1.Content Determination of Domiphen by Potassium Chromate Indicator Method
Xianglan JIANG ; Nannan YANG ; Dongzhi YANG ; Qisi LIN
China Pharmacy 2007;0(29):-
OBJECTIVE: To establish a method for the content determination of domiphen by potassium chromate indicator method.METHODS: The contents of domiphen were determined based on the theory that bromide ion in domiphon could react with AgNO3 to produce silver bromide precipitation.The method was compared with the sodium tetraphenylborate method issued in China Pharmacopeica(2005 edition).RESULTS: The RSD of contents was 0.18%,and the average recovery was 100.2% in the potassium chromate indicator method.There was no significant difference between the results of two determination methods by t-test.CONCLUSION: The potassium chromate indicator method is simple,fast and accurate,which can be used for the content determination of domiphen.
2.Pax5 expression in Non-Hodgkin's Lymphomas and Acute Leukemias.
Xianglan ZHANG ; Zhenhua LIN ; Insun KIM
Journal of Korean Medical Science 2003;18(6):804-808
The Pax5 gene encodes the B-cell-specific activator protein which is a key regulator in development and differentiation of B-cell. We studied the expression of Pax5 in hematologic malignancies to evaluate the diagnostic utility as a B cell marker. Materials included 70 B cell lymphomas, 26 T cell lymphomas, 53 acute leukemias, and 6 multiple myelomas (MMs). Representative areas from the paraffinembedded tissues were selected for tissue microarray, and the expressions of Pax5 was immunohistochemically evaluated. Pax5 was strongly expressed in most of the B cell lymphomas; 44 of 47 diffuse large B cell lymphomas (93.6%), 15 of 16 marginal zone B cell lymphomas (93.8%), all 3 mantle cell lymphomas, 2 follicular lymphomas, and 2 Burkitt's lymphomas (100%). However, Pax5 was expressed in only one of 26 T cell lymphomas. Among leukemias, it was expressed in 10 of the 14 B acute lymphocytic leukemias (ALLs) (72.4%), but also in 3 of the 6 T ALLs (50%), 13 of the 26 acute myelogenous leukemias (AMLs) (50%) and in all 3 ALL arising in chronic myelogenous leukemias and 4 mixed B ALL and AML. In MMs, Pax5 was negative in all cases. We concluded that Pax5 is very useful B cell marker in classification of lymphomas, but not of acute leukemias.
B-Lymphocytes/pathology/physiology
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DNA-Binding Proteins/genetics/*metabolism
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Human
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Leukemia/classification/*metabolism/pathology
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Lymphoma, Non-Hodgkin/classification/*metabolism/pathology
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Support, Non-U.S. Gov't
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Tonsil/cytology/metabolism/pathology
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Transcription Factors/genetics/*metabolism
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Tumor Markers, Biological/*metabolism
3.Application of homemade aromatic masks in non-small cell lung cancer patients with chemotherapy
Yuxin WU ; Ni LI ; Naying YU ; Danping YOU ; Qing LIN ; Xianglan LIN
Chinese Journal of Modern Nursing 2021;27(2):256-260
Objective:To explore the effect of homemade aromatic masks on nausea, vomiting and pain in non-small cell lung cancer patients with chemotherapy.Methods:From October 2018 to August 2019, convenience sampling was used to select 82 patients with non-small cell lung cancer admitted to the 900th Joint Logistic Support Unit of the People's Liberation Army of China. All patients were randomly divided into control group and experimental group, each with 41 cases. Control group carried out the routine care, and experimental group was treated with the homemade aromatic mask on this basis. The Chinese version of Index of Nausea and Vomiting and Retching (INVR) and the Brief Pain Index (BPI) were used to compare nausea, vomiting and pain indicators of patients between two groups during chemotherapy.Results:On the third day of chemotherapy, the total score of nausea and vomiting, and the average pain score of experimental group were (11.00±5.46) and (1.63±1.14) respectively, lower than those of control group, and the differences were statistically significant ( t=-6.635, -4.781; P<0.01) . Conclusions:The homemade aromatic mask can relieve chemotherapy-induced nausea and vomiting in non-small cell lung cancer patients with chemotherapy, and reduce the pain of patients.
4.cDNA Microarray Expression Analysis in HPV-Infected Uterine Cervical Cancer Cell Line.
Kuol HUR ; Zhenhua LIN ; Xianglan ZHANG ; Chan Woo PARK ; Hye Ok KIM ; Jun Hyung CHO ; In Soo KANG ; Young Sik KIM ; In Sun KIM
Korean Journal of Obstetrics and Gynecology 2003;46(4):810-819
OBJECTIVE: To estimate the difference in gene expression related to carcinogenesis between HPV 16 positive squamous cell carcinoma and HPV 16 positive adenocarcinoma of cervix. METHODS: We used cDNA microarray technology to identify alterations in gene expression of human cervical cancers. Gene expression of three cell lines, CaSki and SiHa (HPV 16 positive squamous cell carcinoma) and HeLa (HPV 16 positive adenocarcinoma) were compared with HT3 (HPV 16 negative squamous cell carcinoma). The microarray contains twin spots for 344 cancer-associated genes. RESULTS: The analysis showed several interesting findings: (1) In all three squamous cell lines, CD4, CSF1, MMP15 and TNFR6 were increased, whereas SLC3A2 were decreased, (2) Only in adenocarcinoma cell line HeLa, CDC25A, CDK2, CDK9, IL2, PF4, MAD, FCER2, MAP4K1 and MS4A1 were increased, and PLAU, IL8, IL9R and ATK were decreased. (3) In both squamous cell carcinoma cell lines CaSki and SiHa, 61 genes which belong to chemokine, cell cycle, growth factor, interleukin, adhesion molecule, protein kinase and TNF were increased, whereas 10 genes which are associated with apoptosis and cytokine were increased only in SiHa, and 97 genes which are associated with a variety of cell functions were increased only in CaSki. CONCLUSION: We suggest that there might be common, but also different carcinogenic mechanisms involved in HPV 16 related cervical cancers according to the histologic subtypes and different tumors.
Adenocarcinoma
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Apoptosis
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Carcinogenesis
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Carcinoma, Squamous Cell
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Cell Cycle
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Cell Line*
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Cervix Uteri
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DNA, Complementary*
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Female
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Gene Expression
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Human papillomavirus 16
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Humans
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Interleukin-2
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Interleukin-8
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Interleukins
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Oligonucleotide Array Sequence Analysis*
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Protein Kinases
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Uterine Cervical Neoplasms*