Soyeon Kim
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Soyeon Kim has a total of 14 co-authors. Here are the top co-authors by number of shared publications:
- Gi Ryang Kweon
Department of Biochemistry, College of Medicine, Chungnam National University School of Medicine, Daejeon 35015, Republic of Korea
1 shared publication - Jeongsu Han
Department of Biochemistry, Chungnam National University School of Medicine, Daejeon 35015, Republic of Korea
1 shared publication - Ji-Hoon Park
Department of Biochemistry, School of Medicine, Chungnam National University, Daejeon 301-747, Korea
1 shared publication - Jong-Il Park
Department of Biochemistry, College of Medicine, Chungnam National University, Daejeon 35015, Republic of Korea; Translational Immunology Institute, Chungnam National University College of Medicine, Daejeon, Republic of Korea; Brain Korea 21 FOUR Project for Medical Science, Chungnam National University, Daejeon, Republic of Korea
1 shared publication - Jun Young Heo
Department of Medical Science, Chungnam National University School of Medicine, Daejeon 35015, Republic of Korea
1 shared publication - Kaipeng Jing
Infection Signaling Network Research Center, School of Medicine, Chungnam National University, Daejeon 301-747, Korea
1 shared publication
Latest Publications
- Open Access
- 3 July 2014
- Published by Springer Nature in BMC Cancer
- Vol. 14 (1) , 481
Docosahexaenoic acid-induced apoptosis is mediated by activation of mitogen-activated protein kinases in human cancer cells
The role of omega-3 polyunsaturated fatty acids (ω3-PUFAs) in cancer prevention has been demonstrated; however, the exact molecular mechanisms underlying the anticancer activity of ω3-PUFAs are not fully understood. Here, we investigated the relationship between the anticancer action of a specific ω3-PUFA docosahexaenoic acid (DHA), and the conventional mitogen-activated protein kinases (MAPKs) including extracellular signal-regulated kinase (ERK), c-JUN N-terminal kinase (JNK) and p38 whose dysregulation has been implicated in human cancers.
- 3 July 2014
- Published by Springer Nature in BMC Cancer
- Vol. 14 (1) , 481
Open AccessDocosahexaenoic acid-induced apoptosis is mediated by activation of mitogen-activated protein kinases in human cancer cells
The role of omega-3 polyunsaturated fatty acids (ω3-PUFAs) in cancer prevention has been demonstrated; however, the exact molecular mechanisms underlying the anticancer activity of ω3-PUFAs are not fully understood. Here, we investigated the relationship between the anticancer action of a specific ω3-PUFA docosahexaenoic acid (DHA), and the conventional mitogen-activated protein kinases (MAPKs) including extracellular signal-regulated kinase (ERK), c-JUN N-terminal kinase (JNK) and p38 whose dysregulation has been implicated in human cancers.