Traditional Chinese Medicine Treatment of Psoriasis by Regulating microRNA： A Review / 中国实验方剂学杂志

The incidence of psoriasis which is characterized by dryness， scaling and itching of the skin has been on the rise. It can have a profound psychological impact on patients' quality of life. Accumulating research has been conducted on the mechanisms of psoriasis in western medicine， from the difference of pathological manifestations of terminal keratinocytes， the disorder of expression of related factors and cells， to the immune imbalance of T lymphocytes and their subsets， or the abnormal transcription dominated by genetic genes. As a result， a complex and huge mechanism network has formed and many hypotheses have emerged. In recent years， with the in-depth research on non-coding genes， it has been clarified that microRNA-modified multi-pathway effect interferes with the occurrence and development of psoriasis and affects the proliferation， apoptosis， and differentiation of keratinocytes. The research on microRNA involves both genetics and immunology， which can help improve the key links in the micro pathway of psoriasis. Thus， it is a key part in the pathogenesis of psoriasis and has also become the hotspot and difficulty of modern research on psoriasis. At the same time， we should give full play to the advantages of traditional Chinese medicine （TCM） in syndrome differentiation and treatment. To be specific， microRNA targets of compound Chinese medicine preparations with the functions of clearing heat， cooling blood， detoxifying and removing blood stasis or effective medicinal monomers such as paeonol， tripterygium glycosides， shikonin， curcumin， total glucosides of paeony and indirubin should be explored， and microRNA can be used as the basis for blood syndrome differentiation of psoriasis. Thereby， the syndrome differentiation theory of TCM and micro indicators of western medicine are integrated， to make full use of characteristics of TCM and guide the clinical syndrome differentiation and treatment. At present， the intervention on microRNA in TCM is rarely studied， and available studies mainly focus on several targets such as microRNA-155， microRNA-210， microRNA-21， microRNA-203， microRNA-320， microRNA-124， microRNA-330， microRNA-146a， and microRNA-15a-5p. This paper summarizes the research on compound Chinese medicine prescriptions and monomers in the treatment and syndrome differentiation of psoriasis through the intervention of microRNA， which is expected to provide a reference for the research on psoriasis in TCM and western medicine and the establishment of microRNA-based database.

Follicular Helper T Cells， Psoriasis， and Chinese Medicine Intervention： A Review / 中国实验方剂学杂志

Follicular helper T （Tfh） cells are a newly discovered subset of CD4+ T cells. As reported， abnormalities in their development， differentiation， and function are closely related to the occurrence of autoimmune diseases. Psoriasis is an autoimmune skin disease and it is intractable with a prolonged course. At present， it is generally believed that immune imbalance mediated by T cells is the core mechanism of the pathogenesis of psoriasis. In the context of this mechanism， Tfh cells are associated with psoriasis， and their cellular level and abnormal expression of related candidates can promote the occurrence of psoriasis. In terms of treatment， Chinese medicine， by virtue of the characteristics of wide application and low price， serves as a good complementary and alternative treatment option for psoriasis. As confirmed by previous findings， some active ingredients or preparations of Chinese medicine used in the treatment of psoriasis can also intervene in and regulate the immune response mediated by Tfh cells and the related candidates. Based on the research reports and experimental data， the present study reviewed the research progress from the differentiation of Tfh cells， the relationship between Tfh cells and psoriasis， and the intervention and regulation of Tfh cells and related molecules by Chinese medicine， which is expected to provide certain theoretical support and references for the determination of new strategies for psoriasis treatment and research in related fields.

Effect of Intervention with Traditional Chinese Medicine on Th17/Treg Balance in Psoriasis： A Review / 中国实验方剂学杂志

Psoriasis is an autoimmune disease presented in the context of inflammation， and it mainly results from proliferation and differentiation defects of keratinocytes and abnormal immune response. However， some cellular and molecular mechanisms remain unclear. Although a variety of drugs and physiotherapies are applicable to this disease， they can only be utilized for a short-term period considering their transient effect， high cost， and serious adverse reactions. It is difficult to achieve satisfactory long-term results in the treatment of psoriasis. With the development of network pharmacology and molecular biology and the modernization of traditional Chinese medicine （TCM）， the multi-component and multi-target characteristics of TCM have become prominent， promoting the in-depth research on TCM by doctors and scholars. Nevertheless， there is no detailed summarization on the mechanisms of TCM in interfering with T helper 17 （Th17）/regulatory T （Treg） cell balance to prevent and treat psoriasis. After reviewing the recent literature data， this paper has found that Chinese herbal monomers， active ingredients， and compounds obviously regulate the Th17/Treg axis in psoriasis. Th17 cells have a pro-inflammatory effect， while Treg cells are responsible for maintaining peripheral tolerance. They function in a mutually exclusive manner， and maintaining the Th17/Treg balance helps to effectively reduce inflammatory reaction and regulate immune homeostasis. As revealed by a series of clinical and experimental studies carried out based on the Th17/Treg axis in psoriasis， reducing the percentage of Th17 cells，increasing the percentage of Treg cells，and regulating the levels of related cytokines and transcription factors are conducive to alleviating inflammation and regaining immune homeostasis，which has provided new ideas for further elucidating the pathological mechanism of psoriasis and alternative plans for developing new treatments against psoriasis.

Maternal Genistein Intake Can Reduce Body Weight in Male Offspring / 生物医学与环境科学（英文）

The study objectives were to investigate the relationship between early exposure to genistein and obesity in young adulthood and to evaluate changes in reproductive health during puberty and adulthood following in utero exposure to genistein. Thirty-two female rats were randomized into four groups; low dose 400 mg genistein/kg diet group (LG), mid-dose 1200 mg genistein/kg diet group (MG), high dose 3600 mg genistein/kg diet group (HG), and control group without genistein diet (CON). Rats were fed genistein at the beginning of pregnancy along with a high-fat diet. Pups were sacrificed at week 4 and week 8 after birth. High performance liquid chromatography (HPLC) results showed a correlation between maternal genistein intake and genistein concentration in pups' plasma. Compared to CON, body weight reduced significantly in male HG group at week 8. No statistical differences were found in plasma estradiol (E2), testosterone (T), interleukin (IL)-6, and C-reactive protein (CRP) levels with early genistein exposure. Furthermore, uterine histopathology showed notable changes in groups HG and MG compared with CON at week 4 and week 8. In conclusion, maternal genistein supplement could reduce body weight in male pups and alter uterine histopathology in female pups.

Comparison of DNA-dependent protein kinase catalytic subunit expression in two lung adenocarcinoma cell lines with different radiosensitivity / 南方医科大学学报

<p><b>OBJECTIVE</b>To investigate DNA-dependent protein kinase catalytic subunit (DNA-PKcs) content and activity in lung adenocarcinoma cell lines and its correlation with radiosensitivity.</p><p><b>METHODS</b>The content and activity of DNA-PKcs were analyzed in two lung adenocarcinoma cell lines A549 and H1299 by Western blotting and the Signa TECT DNA-PK assay kit. The dose-survival relationship for two cell lines was analyzed using clonogenic formation assay.</p><p><b>RESULTS</b>A549 was more radiosensitive than H1299. The survival fractions at 2 Gy (SF2) were 0.7412 in A549 cell line and 0.2473 in H1299 cell line. The content of DNA-PKcs was significantly higher in A549 cells than in H1299 cells (t=10.37, P<0.001). The integrated optical densities were 3.29-/+0.44 in A549 cells and 0.50-/+0.17 in H1299 cells. DNA-PKcs activities in A549 and H1299 cells were 8.29-/+1.37 and 2.47-/+1.09, respectively, showing a significant difference between them (t=5.76, P=0.005).</p><p><b>CONCLUSION</b>DNA-PKcs is an important factor to affect the radiosensitivity of lung adenocarcinoma cell lines.</p>

Association of XAGE-1b gene expression with clinical characteristics of non-small cell lung cancer / 南方医科大学学报

<p><b>OBJECTIVE</b>To explore the association between XAGE-1b gene expression and the clinical characteristics of non-small cell lung cancer (NSCLC).</p><p><b>METHODS</b>Tumor tissue and adjacent normal lung tissue specimens were obtained surgically from 30 patients with resectable NSCLC, from which the total RNA was extracted for RT-PCR to amplify full-length XAGE-1b gene. The products of RT-PCR were identified by electrophoresis and sequencing. The expression of XAGE-1b gene and its association with the clinical characteristics of the patients were analyzed.</p><p><b>RESULTS</b>In the 30 tumor tissue specimens, the expression rate of XAGE-1b gene was 40%, but none of the normal lung tissues expressed this gene. The gene expression was not related to the patients' age, gender, tumor differentiation or clinical stages, but showed significant correlation to their pathological classification. The expression rate of XAGE-1b gene in adenocarcinoma was much higher than that in tumors of other pathological types (61.1% vs 8.3%, P=0.015). XAGE-1b gene expression tended to increase with the TNM stages, which, however, failed to find statistical data support (P>0.05).</p><p><b>CONCLUSIONS</b>XAGE-1b gene is highly expressed in lung adenocarcinoma, and can be an ideal target for tumor immunotherapy.</p>