Qi Zhang

Inspired by the hydrophilicity effect of arginine (Arg) in water channel aquaporins (AQPs), Arg was incorporated into the polyamide layer during interfacial polymerization to enhance the permeation and antifouling performance of the nanofiltration (NF) membranes. Due to the presence of active amine groups, Arg became another aqueous phase monomer along with piperazine (PIP) to react with trimesoyl chloride (TMC) during interfacial polymerization, which was incorporated into the polyamide network. The resulting polyamide NF membranes were characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), atomic force microscopy (AFM), static water contact angle, zeta potential, and positron annihilation spectroscopy (PAS) measurement. The effects of incorporating Arg in aqueous phase on water permeability and the rejection of dyes and inorganic salts of the NF membranes were studied, respectively. Similar to its function in AQPs, Arg apparently increased the hydrophilicity and the negative charges of the membrane surface and, consequently, the permeation performance. When the addition of Arg reached 40% to PIP, the water flux was doubled and the rejection ratios of Congo red and Orange GII were still >90%. Meanwhile, the antifouling experiments verified that the modified polyamide NF membranes possessed excellent fouling-resistant performance for negatively charged foulants of BSA, emulsified oil droplet, and humic acid. The flux was decreased below 15%, and recovery even rose to 89%.

Recently, evidences show that cancer stem cells (CSCs) are a type of cancer cell group with self-renewal and play a huge role in tumor recurrence, metastasis, and drug resistance. Finding new treatment directions and targets for cancer prognosis and reducing mortality has become a top priority. OCT4, as a transcription factor, participates in maintaining the stem characteristics of CSCs, but the mechanism of OCT4 is often overlooked. In this review, we try to illustrate the mechanism by which OCT4 plays a role in CSCs from the perspective of genetic modification of OCT4, non-coding RNA, complexes and signaling pathways associated with OCT4. Our ultimate goal is to provide new targets for cancer treatment to prolong the survival of cancer patients.

Early simulation work in the decision-making stage faces several challenges, including, for example, rapid changes of design, input variable uncertainties, and the lack of design information, although early design work represents a large percentage of energy saving potential. The availability of simulation tools for early design stages can help the architect analyze more alternatives. In this study, the existing simulation tools were explored and classified into three categories: simulation plugins based on the design software, geometry user interfaces for a simulation engine, and self-governing simulation tools. Each category’s typical tools were illustrated with their use, and a uniform standard comparison was conducted to screen tools that are available in the early design stages. The future trends of simulation tools are discussed in the second part: building databases based on existing knowledge, uncertainty and sensitivity analyses, and optimization. Time-consuming simulation is a problem in the use of simulation tools in early design stages. Advanced techniques were developed in this part for fast computing, i.e., cloud computing, parallel computing, meta-models, and more statistical methods. This paper illustrates the practical application of particular simulation tools in the early design stage, presents their limitations, and discusses decision-support tools for specific building design activities.

Cancer stem cells (CSCs) play an essential role in the progression of many tumors. Sonic hedgehog (Shh) and Wnt/β-catenin pathways are crucial in maintaining the stemness of CSCs. Curcumin has been shown to possess anticancer activity. However, the interventional effect of curcumin on breast CSCs has not been elucidated. In the present study, we investigated the role of Shh and Wnt/β-catenin pathway in curcumin inhibition of breast CSCs. We showed that the levels of breast CSCs markers were significantly elevated in SUM159 and MCF7 sphere-forming cells. We further illustrated that curcumin effectively decreased breast CSCs activity by inhibiting tumor sphere formation, decreasing breast CSCs markers (CD44, ALDH1A1, Nanog, and Oct4), as well as inhibiting proliferation and inducing apoptosis. Moreover, we showed that downregulation of Shh and Wnt/β-catenin activity resulted in breast CSCs inhibition; curcumin exerted an inhibitory effect on breast CSCs by suppressing both Shh and Wnt/β-catenin pathways. Taken together, these results indicated curcumin inhibition of breast CSCs by downregulation of Shh and Wnt/β-catenin pathways. Findings from this study could provide new insights into the potential therapeutic application of curcumin in breast CSCs elimination and cancer intervention.