Yeeun Kim

Ms. Yeeun Kim

orcid

Research Focus & Metrics

Academic Career Length

2Years (2025-Present)

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

Representative Publications

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28 February 2025 in Preventive Nutrition and Food Science
Verified
Journal Article
Open access
PDF file
CKChanghee Kim
Changhee Kim
MKMinseong Kang
Minseong Kang
YKYeeun Kim
Yeeun Kim
JHJae-Kwan Hwang
Jae-Kwan Hwang
Changhee Kim, Minseong Kang, Yeeun Kim, and Jae-Kwan Hwang. Prev Nutr Food Sci 2025;30:47-55. https://doi.org/10.3746/pnf.2025.30.1.47

6 December 2025 in Food Science and Biotechnology
Verified
Journal Article
Closed access
PDF file
YKYeeun Kim
Yeeun Kim
MKMi-Bo Kim
Mi-Bo Kim
SLSeungok Lee
Seungok Lee
Sang Gil LeeSang Gil Lee
Sang Gil Lee
JHJae-Kwan Hwang
Jae-Kwan Hwang

18 February 2026 in Nutrients
Verified
Journal Article
Open access
PDF file
JLJunhee Lee
Junhee Lee
YKYeeun Kim
Yeeun Kim
MKMi-Bo Kim
Mi-Bo Kim
JPJu Hyun Park
Ju Hyun Park
DKDaedong Kim
Daedong Kim
JHJae-Kwan Hwang
Jae-Kwan Hwang
Background/Objectives: Cancer cachexia involves progressive skeletal muscle and adipose tissue loss, which is further aggravated by cisplatin chemotherapy via increased systemic inflammation, tissue catabolism, and renal toxicity. The present study aimed to evaluate whether a combination of amaranth protein hydrolysate and Agastache rugosa extract (AKE) could attenuate cisplatin-associated cachexia and nephrotoxicity in CT26 tumor-bearing mice. Methods: Cancer cachexia was induced by subcutaneous CT26 cell inoculation in 6-week-old male BALB/c mice, followed by a 7-day tumor establishment period. Cisplatin was then administered intraperitoneally, and AKE (125 or 250 mg/kg/day) was given daily by oral gavage for 14 days. Results: AKE administration significantly alleviated cisplatin-induced body weight loss and systemic inflammation, accompanied by preservation of skeletal muscle and adipose tissue mass, as well as increased myofiber cross-sectional area and adipocyte size. AKE markedly reduced serum inflammatory cytokines, blood urea nitrogen, and creatinine levels, indicating protection against cisplatin-induced renal injury. Mechanistically, AKE suppressed renal apoptosis through inhibition of mitogen-activated protein kinase signaling. In skeletal muscle, AKE attenuated muscle atrophy by modulating protein turnover pathways, including downregulation of muscle-specific ubiquitin ligases and restoration of Akt/mTOR and FoxO3a signaling. Furthermore, AKE mitigated adipose tissue wasting by suppressing AMP-activated protein kinase-dependent browning and restoring adipogenic signaling involved in lipid storage and differentiation. Conclusions: These findings demonstrate that AKE confers comprehensive protection against cisplatin-induced cachexia and nephrotoxicity by coordinately preserving muscle and adipose tissue and attenuating renal injury, suggesting its potential as a functional nutritional strategy to alleviate chemotherapy-associated tissue wasting.

29 June 2026 in The Journal of Nutritional Biochemistry
Verified
Journal Article
Closed access
YKYeeun Kim
Yeeun Kim
JKJunhui Kang
Junhui Kang
SHSungmin Han
Sungmin Han
JLJunhee Lee
Junhee Lee
HKHyunju Kang
Hyunju Kang
MKMi-Bo Kim
Mi-Bo Kim