1.Synthesis and antitumor activities of triazacyclodecane and its platinum (II) complex.
Shuang-Sheng ZHOU ; Qun-Ying ZHANG ; Kei QIN ; Chuan-Hua LU ; Fu-Xing XIE
Acta Pharmaceutica Sinica 2008;43(5):490-494
To search for potential antitumor drugs with potent efficiency and low toxicity, a novel 1,4,7-triazacyclodecane and its platinum (II) complex were synthesized. These compounds were characterized by elemental analysis, IR, 1H NMR, 13C NMR, MS spectra, thermoanalysis and conductivity measurement. Antitumor activity study indicated these compounds had strong antitumor activity in vitro to some extent. Inhibition of human liver tumor of CA was examined by antitumor rate and growth rate, complex C showed inhibition activity on transplanting-tumor growth of CA, 12 mg x kg(-1) was as potent as cisplatin, its ID50 was 853.6 mg x kg(-1).
Animals
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Antineoplastic Agents
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chemical synthesis
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chemistry
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pharmacology
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Cell Line, Tumor
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Cell Proliferation
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drug effects
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Drug Screening Assays, Antitumor
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Female
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Humans
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Inhibitory Concentration 50
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Liver Neoplasms
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pathology
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Male
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Mice
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Neoplasm Transplantation
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Organoplatinum Compounds
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chemical synthesis
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chemistry
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pharmacology
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Random Allocation
2.Effect of genetic polymorphism of MTNR1A gene on adolescent idiopathic scoliosis.
Xu-sheng QIU ; Leung-sang TANG ; Hiu-yan YEUNG ; Hoi-kei KWOK ; Kwong-man LEE ; Ling QIN ; Yong QIU ; Chun-yiu CHENG
Chinese Journal of Surgery 2007;45(18):1264-1266
OBJECTIVETo investigate whether the MTNR1A gene promotor polymorphism (rs2119882) are associated with the occurrence or curve severity of adolescent idiopathic scoliosis (AIS).
METHODS226 AIS patients and 277 normal controls were recruited. The maximum Cobb angles were recorded in AIS patients. PCR-RFLP was used for the genotyping.
RESULTSThe genotype and allele frequency distribution were comparable between AIS and normal control, the mean maximum Cobb angle of different genotypes of rs2119882 were similar with each other among AIS patients.
CONCLUSIONThe MTNR1A gene promoter polymorphism was neither associated with the occurrence nor the curve severity of AIS.
Adolescent ; Adult ; Child ; Female ; Gene Frequency ; Genetic Predisposition to Disease ; Genotype ; Humans ; Male ; Polymerase Chain Reaction ; Polymorphism, Genetic ; Polymorphism, Restriction Fragment Length ; Receptor, Melatonin, MT1 ; genetics ; Scoliosis ; genetics
3.The association between new generation oral contraceptive pill and the development of inflammatory bowel diseases.
Santosh SANAGAPALLI ; Yanna KO ; Viraj KARIYAWASAM ; Siew C NG ; Whitney TANG ; Hithanadura Janaka DE SILVA ; Minhu CHEN ; Kaichun WU ; Satimai ANIWAN ; Ka Kei NG ; David ONG ; Qin OUYANG ; Ida HILMI ; Marcellus SIMADIBRATA ; Pises PISESPONGSA ; Saranya GOPIKRISHNA ; Rupert W LEONG
Intestinal Research 2018;16(3):409-415
BACKGROUND/AIMS: To examine the association between use of oral contraceptive pills (OCPs) and the risk of developing inflammatory bowel diseases (IBD), in a modern cohort. METHODS: A prospective nested case-control study across sites in the Asia-Pacific region was conducted; involving female IBD cases and asymptomatic controls. Subjects completed a questionnaire addressing questions related to OCP use. Primary outcome was the risk of development of IBD of those exposed to OCP versus non-exposure. Secondary outcomes were development of Crohn's disease (CD) versus ulcerative colitis (UC), and whether age of first use of OCP use may be associated with risk of IBD. RESULTS: Three hundred and forty-eight female IBD cases (41% CD, median age: 43 years) and 590 female age-matched controls were recruited. No significant association was found between OCP use and the risk of IBD (odds ratio [OR], 1.65; 95% confidence interval, 0.77–3.13; P=0.22), CD (OR, 1.55) or UC (OR, 1.01). The lack of association persisted when results were adjusted for age and smoking. IBD cases commenced OCP use at a younger age than controls (18 years vs. 20 years, P=0.049). CONCLUSIONS: In this large cohort of subjects from the Asia-Pacific region, we found a modest but not significantly increased risk of developing IBD amongst OCP users.
Case-Control Studies
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Cohort Studies
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Colitis, Ulcerative
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Contraceptives, Oral
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Crohn Disease
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Female
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Humans
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Inflammatory Bowel Diseases*
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Prospective Studies
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Smoke
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Smoking