Meta-analysis on the relationship between the SNP of MMP-2-1306 C>T and susceptibility to breast cancer.

OBJECTIVE: Current conclusions on the potential influence of the single nucleotide polymorphism (SNP) of Matrix metalloproteinase-2 (MMP)-2-1306 C>T on Breast cancer (BCa) susceptibility remain controversial. This study aims to accurately clarify their relation. MATERIALS AND METHODS: The relevant literature on the relation between genetic variation of MMP-2 and BCa susceptibility was searched in PubMed, Web of School, VIP, and CNKI published before March 2019. The keywords used were as follows: "MMP-2, breast/mammary cancer/carcinoma/tumor" or "SNPs of MMP-2, breast/mammary cancer/carcinoma/tumor". Odds ratio (OR) and 95% CI of extracted data from eligible literature were calculated. RESULTS: A total of 7 studies involving 1823 BCa patients and 1899 healthy controls were included. All control genes were consistent with HWE (p>0.05). Different genetic models were utilized to clarify the potential influence of MMP-2-1306 C>T (rs243865) on BCa susceptibility. No significant correlation was identified between the SNP of MMP-2-1306 C>T and BCa susceptibility based on the calculated OR and 95% CI in different genotypes: CC vs. CT&TT: p=0.54, OR=0.88 (95% CI=0.58-1.33); TT vs. CC&CT: p=0.67, OR=1.07 (95% CI=0.79-1.44); CC vs. TT: p=0.73, OR=0.95 (95% CI=0.70-1.29); C Allele vs. T Allele: p=0.93, OR=1.02 (95% CI=0.70-1.47). CONCLUSIONS: The SNP of MMP-2-1306 C>T did not correlate to the susceptibility to BCa.

IL-10 treatment is associated with prohibitin expression in the Crohn's disease intestinal fibrosis mouse model.

Prohibitin, which can inhibit oxidative stress and mitochondrial dysfunction, has been shown to have significant anti-inflammatory activities. Here, we investigate the effects of altering prohibitin levels in affected tissues in the interleukin-10 knockout (IL-10KO) mouse model with intestinal fibrosis. The aim of this study is to investigate the effects of IL-10 on prohibitin and the role of prohibitin in intestinal fibrosis of murine colitis. After the mice were treated with IL-10, prohibitin expression and localization were evaluated in IL-10KO and wild-type (WT, 129/SvEv) mice. The colon tissue was then investigated and the potential pathogenic molecular mechanisms were further studied. Fluorescence-based quantitative polymerase chain reaction (FQ-PCR) and immunohistochemistry assays revealed a significant upregulation of prohibitin with IL-10 treatment. Furthermore, IL-10 decreases inflammatory cytokines and TGF-ß1 in the IL-10KO model of Crohn's disease and demonstrates a promising trend in decreasing tissue fibrosis. In conclusion, we hypothesize that IL-10 treatment is associated with increased prohibitin and would decrease inflammation and fibrosis in an animal model of Crohn's disease. Interestingly, prohibitin may be a potential target for intestinal fibrosis associated with inflammatory bowel disease (IBD).

Down-regulation of four arsenic antagonists on apoptosis and telomerase activity induced by arsenic trioxide in three myelocytic leukemia cell lines.

AIM: To investigate regulative effects of thiol reagents, N-acetyl-l-cysteine (NAC) and natrii dimercaptosussinas (NDMS), catalase (CAT), and calcium chelator 2-[(2-bis-[carboxymethyl]-amino-5-methyl-phenoxy)-met]-6-methoxy-8-bis-[carboxy-methyl]-aminoquinoline (Quin 2) on apoptosis and telomerase activity induced by arsenic trioxide (As2O3) in three myelocytic leukemia cell lines. METHODS: Flow cytometry was used to examine apoptosis and a PCR ELISA kit was used to detect telomerase activity. RESULTS: As2O3 induced about 40 % - 60 % of apoptosis in NB4, K562, and HL-60 cells at the concentration of 0.6, 2.7, and 8.1 micromol/L respectively, as well as down-regulated telomerase activities in three cell lines. NAC 4 mmol/L, NDMS 200 micromol/L, CAT 80 kU/L, and Quin 2 20 micromol/L could down-regulate apoptosis variously induced by As2O3. NAC and CAT alone could decline telomerase activity in three cell lines and further decline telomerase activities that had been decreased by As2O3, whereas Quin 2 antagonized the decline in K562 and HL-60 cells. CONCLUSION: Thiol activity loss, free radical alteration, intracellular calcium changes, and decline of telomerase activity might be involved in As2O3-induced apoptosis. NAC, NDMS, CAT, and Quin 2 antagonized in some extent the effect of As2O3 on the three tested cell lines.

[Sequential observation on the influence of artificial wind-cold environment to immunologic function of mononuclear phagocytic system in mice].

According to TCM theory of Six Evils, the Wind-Cold is one of the pathogen. In order to find the mechanism of Wind-Cold in causing disease, the effect of subacute Wind-Cold stimulation on the phagocyte immunization in mice was observed. Results showed that through exposing in the Wind-Cold environment, the reticuloendothelial system (RES) clearance function and the hydrogen-peroxide releasing of peritoneal macrophage were suppressed. Sequential observation showed that the peak of immunosuppression occurred on the 3rd day after stimulation and began to normalize at 5th day. These results suggested that Wind-Cold stimulation could inhibit temporary phagocytosis of macrophage and bacteriocidal effect. Action of immunosuppression was believed to be produced by the increase of stress hormone after stimulation. Results also suggested that the pathogenic action of Wind-Cold on disease is somewhat related with the suppression of nonspecific cellular immunity.

Prolonged disease-free survival after ablative chemoradiotherapy and autologous bone marrow transplantation in adult malignant lymphoma.

From June 1983 to December 1991, 21 adult patients with intermediate or high-grade malignant lymphoma (ML) were treated by ablative chemoradiotherapy, including vincristine, cytosine arabinoside, BCNU and cyclophosphamide plus total lymphoid or body irradiation with boost irradiation over bulky and original tumor areas (Hd-VCCA+TL(B) I) together with autologous bone marrow transplantation (ABMT). Five patients were in advanced stage, 2 in drug-resistant relapse, 6 in drug sensitive relapse, 6 in first complete remission (CR1) and 2 in CR2. One with marrow involvement at ABMT. The 8-year disease-free survival after ABMT in patients with Hodgkin's disease (HD) and non-Hodgkin's lymphoma (NHL) in 89% and 63%, respectively, with a median follow-up up to 34 months. This study demonstrated that our Hd-VCCA+TL(B) I regimen and ABMT performed early in CR or drug-sensitive relapse of adult poor prognosis lymphoma, may potentially cure more than 70% of them. The toxicity of the present treatment is tolerable. The results confirm the value of ABMT in the treatment of adult ML, and suggest that it is necessary to purge the residual tumor cells in the bone marrow at ABMT in patients with marrow infiltration, or lymphoblastic lymphoma.

[Effects of thyroxine and methimazolum on monamine transmitters in preoptic/anterior hypothalamic area and peripheral serum in rats].

The contents of monamine transmitters in preoptic/anterior hypothalamic (PO/AH) area and in the serum of rats injected with thyroxine (T4, 1 mg/100 g body wt/d, for 10 d, hypodermic i.) and fed with methimazolum (10 mg/100 g body wt/d, for 15 d) were assayed by high pressure liquid chromatography with electrochemical detector (HPLC-ECD). It was found that the content of dopamine and homovanillic acid in PO/AH area showed significant increase (P less than 0.01) associated with a slight rise (P greater than 0.05) of 5-hydroxytryptamine (5-HT) and 5-hydroxyindoleacetic acid (5-HIAA), and with no change of norepinephrine in the thyroxine group. After fed with methimazolum, the content of norepinephrine decreased significantly (P less than 0.05), but no obvious changes occurred in dopamine, homovanillic acid, 5-HT and 5-HIAA. By synchronous analysing of monamine transmitters in peripheral serum, it was showed that there was no significant linear relationship between the changes of monamine transmitters in the brain and in the serum. The correlation between thyroxine and methimazolum on the content of monamine transmitters and on the change of body temperature was also discussed.