• 대한화장품학회:학술대회논문집
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• 대한화장품학회 2003년도 IFSCC Conference Proceeding Book I
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• pp.780-803
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• 2003

Exposure of skin cells, particularly keratinocytes to various nuclear factor-kappaB ($\textrm{NF}_{-{\kappa}}\textrm{B}$) activators [e.g. tumor necrosis factor-$\alpha$, interleukin-1, lipopolysaccharides, and ultraviolet light] leads to phosphorylation and degradation of the inhibitory protein, $\textrm{I}_{{\kappa}}\textrm{B}$. Liberated $\textrm{NF}_{-{\kappa}}\textrm{B}$ is translocated into the nucleus where it can change or alter expression of target genes, resulting in the secretion of extracellular signaling molecules including melanotrophic factors affecting melanocyte. In order to demonstrate the possible role of $\textrm{NF}_{-{\kappa}}\textrm{B}$ activation on the synthesis of melanotrophic factors from the keratinocytes, the activities of $\textrm{NF}_{-{\kappa}}\textrm{B}$ induced by melanogenic inhibitors (MIs) were determined in human HaCaT keratinocytes transfected with $\textrm{pNF}_{-{\kappa}}\textrm{B}$-SEAP-NPT plasmid. Transfectant cells released the secretory alkaline phosphatase (SEAP) as a transcription reporter in response to the $\textrm{NF}_{-{\kappa}}\textrm{B}$ activity and contain the neomycin phosphotransferase (NPT) gene for the dominant selection marker for geneticin resistance. MIs such as niacinamide, kojic acid, hydroquinone, resorcinol, arbutin, and glycolic acid were preincubated with transfectant HaCaT cells for 3 h and then ultraviolet B (UVB) was irradiated. $\textrm{NF}_{-{\kappa}}\textrm{B}$ activation was measured with the SEAP reporter gene assay using a fluorescence detection method. Of the Mis tested, kojic acid ($IC_{50}$/ = 60 $\mu$M) was found to be the most potent inhibitor of UVB-upregulating $\textrm{NF}_{-{\kappa}}\textrm{B}$ activation in transfectant HaCaT cells, which is followed by niacinamide ($IC_{50}$/= 540 $\mu$M). Pretreatment of the transfectant HaCaT cells with the Mis, especially kojic acid and niacinamide, effectively lowered $\textrm{NF}_{-{\kappa}}\textrm{B}$ binding measured by electrophoretic mobility shift assay. Furthermore, these two inhibitors remarkably reduced the secretion level of IL-6, one of melanotrophic factors, triggered by UV-radiation of the HaCaT cells. These observations suggest that Mis working at the in vivo level might act partially through the modulation of the synthesis of melanotrophic factors in keratinocyte.

• 대한원격탐사학회지
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• 제29권4호
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• pp.361-373
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• 2013

공간해상도 약 1 m의 고해상도 X-band SAR 위성이 이용되면서 SAR를 이용한 도심지 모니터링, 표적탐지, 건물 재구성에 관한 연구가 진행되고 있다. 본 연구에서는 고해상도 TerraSAR-X SAR 영상을 이용한 도심지 건물 재구성을 수행하였다. 도심지 건물 재구성을 위하여 1:25,000 수치지형도로부터 건물의 외곽선을 추출하였으며, 추출한 건물의 외곽선을 기반으로 SAR 영상에서 모서리반사 위치를 찾았다. KS 테스트(Kolmogorov-Smirnov Test)에 기반하여 고해상도 SAR 진폭영상의 건물 모서리반사 위치로부터 레이오버 길이를 측정하여 건물의 초기 높이를 설정하였다. 진폭영상을 이용하여 추출한 건물의 초기 높이 기준 -10 m에서 +10 m로 건물의 높이를 변화시키며 도심지에 적합한 간섭위상 시뮬레이션을 수행하여 TerraSAR-X 간섭위상과의 위상 일치성 계산을 하였다. 위상 일치의 경향성 분석을 통해 건물의 높이를 설정해 줌으로써 고해상도 SAR 영상을 이용한 도심지 건물 재구성 연구를 진행하였다. 대전지역의 아파트 단지에 적용한 결과, 진폭영상과 간섭위상을 이용하여 추정된 건물 높이는 LiDAR로부터 추출된 높이를 기준으로 약 1~2 m 정도의 RMSE (Root Mean Square Error)를 보였다. 개발된 알고리즘은 향후 TerraSAR-X와 TanDEM-X 간섭쌍 자료에 적용할 경우, 보다 도심지 모니터링에 효과적으로 이용될 수 있을 것이다.

• Asian Pacific Journal of Cancer Prevention
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• 제17권8호
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• pp.3763-3767
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• 2016

Background: Cervical cancer is the second most common cancer among females across the world. It is a preventable cancer and early detection is very feasible. This study aimed to identify which women characteristics are potentially associated with and may have an important in uence on the uptake of cervical cancer screening in Kurdish women living in the west of Iran.. Materials and Methods: A cross sectional study was conducted in late 2014. A random sample of women aged 40 years and above without history of cervical cancer and identi ed as Kurdish background were selected and interviewed by two trained interviewers. Information about sociodemographic and reproductive factors, history of diseases, and cervical screening was collected using a questionnaire and women who had undergone a hysterectomy were excluded. Univariate analyses were used to describe the general characteristics of the study population. Multivariable logistic regression models with self-reported screening history were used to estimate odds ratios (ORs) with 95% con dence intervals (CI). Signi cance was considered at the 5% level. Results: A total of 561 women were included in this study (mean age $43.6{\pm}5.17$ years) participation in cervical screening at least once was about 32%. Cervical screening uptake percentage was signi cantly lower among people over 60 years of age (adjusted OR= 0.26, 95% CI: 0.11-0.64), and those who were illiterate (OR= 0.41 95% CI: 0.23-0.73) and post-menopausal (OR= 0.56, 95% CI: 0.35-0.91). Women with ${\leq}1$ child were less likely to report a Pap test (adjusted OR=0.43 95%CI: 0.13-1.37) Cervical screening uptake was higher among women with health insurance (OR= 2.31, 95% CI: 1.50-3.56). Conclusions: Cervical screening participation in this study was low compared to other studies in developed countries. The screening uptake was different based on age, education, parity, insurance coverage and menopausal status. It is recommended to target these groups of women in cervical screening program.

• 한국환경과학회지
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• 제17권3호
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• pp.287-296
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• 2008

A comprehensive quality survey for heavy metals, organophosphorous and organochlorine residual pesticides, and coplanar PCBs in samples such as water, sediments and soils as well as spiders has been implemented. The samples were undertaken at nine stream sites and their vicinity in August 2006, representing different surrounding environments. The levels of PCBs were expressed as concentrations and WHO-TEFs. Among 12 coplanar PCBs as target compounds in this study, 2,3', 4,4', 5-PentaCB (IUPAC # 118) was the congener with the highest concentration. The total concentrations and TEF values of coplanar PCBs in Siheung stream sediment (heavy industrial complex site located in Ansan city) were 3915.50 pg/g and 0.8366 pg-TEQ/g on a dry weight basis, respectively. Such levels were around 40 times higher compared to sediment from Gapyung stream (green site located in the upper of Myunggi mountain). It is probably due to the direct input of PCBs trom PCBs treatment materials. Organophosphorous (EPN, dementon-s-methyl, diazinon, parathion, and phenthoate) and organochlorine (alpha-BHC, aldrin, 4,4'-DDT, 4,4'-DDE, endosulfan alpha and etc.) pesticides were not detected above 5 ppb of detection limits. The concentrations of Cu and Cd in water and sediment samples from Siheung stream were 44.11 and $0.17ug/m\ell$ and $713.42{\mu}g/g$ and $3.73{\mu}g/g$, respectively, which contained $20\sim40$ times higher concentrations than those from Gapyung stream. In addition to the water and sediment samples, the levels of heavy metals in spider from designated sampling sites were also determined. Heavy metals in spider collected near Siheung stream was appeared to be equivalent and/or a little higher levels with respect to other spiders. Furthermore, the ratio of relative heavy metals (Cu, Cd, and Pb) in spider from each stream site showed a correlation as similar as that of heavy metals in soil samples.

• 한국생물정보학회:학술대회논문집
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• 한국생물정보시스템생물학회 2001년도 제2회 생물정보 워크샵 (DNA Chip Bioinformatics)
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• pp.61-86
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• 2001

All cancers are caused by abnormalities in DNA sequence. Throughout life, the DNA in human cells is exposed to mutagens and suffers mistakes in replication, resulting in progressive, subtle changes in the DNA sequence in each cell. Since the development of conventional and molecular cytogenetic methods to the analysis of chromosomal aberrations in cancers, more than 1,800 recurring chromosomal breakpoints have been identified. These breakpoints and regions of nonrandom copy number changes typically point to the location of genes involved in cancer initiation and progression. With the introduction of molecular cytogenetic methodologies based on fluorescence in situ hybridization (FISH), namely, comparative genomic hybridization (CGH) and multicolor FISH (m-FISH) in carcinomas become susceptible to analysis. Conventional CGH has been widely applied for the detection of genomic imbalances in tumor cells, and used normal metaphase chromosomes as targets for the mapping of copy number changes. However, this limits the mapping of such imbalances to the resolution limit of metaphase chromosomes (usually 10 to 20 Mb). Efforts to increase this resolution have led to the "new"concept of genomic DNA chip (1 to 2 Mb), whereby the chromosomal target is replaced with cloned DNA immobilized on such as glass slides. The resulting resolution then depends on the size of the immobilized DNA fragments. We have completed the first draft of its Korean Genome Project. The project proceeded by end sequencing inserts from a library of 96,768 bacterial artificial chromosomes (BACs) containing genomic DNA fragments from Korean ethnicity. The sequenced BAC ends were then compared to the Human Genome Project′s publicly available sequence database and aligned according to known cancer gene sequences. These BAC clones were biotinylated by nick translation, hybridized to cytogenetic preparations of metaphase cells, and detected with fluorescein-conjugated avidin. Only locations of unique or low-copy Portions of the clone are identified, because high-copy interspersed repetitive sequences in the probe were suppressed by the addition of unlabelled Cotl DNA. Banding patterns were produced using DAPI. By this means, every BAC fragment has been matched to its appropriate chromosomal location. We have placed 86 (156 BAC clones) cytogenetically defined landmarks to help with the characterization of known cancer genes. Microarray techniques would be applied in CGH by replacement of metaphase chromosome to arrayed BAC confirming in oncogene and tumor suppressor gene: and an array BAC clones from the collection is used to perform a genome-wide scan for segmental aneuploidy by array-CGH. Therefore, the genomic DNA chip (arrayed BAC) will be undoubtedly provide accurate diagnosis of deletions, duplication, insertions and rearrangements of genomic material related to various human phenotypes, including neoplasias. And our tumor markers based on genetic abnormalities of cancer would be identified and contribute to the screening of the stage of cancers and/or hereditary diseases

• Journal of Genetic Medicine
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• 제6권2호
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• pp.146-154
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• 2009

Multiplex ligation dependent probe amplification (MLPA)은 탐침자를 표적지에 교잡시킨 후, ligation 시키고, 그 산물을 중합효소연쇄반응으로 증폭시킴으로써 표적지의 존재여부 또는 농도를 확인할 수 있는 방법으로, 그 원리가 소개된 이래로 여러 유전자들에 대한 거대결실 및 중복돌연변이에 대한 탐색에 이용되었다. 유전자진단은 질환에 관련된 유전자에 대한 돌연변이를 탐색함으로써 질환을 진단하는 방법으로, 단일유전자 결핍 질환에 대한 유전자진단은 주로 중합효소연쇄반응과 염기서열 분석 방법을 통한 점돌연변이의 탐색에 집중되어 있다. 거대결실 또는 중복돌연변이의 경우, 특히 이형접합자를 형성하게 되는 경우는 중합효소 연쇄반응을 통하여 결실 또는 중복돌연변이 여부의 확인이 힘들다. PCR 방법에 기초하여 유전자의 농도(gene dosage)를 알 수 있는 방법으로 MLPA 방법이 소개되면서 거대결실 또는중복돌연변이를 포함하고 있던 질병 관련돌연변이들의 규명이 한층 쉬워졌다. MLPA의 원리를 응용하여 단순한 유전자의 농도 측정뿐 아니라 유전자내의 메칠화양상의 차이를 확인하거나, 염색체의 배수체 이상 등 염색체이상의 돌연변이 규명과, 전체 유전자의 크기가 비교적 커서 거대결실 돌연변이를 많이 동반하는, 주로 우성유전의 암 관련 유전자 돌연변이의 규명에 유용하게 이용된다. MLPA는 상용적인 중합효소연쇄반응으로 확인할 수 없는 유전자의 농도를 효과적으로 규명할 수 있는 방법으로, 적은 양의 주형 DNA만을 사용하고, 한가지의 실험원리로 다양한 응용이 가능하며 high-throughput이 가능한 장점을 가지는 반면, 주형 DNA의 질에 결과의 의존도가 높고, 민족 또는 개인간의 차이를 보일 수 있는 표적 DNA 염기서열 내의 single nucleotide polymorphism (SNP) 등으로 인해 분석의 오류가 생길 수 있으며, 양적 차이를 규명하는 것이므로 수 차례의 대조군 검사가 함께 진행되어야 하는 단점이 있다. 여기서는 MLPA를 이용하여 질병유전자의 돌연변이를 밝힌 사례를 바탕으로 MLPA의 원리와 탐색할 수 있는 돌연변이의 종류, 그리고 이 방법의 장단점에 대해 고찰해 보고자 한다.

• Asian Pacific Journal of Cancer Prevention
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• 제16권9호
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• pp.3785-3792
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• 2015

The CCAAT/enhancer-binding protein-alpha (CEBPA) is a transcriptional factor that plays a crucial role in the control of proliferation and differentiation of myeloid precursors. This gene was recognized as the target of genetic alterations and were associated with clinical complexity among AML. We here analyze the frequency and types of CEBPA mutations and polymorphisms in a de novo AML patients from South India and tried to find out associations of these variations with different clinical parameters and the prognostic significance in AML. Study was carried out in 248 de novo AML patients, cytogenetic analysis was performed from the bone marrow samples and was karyotyped. PCR-SSCP analysis and sequencing was performed for the detection of CEBPA gene variations. All the statistical analysis was performed using SPSS 17 (statistical package for social sciences) software. Pearson Chi-square test, Mann-Whitney U test, Kaplan-Meier survival analysis and log rank tests were performed. CEBPA mutations were detected in 18% and CEBPA polymorphisms were detected in 18.9% of AML cases studied. Most of the mutations occured at the C terminal region. Polymorphisms were detected in both N and C terminal region. with most common being, c.584_589dup ACCCGC and c.690G>T. A significant association was not observed for the mutation and polymorphism with respect to clinical and laboratory parameters. Survival advantage was observed for the mutated cases compared to non mutated cases, especially for the normal karyotype groups. Polymorphisms has no effect on the survival pattern of AML patients. CEBPA mutation and polymorphisms were observed with similar frequency and was identified in all the FAB subtypes as well as in cytogenetic risk groups in our study population, but CEBPA mutations alone confer a prognostic value for NK AML patients.

• Asian Pacific Journal of Cancer Prevention
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• 제16권15호
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• pp.6285-6288
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• 2015

Background: Breast cancer is commonly diagnosed at late stages in countries with limited resources. In Morocco, breast cancer is ranked the first female cancer (36.1%) and screening methods could reduce the proportion presenting with a late diagnosis. Morocco is currently adopting a breast cancer screening program based on clinical examination at primary health facilities, diagnosis at secondary level and treatment at tertiary level. So far, there is no systematic information on the performance of the screening program for breast cancer in Morocco. The aim of this study was to analyze early performance indicators. Materials and Methods: A retrospective evaluative study conducted in Temara city. The target population was the entire female population aged between 45-70 years. The study was based on process and performance indicators collected at the individual level from the various health structures in Tamara between 2009 and 2011. Results: A total of 2,350 women participated in the screening program; the participation rate was 35.7%. Of these, 76.8% (1,806) were married and 5.2% (106) of this group had a family history of breast cancer. Of the women who attended screening, 9.3% (190) were found to have an abnormal physical examination findings. A total of 260 (12.7%) were referred for a specialist consultation. The positive predictive value of clinical breast examination versus mammography was 23.0%. Forty four (35.5%) of the lesions found on the mammograms were classified as BI-RADs 3; 4 or 5 category. Cancer was found in 4 (1.95%) of the total number of screened women and benign cases represented 0.58%. Conclusions: These first results of the programme are very encouraging, but there is a need to closely monitor performance and to improve programme procedures with the aim of increasing both the participation rate and the proportion of women eligible to attend screening.

• Asian Pacific Journal of Cancer Prevention
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• 제16권17호
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• pp.7619-7625
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• 2015

Background: Aberrant microRNA expression has been associated with the pathogenesis of a variety of human malignancies including oral squamous cell carcinoma (SCC). In this study, we examined primary oral SCCs for the expression of 6 candidate miRNAs, of which five (miR-34a, miR-143, miR-373, miR-380-5p, and miR-504) regulate the tumor suppressor TP53 and one (miR-99a) is involved in AKT/mTOR signaling. Materials and Methods: Tumor tissues (punch biopsies) were collected from 52 oral cancer patients and as a control, 8 independent adjacent normal tissue samples were also obtained. After RNA isolation, we assessed the mature miRNA levels of the 6 selected candidates against RNU44 and RNU48 as endogenous controls, using specific TaqMan miRNA assays. Results: miR-34a, miR-99a, miR-143 and miR-380-5p were significantly down-regulated in tumors compared to controls. Moreover, high levels of miR-34a were associated with alcohol consumption while those of miR-99a and miR-143 were associated with advanced tumor size. No significant difference was observed in the levels of miR-504 between the tumors and controls whereas miR-373 was below the detection level in all but two tumor samples. Conclusions: Low levels of miR-380-5p and miR-504 that directly target the 3'UTR of TP53 suggest that p53 may not be repressed by these two miRNAs in OSCC. On the other hand, low levels of miR-34a or miR-143 may relieve MDM4 and SIRT1 or MDM2 respectively, which will sequester p53 indicating an indirect mode of p53 suppression in oral tumors.

• 한국음향학회지
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• 제24권6호
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• pp.317-324
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• 2005

복잡한 음파전달과 시끄러운 해상 교통량이 많은 천해 환경에서 조용한 수중 표적의 탐지와 위치 추정은 아직까지 많은 문제점들을 남기고 있다. 정합장처리는 적절한 조향 벡터를 구성하기 위하여 음파전달 모델을 이용함으로써 최적의 배열 이득과 위치 추정 정밀도를 제공한다. 그러나 실제로는 아직까지 몇몇 제약조건들 때문에 정합장처리의 성능이 제한되고 있다. 가장 중요한 제약조건은 일반적으로 수중의 환경에 대한 정확한 자료가 부족하다는 것이다. 한국 주변의 천해에서 정합장처리의 성능을 판단하기 위하여 일련의 해상실험인 MAPLE (matched acoustic properties and localization experiment)을 실시해오고 있으며, 본 논문은 2003년 10월에 수직선배열과 이동음원을 이용하여 동해 연안에서 실시한 정합장처리 실험으로부터 획득한 자료를 분석한 결과이다. 정합장처리 알고리즘을 이용하여 음원위치추정을 수행하였다. 실험 해역의 수온구조는 내부파 등의 단주기 변동의 영향을 크게 받는 것으로 알려져 왔으며, 본 논문의 정합장처리 결과에서도 단주기변동의 영향을 받아 부엽준위가 증가한 것으로 보인다.