Publications by authors named "Jeong Yeon Sim"

Article Synopsis
  • - Chronic obstructive pulmonary disease (COPD) arises from unresolved inflammation due to toxic environmental factors, with particulate matter (PM) being a major risk factor, but the mechanism was previously unclear.
  • - In experiments using a mouse model, repeated exposure to PM led to chronic inflammation driven by macrophages and decreased levels of certain enzymes involved in NAD synthesis, caused by changes in how genes are regulated.
  • - Resveratrol, a natural compound that activates SIRT1, was shown to reduce PM-induced inflammation and COPD progression, suggesting that targeting metabolic and epigenetic shifts in macrophages may offer new treatments for COPD.
View Article and Find Full Text PDF

Background: Programmed death-ligand 1 (PD-L1) has functional roles in cancer stem-like cell (CSC) phenotypes and chemoresistance besides immune evasion. Chemotherapy is a common treatment choice for colorectal cancer (CRC) patients; however, chemoresistance limits its effectiveness of treatment.

Methods: We examined the role of S100A14 (SA14) in CRC by adopting PD-L1 subpopulations within CRC cell lines and patient tumours, by establishing PD-L1 chemoresistant CRC sublines through prolonged exposure to 5-fluorouracil/oxaliplatin-based chemotherapy in vitro and in vivo, and by analysing a public database.

View Article and Find Full Text PDF
Article Synopsis
  • Scientists found that slow-cycling cancer cells (SCCs) can make cancer come back and resist treatment, but it's hard to study them.
  • They discovered a specific group of SCCs in lung cancer that survive tough conditions by using a special gene called RGS2.
  • By blocking RGS2 or using certain medications like Viagra, they can make these cells die, suggesting a new way to help lung cancer patients after chemotherapy.
View Article and Find Full Text PDF

Slow-cycling cancer cells (SCCs) with a quiescence-like phenotype are believed to perpetrate cancer relapse and progression. However, the mechanisms that mediate SCC-derived tumor recurrence are poorly understood. Here, we investigated the mechanisms underlying cancer recurrence after chemotherapy, focusing on the interplay between SCCs and the tumor microenvironment.

View Article and Find Full Text PDF

Quiescent cancer cells are believed to cause cancer progression after chemotherapy through unknown mechanisms. We show here that human non-small cell lung cancer (NSCLC) cell line-derived, quiescent-like, slow-cycling cancer cells (SCC) and residual patient-derived xenograft (PDX) tumors after chemotherapy experience activating transcription factor 6 (ATF6)-mediated upregulation of various cytokines, which acts in a paracrine manner to recruit fibroblasts. Cancer-associated fibroblasts (CAF) underwent transcriptional upregulation of COX2 and type I collagen (Col-I), which subsequently triggered a slow-to-active cycling switch in SCC through prostaglandin E (PGE)- and integrin/Src-mediated signaling pathways, leading to cancer progression.

View Article and Find Full Text PDF

Eremochloa ophiuroides, a perennial warm-season lawn grass, has a characteristic phenotype of red pigmentation in tissues during maturation. The putative gene families associated with the red coloration were previously identified in E. ophiuroides.

View Article and Find Full Text PDF

This study examined the volatile terpenes produced by rice seedlings in response to oxidative stress induced by various abiotic factors. Solid-phase microextraction-gas chromatography-mass spectrometry (SPME-GC-MS) analyses revealed that when exposed to UV-B radiation, rice seedlings emitted a bouquet of monoterpene mixtures in a time-dependent manner. The mixtures comprised limonene, sabinene, myrcene, α-terpinene, β-ocimene, γ-terpinene, and α-terpinolene.

View Article and Find Full Text PDF