1.Induction of steroid sulfatase expression by tumor necrosis factor-alpha through phosphatidylinositol 3-kinase/Akt signaling pathway in PC-3 human prostate cancer cells.
Bo Young SUH ; Jin Joo JUNG ; Nahee PARK ; Cheul Hun SEONG ; Hee Jung IM ; Yeojung KWON ; Donghak KIM ; Young Jin CHUN
Experimental & Molecular Medicine 2011;43(11):646-652
Steroid sulfatase (STS) is responsible for the hydrolysis of aryl and alkyl steroid sulfates and has a pivotal role in regulating the formation of biologically active estrogens. STS may be considered a new promising drug target for treating estrogen-mediated carcinogenesis. However, the molecular mechanism of STS expression is not well-known. To investigate whether tumor necrosis factor (TNF)-alpha is able to regulate gene transcription of STS, we studied the effect of TNF-alpha on STS expression in PC-3 human prostate cancer cells. RT-PCR and Western blot analysis showed that TNF-alpha significantly induced the expression of STS mRNA and protein in a concentration- and time-dependent manner. Treatment with TNF-alpha resulted in a strong increase in the phosphorylation of Akt on Ser-473 and when cells were treated with phosphatidylinositol (PI) 3-kinase inhibitors such as LY294002 or wortmannin, or Akt inhibitor (Akt inhibitor IV), induction of STS mRNA expression by TNF-alpha was significantly prevented. Moreover, activation of Akt1 by expressing the constitutively active form of Akt1 increased STS expression whereas dominant-negative Akt suppressed TNF-alpha-mediated STS induction. We also found that TNF-alpha is able to increase STS mRNA expression in other human cancer cells such as LNCaP, MDA-MB-231, and MCF-7 as well as PC-3 cells. Taken together, our results strongly suggest that PI 3-kinase/Akt activation mediates induction of human STS gene expression by TNF-alpha in human cancer cells.
Blotting, Western
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Fluorescent Antibody Technique
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Humans
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Male
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Phosphatidylinositol 3-Kinase/genetics/*metabolism
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Phosphorylation/drug effects
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Prostatic Neoplasms/genetics/*metabolism
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Proto-Oncogene Proteins c-akt/genetics/*metabolism
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RNA, Messenger/genetics
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Real-Time Polymerase Chain Reaction
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Recombinant Proteins/genetics/isolation & purification/metabolism
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Signal Transduction
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Steryl-Sulfatase/genetics/*metabolism
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Tumor Cells, Cultured
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Tumor Necrosis Factor-alpha/*pharmacology
2.The Differences in Obesity Rates According to Status of Co-Residence with Their Parents in Korean Adolescents: The Implication of the Gender of Single Parent Living with Adolescents
Nahee KIM ; Young Gyu CHO ; Jae Heon KANG ; Hyun Ah PARK ; Kyoungwoo KIM ; Yang Im HUR ; Duho KWON
Korean Journal of Health Promotion 2018;18(4):177-183
BACKGROUND:
Many studies have reported that adolescents living with single parent have a high risk of obesity. However, those studies did not explore the implication of the gender of single parent living with adolescents. This study investigated the differences in obesity rates according to status of co-residence with their parents in Korean adolescents. The family living with single parent was classified into the family living with single father and the family living with single mother.
METHODS:
This cross-sectional study involved 59,602 adolescents who participated in the 2017 Korea Youth Risk Behavior Web-based Survey. The data on height, weight, status of co-residence with parents, and the other variables were obtained through online questionnaires.
RESULTS:
In male adolescents, the family living with single mother was related to a high proportion of obesity (odds ratio [OR] 1.24, 95% confidence interval [CI] 1.09–1.40) and overweight (OR 1.17, 95% CI 1.03–1.34). However, in female adolescents, the family living with single father was related to a high proportion of obesity (OR 1.49, 95% CI 1.23–1.82). In addition, female adolescents living with neither parent were more likely to be obese (OR 1.47, 95% CI 1.13–1.91) and overweight (OR 1.31, 95% CI 1.00–1.70).
CONCLUSIONS
This study showed a risk of obesity in adolescents living with single parent differs according to the gender of single parent living with adolescents. Not adolescents living with a same-gender parent, but those living with an opposite-gender parent have a high risk of obesity.
3.The Differences in Obesity Rates According to Status of Co-Residence with Their Parents in Korean Adolescents: The Implication of the Gender of Single Parent Living with Adolescents
Nahee KIM ; Young Gyu CHO ; Jae Heon KANG ; Hyun Ah PARK ; Kyoungwoo KIM ; Yang Im HUR ; Duho KWON
Korean Journal of Health Promotion 2018;18(4):177-183
BACKGROUND: Many studies have reported that adolescents living with single parent have a high risk of obesity. However, those studies did not explore the implication of the gender of single parent living with adolescents. This study investigated the differences in obesity rates according to status of co-residence with their parents in Korean adolescents. The family living with single parent was classified into the family living with single father and the family living with single mother. METHODS: This cross-sectional study involved 59,602 adolescents who participated in the 2017 Korea Youth Risk Behavior Web-based Survey. The data on height, weight, status of co-residence with parents, and the other variables were obtained through online questionnaires. RESULTS: In male adolescents, the family living with single mother was related to a high proportion of obesity (odds ratio [OR] 1.24, 95% confidence interval [CI] 1.09–1.40) and overweight (OR 1.17, 95% CI 1.03–1.34). However, in female adolescents, the family living with single father was related to a high proportion of obesity (OR 1.49, 95% CI 1.23–1.82). In addition, female adolescents living with neither parent were more likely to be obese (OR 1.47, 95% CI 1.13–1.91) and overweight (OR 1.31, 95% CI 1.00–1.70). CONCLUSIONS: This study showed a risk of obesity in adolescents living with single parent differs according to the gender of single parent living with adolescents. Not adolescents living with a same-gender parent, but those living with an opposite-gender parent have a high risk of obesity.
Adolescent
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Cross-Sectional Studies
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Fathers
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Humans
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Korea
;
Mothers
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Obesity
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Overweight
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Parents
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Risk-Taking
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Single Parent
;
Single-Parent Family
4.Prediction of itching diagnostic marker through RNA sequencing of contact hypersensitivity and skin scratching stimulation mice models.
Young Won KIM ; Tong ZHOU ; Eun A KO ; Seongtae KIM ; Donghee LEE ; Yelim SEO ; Nahee KWON ; Taeyeon CHOI ; Heejung LIM ; Sungvin CHO ; Gwanhui BAE ; Yuseong HWANG ; Dojin KIM ; Hyewon PARK ; Minjae LEE ; Eunkyung JANG ; Jeongyoon CHOI ; Hyemi BAE ; Inja LIM ; Hyoweon BANG ; Jae Hong KO
The Korean Journal of Physiology and Pharmacology 2019;23(2):151-159
Pruritus (itching) is classically defined as an unpleasant cutaneous sensation that leads to scratching behavior. Although the scientific criteria of classification for pruritic diseases are not clear, it can be divided as acute or chronic by duration of symptoms. In this study, we investigated whether skin injury caused by chemical (contact hypersensitivity, CHS) or physical (skin-scratching stimulation, SSS) stimuli causes initial pruritus and analyzed gene expression profiles systemically to determine how changes in skin gene expression in the affected area are related to itching. In both CHS and SSS, we ranked the Gene Ontology Biological Process terms that are generally associated with changes. The factors associated with upregulation were keratinization, inflammatory response and neutrophil chemotaxis. The Kyoto Encyclopedia of Genes and Genomes pathway shows the difference of immune system, cell growth and death, signaling molecules and interactions, and signal transduction pathways. Il1a , Il1b and Il22 were upregulated in the CHS, and Tnf, Tnfrsf1b, Il1b, Il1r1 and Il6 were upregulated in the SSS. Trpc1 channel genes were observed in representative itching-related candidate genes. By comparing and analyzing RNA-sequencing data obtained from the skin tissue of each animal model in these characteristic stages, it is possible to find useful diagnostic markers for the treatment of itching, to diagnose itching causes and to apply customized treatment.
Animals
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Biological Processes
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Chemotaxis
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Classification
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Cytokines
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Dermatitis, Contact*
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Gene Expression
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Gene Ontology
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Genome
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Hypersensitivity
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Immune System
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Interleukin-6
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Mice*
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Models, Animal
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Neutrophils
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Pruritus*
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RNA*
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Sensation
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Sequence Analysis, RNA*
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Signal Transduction
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Skin*
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Transcriptome
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Transient Receptor Potential Channels
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Up-Regulation
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Wound Healing