Publications by authors named "Min-A Seol"

We assembled the complete mitochondrial genome of the green peach aphid, using its genomic DNA isolated from the bell pepper in Korea. The circular mitogenome of is 16,936 bp long and contains the standard 37 genes: 13 protein-coding genes, 2 ribosomal RNA genes, and 22 transfer RNA genes, as well as a single control region of 798 bp. Given the high AT ratio (84.

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Precise mechanisms underlying interleukin-7 (IL-7)-mediated tumor invasion remain unclear. Thus, we investigated the role of IL-7 in tumor invasiveness using metastatic prostate cancer PC-3 cell line derivatives, and assessed the potential of IL-7 as a clinical target using a Janus kinase (JAK) inhibitor and an IL-7-blocking antibody. We found that IL-7 stimulated wound-healing migration and invasion of PC-3 cells, increased phosphorylation of signal transducer and activator of transcription 5, Akt, and extracellular signal-regulated kinase.

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Interleukin-7 (IL-7), which is required for the development and survival of T cells in the thymus and periphery, plays a role in joint destruction. However, it remains unclear how IL-7 affects osteoclast formation. Thus, we investigated the mechanism by which IL-7 induced osteoclast formation through IL-7 receptor α (IL-7Rα) in osteoclast precursors.

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An antifungal protein, AtUSP protein (At3g53990), was isolated from Arabidopsis thaliana leaves by ion and size chromatography and sequenced by N-terminal sequencing. The AtUSP gene amplified from an Arabidopsis leaf cDNA library was transformed to Escherichia coli to express the AtUSP protein. The recombinant protein inhibited the cell growth of various pathogenic fungal strains.

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Age-associated immunological dysfunction (immunosenescence) is closely linked to perturbation of the gut microbiota. Here, we investigated whether syringaresinol (SYR), a polyphenolic lignan, modulates immune aging and the gut microbiota associated with this effect in middle-aged mice. Compared with age-matched control mice, SYR treatment delayed immunosenescence by enhancing the numbers of total CD3 T cells and naïve T cells.

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Although ionizing radiation is known to induce cellular senescence in vitro and in vivo, its long-term in vivo effects are not well defined. In this study, we examined the prolonged expression of senescence markers in mice irradiated with single or fractionated doses. C57BL/6 female mice were exposed to 5 Gy of γ-rays in single or 5, 10, 25 fractions.

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Background: The molecular mechanisms of CC (cholangiocarcinoma) oncogenesis and progression are poorly understood. This study aimed to determine the genome-wide expression of genes related to CC oncogenesis and sarcomatous transdifferentiation.

Methods: Genes that were differentially expressed between CC cell lines or tissues and cultured normal biliary epithelial (NBE) cells were identified using DNA microarray technology.

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Purpose: To investigate changes in gonadal white adipose tissue and lipogenesis-related gene expression induced by radiation exposure.

Materials And Methods: Groups of two-month-old C57BL/6 mice were exposed whole-body to ¹³⁷Cs γ-rays at a single dose (5 gray [Gy]) or fractionated doses (1 Gy x 5 times, 0.5 Gy x 10 times, or 0.

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Article Synopsis
  • Cholangiocarcinoma (CC) is a deadly bile duct cancer with poor survival rates, characterized by aggressive spread and a process called epithelial mesenchymal transition (EMT).
  • The study focused on understanding genetic changes and gene expression linked to the aggressive form of CC, using four established human cell lines (SCK, JCK1, Cho-CK, and Choi-CK) with varying differentiation levels.
  • Key findings included a deletion of the p53 tumor suppressor gene in the aggressive SCK cells and significant differences in the expression levels of 260 over-expressed and 247 under-expressed genes in comparison to well-differentiated cells, indicating a connection between these genetic changes and the aggressive behavior of
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