• Journal of Radiation Protection and Research
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• 제31권2호
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• pp.53-63
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• 2006

원전 종사자를 대상으로 경시적인 코호트 연구를 통하여 저준위 방사선 노출과 암 발생 위해도를 규명하고자 하였다. 방사선 노출에 관한 정보는 한국수력원자력(주)의 방사선 관리 DB에서 수집하였고, 암 발생에 관한 정보는 한국인 중앙 암 등록 자료를, 암 사망에 관한 정보는 통계청 사망원인 자료를 이용하여 수집하였다. 방사선 노출과 암 발생 위해도는 표준화 암 사망비(SMR)와 표준화 암 발생 비(SIR)로 평가하였다. 노출 군에서 암 발생에 대한 상대위험도는 1.08로 평가되었으나 전체 암에 대한 SIR은 0.81로 유의성이 관찰되지 않았다. 암 사망에 대한 상대위험도는 1.21 이었으나 전체 암에 대한 SMR도 0.86으로 역시 유의성은 관찰되지 않았다. 암 유형별 양상은 우리나라 일반인과 유사한 결과를 보였으며, 방사선량 증가에 따른 양-반응 관계 또한 확인되지 않았다.

• 한국산업보건학회지
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• 제16권4호
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• pp.398-412
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• 2006

The purpose of this study is to investigate the relationship between the acceleration of vibration by the powered hand tools used in the shipbuilding industry, and to develop the prospective prevalence model for the hand-arm vibration syndrome among the shipbuilding workers.The acceleration levels and frequencies of six types of grinder were measured using the ISO5349 method along with the time of exposure to the vibration from the powered hand tools. Medical examination for 114 workers were performed using the cold provocation test. Comparisons were made between the estimated prevalence of hand-arm vibration syndrome from ISO5349 and the observed values from the medical examinations. By multiple regression, we developed the prospective prevalence model of hand-arm vibration syndrome produced by the hand tools used in the shipbuilding industry. 4 hour-energy-equivalent frequency-weighted accelerations were $6.23m/s^2$ in the grinding job done after welding, and $13.39m/s^2$ in the grinding job done before painting. The mean exposure time while holding powered hand tools was 4.64 hours. Prevalence rates of Raynaud's Phenomenon were 12.04% in the grinding after soldering, and 42.9% in the grinding before painting measured using the ISO5349 method. After exposure to vibration for 10.79 years, about a half of the workers in the grinding after welding could developed Raynaud's Phenomenon. For the workers in the grinding before painting, the latency was 5.02 years. The ISO equation for dose response relationship was not significantly correlated with observed recovery rates of finger skin temperatures, blood flows and amplitudes of nerve conduction velocities. A multiple regression model for dose-response relationship was proposed from the results. Recovery rate of the skin temperatures = -0.668+ 0.337 ${\times}$ 4 hour energy equivalent frequency-weighted accelerations + 0.767 ${\times}$ duration of vibration exposure(years) The validity was proved by multiple regression analysis after correlation transformation and regression results based on model-building data and validation data.

• 대한방사선치료학회지
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• 제22권2호
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• pp.123-129
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• 2010

목 적: 방사선 치료의 선량평가를 위해 사용되는 Optically stimulated luminescent dosimeters (OSLD) 선량 특성을 분석하여, 선량 측정의 유용성을 알아보고자 한다. 대상 및 방법: $NanoDot^{TM}$와 $Inlight^{TM}$MicroStar Reader, Solid Water Phantom, 의료용 선형가속기 $TRYLOGY^{(R)}$를 사용하였다. 측정 조건은 OSLD를 Solid Water Phantom의 $D_{max}$ 깊이에 위치시킨 후 SSD는 100 cm, Field size는 $10{\times}10\;cm^2$로 하고 300 MU/min으로 6 MV 광자선, 100 cGy의 방사선을 조사하였다. OSLD를 10분 마다 판독하면서 변화값을 측정하였고, OSLD에 선량을 50 cGy와 100 cGy씩 누적시켜 판독하였다. 또한 에너지 의존성은 6 MV, 15 MV, 4~20 MeV를 사용하였다. 선량률은 100~1,000 MU/min로 변화시키면서 측정하였다. 광자선 6 MV의 PDD의 변화를 측정하기 위해 OSLD와 전리함(Ionization chamber) (FC 65P-747)을 사용하였다. 결 과: 시간의 경과에 따른 OSLD의 재현성은 ${\pm}2.5%$였다. OSLD의 선량에 대한 선형성(linearity)을 평가한 결과 300 cGy까지는 선형적으로 증가하였고, 300 cGy 이상에서는 초선형적(supralinearity)으로 증가하였다. 에너지 의존성은 ${\pm}2%$ 이내였고 선량율 의존성은 ${\pm}3%$ 이내였다. 6 MV 광자선에 대하여 OSLD로 측정한 $PDD_{10}$은 66.7%, $PDD_{20}$은 38.4%였고 전리함(Ionization chamber)으로 측정한 $PDD_{10}$은 66.6%, $PDD_{20}$은 38.3%였다. 결 론: OSLD의 특성을 분석한 결과 시간, 에너지, 선량률의 변화에 따른 차이는 ${\pm}3%$ 이내였으며 전리함(Ionization chamber)과 비교한 PDD는 0.3% 이내였다. 또한 300 cGy까지는 선량이 선형적으로 증가하였다. OSLD는 여러 번 반복 측정이 가능하였고 측정과 판독이 용이하여 선량계로서 유용성을 확인하였다.

• IMMUNE NETWORK
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• 제4권4호
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• pp.244-249
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• 2004

Background: Corticotropin-Releasing Hormone (CRH), an important regulator of stress response, has a potent immunoregulatory effect with the ability to promote the growth of various cancer through CRH receptor type 1 under stress. Although the metastasized cancers through cell migration are more aggressive than the primary cancers, little is known about the effect of CRH on cell migration. Gastric cancer is prone to metastasize to other tissues and it is reported that gastric cancer is response to various stresses such as oxidative stress. Herein, we studied the relationship between CRH and gastric cancer cell migration. Methods: We used gastric cancer cell line, MKN-28 and tested the CRH receptor type 1 expression on MKN-28 by RT-PCR. To examine the change in the ability of migration by CRH in MKN-28, cells were incubated with CRH and then migration ability was measured using a cell migration assay. Results: We confirmed that CRH receptor type 1 was expressed in MKN-28 and HaCaT cells. The migration ability of MKN-28 cells was increased by CRH in a time-, dose- dependent manner. Conclusion: These data suggest that CRH increases migration ability in gastric cancer cell line and that CRH may be a critical regulator in the metastasis of gastric cancer cell.

• 멤브레인
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• 제27권2호
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• pp.138-146
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• 2017

새로운 형태의 페녹시-카르복시레이토페녹시기가 함께 치환된 포스파젠 고분자를 여러 치환율을 가지고 합성하였다. 이러한 형태의 포스파젠 고분자를 이용해 당뇨병 진단막을 제조하여 혈액 속의 글루코우즈의 농도를 변화시켜가며 680 nm에서의 흡광도를 측정하였다. 기본적으로 흡광도가 시간에 따라 변화하는 양(K/S)과 글루코우즈의 농도가 직선적인 관계를 가지는 것으로 나타났다. 소수성기인 페녹시기와 친수성기인 카르복시레이토페녹시기의 치환율이 글루코우즈 농도 측정에 미치는 영향을 조사하였다. 친수성기의 치환율이 10% 이하인 경우에는 글루코우즈의 침투속도가 너무 느려 글루코우즈의 농도 측정이 어려웠다. 그러나 친수성기의 치환율이 10% 이상으로 증가함에 따라 글루코우즈의 농도와 K/S의 기울기 값(Dose-Response Slope : DRS)이 점차 증가하였다. 하지만 친수성기의 치환율이 30% 이상일 경우에는 글루코우즈가 너무 빨리 침투하여 DRS가 급격히 증가하였다.

• Asian Pacific Journal of Cancer Prevention
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• 제13권9호
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• pp.4777-4781
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• 2012

Objective: To investigate the relationship between the efficacy and safety of different doses of thalidomide (Thal) plus dexamethasone (Dex) as the initial therapy in elderly patients with newly diagnosed multiple myeloma (MM). Methods: Clinical data of 28 elderly patients with newly diagnosed MM who underwent the TD regimen as the initial therapy were analyzed retrospectively. The patients were divided into two groups according to the maximal sustained dose of Thal: lower dose (group A) and higher dose (group B). The overall response rate (ORR), progression free survival (PFS), overall survival (OS), and adverse events (AES) were compared between the two groups. Results: A total of 28 patients were followed up with a median of 18 months. The ORR was 60.1%. The median response time and PFS were 2.0 and 17.0 months, respectively. The mean sustained dose of Thal in group B was significantly higher than group A (292.9 mg v 180.4 mg, P=0.01). There was no significantly difference in ORR (57.1% v 64.3%, P=1.00) and PFS (9.63months v 17.66 months, P=0.73) between groups A and B. During the follow up, only five patients died (<40%) and, therefore, median OS values were not available. It is estimated, however, that the mean survival time in the two groups was 35.6 and 33.4 months (P>0.05), respectively. All of the patients tolerated the treatment well. The incidence of AES in patients with a grading above 3 in group B was significantly higher than in group A (P=0.033). Conclusions: The TD regimen results in a high response rate and manageable AES as the initial therapy in elderly patients with MM. TD should be considered as the front line regimen for the treatment of elderly patients with MM in areas with financial constraints. The clinical response can be achieved at a low dose Thal with minimal toxicity.

• Bulletin of the Korean Chemical Society
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• 제30권10호
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• pp.2318-2328
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• 2009

Massive deadenylation of adenine based-nucleosides induced by halogenated alkanes at the physiological condition have been observed. For the study of deadenylation effects by the different substituents and/or functionality in halogenated alkanes, diverse kinds of halogenated alkanes were incubated with adenine based-nucleosides (ddA, dA and adenosine) for 48 h at the physiological condition (pH 7.4, $37\;{^{\circ}C}$), which were analyzed by HPLC and further confirmed by LC-MS. Among the sixteen different halogenated alkanes, we observed massive deadenylation of nucleosides by 2-bromo-2-methylpropane, 2,3-dibromopropene, 2-bromopropane, bromoethane and 2-iodopropane. The order of deadenylation rate was highest in 2-bromo-2-methylpropane followed by 2,3-dibromopropene, 2-bromopropane, bromoethane and 2-iodopropane. In addition, time and dose response relationship of deadenylation in adenine based-nucleosides induced by 2-bromo-2-methylpropane, 2,3-dibromopropene, 2-bromopropane, bromoethane and 2-iodopropane at the physiological condition were investigated. In addition, deadenylation of calf thymus DNA induced by halogenated alkanes was also investigated. These results suggest that the toxic effect of certain halogenated alkanes might be from the depurination of nucleosides.

• Bulletin of the Korean Chemical Society
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• 제30권12호
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• pp.2949-2958
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• 2009

Massive deguanylation of guanine based-nucleosides induced by halogenated alkanes at the physiological condition have been observed. For the study of deguanylation effects by the different substituents and/or functionality in halogenated alkanes, diverse kinds of halogenated alkanes were incubated with guanine based-nucleosides (ddG, dG and guanosine) for 48 h at the physiological condition (pH 7.4, 37$^{\circ}C$), which were analyzed by HPLC and further confirmed by LC-MS. Among the sixteen different halogenated alkanes, we observed massive deguanylation of nucleosides by 2-bromo-2-methylpropane, 2,3-dibromopropene, 2-bromopropane, bromoethane and 2-iodopropane. The order of deguanylation rate was highest in 2-bromo-2-methylpropane followed by 2,3-dibromopropene, 2-bromopropane, bromoethane and 2-iodopropane. In addition, time and dose response relationship of deguanylation in guanine basednucleosides induced by 2-bromo-2-methylpropane, 2,3-dibromopropene, 2-bromopropane, bromoethane and 2-iodopropane at the physiological condition were investigated. Deguanylation of calf thymus DNA induced by halogenated alkanes was also investigated. These results suggest that the toxic effect of certain halogenated alkanes might be from the depurination of nucleosides.

• Toxicological Research
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• 제18권4호
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• pp.355-362
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• 2002

Pathophysiological elevation of intracellular calcium concentration ($[Ca^{2+}]_1$) in the neuron has been considered as an important responsible factor in the neuronal cell damages. However the mechanism of increase of $[Ca^{2+}]_1$ and the relationship between $[Ca^{2+}]_1$ level and cytotocixity have not been fully demonstrated. In the present study, real-time alteration of $[Ca^{2+}]_1$and cellular response (cell damages) in the pheochromocytoma cells (PC12) stimulated by glutamate were investigated. Glutamate dose dependently decreased cell viability determined propidium iodide fluorescence method and morphology change. Conversely related with cell damages, glutamate dose dependently increased the level of［Ca$^{2+}$］$_{i}$ . To investigate the mechanism of glutamate-induced increase of $[Ca^{2+}]_1$,$[Ca^{2+}]_1$, was first measured in the cell cultured in calcium free media and in the presence of dantrolene, an inhibitor of calcium release from ryanodine receptor located in endoplasmic reticulum (ER). Similar to the increase$[Ca^{2+}]_1$ in the calcium-containing media, glutamate dose dependently increased $[Ca^{2+}]_1$ in the cell cultured in free calcium media. However pretreatment (2 hr) with 20~50 $\mu\textrm{M}$ dantrolene substantial lowered glutamate-induced increase of $[Ca^{2+}]_1$, suggesting that release of calcium from ER may be major sourse of increase of $[Ca^{2+}]_1$ in PC12 cells. Dantrolene-induced inhibition of $[Ca^{2+}]_1$ resulted in recovery of cytotoxicity by glutamate. Relevance of N-methy-D-aspartate (NMDA) receptor, a type of glutamte receptor on glutamate-induced incense of $[Ca^{2+}]_1$,$[Ca^{2+}]_1$ was also determined in the cells pretreated (2 hr) with NMDA receptor antagonist MK-80l. Glutamate-induced increase of $[Ca^{2+}]_1$ was reduced by MK-801 dose dependently. Furthermore, glutamate-induced cytotoxicity was also prevented by MK-80l. These results demonstrate that glutamte increase $[Ca^{2+}]_1$ dose dependently and thereby cause cytotoxicity. The increase of $[Ca^{2+}]_1$ may release from ER, especially through ryanodine receptor and/or through NMDA receptor Alteration of calcium homeostasis through disturbance of ER system and/or calcium influx through NMDA receptor could contribute glutamate-induced cell damages.s.

• IMMUNE NETWORK
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• 제5권4호
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• pp.247-251
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• 2005

Background: Natural killer (NK) cells are CD3 (-) CD14 (-) CD56 (+) lymphocytes. They play an important role in the body's innate immune response. They can induce spontaneous killing of cancer cells or virus-infected cells via the Fas/Fas ligand or the granzyme/perforin systems. The corticotropin-releasing hormone (CRH) is an important regulator for the body's stress response. It promotes proliferation and migration of various cancer cells through the CRH type 1 receptor under stress, and also inhibits NK or T cell activity. However, the relationship of CRH and NK cell migration to the target has not been confirmed. Herein, we study the effect of CRH on NK cell migration. Methods: We used the human NK cell line, NK-92MI, and tested the expression of CRH receptor type 1 on NK-92MI by RT-PCR. This was to examine the effect of CRH on tumor and NK cell migration, thus NK cells (NK-92MI) were incubated with or without CRH and then each CRH treated cell's migration ability compared to that of the CRH untreated group. Results: We confirmed that CRH receptor type 1 is expressed in NK-92MI. CRH can decrease NK cell migration in a time-/dose-dependent manner. Conclusion: These data suggest CRH can inhibit NK cell migration to target cells.