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이정웅 ( Lee Jeong Ung ),허수영 ( Heo Su Yeong ),이귀세라 ( Lee Gwi Se La ),김사진 ( Kim Sa Jin ),김은중 ( Kim Eun Jung ),남궁성은 ( Namgung Seong Eun ) 대한산부인과학회 2003 Obstetrics & Gynecology Science Vol.46 No.5
Leiomyomas are most common mesenchymal tumors of the vulva, which have an extremely low incidence. Although these tumors are known a low grade tumor, they have to be removed immediately to prevent further growing and sarcomatous change in the future. We experienced a case of leiomyoma of the vulva, and reported it with a brief review of literatures.
OVCAR-3 세포주에서 Annexin V, Propium Iodide와 Cytokeratin 염색에 의한 고사세포의 측정
송민경 ( Song Min Gyeong ),권문기 ( Kwon Mun Gi ),이정웅 ( Lee Jeong Ung ),최예훈 ( Choi Ye Hoon ),김태우 ( Kim Tae U ),류기성 ( Ryu Ki Sung ),나종구 ( Rha Jong Gu ),한구택 ( Han Gu Taeg ) 대한산부인과학회 2003 Obstetrics & Gynecology Science Vol.46 No.7
Objective : This study was designed to estimate the chemosensitivity by a quantitative evaluation of the apoptotic cell fractions using flow cytometry. Methods : The OVCAR-3 cells were exposed to 20 nM or 30 nM taxol for 0 (control), 24 and 48 hours, then removed the taxol contained media, and cultured further with fresh media without taxol. (1) Fluorescin isothiocyanate-conjugated Annexin V (Annexin V-FTTC) and propidium iodide (PI) were added to one test tube to detect the apoptotic cell fractions and at the same time, PI was added to the other tube to stain the DNA. (2) Annexin V-FITC and cytokeratin (clone CAM5.2 and MNF116) were added to the test tube. They were fixed and permeabilized with 1% paraformaldehyde solution and 100% methanol. They were then incubated with phycoerythrin (PE)-conjugated goat anti-mouse immunoglobulin G (GAM IgG_1-PE or GAM IgG_2a-PE) and sequentially stained with PI for DNA. All the stained cells were analyzed by a FACScan flow cytometer. Results : (1) After treatment of 20 nM or 30 nM of taxol, G_2M arrest was observed in both of treatment groups, which increased with time. (2) The G_0G_1 sub-fraction indicative of apoptosis increased with increase of culturing time from 24 hrs to 48 hrs. (3) The early apoptotic cell fraction with positive annexin V-FITC and negative PI increased with increase of culturing time. (4) In cells stained sequentailly with annexin V-FITC, cytokeratin (CAM5.2 and MNF116), and PI after 30 nM taxol treatment, the early apoptotic cell fractions increased with increase of culturing time. However, their extent was somewhat lower than those observed by positive annexin V-FITC and negative PI in cells treated with 20 nM of taxol. Conclusion : The results of sequential stainings with annexin V-FITC, cytokeratin, and PI were consistent with the those of annexin V-FITC and PI with parallel DNA staining. Our results suggested that the level of apoptosis detected by flow cytometry could be a marker of chemosensitivity which could select the sensitive anti-cancer agents before administration to gynecologic cancer patients.