• 대한후두음성언어의학회지
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• 제20권1호
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• pp.36-41
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• 2009

Background and Objectives: Topical administration of mitomycin-C (MMC) has been reported to reduce or delay scar formation in airway surgery. However, it is not infrequent to experience recurrent stenosis or adhesion of operative wound even after a meticulous MMC application during the laryngeal surgery. Therefore we aimed to evaluate the effectiveness of repeated postoperative MMC applications and the technical feasibility of MMC applications to the laryngeal wound at an outpatient clinic. Methods: We reviewed medical records of 13 consecutive patients who received office-based MMC applications after laryngeal airway surgery at Samsung Medical Center, Seoul, Korea. The patients were grouped into 3 categories according to the site of surgical wound and the purpose of MMC application; group I : supraglottic stenosis (n=5), group II : cordectomy and arytenoidectomy site granulation prevention (n=3), Group III : laryngeal web prevention (n=5). Outcomes in each group and adverse effects of repeated MMC applications were evaluated. Results: Office-based MMC application was successfully performed one to four times with a week interval for each patient. No significant complications were observed except slightly decreased mucosal wave in one female patient who received 4 times of MMC application at the anterior commissure of vocal fold. Repeated MMC applications at the outpatient clinic resulted in wide or acceptable supraglottic airway in group I, clean wound healing without granulation formation in group II, and negligible or no web formation at the anterior commissure in group III. Conclusion : Office-based topical administration of MMC to the larynx was technically feasible. Postoperative repeated MMC applications were effective to reduce recurrent stenosis or adhesion of supraglottic structures, to prevent granuloma formation after laser arytenoidectomy and glottic web formation after anterior commissure resection.

• 한방안이비인후피부과학회지
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• 제9권1호
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• pp.1-15
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• 1996

The purpose of this research was to investigate effect of water extract of DangKwi-Eum-Ja ka Sumsoo(DESE) on the cytotoxicity of human epidemloid cell, A431 cells. The effects of DESE on the proliferation of A431 cells, Balb/c 3T3 cells, mouse thymocytes and splenocnes were estimated by MTT colorimetric assay, and nitric oxide production from mouse peritoneal macrophage was estimated by Griess method. DESE inhibited the proliferation of A431 cells at $10{\mu}g/ml$, and did not affect the proliferation of Balb/c 3T3 cells. DESE decreased the cytotoxicity of mitomycin C or cisplatin on A431 cells, increased the cytotoxicity of mitomycin C or cisplatin on Balb/c 3T3 cells. DESE inhibited the proliferation of mouse thymocytes and splenocytes at $100{\mu}g/ml$. DESE did not affect the nitric oxide production from mouse peritoneal macrophage in vitro, but decreased the nitric oxide production from DESE-treated mouse peritoneal macrophage.

• Applied Biological Chemistry
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• 제48권3호
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• pp.222-227
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• 2005

특수미인 거대배아미와 유색미의 발아처리에 의한 항돌연변이 활성의 변화를 평가하고자, 70% 에탄올 추출물이 in vitro에서 산화적 손상에 의한 DNA strand scission을 억제하는 효과와 함께 E. coli 및 V79 배양세포에 화학적으로 유발된 돌연변이에 대한 억제효과를 측정하였다. Mitomycin C로 유발된 돌연변이에 대한 억제활성을 E. coli에서 SOS chromotest로 조사한 결과, 활성은 발아유색미(40.4%) > 발아거대배아미(37.1%) > 무발아유색미(35.5%) > 발아현미(15.7%) > 무발아거대배아미(14.0%) > 무발아현미(0.8%)의 순서였다. Mitomycin C가 유도한 DNA strand scission에 대한 억제 효과는 무발아유색미 > 무발아거대배아미 > 발아유색미 > 발아현미 > 무발아현미 > 발아 거대배아미로 나타났다. V79 세포주에서 4-NQO로 유도된 6-TG 저항성 colony의 형성을 저해하는 활성을 지표로 항돌연변이 활성을 조사한 결과, 발아거대배아미(53.2%) > 무발아유색미(40.0%) > 무발아현미(21.2%) > 발아현미(14.4%) > 무발아거대배아미(0.23%)의 순서로 돌연변이를 저해하였는데, 발아유색미는 돌연변이를 촉진하는 것으로 나타났다(-69%).

• Journal of Yeungnam Medical Science
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• 제24권2호
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• pp.232-242
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• 2007

녹내장으로 수술적 치료가 필요한 무수정체안과 인공수정체안 환자들에게서 Mitomycin C(MMC)를 사용한 섬유주절제술을 시행하고 유용성을 알아보고자 하였다. 1994년 5월부터 2002년 2월까지 영남대학교 의과대학 부속병원 안과에서 무수정체안과 인공수정체안에 녹내장 치료로 MMC의 국소접촉법을 이용한 섬유주 절제술을 시행하고 6개월 이상 추적관찰 가능 하였던 45명 51안을 대상으로 녹내장의 유형, 기왕의 안수술, 백내장수술의 종류, 수정체 후낭의 상태, 인공수정체 유뮤에 따른 성공률과 수술 실패의 위험인자 및 합병증 등을 의무기록을 바탕으로 후향적으로 조사하였다. 수술 성공 여부의 기준은 술 후 안압하강제 사용에 관계없이 술 후 최종 안압이 21 mmHg이하이며 시력상실이 없는 경우를 성공으로 판정하였다. MMC를 사용한 일차 섬유주절제술 후 평균 관찰 기간은 27.7개월이었으며 수술 성공률은 70.6%(36안/51안)이었다. Kaplan-Meier 생존분석을 이용한 누적 성공률은 3개월에 98.0%, 6개월에 94.1%, 12개월에 91.9%, 24개월에 83.4%, 36개월에 75.5%로서 보고된 고식적 섬유주 절제술의 성공률보다 높았다. 술 전 안압이 30mmHg 미만으로 낮았던 환자들과 이전 백내장 수술을 제외한 안 수술의 기왕력이 없었던 환자들에게 의미있게 수술 성공률이 높은 것으로 조사되었다. 술 후 합병증으로는 전방출혈과 맥락막박리가 각 4안에서, 저안압이 3안, 그리고 얕은 전방과 안내염이 각 1안에서 발생하였다. 결론적으로 무수정체안과 인공수정체안의 녹내장에서 MMC 섬유주절제술은 기존 보고된 방수유출장치술의 수술 성공률에 비해 낮지 않으면서도 합병증이 적다는 점에서 방수유출장치삽입술에 앞서 우선적으로 선택할 수 있는 유용한 수술 방법이라고 생각된다.

• 한국환경성돌연변이발암원학회지
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• 제18권2호
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• pp.89-92
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• 1998

The results of chromosome aberration test in mammalian cells in culture (Chinese hamster lung fibroblast cells) showed no induction of structural and numerical aberrations by YH1226, a cephalosporin antibiotic regardless of metabolic activation, while positive control group (mitomycin C and benzo(a)pyrene) showed structural chromosome aberrations of 25% and 10%, respectively. The in vivo induction of micronuclei was measured in polychromatic erythrocytes in bone marrow of male ddY mouse given YH1226 at 500, 250, 125 mg/kg by i.p. once. After 24 hours, animals were sacrificed and evaluated for the incidence of micronucleated polychromatic erythrocytes in whole erythrocytes. Although a positive response for induction of micronuclei in animals treated with mitomycin C demonstrated the sensitivity of the test system for detection of a chemical clastogen, YH1226 did not induce microunclei in bone marrow of ddY male mice.

• 한국환경성돌연변이발암원학회:학술대회논문집
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• 한국환경성돌연변이발암원학회 2003년도 추계학술대회
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• pp.109-110
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• 2003

• 한국미생물·생명공학회지
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• 제19권6호
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• pp.553-560
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• 1991

Bacillus circulans로부터 mitomycin C처리에 의해 유발되는 Bacteriophage Sigma FA1을 서당밀도균배 원심법 (sucrose gradient centrifugation)에 의해 분리, 정제하였다. Sigma FA1의 감수성숙주에 대한 치사작용은 single-hit 방식이었다. 한편, 세포에 감여된 후 phage DNA는 천천히 분해되기 시작했으며, 본 연구의 결과는 Sigma FA1의 세포에 대한 치사작용이 기존의 것과는 다른 것임을 입증시켰으며, 이는 단 백질분해기능에서 유래되는 듯 했다.

• 약학회지
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• 제43권1호
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• pp.104-110
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• 1999

We investigated effects of methanol extract of Aloe vera on anticancer drugs(cisplatin, mitomycin C, 5-fluorouracil)-induced growth inhibition in p388, L1210, HCT-15, SK-HepG-1 as cancer cell lines and mouse splenocytes as a normal cell by MTT assay, respectively. We also examined the effects of aloe extract and mitomycin C on the mitogen(Con, A, LPS)-induced splenocyte proliferation. Aloe extract(0.25 mg/m , 1.25 mg/m , 2.5 mg/m , 5.0 mg/m ) showed dose-dependently selective cytotoxicity against the cancer cell lines. In contrast, Aloe extract increased the growth and proliferation of the normal mouse splenocytes. The combination of aloe extract with anticancer drugs showed an additive effect for the cytotoxicity against cancer cell lines. However, that combination reduced clealy the anticancer drugs-induced toxicity against the normal mouse splenocytes.

• 한국미생물·생명공학회지
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• 제21권2호
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• pp.132-138
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• 1993

The s-type pyocin was purified from the lysate of the mitomycin C-induced Pseudomonas aeruginosa 90-2-2205 cells by the other of ammonium sulfate precipitation, DEAE-Sephadex A-50 chromatography and Sephadex G-200 gel filtration. The purity was confirmed by the polyacry-lamide gel electrophoresis. The molecular weight of the purified pyocin was estimated 180, 000 by gel filtration. The pyocin was analyzed to be a complex of some polypeptides by the SDS-PAGE. The pyocin was stable by heat treatment and at pH 6-7.5 by adding 10-3% gelatin and 0.2M NaCl to the 10mM Tris-HCl buffer (pH7.5). Its killing action against the sensitive cells was assumably a single hit process.

• BMB Reports
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• 제29권6호
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• pp.489-492
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• 1996

A number of anticancer-chemotherapeutic agents induce cell death through the process of apoptosis. Effects of echinomycin, an anticancer agent on cancer progression, were investigated in P388 murine leukemia cells. First, according to the results of cytotoxicity measurement. $IC_{50}$ of echinomycin was 1.12 nM, a relatively lower value than the other examined anticancer agents, mitomycin-C and etoposide Second, the DNA fragmentation assay for echinomycin-treated cells exhibited that echinomycin was able to induce apoptosis in a shorter period of time and with a lower dose than mitomycin-C or etoposide. The data of DNA fragmentation were quite comparable to those of cytotoxicity measurement. Finally we showed that mitogen-activated protein (MAP) kinase, a key protein in cell mitosis, was translocated into the nucleus from the cytosol after treatment with echinomycin. These findings suggest that a MAP kinase-related process may be involved in apoptosis induced by echinomycin.