• 제목/요약/키워드: oncogene expression

검색결과 185건 처리시간 0.034초

Expression of the Type IV Collagenase Genes and ras Oncogene in Various Human Tumor Cell Lines

  • Moon, A-Ree;Park, Sang-Ho;Lee, Sang-Hun
    • BMB Reports
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    • 제29권5호
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    • pp.484-487
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    • 1996
  • The matrix metalloproteinases (MMPs) are members of a unique family of proteolytic enzymes that degrade components of the extracellular matrix. Significant evidence has accumulated to directly implicate members of the MMPs in tumor invasion and metastasis formation. To investigate the correlation between ras oncogene and MMP gene expression in various tumor cells, we detected mRNAs for the ras, MMP-2 and MMP-9 (72 kD and 92 kD type IV collagenases, respectively) genes in nine human tumor cell lines. The ras gene was expressed in seven cell lines; MMP-2 in three; MMP-9 in two cell lines tested. There was no direct correlation between the ras oncogene and MMP expression. A clear difference in the mRNA expression between MMP-2 and MMP-9 was observed among the cell lines. As an approach to study the effect of the ras oncogene on metastasis, we examined the expressions of MMP-2 and MMP-9 in HT1080 cells transfected with the v-H-ras gene. MMP-9 expression was Significantly enhanced in the ras-transfected HT1080 cells compared with the nontransfectants while ras transfection did not affect the expression of MMP-2. These results suggest the possible inducing effect of the ras oncogene on the metastasis by activation of the MMP-9 gene in HT1080.

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식이 Capsaicin이 마우스의 주요 장기조직에서의 Proto-oncogenes Expression에 미치는 영향 (Effect of Dietary Capsaicin on Proto-oncogenes Expression in Various in Mice)

  • 김정미;한인섭;김병삼;유리나
    • 한국식품영양과학회지
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    • 제25권6호
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    • pp.1024-1030
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    • 1996
  • 매운맛 성분(capsaicin, CAP)이 암발생에 미치는 영향에 대한 분자적인 수준에서의 기초 정보를 확보하기 위해, 식이 CAP의 투여가 동물 조직 중 proto-oncogene 의 발현에 미치는 영향을 조사하였다. ICR mouse를 4 group으로 분류하여 각각 식이CAP 농도가 0, 5, 20, 100ppm이 되도록 조제한 먹이로 4주 동안 사육하였다. 사육기간 종료 후 동물들의 중요장기를 적출하여 total RNA를 분리하고, proto-oncogene(c-jun, c-myc, H-ras, erbB, p53)의 발현 수준을 slot blot hybridization assay를 통해 살펴 보았다. 이때, control probe로는 18SrRNA를 사용하였다. 그 결과, c-jun proto-oncogene의 발현은 각 주요 장기조직에 따라 다른 양상을 나타내었는데, 식이CAP 투여량이 증가함에 따라 간과 신장에서 그 발현이 증가하며, 위에서는 CAP 20ppm까지는 c-jun의 발현이 증가하다. 100ppm 투여시에는 감소하는 것으로 나타났으며, 비장에서는 식이CAP 투여량이 증가함에 따라 감소하는 경향을 보였다. 한편, tumor suppressor gene인 p53의 경우, 간에서만 CAP 20, 100ppm 처리시 약하게 발현되었다. 이들 결과로 보아, 식이 CAP에 의한 proto-oncogene의 발현은 CAP 투여량에 따라 그 정도를 달리하며, 그 발현 정도는 조직 특이성을 나타내는 것으로 평가된다.

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Sarcoma 180 세포에서 비파엽에서 분리한 올솔레산이 c-myc 과 c-Ha-ras 암유전자 발현에 미치는 영향 (Effects of Ursolic Acid Isolated from Eriobotrya Japonica on c-myc and c-Ha-ras Oncogene Expression at Sarcoma 180 cell)

  • Yang-Ae Choi;Tae Hyong Rhew;Kun-Young Park;Hae-Young Chung;Jae-Chung Hah
    • 한국식품영양과학회지
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    • 제21권3호
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    • pp.314-318
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    • 1992
  • 비파엽에서 분리동정한 활성성분인 울솔레산을 sarcoma 180 cells에 처리하여 c-myc과 c-Ha-ras 암유전자 발현에 있어서 변화를 조사하였다. 그 결과 c-myc 유전자의 발현에서는 뚜렸한 감소가 관찰되었으나 c-Ha-ras 유전자 발현은 대조군과 거의 차이가 없었다. Cell proliferation에 중요한 역할을 하는 것으로 추측되고 있는 c-myc 유전자 발현의 감소는 지금까지 보고된 그 물질의 antipromotional effect와 관계있는 것으로 보여진다.

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생쥐에서 종양세포의 암유전자발현에 대한 울솔산의 효과 (Effects of Ursolic Acid on Oncogene Expression Detected by In Situ Hybridization in Mice)

  • 류태형;박성미;박건영;정해영;하재청;이정규
    • 약학회지
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    • 제36권6호
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    • pp.529-537
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    • 1992
  • To investigate the effect of ursolic acid on the expression of oncogenes in tumor cells of mice, sarcoma 180 ascites tumor cells were implanted into the left groin of ICR mice and the tumor bearing mice were treated with ursolic acid. The expression of oncogenes were measured by in situ hybridization method. Ursolic acid significantly reduced the expression of oncogenes in the tumor cells. Therefore, it can be said that the prestated anticarcinogenic effect of ursolic acid could be partly ascribed to the mechanism included in the oncogene´s transcription level.

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Reduced Expression of Limd1 in Ulcerative Oral Epithelium Associated with Tobacco and Areca Nut

  • Maiti, Guru Prasad;Ghosh, Amlan;Chatterjee, Ramdas;Roy, Anup;Sharp, Tyson V.;Roychoudhury, Susanta;Panda, Chinmay Kumar
    • Asian Pacific Journal of Cancer Prevention
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    • 제13권9호
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    • pp.4341-4346
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    • 2012
  • Purpose: The aim of this study was to cast light on initiating molecular events associated with the development of premalignant oral lesions induced by tobacco and/or areca nut. Method: Immunohistochemical analyses of cell cycle regulatory proteins (LIMD1, RBSP3, p16, RB, phosphorylated RB, p53), EGFR and SH3GL2 (EGFR associated protein) were performed with inflammatory/ulcerative epithelium and adjacent hyperplastic/mild dysplastic lesions. Results: No change in expression of the proteins was seen in inflammatory epithelium. Reduced nuclear expression of LIMD1 was evident in ulcerative epithelium. In hyperplastic lesions, reduced expression of RBSP3, p16, SH3GL2 and overexpression of p-RB and EGFR were apparent. Reduced nuclear expression of p53 was observed in mild dysplastic lesions. Conclusion: Our data suggest that inactivation of LIMD1 in ulcerative epithelium might predispose the tissues to alterations of other cell cycle regulatory and EGFR signaling proteins needed for the development of premalignant oral lesions.

TGIF에 의한 Human cervical cancer oncogene (HCCR) 발현 조절 (TGIF Site is Involved in Expression of Human Cervical Cancer Oncogene (HCCR) 발현 조절)

  • 조광원
    • 생명과학회지
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    • 제19권9호
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    • pp.1289-1293
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    • 2009
  • 원암단백질로 알려진 Human cervical cancer oncogene (HCCR)은 발암억제 단백질인 p53과 작용하여 다양한 암조직에서 암의 유발을 촉진한다. 그러나, 아직 정확한 발암 유도기전이 알려져 있지 않다. 이러한 의문을 해소하기 위한 일환으로 본 연구에서는 HCCR의 발현이 어떻게 조절되는지를 조사하였다. 이를 위해 먼저 HCCR 5' 쪽의 promoter 영역을 분리하여 Luciferase assay법을 이용하여 K562, HEK293, A549 세포에서 분석하였고, Promoter의 -370에서 -406사이 36bp의 첨가로 promoter활성이 의미 있게 억제됨을 관찰하였다. 또한, 36 bp만을 포함하는 probe를 이용한 mobility shift assays (EMSA)에서 핵단백질이 결합함을 관찰하였고, 컴퓨터를 이용한 분석에서 TG-interacting factor (TGIF)에 대한 consensus sequences 존재함을 관찰하였다. TGIF 만을 포함하는 probe (TC)와 돌연변이를 유발한 probe (mTG)를 이용한 EMSA에서 이 자리에 TGIF가 결합함을 보였다. 또한, TGIF 자리에 돌연변이를 유발하면(pGL3-mTGIF) 발현의 억제가 회복됨을 관찰하였다. 본 연구에서는 HCCR promoter의 특성을 분석하였고, 이 과정에서 -390에서 -366 사이에 TGIF 전사인자가 결합하여 전사활성을 조절함을 증명하였다.

Expression of the Pokemon Proto-oncogene in Nasopharyngeal Carcinoma Cell Lines and Tissues

  • Jiao, Wei;Liu, Fei;Tang, Feng-Zhu;Lan, Jiao;Xiao, Rui-Ping;Chen, Xing-Zhou;Ye, Hui-Lan;Cai, Yong-Lin
    • Asian Pacific Journal of Cancer Prevention
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    • 제14권11호
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    • pp.6315-6319
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    • 2013
  • To study the differentiated expression of the proto-oncogene Pokemon in nasopharyngeal carcinoma (NPC) cell lines and tissues, mRNA and protein expression levels of CNE1, CNE2, CNE3 and C666-1 were detected separately by reverse transcription polymerase chain reaction (RT-PCR), real-time PCR and Western-blotting. The immortalized nasopharyngeal epithelial cell line NP69 was used as a control. The Pokemon protein expression level in biopsy specimens from chronic rhinitis patients and undifferentiated non keratinizing NPC patients was determined by Western-blotting and arranged from high to low: C666-1>CNE1>CNE2> CNE3>NP69. The Pokemon mRNA expression level was also arranged from high to low: CNE1>CNE2>NP69>C666-1>CNE3. Pokemon expression of NP69 and C666-1 obviously varied from mRNA to protein. The Pokemon protein level of NPC biopsy specimens was obviously higher than in chronic rhinitis. The data suggest that high Pokemon protein expression is closely associated with undifferentiated non-keratinizing NPC and may provide useful information for NPC molecular target therapy.

DIFFERENTIAL EXPRESSION OF ORNITHINE DECARBOXYLASE AND HA-RAS CELLULAR ONCOGENE DURING DEVELOPMENT OF THE FEMALE RAT

  • Baik, M.G.;Park, C.S.
    • Asian-Australasian Journal of Animal Sciences
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    • 제7권1호
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    • pp.119-124
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    • 1994
  • Experiments were performed to determine age-associated changes in ornithine decarboxylase (ODC) gene and Ha-ras cellular oncogene expression in tissues of female rats. In the kidney, ODC mRNA levels did not show age-associated changes, while ODC enzyme activities were decreased with advancing age from 3 to 10 months. These results suggest that post-transcriptional mechanism (s) are involved in the age-dependent decrease in renal ODC enzyme activity. In addition, we found no correlation between testosterone-induced renal ODC expression and DNA methylation pattern. Ha-ras mRNA levels in brain decreased as animals aged from 3 to 6 months, while renal Ha-ras mRNA levels were not influenced by age. Results demonstrate the age-dependent expression of Ha-ras in a tissue-specific manner.

Diagnostic Relevance of Overexpressed Serine Threonine Tyrosine Kinase/Novel Oncogene with Kinase Domain (STYK1/NOK) mRNA in Colorectal Cancer

  • Orang, Ayla Valinezhad;Safaralizadeh, Reza;Hosseinpour Feizi, Mohammad Ali;Somi, Mohammad Hossein
    • Asian Pacific Journal of Cancer Prevention
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    • 제15권16호
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    • pp.6685-6689
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    • 2014
  • Background: Alterations in gene expression levels or mutations of tyrosine kinases are detected in some human cancers. In this study, we examined whether serine threonine tyrosine kinase 1 (STYK1)/novel oncogene with kinase domain (NOK) is overexpressed in patients with colorectal cancer. We also examined the clinical relevance of STYK1/NOK expression in cancer tissues. Materials and Methods: In tumor samples of patients with colorectal cancer and their matched non-cancerous samples, STYK1/NOK messenger RNA (mRNA) expression was analyzed by quantitative reverse transcriptase polymerase chain reaction. Associations between the expression levels of STYK1/NOK and clinicopathological characteristics of colorectal cancer were also assessed using Mann-Whitney U and Kruskal-Wallis tests. Results: Upregulation of STYK1/NOK was found in cancer tissues even at early stage of colorectal cancer compared to normal adjacent tissues. The optimal cutoff point of 0.198 the STYK1/NOK expression showed 0.78 sensitivity and 0.75 specificity for diagnosis. Overexpressed STYK1/NOK was correlated with tumor size but had no association with other clinicopathological characteristics of colorectal cancer. Conclusions: These results indicate that STYK1/NOK mRNA is widely expressed in the patients with colorectal cancer and suggest that inhibition of this molecule could potentially serve as a novel therapeutic target.

생쥐 초기배아에서 c-myc Proto-Oncogene Promoter의 기능적 활성화 (Zygotic Expression of c-myc Gene in Mouse Early Embryos: Functional Role of c-myc Promoter)

  • 박기수;강해묵;심찬섭;선웅;김재만;이영기;김경진
    • 한국동물학회지
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    • 제38권4호
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    • pp.550-556
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    • 1995
  • c-myc proto-oncogene은 여러 세포들의 분화와 형질전화에 뿐만 아니라 정상세포의 분열조절에도 관여한다고 알려져왔다. 특히 생쥐의 초기배아에서 c-myc mRNA가 발현되고 antisense c-myc oligomer의 미세주입에 의해 배발생이 억제된다는 연구결과는 c-myc이 초기배아의 발생 및 분열에 관여하는 것을 시사한다. 그러나 최근까지 초기배아에 존재하는 c-myc promoter의 기능적 활성화에 관한 연구는 미진하였다. 이를 위하여, c-myc promoter와 대장균의 lacZ 유전자를 결합시킨 두 종류의 vector(pcmyc-Gall, pcmyc-Ga12)를 만들어 수정란의 전핵에 미세주입한 후, 배 발생에 따른 c-myc promoter의 활성화를 lacZ 유전자의 산물인 $\beta$-galactosidase 에 의한 X-gal 염색으로 조사하였다. 미세주입된 초기 배아는 2세포기 배아를 포함하는 여러 발생단계에서 $\beta$-galactosidase 의 활성을 보였다. 이는 c-myc 유전자가 배아의 게놈유전자로부터 발현되며, 또한 궁극적으로 초기 배아의 발생과정에 중요한 역할을 하고 있음을 시사하고 있다.

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