• 대한한방내과학회지
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• 제41권5호
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• pp.911-925
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• 2020

Objectives: The purpose of this study was to report a case of a patient with advanced gastric cancer with peritoneal metastasis treated with chemotherapy and Korean medicine Methods: A patient with advanced gastric cancer with peritoneal metastasis was treated with Xeloda/cisplatin since April 2019. The cycle was repeated every three weeks for a total of 11 times. At the same time, the patient was treated with Korean medicine. The tumor size was measured by computed tomography (CT) and esophagogastroduodenoscopy (EGD). Adverse events were evaluated by the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE), version 5.0. Results: After treatment with Xeloda/cisplatin and Korean medicine for nine months, the extent of the proximal portion of the primary tumor and the size and number of multiple nodules around the stomach decreased and the cancer cells with peritoneal metastasis disappeared. The symptoms of discomfort and physical activity were gradually improved. As a result, the patient underwent conversion surgery. Conclusions: This case study suggests that the combination of chemotherapy and Korean medicine may contribute to the reduction in tumor size as well as the improvement in the quality of life.

• 한국수산과학회지
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• 제47권5호
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• pp.501-507
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• 2014

Norovirus (NoV) is a major cause of food poisoning outbreaks in Korea. Most NoV outbreaks originate from environmental contamination, but bivalves such as oysters are also important vectors. Oyster Crassostrea gigas contamination by NoV has been reported in Korea, but no quantitative analyses of NoV have been performed. We investigated the NoV concentration in 21 oyster samples from a Korean commercial oyster-growing area with confirmed fecal contamination from January to December 2012, using real-time reverse transcription-polymerase chain reaction. Additionally, we assessed the NoV concentration after heating to investigate the effects of heat treatment on NoV-infected oysters. In NoV-positive samples, the cycle threshold (Ct) values were 37.43-39.41 and 36.77-39.30, while viral concentrations were $8.97{\times}10^2-2.24{\times}10^2$ and $3.05{\times}10^2-7.47{\times}10^1$ copies/g for genogroups I and II, respectively. After heat treatment, NoV genogroup I decreased by 83.4%, 88.0%, 89.4% and 100% at $60^{\circ}C$, $68^{\circ}C$, $70^{\circ}C$, and $100^{\circ}C$, respectively, for 15 min, while genogroup II respectively decreased by 67.3%, 76.3%, 80.1%, and 89.8% under the same conditions.

• 대한한방내과학회지
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• 제41권2호
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• pp.166-176
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• 2020

Objectives: This study reports on the effect of Integrative Medicine Therapy (IMT) on a patient with pancreatic cancer with liver metastasis. Methods: One pancreatic cancer with liver metastasis patient was treated using IMT in conjunction with Gemcitabine/Abraxane since September 2019. The cycle was repeated every four weeks for a total of 11 times. At the same time, the patient was treated with IMT. Tumor size was measured by scanning with Computed Tomography (CT). Adverse events were evaluated using the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE), version 5.0. Results: After treatment with Gemcitabine/Abraxane and IMT for eight months, the size of the body and tail of the cancer tumor and several hepatic metastatic regions decreased (partial response, [PR]), size, and number of multiple nodules in both lungs decreased. No evidence of newly developed metastatic lesions was found. The patient has maintained a good treatment outcome and has shown prolonged overall survival. Conclusions: This case demonstrates that treatment with IMT may have substantial benefits for patients with end-stage pancreatic cancer.

• 한국수정란이식학회지
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• 제24권3호
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• pp.225-230
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• 2009

Sex-sorting of sperm is an assisted reproductive technology (ART) used by the livestock industry for the mass production of animals of a desired sex. The standard method for sorting sperm is the detection of DNA content differences between X and Y chromosome-bearing sperm by flow cytometry. However, this method has variable efficiency and therefore requires verification by a second method. We have developed a sex determination method based on quantitative real-time polymerase chain reaction (qPCR) of the porcine amelogenin (AMEL) gene. The AMEL gene is present on both the X and the Y chromosome, but the length and sequence of its noncoding regions differ between the X and Y chromosomes. By measuring the threshold cycle (Ct) of qPCR, we were able to calculate the relative frequency of X chromosome. Two sets of AMEL primers were used in these studies. One set (AME) targeted AMEL gene sequences present in both X and Y chromosome, but produced PCR products of different lengths for each chromosome. The other set (AXR) bound to AMEL gene sequences present on the X chromosome but absent esholthe Y-chromosome. Relative product levels were calculated by normalizing the AXR fluorescence to the AME fluorescence. The AMEL method accurately predicted the sex ratios of boar sperm, demonstrating that it has potential value as a sex determination method.

• Tuberculosis and Respiratory Diseases
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• 제63권2호
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• pp.154-164
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• 2007

배경: Irinotecan hydrochloride는 topoisomerase I inhibitor로서 소세포 폐암에 효과적인 약제로 알려져 있다. Irinotecan은 cisplatin과 더불어 방사선감작물질로 작용하기도 한다. 본 연구는 이전에 치료받은 경험이 없는 제한성 병기의 소세포 폐암 환자에서 irinotecan과 cisplatin(IP)의 방사선 동시화학요법의 효과를 평가하기 위하여 시행되었다. 방법: 2002년 12월부터 2004년 11월까지 충남대학교 병원에서 새로이 제한성 병기의 소세포 폐암으로 진단된 24명의 환자들을 대상으로 하였다. Irinotecan $60mg/m^2$을 제 1일과 제 8일째 투여하였고 cisplatin $60mg/m^2$을 제 1일째 투여하였으며 매 3주 간격으로 시행되었다. 제 3차 항암화학요법을 시작하는 날과 동시에 과다 분할방사선 치료(twice-daily thoracic irradiation; 45 Gy total)을 시작하였다. 예방적 전 뇌 방사선 조사(Prophylactic cranial irradiation)가 방사선 동시화학요법이 끝난 후 완전반응(complete response)을 나타낸 환자에서 시행되었다. 제 2차 항암요법과 제 6차 항암요법이 끝난 후에 흉부 전산화 단층촬영과 기관지경 등을 통한 병기의 재평가가 이루어졌다. 결과: 병기의 재평가는 19명의 환자에게 이루어졌다. 중앙 추적관찰기간은 12.5개월이고 전체 99회의 항암치료가 시행되었다. 평균 한 환자당 5.2회의 항암치료가 시행되었다. 실제 용량강도는 cisplatin $19.6mg/m^2$/week과 irinotecan $38.2mg/m^2$/week이었다. 9명의 환자가 완전반응을 보였고 10명의 환자가 부분반응(partial response)을 보여서 전체 반응률은 95%였다. 3에서 4도의 혈액학적 독성은 백혈구 감소증(35% of cycles), 빈혈(7% of cycles), 혈소판 감소증(7% of cycles) 등으로 나타났다. 3에서 4도의 비 혈액학적 독성은 설사(5% of cycles)였다. 3에서 4도의 방사선 식도염(10% of patients)을 제외하고는 과다 분할 방사선 치료를 이용한 방사선 동시 화학요법의 기존의 방법과 독성 면에서는 큰 차이가 없었다. 치료와 관련된 사망은 관찰되지 않았다. 평가가 가능한 환자들에서 1년 생존율과 2년 생존율은 각각 89% (16/18)와 47% (9/18)였다. 결론: 3주 간격으로 시행된 irinotecan과 cisplatin을 이용한 과다분할 방사선 동시 요법은 제한성 병기의 소세포 폐암 환자에서 부작용은 높지 않으면서 효과적인 치료법으로 고려될 수 있을 것이다.

• Tuberculosis and Respiratory Diseases
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• 제70권4호
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• pp.301-306
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• 2011

Background: It is well-known that cell-free nucleic acids rise in patients with many types of malignancies. Several recent experimental studies using cancer cell lines have shown that changes in cell-free RNA are predictive of the response to chemotherapy. The objective of this study was to determine whether quantification of free RNA can be used as a biomarker for clinical responses to chemotherapy in patients with lung cancer. Methods: Thirty-two patients with lung cancer (non-small cell lung cancer, n=24; small cell lung cancer, n=8) were divided into 2 groups according to their responses to chemotherapy (response group, n=19; non-response group, n=13). Blood samples were collected before and after two cycles of chemotherapy. Real-time quantitative RT-PCR was used for transcript quantification of the glyceraldehyde-3-phosphate dehydrogenase gene. Results: The pre chemotherapy values (Response group $41.36{\pm}1.72$ vs. Non-response group $41.33{\pm}1.54$, p=0.78) and post chemotherapy values (Response group $39.92{\pm}1.81$ vs. Non-response group $40.41{\pm}1.47$, p=0.40) for cell free RNA concentrations, expressed as Ct GAPDH (threshold cycle glyceraldehyde-3-phosphate dehydrogenase gene) levels, was not different between the two groups. There was no significant relationship between changes in the cell free RNA level clinical responses after chemotherapy (p=0.43). Conclusion: We did not find a correlation between quantification of serum cell free RNA levels and clinical responses to chemotherapy in patients with lung cancer. Further investigations are needed to determine whether the cell free RNA level is a useful predictor of responses to chemotherapy in patients with lung cancer.

• 대한방사선치료학회지
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• 제28권2호
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• pp.149-159
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• 2016

목 적 : 폐암환자의 호흡동조 방사선 치료 계획 시 호흡 훈련 전후 RPM 신호와 횡격막 위치 변화를 분석하여 호흡 훈련의 유용성을 평가하고자 한다. 대상 및 방법 : 2016년 4월부터 8월까지 호흡 동조 방사선 치료를 받는 환자 11명을 대상으로 호흡 훈련을 시행하였고 동시에 RPM 신호 및 횡격막 영상을 획득하였다. 호흡 훈련은 총 3단계로 1단계 자유 호흡 상태의 신호 획득, 2단계 호흡 신호 가이드를 통한 1차 호흡 신호 획득, 3단계 설명과 반복 훈련으로 규칙성과 안정을 유도한 최종 호흡 신호를 획득 하였다. 각 단계의 흡기와 호기시 RPM 신호와 투시 영상의 횡격막 위치의 평균값, 표준편차, 최대값, 최소값을 구하고, 이를 1단계 값으로 표준화 하여 2, 3단계를 상대분포 백분율(%)로 변환하여 환자의 호흡 변화와 내부 움직임을 분석 함으로써 각 환자의 호흡훈련 유용성을 평가 하였다. 결 과 : RPM 신호와 횡격막 진폭을 측정한 뒤, 1단계를 100%으로 표준화하여 각 단계의 평균값과 표준편차의 오차 평균을 구하였다. 그 결과, 3단계 최종호흡 획득 시 진폭의 상대평균 및 표준편차 모두 감소가36.4%, 표준편차만 감소가 18.2%, 진폭만 감소가 36.4%로 나타났으며, 횡격막 영상의 위치 측정 시 3단계에서 전체 81.8%의 환자에게서 상대평균 진폭 값이 30% 감소함을 보였다. 그러나 모든 환자들에게서 2단계 대비 3단계의 RPM 신호와 횡격막 진폭이 각각 평균 52.6%, 42.1% 감소함을 보였다. 또한, RPM 신호와 횡격막 영상 진폭 차이의 연관성은 2번 10번 환자를 제외하고 각각 1, 2, 3단계 움직임의 패턴이 상관관계를 보였다. 결 론 : 호흡 동조 방사선치료에서 호흡 훈련을 시행하였을 때 최적화된 호흡 주기를 유도할 수 있었으며, 모의 호흡 훈련을 치료 전 시행함으로써 불규칙적인 호흡에 의한 환자의 호흡을 제어해 폐의 움직임을 예측 가능 하게 해주는 효과를 기대할 수 있었다. 궁극적으로는 방사선 치료의 체계적 오류를 최소화해 보다 정확한 치료를 기대할 수 있어 호흡 훈련이 유용하다고 할 수 있겠다.그러나 본 연구는 치료 전 호흡 훈련을 시행한 자료를 바탕으로 분석한 연구로 제한되어 있으며 추후 실제 CT 계획과 치료 시 획득한 자료를 가지고 검증하는 것도 필요할 것으로 사료된다.

• 대한방사선치료학회지
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• 제22권2호
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• pp.113-122
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• 2010

목 적: 호흡동조방사선 치료 시 종양의 실제 움직임과 호흡추적장치로 측정한 피부 움직임의 차이를 자체 제작한 구동팬텀에서 가상의 종양을 이용하여 호흡과 유사하게 움직임에 따른 정적 상태, 동적 상태 및 호흡동조상태에서 표적 위치의 정확성의 측정치와 실측치를 평가하고 선량분포를 분석, 비교하고자 한다. 대상 및 방법: 호흡에 의해 움직이는 종양 측정을 위해 2차원적으로 움직이는 구동팬텀을 자체 제작하였다. 구동 팬톰의 움직임은 위. 아래 방향(SI) 각각 1.5 cm 왕복운동, 상 하 방향 2 cm으로 속도조절(1-5단계)이 되도록 하였다. 가로 4 cm, 세로 4 cm, 높이 0.5 cm의 아크릴 슬라이스에 직경 0.5 cm 종양을 납으로 표시하고, 위아래로 동일한 아크릴 슬라이스를 2장씩 쌓은 후 아크릴 슬라이스 세 번째와 네 번째 사이 Dmax 1.5 cm film을 삽입하였다. 가상의 타겟을 구동 팬텀 위에 위치시키고 6 MV X-선이 조사되는 정적인 상태, 호흡동조 및 동적인 상태에서 각각 5 Gy를 조사하였다. 구동팬텀 위에 표식자를 올린 후, 호흡추적장치를 이용하여 사전에 설정한 호흡시간의 변화에 따른 진폭과 위상변화를 분석하였다. 결 과: RPM respiratory gating system을 이용하여 호흡주기를 8단계로 나누어 각각을 12회씩 위상변화를 분석하여 평균과 표준편차를 구한결과 평균은 3.0 (1.5~1.5) sec에서 1.7 cm로 가장 크고, 3.0 (1.3~1.7) sec 5.0 (2.0~3.0) sec에서 0.2602 cm로 가장 크고 4.0 (2.0~2.0) sec에서 0.0866 cm로 가장 작았다. 또한 실측치에서 평균 및 표준편차를 구한 결과 t0에서 9.9 (6.6) mm $t_{10}$에서 10.6 mm (7.3), $t_{20}$ 16.5 mm (10.3), $t_{30}$ 10.2 mm (7.6)으로 나타났으며, 호기나 흡기 시간의 차이에 따른 규칙은 없고 대체로 균일한 평균과 표준편차의 분포를 나타내었다. 또한 정적 상태, 동적 상태 및 호흡동조상태에서 Gafchromic EBT film 의 방사선량을 분석한 결과, ICRU 62에서 권고한 90% 선량분포가 3 mm 이내에 포함되므로 정확성과 정도관리 측면에서 적합한 것으로 사료된다. 결 론: 구동팬톰을 이용하여 호흡움직임에 따른 정확성 및 선량분포차이를 Gafchromic film을 통하여 확인하였으며 결과를 바탕으로 호흡에 의해 변화가 생기는 장기에 대한 차이를 고려하여 치료계획을 한다면 종양과 정상조직에 적절한 선량계획을 세울 수 있어 치료효과 향상에 도움을 주게 될 것으로 생각한다.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2013년도 제45회 하계 정기학술대회 초록집
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• pp.88-89
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• 2013

A variety of influenza A viruses from animal hosts are continuously prevalent throughout the world which cause human epidemics resulting millions of human infections and enormous industrial and economic damages. Thus, early diagnosis of such pathogen is of paramount importance for biomedical examination and public healthcare screening. To approach this issue, here we propose a fully integrated Rotary genetic analysis system, called Rotary Genetic Analyzer, for on-site detection of influenza A viruses with high speed. The Rotary Genetic Analyzer is made up of four parts including a disposable microchip, a servo motor for precise and high rate spinning of the chip, thermal blocks for temperature control, and a miniaturized optical fluorescence detector as shown Fig. 1. A thermal block made from duralumin is integrated with a film heater at the bottom and a resistance temperature detector (RTD) in the middle. For the efficient performance of RT-PCR, three thermal blocks are placed on the Rotary stage and the temperature of each block is corresponded to the thermal cycling, namely $95^{\circ}C$ (denature), $58^{\circ}C$ (annealing), and $72^{\circ}C$ (extension). Rotary RT-PCR was performed to amplify the target gene which was monitored by an optical fluorescent detector above the extension block. A disposable microdevice (10 cm diameter) consists of a solid-phase extraction based sample pretreatment unit, bead chamber, and 4 ${\mu}L$ of the PCR chamber as shown Fig. 2. The microchip is fabricated using a patterned polycarbonate (PC) sheet with 1 mm thickness and a PC film with 130 ${\mu}m$ thickness, which layers are thermally bonded at $138^{\circ}C$ using acetone vapour. Silicatreated microglass beads with 150~212 ${\mu}L$ diameter are introduced into the sample pretreatment chambers and held in place by weir structure for construction of solid-phase extraction system. Fig. 3 shows strobed images of sequential loading of three samples. Three samples were loaded into the reservoir simultaneously (Fig. 3A), then the influenza A H3N2 viral RNA sample was loaded at 5000 RPM for 10 sec (Fig. 3B). Washing buffer was followed at 5000 RPM for 5 min (Fig. 3C), and angular frequency was decreased to 100 RPM for siphon priming of PCR cocktail to the channel as shown in Figure 3D. Finally the PCR cocktail was loaded to the bead chamber at 2000 RPM for 10 sec, and then RPM was increased up to 5000 RPM for 1 min to obtain the as much as PCR cocktail containing the RNA template (Fig. 3E). In this system, the wastes from RNA samples and washing buffer were transported to the waste chamber, which is fully filled to the chamber with precise optimization. Then, the PCR cocktail was able to transport to the PCR chamber. Fig. 3F shows the final image of the sample pretreatment. PCR cocktail containing RNA template is successfully isolated from waste. To detect the influenza A H3N2 virus, the purified RNA with PCR cocktail in the PCR chamber was amplified by using performed the RNA capture on the proposed microdevice. The fluorescence images were described in Figure 4A at the 0, 40 cycles. The fluorescence signal (40 cycle) was drastically increased confirming the influenza A H3N2 virus. The real-time profiles were successfully obtained using the optical fluorescence detector as shown in Figure 4B. The Rotary PCR and off-chip PCR were compared with same amount of influenza A H3N2 virus. The Ct value of Rotary PCR was smaller than the off-chip PCR without contamination. The whole process of the sample pretreatment and RT-PCR could be accomplished in 30 min on the fully integrated Rotary Genetic Analyzer system. We have demonstrated a fully integrated and portable Rotary Genetic Analyzer for detection of the gene expression of influenza A virus, which has 'Sample-in-answer-out' capability including sample pretreatment, rotary amplification, and optical detection. Target gene amplification was real-time monitored using the integrated Rotary Genetic Analyzer system.