Songhwa Choi

Dr. Songhwa Choi

orcid

Research Focus & Metrics

Academic Career Length

9Years (2018-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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16 May 2018 in The FASEB Journal
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Journal Article
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SCSonghwa Choi
Songhwa Choi
JSJustin M. Snider
Justin M. Snider
NONicole Olakkengil
Nicole Olakkengil
JLJohana M. Lambert
Johana M. Lambert
AAAndrea K. Anderson
Andrea K. Anderson
Ashley J SniderAshley J Snider
Ashley J Snider
Saturated fatty acids (SFAs) have been shown to induce endoplasmic reticulum (ER) stress and chronic inflammatory responses, as well as alter sphingolipid metabolism. Disruptions in ER stress and sphingolipid metabolism have also been implicated in intestinal inflammation. Therefore, to elucidate the roles of SFAs in ER stress and inflammation in intestinal epithelial cells, we examined myristate (C14:0) and palmitate (C16:0). My‐ ristate, but not palmitate, induced ER stress signaling, including activation of inositol‐requiring enzyme 1 (IRE1) and X‐box binding protein 1 (XBP1) signaling. Myristate significantly increased C14‐ceramide levels, whereas palmitate increased several long‐chain ceramides. To define the role of ceramide synthases (CerSs) in myristate‐induced ER stress, we used the pharmacologic inhibitor, fumonisin B1 (FB1), and small interfering RNA (siRNA) for CerS5 and 6, the primary isoforms that are involved in C14‐ceramide generation. FB1 and siRNA for CerS5 or 6 suppressed myristate‐induced C14‐ceramide generation and XBP1 splicing (XBP1s). Moreover, increased XBP1s induced the downstream expression of IL‐6 in a CerS5/6‐dependent manner. In addition, a myristate‐enriched milk fat‐ based diet, but not a lard‐ based diet, increased C14‐ ceramide, XBP1s, and IL‐ 6 expression in vivo. Taken together, our data suggest that myristate modulates ER stress and cytokine production in the intestinal epithelium via CerS5/6 and C14‐ ceramide generation.—Choi, S., Snider, J. M., Olakkengil, N., Lambert, J. M., Anderson, A. K., Ross‐Evans, J. S., Cowart, L. A., Snider, A. J. Myristate‐induced endoplasmic reticulum stress requires ceramide synthases 5/6 and generation of C14‐ceramide in intestinal epithelial cells. FASEB J. 32, 5724–5736 (2018). www.fasebj.org


19 December 2018 in Genes & Nutrition
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Journal Article
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SCSonghwa Choi
Songhwa Choi
HKHyeonyoung Ko
Hyeonyoung Ko
KLKayoung Lee
Kayoung Lee
JSJoohon Sung
Joohon Sung
YSYun-Mi Song
Yun-Mi Song
Hypovitaminosis D is prevalent worldwide. It is more prevalent in Eastern Asia region, including Korea. In addition to various environmental factors that influence serum 25-hydroxyvitamin D (25(OH)D) concentration, genetic influence also plays a significant role based on studies estimating the heritability of 25(OH)D in non-Asian populations. The objective of this study was to determine the genetic influence on serum 25(OH)D concentration in Korean men using the twin and family data. A total of 1126 Korean male adult twins and family members from the Healthy Twin Study with serum 25(OH)D measurement were included in this cross-sectional study. Intraclass correlation coefficients (ICCs) and heritability were calculated by mixed linear regression analysis and quantitative genetic analysis after adjusting for environmental and lifestyle factors. Mean (± standard deviation; SD) of serum 25(OH)D concentration was 15.34 ± 6.18 ng/ml. The prevalence of vitamin D insufficiency was 19.8% and that of vitamin D deficiency was 77.9%. After adjusting for age, the highest ICC (0.61) was observed for monozygotic twin pairs while the lowest ICC (0.31) was found for father-son pairs. Age-adjusted heritability was estimated to be 58%. When physical activity, multivitamin intake and season of blood sampling were further considered, the ICC and heritability did not materially change. In the sensitivity analysis after excluding known multivitamin users, age-adjusted heritability was reduced to 44%. In our study of Korean male twins and family members, heritability of 25(OH)D was moderately high. This supports the finding that genetic factors have significant influence on vitamin D status.

31 August 2022 in Clinical Psychopharmacology and Neuroscience
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SRSungwon Roh
Sungwon Roh
KLKang Soo Lee
Kang Soo Lee
SCSonghwa Choi
Songhwa Choi
JKJae-Min Kim
Jae-Min Kim
Sungwon Roh, Kang Soo Lee, Songhwa Choi, Jae-Min Kim. Clin Psychopharmacol Neurosci 2022;20:548-59. https://doi.org/10.9758/cpn.2022.20.3.548

Verified
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SLSoo Yong Lee
Soo Yong Lee
IKIl Young Kim
Il Young Kim
SASung-Ho Ahn
Sung-Ho Ahn
SKSu Jin Kim
Su Jin Kim
HLHyun min Lee
Hyun min Lee
CCChong Kun Cheon
Chong Kun Cheon
Fabry disease (FD) is a lysosomal storage disorder caused by pathogenic variants in the gene encoding alpha-galactosidase A (GLA). Deficiency of GLA results in the progressive accumulation of glycosphingolipids in virtually all organs, resulting in a progressive multisystem disease. Due to multi-organ involvement in FD, a comprehensive, multidisciplinary approach to diagnosis and treatment with regular follow-ups is essential. The Pusan National University Yangsan Hospital (PNUYH) multidisciplinary care model of FD aims to provide detailed practice guidelines and evidence-based recommendations for the diagnosis, screening, and treatment of FD according to specialty. This guideline focuses on the “quarterback” type of multidisciplinary team (MDT) operation and is limited in its applicability to the Korean insurance system. However, it reflects our team’s extensive experience and insights into optimizing MDT operations within these constraints and is expected to be highly beneficial for centers initiating MDTs for the effective treatment of FD.

20 April 2019 in Korean Journal of Family Practice
Verified
Journal Article
Closed access
SCSonghwa Choi
Songhwa Choi
MSMIN SEOB SIM
MIN SEOB SIM
HSHyoung Gon Song
Hyoung Gon Song
YSYun-Mi Song
Yun-Mi Song