• 제목/요약/키워드: Neoplastic

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RGB 채널치환을 이용한 내시경영상 향상을 위한 예비 연구 (Enhancement of Endoscopic Images by RGB Channel Substitution Image Processing, a Preliminary Report)

  • 이동환;양찬주;정훈용;이재령;남수정;최승호
    • 대한기관식도과학회지
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    • 제18권2호
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    • pp.45-48
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    • 2012
  • Background Neoplastic vessels tend to proliferate on the surface of malignant lesions in the aerodigestive tract. So, superficial malignant lesions can be detected earlier by enhancing mucosal vascular clarity. To enhance mucosal vascular clarity on endoscopic image, we developed an image processing algorithm of RGB (red-green-blue) channel substitution image (CSI). Methods Each pixel in original white light image (WLI) has its own value of red, green and blue channel. Various combinations of RGB channel substitution was tried on original WLI. Results To make superficial blood vessels darker than brighter background mucosa, in the CSI algorithm, RGB value in each pixel of WLI is substituted; red value to green one, green value to blue one. There was a good contrast between superficial mucosal vessels and background brighter mucosa in the CSI image. Conclusion By RGB CSI algorithm, WLI could be successfully converted to new images with enhanced mucosal vascular clarity. Using RGB CSI algorithm could provide added vascular visibility on original WLI.

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DNA복제 및 회복에 미치는 수종항암 항생제의 영향에 관한 연구 (Effects of Anti-Neoplastic Antibiotics on DNA Replication and Repair)

  • Park, Sang-Dai;Rie, Myung-Chull;Lee, Chun-Bok
    • 한국동물학회지
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    • 제26권1호
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    • pp.19-28
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    • 1983
  • 본 연구는 알킬화제이며 항암항생제인 Mitomycin C(MMC)와 Bleomycin(BLM)이 DNA 복제 및 회복에 미치는 영향을 규명하고, 아울러 MMC에 의한 "유발상해회복"이 포유동물세포에 유발되는지 밝히고자 수행하였다. 이를 위해 자기방사법에 의한 비주기 DNA 합성율과 알카리 유출법에 의한 DNA단사절단율을 측정하였다. CHO세포에 MMC를 제 1차 $(MMC_1)$ 처리한 후 5시간 뒤에 제 2차 $(MMC_2)$로 처리하여 얻은 결과는 다음과 같았다. 1. BLM은 비주기 DNA합성을 매우 적게 유발시켰으며, BLM $5\\mug/ml$의 농도에서 부터 비주기 DNA합성율은 증가를 보이지 않았다. BLM은 처리후 1.5시간까지 DNA합성억제를 보였으며, 1.5시간후 DNA합성율이 증가되었으나, 대조군의 60% 수준까지 회복되었을 뿐이다. 2. MMC에 의해 유발된 비주기 DNA합성은 농도에 따라 비례하였으며, 배양후 시간의 간격에 따라 비례하여 감소하였다. 제 1,2차 MMC를 처리한 세포의 비주기 DNA합성은 제 1차만 처리한 세포의 비주기 DNA합성보다 많았다. 3. 알카리 유출법 결과는 MMC에 의하여 유발된 DNA 단백질 연결로 인한 DNA 단사절단율이 농도에 비례함을 나타내었다. DNA 단백질 연결로 인한 DNA 단사절단율은 배양후의 시간에 비례해서 감소되었다. 이러한 결과는 MMC와 BLM 모두가 DNA 상해제임과 MMC에 의한 DNA 상해 부위의 복제율이 어떠한 유발기작에 의하여 촉진됨을 시사한다.촉진됨을 시사한다.

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Thymoquinone (TQ) regulates cyclooxygenase-2 expression and prostaglandin E2 production through PI3kinase (PI3K)/p38 kinase pathway in human breast cancer cell line, MDA-MB-231

  • Yu, Seon-Mi;Kim, Song-Ja
    • Animal cells and systems
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    • 제16권4호
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    • pp.274-279
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    • 2012
  • Thymoquinone (TQ), a drug extracted from the black seeds of Nigella sativa, has been shown to exhibit anti-inflammatory, anti-oxidant, and anti-neoplastic effects in numerous cancer cells. The effects of TQ on cyclooxygenase-2 (COX-2) expression and prostaglandin $E_2$ ($PGE_2$) production in MDA-MB-231, however, remain poorly understood. Western blot analysis and immunofluorescence staining were performed to study the expression levels of inflammation regulatory proteins in MDA-MB-231. $PGE_2$ assay was conducted to explore the TQ-induced production of $PGE_2$. In this study, we investigated the effects of TQ on COX-2 expression and $PGE_2$ production in MDA-MB-231. TQ significantly induced COX-2 expression and increased $PGE_2$ production in a dose-dependent manner, as determined by a Western blot analysis and $PGE_2$ assay. Furthermore, the activation of Akt and p38 kinase, respectively, was up-regulated in TQ treated cells. Inhibition of p38 kinase with SB203580 and PI3kinase (PI3K) with LY294002 abolished TQ-caused COX-2 expression and decreased $PGE_2$ production. These results collectively demonstrate that TQ effectively modulates COX-2 expression and $PGE_2$ production via PI3K and p38 kinase pathways in the human breast cancer cell line MDA-MB-231.

전완부에 발생한 내혈관 유두내피 증식증(Masson 혈관종) (Intravascular Papillary Endothelial Hyperplasia (Masson's hemangioma) Presenting as a Forearm Mass)

  • 전영수;유기형;김상환
    • 대한골관절종양학회지
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    • 제15권1호
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    • pp.59-64
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    • 2009
  • 내혈관 유두내피 증식증 (Masson 혈관종)은 피부나 피하조직에 주로 발생하는 흔하지 않은 양성의 혈관 병변으로 혈관 내피세포의 과도한 증식으로 발생할 수 있다. 이 질환은 정상 또는 기형적인 혈관에서 일차적으로 발생할 수 있으며, 혈관종, 화농성 육아종, 또는 림프관종등과 동반될 수 있다. 혈관내 유두상 내피성 과형성증은 임상적, 조직학적으로 저등급의 혈관육종으로 오인하여 진단, 치료할 수 있으므로 감별하여야 한다. 저자는 27세 환자가 전완부의 종물을 주소로 내원하여 상기 병명으로 진단한 예를 경험하였기에 문헌 고찰과 함께 이를 보고하는 바이다.

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Prognostic and Clinicopathological Significance of Transducer-Like Enhancer of Split 1 Expression in Gastric Cancer

  • Lee, Ji-Hye;Son, Myoung-Won;Kim, Kyung-Ju;Oh, Mee-Hye;Cho, Hyundeuk;Lee, Hyun Ju;Jang, Si-Hyong;Lee, Moon Soo
    • Journal of Gastric Cancer
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    • 제16권1호
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    • pp.21-27
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    • 2016
  • Purpose: Transducer-like enhancer of split 1 (TLE1) is a member of the Groucho/TLE family of transcriptional co-repressors that regulate the transcriptional activity of numerous genes. TLE1 is involved in the tumorigenesis of various tumors. We investigated the prognostic significance of TLE1 expression and its association with clinicopathological parameters in gastric cancer (GC) patients. Materials and Methods: Immunohistochemical analysis of six tissue microarrays was performed to examine TLE1 expression using 291 surgically resected GC specimens from the Soonchunhyang University Cheonan Hospital between July 2006 and December 2009. Results: In the non-neoplastic gastric mucosa, TLE1 expression was negative. In GC, 121 patients (41.6%) were positive for TLE1. The expression of TLE1 was significantly associated with male gender (P=0.021), less frequent lymphatic (P=0.017) or perineural invasion (P=0.029), intestinal type according to the Lauren classification (P=0.024), good histologic grade (P<0.001), early pathologic T-stage (P=0.012), and early American Joint Committee on Cancer stage (P=0.022). In the Kaplan-Meier analysis, the TLE1 expression was significantly associated with longer disease-free (P=0.022) and overall (P=0.001) survival rates. Conclusions: We suggested that TLE1 expression is a good prognostic indicator in GCs.

복수를 침범한 소세포형 T-세포 전림프구성 백혈병의 세포소견 -1예 보고- (Cytologic Features of Ascitic Fluid Complicated by Small Cell Variant T-cell Prolymphocytic Leukemia -A Case Report -)

  • 한지영;김진수;김동훈;김루시아;박인서;김준미;주영채;최석진
    • 대한세포병리학회지
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    • 제19권2호
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    • pp.168-172
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    • 2008
  • T-cell prolymphocytic leukemia (T-PLL) is a rare, mature T-cell lymphoproliferative disorder with a post-thymic mature T-cell phenotype. The disease is characterized by rapidly rising lymphocytosis, lym-phadenopathy, and splenomegaly. The clinical course is usually aggressive and progresses with frequent skin lesions and serous effusions. In 25% of cases, leukemic cells are small and tumor cells may not have a discrete nucleolus under light microscopy. Although the presence of characteristic cytoplasmic protrusions or blebs in tumor cells is a common morphologic finding in the peripheral blood film irrespective of the nuclear features, small cell variants lacking the typical nuclear features can cause diagnostic problems in clinical cytology. Furthermore, the small leukemic cells can share some cytologic findings with lymphocyte-rich serous effusions caused by non-neoplastic reactive lymphocytosis as well as other small lymphocytic lymphoproliferative disorders. Here, we describe the cytological findings of ascitic fluid complicated by small cell variant T-PLL in a 54-year-old man, the cytology of which was initially interpreted as small lymphocytic malignancy such as small lymphocytic lymphoma/chronic lymphocytic leukemia.

Anti-apoptotic Effect of Bojungbangam-tang Ethanol Extract on Cisplatin-Induced Apoptosis in Rat Mesangial Cells

  • Kim, Nam-Su;Ju, Sung-Min;Kwon, Young-Dal;Shin, Byung-Cheul;Ahn, Kyoo-Seok;Kim, Sung-Hoon;Song, Yung-Sun;Jeon, Byung-Hun
    • 동의생리병리학회지
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    • 제20권6호
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    • pp.1664-1671
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    • 2006
  • Cisplatin is a anti-neoplastic agent which is commonly used for the treatment of solid tumor. Cisplatin activates multiple signal transduction pathways involved in the stress-induced apoptosis in a variety of cell types. Cytotoxicity of cisplatin was detected in rat mesangial cells and the value of $IC_{50}$ is about 20 ${\mu}M$. The treatment of cisplatin to rat mesangial cells showed the apoptotic bodies and DNA fragmentation. The activation of caspase-3, -8, and -9 and proteolytic cleavage of PARP were observed in the rat mesangial cells treated time-dependently with cisplatin. The activation of ERK, p38 and JNK was also observed in the apoptosis induced by cisplatin in rat mesangial cells. The ethanol extract of Bojungbangam-tang (EBJT), a new hergal prescription composed of nine crude drugs, inhibited cisplatin-induced apoptosis in rat mesangial cells. EBJT reduced sub-G1 peak (apoptotic peak) in cisplatin-treated rat mesangial cells. The cisplatin-induced ERK and JNK activation in rat mesangial cells were blocked by EBJT, but EBJT had no effect on p38 activation. Taken together, these results con suggest that EBJT prevents cisplatin-induced apoptotic cell death in rat mesangial cells through inhibition of ERK and JNK activation.

랫드의 실험적 간암발생과 자연살해세포의 활성에 미치는 녹용의 효과 (Effects of the Pilose Antler on the Experimental Hepatocarcino- genesis and the Natural Killer Cell Activity in Rats)

  • 정자영;길광섭;이영순
    • Toxicological Research
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    • 제14권4호
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    • pp.475-481
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    • 1998
  • This study was performed to investigate the modifying effect of the general (GPA) and the fermented pilose antler (FPA) on experimental hepatocarcinogenesis and Natural Killer cell activity in rats. Specific pathogen free, 5-week male Sprague-Dawley rats were divided into four groups. To induce hepatocarcinogenesis, diethylnitrosamine (DEN, 200 mg/kg, i.p.) was used as a tumor initiator and was given in a single dose at experimental onset. All rats were given a partial hepatectomy (PH) at 3 weeks after experimental onset. Sodium phenobarbital (PB, 0.05% in diet), GPA (0.075% in diet) and FPA (0. 075% in diet) were given from 2 to 8 weeks. Group I of the initiation control group was only given DEN. As initiation-promotion group, Group II was given DEN and then PB. Group III and IV were given DEN-PB-GPA and DEN-PB-FPA, respectively. In hematological analysis, as compared with Group I. the number of white blood cells were significantly increased in the GPA (p<0.01) and the FPA treated group (p<0.05), respectively. Natural killer (NK) cell activity by flow cytometer (FCM) analysis was higher in group of treated with the GPA (35%) than that of the FPA (27.5%), but not significant. Result of the immunohistochemical staining of the glutathione S-transferase placental form (GST-p) indicated that the number of and area of the pre-neoplastic lesions was not significantly changed in Group III and IV compared Group II, respectively. In conclusion, the GPA and the FPA treatment significantly increased the number od WBC in peripheral blood, but the enhancing NK activity and the modifying effect on the experimental hepatocarcinogenesis were not observed.

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소아에서 신장 이식 후 발생한 Posttransplant Lymphoproliferative Disease 1례 (A Case of Posttransplant Lymphoproliferative Disease Following Renal Transplantation in a Child)

  • 장원경;한혜원;이미정;김태형;박영서
    • Childhood Kidney Diseases
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    • 제7권2호
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    • pp.245-252
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    • 2003
  • Posttransplant lymphoproliferative disease(PTLD)는 이식 후 발생하는 림프증식성 질환으로 이식장기의 거부반응을 억제하기 위한 면역억제제의 사용 및 이에 따른 EBV 감염과 연관이 있다고 알려져 있다. 소아 PTLD의 경우 성인에 비해 EBV의 초감염 또는 재활성이 더 많은 것으로 보고되고 있으며 최근 더 강력한 면역억제제들의 개발 및 사용에 따라 발생이 증가하고 있다. 본 증례는 14세 여아로 신이식 44개월 후에 EBV 감염의 증거 없이 지발성 PTLD가 발생하였으며 골수 검사상 B-세포 급성 림프구성 백혈병으로 진단되어 항암화학요법 치료를 시작하였고, 치료 후 완전 관해는 이루어졌으나 심한 중성구 감소증에 따른 패혈성 쇼크로 입원 77일만에 사망하였다.

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자궁경부상피내종양과 침윤성 편평상피암종의 혈관신생에서 비만세포와 혈관내피성장인자의 발현 (Mast Cells and Vascular Endothelial Growth Factor Expression in Neoangiogenesis of Cervical Intraepithelial Neoplasia and Invasive Squamous Cell Carcinomas of the Uterine Cervix)

  • 제갈승주;이정아;노종섭
    • 대한임상검사과학회지
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    • 제37권3호
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    • pp.197-206
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    • 2005
  • To determine the correlation between mast cells(MCs) and neoangiogenesis in the growth and progression of cervical cancer, we investigated mast cell density(MCD), microvessel density(MVD) and the expression of vascular epithelial growth factor(VEGF) in cervical intraepithelial neoplasia and invasive suqamous cell carcinoma of the uterine cervix. Forty-five cervical intraepithelial neoplasia(CIN I, II and III), 15 microinvasive carcinomas, 15 invasive squamous cell carcinomas and 20 normal cervical epithelia were included in this study. MCs were stained with anti-c-Kit antibody and alcian blue, microvessels with anti-factor VIII antibody and VEGF with anti-VEGF antibody. The adjacent fields of both normal and neoplastic epithelium were used for counting MCs and microvessels. Computerized image analysis was used to evaluate MCD and MVD. MCD and MVD were the mean numbers per $1mm^2$ counted in 5-10 high and low power fields respectively. In both c-Kit and alcian blue stained sections, MCD progressively increased along the continuum from CIN I to invasive squamous cell carcinoma(p<0.001). MVD increased significantly with cervical neoplasia progression, from CIN to invasive squamous cell carcinoma (p<0.001). In double c-Kit and Factor VIII-stained sections, MCs were mainly present in the areas adjacent to newly formed blood vessels. However, there were no significant differences in MCD and MVD between normal epithelum and CIN I. A strong correlation was also observed between MCD and MVD. In double VEGF and alcian blue-stained sections, VEGF was expressed in only MCs. Strong VEGF-positive MCs were particularly abundant around the tumorous region. Our results suggest that MCs may upregulate neoangiogenesis by VGEF secretion in the development and progression of cervical neoplasia.

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