+＞La3+. For the desorption of interlayer RE3+, NH4+ is better than Mg2+ because the larger change of the basal spacings (Δd) provides more minor activation energy barriers (ΔE) for NH4+ diffusion within interlayers. It can enrich the metallogeny theory of weathered crust elution-deposited rare earth ores and provide a certain theoretical basis for its efficient exploitation

Development Review on Leaching Technology and Leaching Agents of Weathered Crust Elution-Deposited Rare Earth Ores

Weathered crust elution-deposited rare earth ores are key strategic resources and the main source of medium and heavy rare earths. This paper summarizes the development of leaching technology of rare earth ores, compares the advantages and disadvantages of the three generations of leaching technology, and introduces the improved heap leaching technology and the new technology of the leaching–extraction integration and enhanced leaching, focusing on the leaching of weathered crust elution-deposited rare earth ores. In this paper, the development of the leaching agents is expounded, and the research status and the development trend of the composite ammonium salt leaching agent, impurity inhibition leaching agent, swelling inhibition leaching agent, and seepage-promotion leaching agent are also introduced. And this paper summarizes the leaching mechanism and the development direction of leaching agents. Moreover, the future key research direction of weathered crust elution-deposited rare earth ores is proposed, which is green, efficient, safe development and utilization

Study on the Leaching Kinetics of Weathered Crust Elution-Deposited Rare Earth Ores by Hydroxypropyl Methyl Cellulose

In the process of the in situ leaching of weathered crust elution-deposited rare earth ores (WCE-DREOs), there are many problems in the conventional leaching agent, such as a slow leaching rate, low leaching yield and long leaching period. In order to solve the above problems, 2.0 wt% ammonium sulfate was mixed with hydroxypropyl methyl cellulose (HPMC). The effects of the HPMC concentration, temperature, pH and flow rate on the leaching kinetics of rare earth (RE) and aluminum (Al) were investigated. The results showed that when the concentration of HPMC was 0.05 wt%, the leaching equilibrium time of RE and Al was about 60% shorter than that of single ammonium sulfate. With an increase in the leaching temperature, the leaching equilibrium time of RE and Al decreased, and the apparent activation energy of RE and Al was 23.13 kJ/mol and 17.31 kJ/mol, respectively. The leaching process was in line with the internal diffusion kinetic control model. When the pH of the leaching agent was 4.02~8.01, the leaching yield of RE and Al was basically the same, but the leaching yield of Al was greatly increased at pH 2.0 due to a large amount of adsorbed hydroxy-Al in the RE ore eluded. The leaching yield reached the maximum when the flow rate was 0.7 mL/min. The leaching time and the leaching cost of RE can be saved by the composite leaching agent. The results provide theoretical guidance for the development and industrial application of the new composite leaching agent